Job Roles
Support clinical research activities in accordance to the applicable International & National Acts , Regulations and NKF policies.
Main Responsibilities
Research Projects management
- Work closely with clinical Principle Investigators (PIs) , to assist them with IRB preparation & submission, protocol development, preparation of study logistics, subject pre-screening , etc.
- Coordinate the schedules of all study team members, book meeting room, and take meeting minutes, prepare presentations and documents required for the meeting .
- Assist the investigators in recruitment and conduct of studies according to protocols.
- Assist with consent taking for subject when required
- Maintain study files as required , data collection and management, study documentation, study monitoring and event report
- Prepare relevant progress report and research papers under the supervision of the Principal Investigators
- Able to manage more than one research projects concurrently when required
- Self driven for learning, actively conduct literature review to gain relevant information
- Cross cover other project teams when assistance is required
Other Duties
- Participate in research group discussion
- Contribute ideas to new research projects initiated
- Provide administrative support to Research Office where needed.
- Perform any other ad-hoc duties as assigned
Qualifications
- Bachelor in Nursing /Health Science or diploma in Clinical Research management
Experience
- Minimal 3 years of working experience, of which 2 years of relevant experience in research coordination (experience in data analytic will be added asset)
- Proficient in using Microsoft Words, Excel & Powerpoint
- Familiar with local ethical guidelines and regulatory requirement in research
Soft Skills
- Excellent interpersonal skill
- Good communication skills in both verbal and written, bilingual and/or knowledge of local dialects desired.
Note
- Candidate should be comfortable with travelling to dialysis centres islandwide
