We are seeking a reliable, detail-orientated engineer to join our team in Singapore Research Centre (SRC). The key responsibilities include: Participating in research and development of advanced intelligent speech and audio algorithms for embedded system including, but not restricted to:

earphones, smart watches, IoT devices and etc.

Required Skills:

Be independent in research of advanced speech and audio algorithms and the development or implementation of such algorithms for embedded systems.

• Experience or knowledge of acoustic tests measurements for data acquisition and be familiar with state-of-the-art testing equipment.
• Experience of conducting objective/subjective evaluation of various audio algorithms on speech enhancement, active noise control, binaural rendering.
• Extensive experience in signal processing, acoustic modelling, adaptive filtering, noise suppression, active noise cancellation, hearing through etc.
• Ability handling C, Python, and script codes for system modelling, simulation and system implementation.

Qualifications Requirement:

• PhD with relevant experience (fresh PhD graduates are welcome).
• Extensive knowledge in at least one of the areas including: signal processing applied to audio, active noise control, speech enhancement, adaptive filtering and microphone array signal processing.
• Solid mathematical background.
• Working knowledge of C/C++ and/or Matlab/Python scripting as well as DSP algorithm optimizations
• Highly Desired:
  • Expertise in AI applied to audio, with hands-on experience in at least one deep learning framework in Python
  • Hands on experience in DSP code optimization and deployment for embedded audio systems
  • Knowledge and expertise of earphone active noise cancellation/hear through algorithm design and tuning, measurements and etc.
  • Top-ranking and/or award receivers in world competition in speech/audio signal processing field
  • Interested candidate who wish to apply for this position, please click on APPLY NOW

EA License No.: 01C4394 | PERSOLKELLY Singapore Pte Ltd

EA Registration No.: R23117518 | Heah Sian Wei

By sending us your personal data and curriculum vitae (CV), you are deemed to consent to PERSOLKELLY Singapore Pte Ltd and its local and overseas subsidiaries and affiliates collecting, using and disclosing your personal data to prospective employers/companies based in any country for purposes of evaluating suitability for employment, conducting reference checks, administering employment related services, complying with Government’s COVID-19 health advisories and such other purposes stated in our privacy policy. Our full privacy policy is available at www.persolkelly.com.sg. If you wish to withdraw your consent, please drop us an email to let us know. Please feel free to contact us if you have any queries.

Responsibilities:

• Assist physiotherapists in implementing treatment plans for patients.
• Conduct therapeutic exercises and activities with patients under the supervision of a physiotherapist.
• Provide support in the application of modalities such as heat, cold, ultrasound, and electrical stimulation.
• Guide and educate patients on proper exercise techniques and home care programs.
• Assist in the maintenance and organization of treatment areas and equipment.
• Monitor and record patient progress and report to the supervising physiotherapist.
• Collaborate with other healthcare professionals to ensure comprehensive patient care.
• Adhere to ethical and professional standards in the delivery of physiotherapy services.

Requirements:

• Degree in Physiotherapy or equivalent
• At least 2 – 3 years of experience in a clinical setting with pediatric background.
• Ability to work within short notice.

Interested candidates who wish to apply for the advertised position, please click on the APPLY button below to send in your resume or send to [email protected].

EA License No: 13C6305

Reg. No.: R24120209

For candidate who applied for the advertised position is deemed to have consented to us that we may collect, use or disclose your personal information for purpose in connection with the services provided by us.

Introduction

In collaboration with the Woodlands Health (WH) and the National Health Group (NHG), the Rehabilitation Research Institute of Singapore (RRIS), the Nanyang Technological University (NTU), and SingHealth, SEC is undertaking a research programme on "Built Environment and physical activity in Falls and Arthritis study (BE FIT)". It addresses imminent health challenge on moving away from “sickcare” and pivoting towards preventive healthcare as part of the nationwide effort on Healthier SG. Within BE-FIT we envision motivating vulnerable older adults to engage in healthy behavior by providing recommendations on improving accessibility (as well as preception thereof), in urban environment for uptake of physical activity. A deeper understanding of the interactions and interplay between Built Environment (BE) and the high burden of falls and osteo-arthritis (OA) as proposed within the BE-FIT is crucial towards informing data-driven decisions on urban design and how the mobility-impaired elderly interact with their physical environment. Within the BE-FIT framework we are advertising the job position for a postdoctoral researcher.

Project Background

Falls result in severe physical as well as psychological impact among older adults. Beyond physical implications on injury-related trauma and in severe cases death, the psychosocial impact of falling can also be excruciating. Fear of falling can result in vicious cycles of decreased activity as well social isolation. These in turn lead to lower muscle strength and higher risk of future falls. In a similar manner, osteo-arthritis (OA) can lead to fear of movement (kinesiophobia) resulting in reduction of physical activity levels.

Task/Job Description

We will investigate movement patterns and features of walking outdoors and in the neighbourhoods among vulnerable older adults (suffering from OA as well as at high risk of falling) in order to understand perceptions on interacting with built environment. We will acquire these movement patterns and features using the state-of-the art inertial measurement units (wearables such as ZurichMOVE or Axivity) sensors. These sensors are equipped with triaxial accelerometers and gyrospcopes and provide assessment of aspects such as impact and swing behaviour during different movements. Specifically we will be addressing the following research questions:

1. What are the kinematic characteristics of walking among older adults with OA and/or previous falls under ecological settings (neighbourhoods)?
2. Do the kinematic characteristics of naturalistic walking predict physical activity rates?
3. Does the design of walkways (including overall layout, e.g. design of curbs, pathways etc and accessibility features e.g. size of the curbs, or height of side walk, ramps vs stairs) impact overall levels of physical activity as well as specifics of walking quality?

Specific to the Position:

The general concept is to generate machine learning as well as statistics-based models to extract movement patterns from movement/locomotion/walking/gait dataset collected via wearable sensors. The gait data from multiple sensors will be collected while participants (older adults) move/walk/transition for both short (up to 10 minutes) as well as long (over multiple days) periods of time. This data will be complemented with data from our collaborators on walkability assessment, where we evaluate naturalistic observation on individual’s daily routes and outdoor activities. Finally, we will also tap into questionnaire data involving individuals’ fall history, psychosocial status as well as cognitive ability, as well as their perception of the built environment. The primary task will be to extract features (gait signatures, but also artificial “machine learned” features) that allow us to assess fall risk in an individualized manner. Crucial aspects are the interpretability and repeatability of these signatures as these aspects will allow clinical as well as stakeholder uptake. Another important aspect for uptake is the association (via analysis as well as interpretation) of these features to the walkability as well as clinical assessment to provide a hybrid ‘mapping’ of the manner in which older adults interact with their environment.

Requirements:

• Minimum 2 years of experience in machine or deep learning with a background (PhD) in computer science, computer vision, neuroscience, physics or biomedical and/or other engineering fields.
• Expertise in predictive model development, especially for healthcare applications.
• A solid understanding in experimental design, feature extraction, selection, and analysis, as well as tailoring machine/deep learning techniques to hybrid datasets including clinical battery, and objective physiological (movement) datasets.
• A strong foundation in deep and machine learning algorithms, statistical analysis, and study design from ideation to evaluation and validation.
• A strong publication record especially in area of artificial intelligence and machine learning.
• Presentations at conferences and participation in workshops is desired.
• Programming skills: Expert in Python (PyTorch as well as the use of libraries).
• Experience/expertise in working with Matlab and/or R (or any other statistical software e.g. SAS).
• Previous experience with physiological (such as heart rate via an ECG or also EEG) datasets is desired, but not a must-have.
• A solid foundation of machine learning frameworks such as Tensorflow and algorithms, statistical analysis, and study design from ideation to evaluation and validation.
• Experience with GUI development is desired.
• Personal: Are you motivated to work on challenging problems? Can you work independently on a project level demonstrating problem solving skills? Do you see yourself fitting in with the team of multinational group of biomechanists, engineers as well as health-care and clinical scientists? Do you have a penchant for collaborating - maintaining channels of communication - with lab/team members but also worldwide? If yes, this job might just be for you.

Information about the application process and contact for applicants

Questions regarding the position should be directed to Navrag Singh, PhD, via email [email protected].

We look forward to receiving your online application with the following documents:

• A cover letter outlining your motivation and experience in the field of machine-learning and bioengineering with a focus towards practical applications in healthcare
• Curriculum Vitae or Resume
• List of publications and abstracts of presentations at conferences
• Certificates (e.g. PhD and Master’s degree)
• Transcripts of records

Please note that we exclusively accept applications submitted through our online application portal. Applications via email or postal services will not be considered.

Further information about BE-FIT Project can be found on our website: https://sec.ethz.ch; https://fht.ethz.ch

Work location: 1 Create Way, CREATE Tower, Singapore 138602 (NUS University Town)

The Singapore-ETH-Centre is an equal opportunity and family-friendly employer. All candidates will be evaluated on their merits and qualifications, without regards to gender, race, age or religion.

Responsibilities

• Provides assistance to the research team
• Screens and recruits suitable patients to participate in the research project
• Briefs patients on research background and rationale and to obtain their consent of participation
• Collects data from patients' medical records and research statistics
• Helps document adverse events / reactions that arise
• Performs phlebotomy and venepuncture when required
• Other ad-hoc roles as assigned

Requirements

• Minimum Diploma in Nursing
• Phlebotomy skills are a MUST

Interested candidates please send in your resume to:

[email protected]

EA Personnel: Valerie Yong Kian Fung
CEI No.: R1103704

Recruit Express Pte Ltd, EA License No.: 99C4599

Duties and Responsibilities

• Perform research to discover vulnerabilities in operating systems, software applications and hardware devices through code audit, black box testing and reverse engineering.
• Develop and enhance processes and tools for the discovery and triage of vulnerabilities.
• Research into new vulnerability discovery techniques and processes.

Requirements

• Bachelor's degree in a computer science or engineering field or equivalent a minimum of 3 years of relevant experience.
• Strong reverse engineering skills and experienced in reverse engineering complex software applications or operating system components.
• Up-to-date knowledge on different type of software vulnerabilities, and experienced in performing vulnerability discovery on any operating system, software applications or hardware devices.
• Up-to-date knowledge on modern exploitation techniques and hands-on experience in bypassing exploitation mitigation technologies gained through developing proof-of-concept exploits.
• Experience in using and current static and dynamic software analysis tools and techniques in reverse engineering and vulnerability discovery process. Able to adapt and extend existing manual or automated tools to better support the work.
• Development experience in C /C++ or scripting languages (e.g. Python, Ruby).

As a Cyber Security Researcher, you will be conducting research and development work to deliver comprehensive security assessment on cyber security technologies (e.g. network-based and host-based threat detection and protection systems).

Specifically, successful applicants will:

• Evaluate the effectiveness of cyber security products in protecting cyber assets (i.e. against their stated capabilities).
• Research, reverse engineer and analyze cyber security products for potential weaknesses and propose mitigation and remediation solutions.
• Create proof of concept code to demonstrate the identified security issues.
• Develop and enhance processes and tools for the testing and evaluation of cyber security products.

Requirements:

• Bachelor's degree in a computer science or engineering field or equivalent practical experience.
• Have strong interest or relevant experience in the following:

o Analyzing system and network behavior and activities on common operating systems such as Windows.

o Monitoring and analyzing network traffic and packet captures.

o Reverse engineering of software applications or systems.

o Understanding of Operating System Kernels.

o Developing host-based or network-based cyber security products.

• Proficient in some programming or scripting language, e.g. C /C++, x86/x64 assembly, Java, Ruby, or Python.
• Familiarity with major Operating Systems (Microsoft Windows, Linux).
• Prior developing/reversing experience with Operating System’s Driver will be an advantage.

Preferred Skills /Qualities:

• Good analytical and technical skills

Eurofins Clinical Diagnostics Pte Ltd, a subsidiary of Eurofins Scientific, a leading international life sciences company with a long history of global excellence in Testing for Life, analyzing everything that impacts health and safety is seeking highly motivated and service oriented sales executives to join our expanding operations in Singapore.

Responsibilities:

• Ensure sales targets are met within a specific time period for the assigned territory.
• Implement and execute sales strategies to improve market share and overall business growth.
• Ensure consistent sales growth through identifying business opportunities and developing strategic accounts.
• Manage existing and build new accounts.
• Provide clinical information and benefits of the designated portfolio to medical professionals
• Provide market intelligence and trends to remain current on industry and customer needs.
• Optimize quality of service and contribute to client’s satisfaction.
• Build company image in the market as a reliable partner to the clients

Responsibilities

• Provides assistance to the research team
• Screens and recruits suitable patients to participate in the research project
• Briefs patients on research background and rationale and to obtain their consent of participation
• Collects data from patients' medical records and research statistics
• Helps document adverse events / reactions that arise
• Performs phlebotomy and venepuncture when required
• Other ad-hoc roles as assigned

Requirements

• Minimum Diploma in Nursing
• Phlebotomy skills are a MUST

Interested candidates please send in your resume to:

[email protected]

EA Personnel: Valerie Yong Kian Fung
CEI No.: R1103704

Recruit Express Pte Ltd, EA License No.: 99C4599

Responsibilities

· Responsible for providing strategic level/long-term planning

· Drive continuous improvement projects to optimize operations and improve productivity to meet and exceed business objectives; work on strategic projects that have total building and network-wide impact.

· Effectively leverage the Operations and Area Managers to solicit ideas and understand problems and challenges

· Anticipate needs; make administrative decisions and requests for information

· Domestic and international travel logistics management, trip preparation and expense reporting

· Forecast and manage budgets and team procurement

· Coordinate department facility operations, including space planning and office moves

· Daily team support including: new hire set up; purchase of goods & services, process invoices

· Ensure compliance with administrative operations policies and procedures

· Develop and prepare reports and maintain database

Requirements

· Min dip/deg in any discipline

· Ability to work in a fast pace environment

· Team player and collaborator

· Excellent communication skills

· No experience needed, training will be provided

If you are interested in any of the positions, do kindly drop your most updated resume to [email protected]

Thank You.

Victoria Yam Wen Ting

R21103142

Recruit Express Pte Ltd (Healthcare & Lifesciences Division)

EA License: 99C4599

Job Summary:

• Industry: Healthcare
• Location: Redhill/Queenstown
• Employment type: 1-year contract

Job Responsibilities:

• Assist in the recruitment of trial participants daily and ensure smooth facilitation
• Facilitate the administration of surveys, questionnaires and interviews related to the research
• Work closely with the research team in data collection, data analysis, and academic writing
• Coordinate the administrative aspects of research planning and execution, which includes familiarisation with ethics-related approval requests and meeting organization
• Handle administrative and logistics planning of the research study
• Reply timely to the ethics board and other administration-related requests

Job Requirements:

• A diploma or equivalent in qualifications in Science/Public Health/Social Science with 2 years of relevant experience
• Able to adapt to a fast-paced environment, with a strong focus on meeting research deliverables and targets.
• Independent and mature.
• Able to work independently, as well as in a team.
• Meticulous, well-organized and able to multi-task
• Able to work in an interdisciplinary environment with different groups of stakeholders.
• Good verbal and written communication skills

By submitting any application or resume to us, you will be deemed to have agreed and consented to us disclosing your personal information to prospective employers for their consideration.
We regret that only shortlisted candidates will be notified.
Registration No: R23113834

Our client, a leading Multinational American Technology company, is in search of a Senior Marketing Insights Researcher to join their APAC Team. This role will design, implement, and deliver impactf ul research—both quantitative and qualitative—and translate these insights into actionable strategies for our business partners.

Responsibilities:

• Develop comprehensive learning plans to address key business questions.
• Conduct and design research focused on understanding audiences, developing campaigns, and testing creative messages.
• Utilize multiple research methodologies as needed to meet objectives.
• Determine the best recruitment strategies and make decisions on country selection for fieldwork.
• Craft detailed questionnaires.
• Translate research findings into actionable insights with clear recommendations that motivate stakeholders to apply these learnings in marketing and other organizational areas.
• Collaborate closely with cross-functional teams, including Marketing, Creative, Decision Science, and Global Marketing Insights, to both design research inputs and embed the resulting insights.

Qualifications:

• At least 8-10 years of experience with a strong background in both quantitative and qualitative research, particularly within the APAC region.
• Proven ability to tackle both undefined and well-defined problems with appropriate methodologies.
• Expertise in synthesizing insights from various sources to create comprehensive and persuasive recommendations.
• Strong collaboration, communication and presentation skills.
• Regional exposure is a plus
• Open to 8 months contract - renewable!

What We Provide:

• A highly competitive remuneration package.
• An opportunity to interface with cutting-edge technology.
• An inclusive and collaborative work milieu.
• A clear trajectory for career advancement and professional growth

Interested candidates may apply through the application system or send it to [email protected]. Shortlisted candidates will be notified.

By sending us your personal data and curriculum vitae (CV), you are deemed to consent to Morgan Mckinley Pte Ltd and its affiliates to collect, use and disclose your personal data for the purposes set out in the Privacy Policy available at https://www.morganmckinley.com/sg/privacy-policy. You acknowledge that you have read, understood, and agree with the Privacy Policy.

Morgan McKinley Pte Ltd

Koh Boon Sien

EA Licence No: 11C5502

EA Registration No. R1110345

1. Develop enrolment/follow-up mechanisms

2. Enrolment and follow-up of study subjects

3. Subject follow-up procedures

4. Case report form (CRF) completion and study documentation

5. Adverse event monitoring and reporting responsibilities

6. Regulatory documents

7. Any other ad-hoc duties as assigned by Supervisor

Min Requirements

• Diploma in any health science courses
• Able to commence work within short notice

We regret that only shortlisted candidates will be contacted

Interested candidates please send your resume to [email protected]

Consultant: Tan Ming Hui, Magdelene (R21101623)

Recruit Express Pte Ltd (99C4599)

Responsibilities:

• Provide secretarial support to clinical quality assurance committees, workgroups and associated meetings.
• Work with relevant stakeholders in areas of quality assurance, patient safety, continual improvement, and risk management.
• Plan, develop and implement quality improvement projects.
• Assist with other clinical governance functions such as preparation of reports and analysis.
• Serve as a resource-person and maintain positive relationships with doctors, nurses, allied health and administrative colleagues.
• Support in the licensing of hospital, internal audits, incident management and clinical quality records review programme.
• Undertake any other tasks and duties as assigned by the Manager or Head of Department

Job Requirements:

• Degree in Life / Pharmaceutical Sciences, Healthcare Administration / Management, Biomedical Engineering, Pharmacy, Nursing, or Occupational, Physio or Speech therapy.
• Preferably 3 to 4 years of healthcare experience.
• Experience in healthcare administration, clinical quality methodologies such as JCI, LEAN, Six Sigma, Root Cause Analysis, and / or risk management will be of added advantage.
• Good PC skills and proficient in MS Office applications
• Meticulous with strong problem-solving, interpersonal, oral and written communication skills.
• Positive work attitude and ability to work with all levels of staff and diverse stakeholders in both independent and collaborative work environments.
• Self-motivated, able to multi-task, work independently, and produce well written reports, papers, minutes, etc.
• Has compassion and a heart for patient safety and ethics.

Interested candidates kindly click the APPLY NOW button or email updated resume to [email protected]

By submitting any application or résumé to us, you will be deemed to have agreed and consented to us disclosing your personal information to prospective employers for their consideration.

We regret to inform you that only shortlisted applicants would be notified.

Tan Chee Meng (Gavin)
Registration Number: R1546873
Dynamic Human Capital Pte Ltd | EA License No.: 12C6253

Job Description:

• Develop enrolment/follow-up mechanisms
• Enrolment and follow-up of study subjects
• Subject follow-up procedures
• Case report form (CRF) completion and study documentation
• Adverse event monitoring and reporting responsibilities
• Regulatory documents
• Any other ad-hoc duties as assigned by Supervisor

Job Requirements:

• Diploma either in Nursing, health sciences or para-clinical disciplines
• Possess working knowledge of applicable regulations and guidelines e.g. SG-GCP, ICH-GCP, Code of Federal Regulations, Declaration of Helsinki, etc.
• Proficient in Microsoft Words, Excel

Interested candidates do attach your resume to [email protected]

Attn: Angela Celeste Poh Li Ying (R2095367)

Recruit Express Pte Ltd (99C4599)

The Opportunity

Esco Lifesciences Group is Singapore’s most globalized life sciences company, with annual revenues close to SGD 200M and global operations in over 42 locations and 26 direct countries across North America, Europe, Asia, Oceania.

Esco Aster Pte Ltd is an affiliate of Esco Lifesciences Group and was first incorporated in 2017.

Esco Aster is a contract research development and manufacturing organization founded and deeply rooted by scientists enabling fellow scientists to translate their bench work into commercially available products at affordable prices.

Our scientific work is in emerging and frontier biology utilizing cells as a final product or deriving products from cells which often we use cells as the factory to derive our target product.

Our first commercial breakthrough success is Esco Aster is commercially first in class being first in the world to be certified for cultivated/cell-based meat to FSSC 22000 and by a competent food regulatory body.

We are first in the region to operate an end-to-end integrated full cell line creation/immortalization or engineered cell line, cell culture process development, analytical development for stem cells and exosomes with full cGMP Capabilities from Drug Substance and small-scale fill & finish for final Cell Therapy Product.

The work we do creates a remarkable and lasting impact on our world. We offer you an opportunity to be part of this exciting journey to own your career and firsthand exposure to new emerging modalities supporting translational sciences.

Join us as we redefine BioSolutions for One World and One Health for the current and future generations to come.

Esco Aster.

One World Biosolutions for One Health.

The Scope

Esco Aster is looking for a Clinical Development Lead to support our internal and external collaborators encompassing pre-clinical development including CMC (Chemistry, Manufacturing and Controls)/regulatory/GLP toxicology as well as clinical sciences and overseeing clinical operations with external clinical research organizations.

This work involves cross department work within the company as well as part of team that works with external collaborators Chief Medical Officer, Research and Clinical Development teams. This role is for a middle management position, and it will in the midterm involve building a team of direct reports of clinical scientists, clinical research associates, clinical research co-ordinators, clinical ops.

Primary work location: Ayer Rajah Crescent, Singapore.

Responsibilities

Scientific Affairs / Writing

· Support the development of publication and scientific/clinical meeting strategy; prepare essential content and coordinate authorship of publications (abstracts, posters, manuscripts, presentations).

· Manage, update and maintain company’s clinical/scientific materials, reference library of appropriate high impact publications.

· Generate, analyses, interpretate scientific/clinical narratives to support clinical, regulatory, and external communication activities.

· Conduct systematic literature reviews, cohesively collates relevant clinical and scientific information to obtain strategic input into clinical program development, including target diseases/patient populations, draft labels, competitive landscape, and market development.

· Support and help to onboard and maintain relationship with company key opinion leaders (KOLs), clinical investigators, clinician scientists, academic organizations to assure incorporation of latest clinical thinking and guidelines into clinical development plans and enable expanded access and compassionate usage.

Regulatory Affairs / Documentation

· Medical writing: Provide scientific/clinical input into and assist in the development, maintenance and review of clinical documents and specified regulatory submission documents including clinical protocol, investigator brochures, informed consent form, annual IND reports, clinical study reports, manuscripts, and different scientific/clinical presentations and subsequent amendments.

· Work across various functions to lead and guide as well as technical writing of phase appropriate clinical, CMC and regulatory strategy working with our collaborators CMC/Regulatory, Scientific/Medical Affairs team.

· Function as in house resource to compile and provide relevant scientific/clinical information to subject matter experts (SMEs) from other functions (e.g Business Development & Product Development, Scientific and Clinical Trial Manufacturing Teams) to support collaborations and new product development.

· Review pre-clinical data of medical products, therapeutic products, medical devices and surgical procedures.

· Develop protocols for transition of products from experimental settings to clinical trials.

· Write and review documents required for conducting clinical trials such as investigator's brochure, patient consent form, inclusion and exclusion criteria, providing expanded access/compassionate usage and patient advocacy, working with outsourced CRO on risk assessment and management of potential adverse events and ensuring absolute safety of the patients.

GLP Studies

· Act as Study Director Support as well as provide oversight to outsourced partnered CRO or client appointed CRO.

· Ensure that animal studies and/or in vitro models are representative of PK/PD/Biodistribution studies for first in man trials.

Medical Studies/Clinical Trials

· Conduct medical studies in accordance with ISO 13485 standards using patented microneedles for hair loss / cartilage repair with naïve exosomes. Data generated from medical studies will subsequently be used for FDA 21 CFR 820 and EU MDR filing as a double-blind, randomized clinical trial, with planned sites in Singapore, Bintan, Japan and Australia. The patented saline control microneedles with/without exosomes (from human and animal source) will be benchmarked against Minoxidil and tested with and without LED light (Red/Blue) wavelengths.

· Future programs include Osteoarthritis/Cartilage Repair for BM-MSCs autologous therapy, Zonal Chondrocytes autologous therapy, Car-T Blood Cancer and associated cancer cell therapies using cells or naïve/engineered exosomes.

· Coordinate with internal and external clients including applicable regulatory bodies and business partners (CROs).

· Serve as primary contact/escalation for clinical trials as assigned.

Others

· Perform tasks in accordance with applicable regulations and site safety requirements.

· Undertake other tasks as assigned.

Requirements

· Minimum MD/PhD or MBBS/MD-PhD degree with relevant publications as a clinician scientist.

· Preferred experience in overseeing as study director for GLP Toxicology.

· Strong technical/ scientific/clinical knowledge on immunology, oncology and/or immunotherapies (CAR-T, TCR-T cell therapies e.g.) is highly preferred.

· Understanding of laboratory techniques in one or more of the following areas: Flow cytometry, serology, toxicology, clinical virology, immunohistochemistry, immunological assays, development of biomarkers to determine efficacy, on target, off target and enable stricter inclusion criteria.

· Have experience the full life cycle of clinical trials from feasibility, selection, initiation and close out activities.

· Ability to conduct and like to read and analyse as well as write documents based on database/literature searches with critical analytical thinking and problem-solving skills using PUBMED, EMBASE, MEDLINE etc.

· Prior experience in preparing entire clinical dossier and previous track record in receiving IND approval and up to phase 2 Clinical Trial Material.

· Minimum 5 years of medicine and/or surgical practice.

· Deep understanding of immunology.

· Experience and knowledge of clinical research/development, Good Clinical Practices (GCP) and/or regulatory requirements for the conduct of clinical trials preferred.

· Proficient in MS Office Suite (Microsoft Word, PowerPoint, Excel).

· Excellent project/process management and communication skills.

· Able to work well independently and in a team.

· Possess strong interpersonal skills and ability to collaborate effectively with internal and external stakeholders.

Apply now by submitting a Cover Letter and CV to [email protected].

Responsibilities

· Responsible for providing strategic level/long-term planning

· Drive continuous improvement projects to optimize operations and improve productivity to meet and exceed business objectives; work on strategic projects that have total building and network-wide impact.

· Effectively leverage the Operations and Area Managers to solicit ideas and understand problems and challenges

· Anticipate needs; make administrative decisions and requests for information

· Domestic and international travel logistics management, trip preparation and expense reporting

· Forecast and manage budgets and team procurement

· Coordinate department facility operations, including space planning and office moves

· Daily team support including: new hire set up; purchase of goods & services, process invoices

· Ensure compliance with administrative operations policies and procedures

· Develop and prepare reports and maintain database

Requirements

· Min dip/deg in any discipline

· Ability to work in a fast pace environment

· Team player and collaborator

· Excellent communication skills

· No experience needed, training will be provided

If you are interested in any of the positions, do kindly drop your most updated resume to [email protected]

Thank You.

Victoria Yam Wen Ting

R21103142

Recruit Express Pte Ltd (Healthcare & Lifesciences Division)

EA License: 99C4599

• Position: Medical Writer (Biomedical/Clinical Trial/Research)
• Location: Near Bras Basah MRT station/Bencoolen MRt
• Working Hours: Monday - Friday| 9.00am to 6.00pm
• Salary (commensurate with experience): Up to $6500+ Performance Bonus + Travel Allowance + 14 Days Annual Leave + Medical Benefits and Annual Check-up + Online Learning Portal for self-development + WFH Opportunities
• Duration: 1 Year Contract (RENEWABLE/CONVERTIBLE TO PERMANENT)
• Industry: Digital Media Marketing
• Career Advancement: YES

Responsibilities:

• Scientific bridge between clinical development and commercial
• Functions in pharmaceutical and device. It requires the ability to work closely with medical
• Regulatory representatives, HCPs and KOLs to deliver high quality writing that is scientifically
• Rigorous, patient focused, and in line with the strategic positioning of the pharmaceutical or medical devices products.

Requirements:

• Candidate should preferably possess a first-degree degree in biomedical science; a
• research-based degree (MSc or Ph.D.)
• At least 3-5 years of experience in Medical Communication Agency
• The ability to adapt complex scientific information into concise content will be
• essential.
• Excellent delivery in providing summary for AD Board Meetings and Scientific Conferences.

Email to [email protected]

Do visit Search Personnel Pte Ltd for more job listings.

***We DO NOT charge our candidates any referral fee nor bind them with any contract.***

Joie Chang

Deputy Consulting Director (APAC)

Reg no.: R2090601 | EA No: 13C6684

Clinical Trial Assistant (Nursing admin) (1-year)

Location: Novena

Salary: 2200 - 2700

Office hours Monday to Friday

Roles & Responsibilities

1. Develop enrolment/follow-up mechanisms

2. Enrolment and follow-up of study subjects

3. Subject follow-up procedures

4. Case report form (CRF) completion and study documentation

5. Adverse event monitoring and reporting responsibilities

6. Regulatory documents

7. Any other ad-hoc duties as assigned by Supervisor

How to Apply:send your resume to: [email protected] or Telegram me @jocelynchan

Jocelyn Chan| Consultant | Recruit Express Pte Ltd (Healthcare & Lifescience)Company EA Licence number : 99C4599Personnel EA License: R1331820

Core Responsibilities

• Develop advanced blockchain protocols involving ZK proofs, FHE, and conventional cryptographic tools relevant to blockchains.
• Help develop practical applications using the above tools.
• Keep up to date on emerging capabilities in a fast-moving domain and identify where and how new capabilities can be applied.
• Analyze and anticipate how adversaries may attempt to subvert or misuse applications.

Analytical/Decision Making Responsibilities

• Ability to clearly articulate both problems and proposed solutions.
• Proactive approach to identifying issues and presenting solutions and options with the underlying trade-offs, and where appropriate, leading to resolution.
• Ability to prioritize personal and team workloads to best meet organizational objectives.
• Empowered to make decisions and recommend approaches based on the results from quality reviews.

Other Responsibilities

• Occasional travel may be required.
• Actively promote the research done through blogposts, twitter threads, podcasts.
• Engage with researchers on a regular basis on open forums and discussion boards.

Job Requirements

• Deep understanding of blockchains, cryptography in particular ZK proof systems, system/network security and distributed systems.
• A Bachelor's degree in mathematics, computer science, physics, or engineering preferred.
• Masters or PhD degree preferred.
• For those with a PhD degree, you must have published high impact research work at top-tier security conferences.

Responsibilities:

• Assist physiotherapists in implementing treatment plans for patients.
• Conduct therapeutic exercises and activities with patients under the supervision of a physiotherapist.
• Provide support in the application of modalities such as heat, cold, ultrasound, and electrical stimulation.
• Guide and educate patients on proper exercise techniques and home care programs.
• Assist in the maintenance and organization of treatment areas and equipment.
• Monitor and record patient progress and report to the supervising physiotherapist.
• Collaborate with other healthcare professionals to ensure comprehensive patient care.
• Adhere to ethical and professional standards in the delivery of physiotherapy services.

Requirements:

• Degree in Physiotherapy or equivalent
• At least 2 – 3 years of experience in a clinical setting with pediatric background.
• Ability to work within short notice.

Interested candidates who wish to apply for the advertised position, please click on the APPLY button below to send in your resume or send to [email protected].

EA License No: 13C6305

Reg. No.: R24120209

For candidate who applied for the advertised position is deemed to have consented to us that we may collect, use or disclose your personal information for purpose in connection with the services provided by us.

• Position: Medical Writer (Biomedical/Clinical Trial/Research)
• Location: Near Bras Basah MRT station/Bencoolen MRt
• Working Hours: Monday - Friday| 9.00am to 6.00pm
• Salary (commensurate with experience): Up to $6500+ Performance Bonus + Travel Allowance + 14 Days Annual Leave + Medical Benefits and Annual Check-up + Online Learning Portal for self-development + WFH Opportunities
• Duration: 1 Year Contract (RENEWABLE/CONVERTIBLE TO PERMANENT)
• Industry: Digital Media Marketing
• Career Advancement: YES

Responsibilities:

• Scientific bridge between clinical development and commercial
• Functions in pharmaceutical and device. It requires the ability to work closely with medical
• Regulatory representatives, HCPs and KOLs to deliver high quality writing that is scientifically
• Rigorous, patient focused, and in line with the strategic positioning of the pharmaceutical or medical devices products.

Requirements:

• Candidate should preferably possess a first-degree degree in biomedical science; a
• research-based degree (MSc or Ph.D.)
• At least 3-5 years of experience in Medical Communication Agency
• The ability to adapt complex scientific information into concise content will be
• essential.
• Excellent delivery in providing summary for AD Board Meetings and Scientific Conferences.

Email to [email protected]

Do visit Search Personnel Pte Ltd for more job listings.

***We DO NOT charge our candidates any referral fee nor bind them with any contract.***

Joie Chang

Deputy Consulting Director (APAC)

Reg no.: R2090601 | EA No: 13C6684

Responsibilities:

• Assist physiotherapists in implementing treatment plans for patients.
• Conduct therapeutic exercises and activities with patients under the supervision of a physiotherapist.
• Provide support in the application of modalities such as heat, cold, ultrasound, and electrical stimulation.
• Guide and educate patients on proper exercise techniques and home care programs.
• Assist in the maintenance and organization of treatment areas and equipment.
• Monitor and record patient progress and report to the supervising physiotherapist.
• Collaborate with other healthcare professionals to ensure comprehensive patient care.
• Adhere to ethical and professional standards in the delivery of physiotherapy services.

Requirements:

• Degree in Physiotherapy or equivalent
• At least 2 – 3 years of experience in a clinical setting with pediatric background.
• Ability to work within short notice.

Interested candidates who wish to apply for the advertised position, please click on the APPLY button below to send in your resume or send to [email protected].

EA License No: 13C6305

Reg. No.: R24120209

For candidate who applied for the advertised position is deemed to have consented to us that we may collect, use or disclose your personal information for purpose in connection with the services provided by us.

Job Scope for a Researcher at Nam Hwa Opera Limited

To Execute and assist in Research, Publication, Seminar and Exhibition Programmes:

(1) Research on Teochew Culture and Art :

· Investigate the historical, social, cultural, and artistic aspects of the Teochew community, and analyse data on their traditions, customs, and heritage.

(2) Documentation and Archiving:

· Maintain detailed research records and manage digital and physical archives of Teochew cultural and art materials.

(3) Collaboration:

· Partner with universities, museums, cultural organizations, clan associations, and Huay Kuan for joint projects, and engage with other researchers and experts.

(4) Educational Programs and Materials:

· Create educational content on Teochew culture and art for workshops, lectures, and courses, and design and implement community outreach programs to promote cultural and art awareness.

(5) Community Engagement:

· Conduct interviews and surveys within the Teochew and art community to foster relationships with community leaders and members to support research initiatives.

(6) Additional Responsibilities:

• Oversee the daily operations of the Research Center.
• Maintain the inventory database for items in the Research Center (e.g., books, magazines, vinyl records, etc.).
• Assist in marketing for the Research Center, including the monthly newsletter, and manage content for social media pages and the website.
• Perform other ad hoc duties, including supporting company in Opera and Music performances.

Qualifications:

· Candidates must possess at least a bachelor’s degree or equivalent.

· Working experience is preferred. Fresh graduates may apply.

· Proficient in MS Office, photo editing and video editing software’s.

· Excellent communication and people skills.

MAJOR DUTIES & RESPONSIBILITIES

• Provide secretariate and administrative support to Review workgroups and Clinical committees, including the provision of secretariat support which will includes curating agenda and take minutes of the meetings.
• Assist in the Programme Management and monitoring support with dashboard visualization reporting to build data analytics capability in evaluating program effectiveness. Track and report on program progress, including key performance indicators and outcomes to ensure successful program execution.
• Supports the coordination and integration of new and existing clinical programmes into integrated care plans and services and standardized care protocols, with the intention to evolve into mainstream bundled care plans/models across
• Collaborate and provide support for stakeholders in various Clinical Steering Committees’ and Workgroups in the development of strategic Population Health programmes roadmap so that integrative care work planning, prioritization and implementation timelines are enabled for success.
• Facilitate the ecosystem mapping to identify current services or gaps and support the framing, strategic planning, and resourcing of integrated care programmes in tandem with the respective Chairs of the clinical Steering Committees and Workgroups.
• Undertake any other tasks or ad-hoc duties as assigned by the Supervisor

Requirement

• Minimally Degree in any discipline, prior experience in similar capacity is preferred
• able to start work on short notice

Interested and qualified candidates, please send in your application to [email protected]

Ivy Yong Shi Mei
R2198995
Recruit Express Pte Ltd 99C4599

Job Scope:

• Support review and investigation of Hospital Incident Reports
• Provide secretariat support to meetings and committees (e.g. Total Quality Management Committee, Incident Review Committee for Serious Reportable Events Various Quality Assurance Committees) and see to the follow-up of all matters arising on all related activities.
• Provide secretarial and admin support for monthly Senior leadership’s Quality & Safety walkabout
• Support and coordinate the efforts in the annual review of departmental policies.
• Support and organize the annual Quality & Safety Day.
• Collaborate with external organizations for quality improvement efforts such as organizing Quality Conferences and cross-institutional improvement projects.
• Support the projects or poster submission to external award platforms.
• Coordinate MOH, AIC, or hospital initiated surveys (e.g. Patient Safety Culture Survey, Patient Experience Survey), analyze data, and follow up with improvement efforts.
• Undertake any special projects or initiatives as assigned by the supervisor and/or Head of Department.
• Any other tasks as assigned by HOD.

Requirements:

• Min Degree in Healthcare Related fields / Nursing
• Prior experience in clinical quality would be an advantage
• Nurses keen to explore clinical quality are welcome too

Interested and qualified candidate , please send in your resume to [email protected]

Ivy Yong Shi Mei

R2198995

Recruit Express Pte Ltd 99C4599