Tenwek Hospital

Health care + 1 more

Research Manager

Closed for applications
Job details

Contract Type

Description

Qualifications & Experience

  • Masters in relevant field from a recognized Institution
  • Certification in Good Clinical Practice (GCP) or a similar research ethics certification
  • At least 3 years of experience in medical research, public health, ethics, epidemiology, or a related biomedical science and a minimum of 2 years in a leadership or supervisory role within a research setting

Method of Application

Interested candidates who meet the above criteria should send their applications enclosing:

  • Resume
  • Cover Letter
  • Statement of Faith


Responsibilities
  • Facilitate communications with investigators at Tenwek Hospital and other institutions together with the Head of Research
  • Monitoring and auditing research budgets under the supervision of the Head of Research
  • Assures compliance with registry and IRB status for research projects (such as clinicaltrials.gov)
  • Assists the Head of Research in publicizing successful research projects and hosting annual Research Day
  • Understands and assures compliance with standards within Kenya and pertinent to funding agencies
  • Supports and helps to write grant applications for funding of research projects
  • Coordinates the submission of invoices for deliverables or services together with the finance team
  • Serving as the ISERC point person to facilitate protocol review
  • Promoting research training at Tenwek Hospital.
  • Collecting and monitoring research project reports and Adverse Event reporting.
  • Scheduling and planning ISERC meetings in consultation with the chair.
  • Receiving, dispatching, and reviewing research proposals.
  • Recording and documenting all research applications and their actions in a spreadsheet.
  • Coordinating with the finance team to ensure proper financial records and audits.
  • Educating staff and others on the ISERC processes and requirements.
  • Maintaining and keeping records of approval deadlines and sending out reminders.
  • Keeping a database of published research studies.
  • Coordinating communications with external IRB stakeholders.
  • Providing administrative support to the hospital and the Head of Research whenever needed.


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