KEMRI Study Coordinator Job

Location: Kisumu

Vacancy No. FN-02-02-2024

Duties and Responsibilities

•  Develop an in-depth understanding of the study protocols, goals and logistics required to conduct research studies and implementation projects
•  Develop clinical trial implementation plans in collaboration with investigators and relevant stakeholders
•  Create Standard Operating Procedures (SOPs) that align with the study protocols
•  Conduct training for research teams to always guarantee adherence to study SOPs at all times.
•  Provide leadership in research studies through coordination and daily oversight of day-to-day implementation of study activities
•  Coordinate the study team to ensure proper performance of study and project activities consistent with study protocols and SOPs
•  Lead study recruitment with the support of study investigators and research team, including evaluating potential participants for inclusion in clinical trials in compliance to the study protocol
•  Perform study visits and clinical assessments of study participants, document study procedures, and interpret laboratory results in collaboration with study PIs.
•  Ensure proper documentation of all research participants in physical and electronic medical records
•  Ensure participant safety through monitoring of clinical and laboratory adverse events
•  Ensure timely reporting of adverse events and protocol deviations.
•  Ensure participant privacy and confidentiality are maintained
•  Compiling weekly clinical and study data and study reports in coordination with data manager
•  Oversee and monitor study budget expenditure, including study resource utilization, cash flow and expenditures
•  Maintain relationships with collaborating partners and the County Ministry of Health
•  Coordinate communication with research staff and PI/Co-PIs/Co-Investigators
•  Maintain regular communication with members of the research team
•  Ensure regular and timely updates of clinical trial recruitment, follow-up, and data collection progress
•  Work professionally and ethically with competence, accountability, and integrity
•  Perform any other relevant duties as assigned by the study PIs

Qualifications:

•  Bachelor of Medicine and Surgery
•  Be duly registered with the relevant professional body, holding valid practice license

Other Desirable Qualifications:

•  Knowledge in Cervical Cancer Screening and Prevention Clinical or research programs
•  Attention to detail, critical thinking and problem-solving skills
•  Interpersonal and communication skills
•  Good communication skills
•  Experience working in HIV care, either in a Clinical or Research setting

How To Apply

All applicants must meet each selection criteria detailed in the minimum requirements.

Must include a current CV with names of at least three referees.

Must include copies of academic and professional certificates.

Indicate Position & Vacancy Number or Reference Number as the subject of the Email

A duly signed application letter indicating the vacancy reference with copies of documents listed above should be sent to the stated email address not later than 19th March, 2024
Send your application to hrrctp@kemri-rctp.org