Summary
Date Posted: Thursday, June 01 2023, Base Salary: Not Disclosed

JOB DETAILS:

Purpose of position
• The Trial Manager will assist the Principal Investigator in Coordinating the NIHR-LSTM administrative, research and community activities at KAVI-ICR site. She/He will be expected to deliver high quality research whilst maintaining excellent GCP standards and practice.

Duties and Responsibilities
• Sub-investigator in all clinical trials and community studies conducted at NIHR-LSTM-KAVIICR site.
• Communicate with the sponsor and the regulatory agencies in all issues relating to the study.
• Setting up, coordinating and supervising clinical trial sites.
• Develop study procedures, methodology and instructions for clinical trials staff, as well as where necessary design data collection tools.
• Ensuring compliance with the Protocol, SOPs, local regulations, ICH and GCP guidelines.
• Collect, verify and finalize collected data to create reports and present results of findings.
• Provide appropriate treatment and where necessary, facilitate referral of volunteers with complications.
• Assist the Principal Investigator in drawing an annual budget for the clinic and community activities.
• Participate in Community Advisory Board and Community Engagement meetings.

Job requirements/Specifications:
• A Bachelor’s degree in any Health Sciences/Medical field plus 3 and above years experience or Diploma in any Health Sciences/Medical field plus 5 and above years experience from a recognized Institute
• Must be registered with the relevant Professional regulatory body in Kenya.
• Must have a valid GCP/ICH Training
• Skills, Knowledge and Abilities in the following areas: carrying out clinical trials; current databases especially RedCap; building staff capacity through mentorship and effective leadership in the management of clinic activities; participatory research approaches and qualitative methods & analysis; data collection software; such as RedCap; publications and other dissemination activities. Note that clinical trials preferably working with fistula patients will be an added advantage

Terms of Appointment
• This a one year full time contract renewable based on performance and by mutual consent.

Work Hours: 8

Experience in Months: 36

Level of Education: Bachelor Degree

Job application procedure
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