Principal Job Responsibilities:

·         Lead and/or serve as study physician in the implementation of an on-going research project through handling clinical activities including recruitment, screening, enrolment and follow-up of research participants.

·         Participate and/or lead in problem identification for research, research designing, research protocol development, data collection, analysis, interpretation and report writing.

·         Writing grants independently and/or in collaboration with senior researchers in the respective Directorate.

·         Provide medical care for study participant as applicable      

·         Conduct and lead clinical examinations and medical follow-up of study participants.       

·         Conduct and coordinate other clinical procedures required in a study protocol.

·         Conduct and/or Lead data collection, CRF completion, verify and review clinical data

·         Lead and provide counselling and medical care of study participants as a physician.         

·         Ensure protection, care and retention of study participants during a study conduct.          

·         Follow-up, recording & reporting of AEs, NEs & SAEs as deemed necessary.   

·         Prepare clinical progress report.         

·         Cooperate in ensuring quality control activities in the conduct of trials.

·         Representing the directorate/institute in any scientific platforms for paper presentation and/or participation when applicable

·         Perform miscellaneous job-related duties as assigned by the director and/or the principal investigator.

Job Requirements

Specifications for the Position:

Qualification, Experiences and Essential Skills

- MD plus specialty/MSc in clinical pharmacology with min 4 years of experience in medical practice; plus

- Experience in clinical research and scientific paper writing with at least one publication point (i.e. minimum one publication with first authorship; or minimum two publications with non-first authorship status) is mandatory.

- Experience in clinical trial and training in research ethics & GCP is an advantage.

Personal Attributes:

-          Initiatives for team work and leadership

-          Personal training/skills in the required position 

-          Excellent interpersonal communication skill and proficient in English  

-          Strong computer literacy

-          Strong organizational skills, flexible to working off-working hours or weekends

-          A high level of attention to details

-          Ability to work with others/team work, including international collaborators

-          Open for discussion and learning

-          Ability to problem solving and willingness to take self-initiatives

-          Willingness to take up additional responsibilities and continuous training as needed

How to Apply

Interested applicants who fulfilled the above requirements should send the following through this LINK

• A CV/resume  (not more than 5 pages)

• A cover letter (not more than one page)

• A one page table summarizing your educational background, technical skills and  competencies to facilitate the screening process

Term of employment: One year full time contract with possibility for extension depending on performance and availability of funding

References:  Please provide three references including their e-mail address.

No. Required: 01 (one)