Vacancy No. FN-06-03-2023

Duties and Responsibilities:

  • Work with study investigators to ensure study procedures are completed, specimens are collected, processed, and properly stored, and required data are collected
  • Locate and contact study participants
  • Administer informed consent to study participants and record the process appropriately
  • Respond to questions about the study posed by participants and other stake holders
  • Develop in-depth understanding of the study’s goals and the logistics required to conduct the study
  • Track/trace participants for their study visits within the prescribed visit windows to ensure good retention and safety monitoring
  • Complete CRFs
  • Administer questionnaires
  • Administer participant reimbursement.
  • Basic data management/data quality review in collaboration with the data science investigator
  • Collection of blood and urine samples from consented study participants
  • Sample handling, including packaging, chain of custody, preparation for transport to testing laboratories both locally and internationally.
  • Travel on short notice to clinics, laboratory centers, and communities within the study regions
  • Coordination with other studies around documentation of participant consent, sample receipt, and sample collection kits
  • Report problems encountered to the study PI and consult appropriately
  • Report adverse events as applicable and document all protocol deviations
  • Communicate with the Scientific Ethics Review Unit (SERU) and submit yearly reports, amendments, protocol deviations and renewals as required.
  • Maintain participant confidentiality at all times
  • Maintain good relationship with participants
  • Maintain communication with team members in Kenya and the U.S., including communication via phone, email, Zoom, and other electronic means
  • Prepare for and attend regularly scheduled team meetings conducted virtually or in person
  • Due to working across time zones with the study team, and for participant recruitment, flexibility in working hours including evenings and occasionally weekends (for travel) is required.
  • Perform any other relevant duties as assigned by the Principal Investigator and designated supervisors

Other required skills:

  • Must be keen and attentive to details and have ability to follow instructions and procedures properly.
  • Excellent written and verbal communication required.
  • Works in a professional and ethical manner with competence, accountability and integrity
  • Must be non-judgmental and flexible to mix with all cadres of people

Required Qualifications:

  • Diploma in Clinical Medicine and Surgery, Nursing or Medical Laboratory Science.
  • Phlebotomy certification from an accredited institution

Preferred Qualifications:

  • Experience working with the Household Socio-Economic (HSE) Survey as part of the Sustainable East Africa Research In Community Health (SEARCH) study
  • At least one year experience in implementing clinical research studies.
  • Experience working in HIV care, either in a clinical or research setting
  • License to ride a motorbike (with a valid riding license)

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 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: [email protected] not later than 16th April, 2023.

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