Principal Job Responsibilities:

·         Develop, conduct and lead clinical trial projects

·         Participate and/or lead implementation of on-going clinical researches through handling clinical activities such as recruitment, screening, enrolment and follow-up of research participants.

·         Lead and provide medical care to study participants as necessary

·         Participate with CTD and beyond team in problem identification for research, research designing, research protocol development, data collection, analysis, interpretation and report writing.

·         Prepare and/or lead grant writing independently and/or in collaboration with senior and junior researchers in the respective Directorates.

·         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 and project 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 certificate in Pediatrics with min 6 years of experience in medical practice as pediatrician; plus

- Experience in clinical research and scientific paper writing with at least two publication points (at least one publication as first author) is mandatory.

- Experience in clinical trial at the position of Principal Investigator is given priority.

How to Apply

Interested applicants who fulfilled the above requirements should send the following through this LINK or before April 22, 2023.

• 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.