Healthcare and MedicalFull-TimeSenior-level(6+ yrs)
Job Description
Role Overview
The Clinical Research Facilities (CRF) Study Manager at ILRI is responsible for the comprehensive management and oversight of research studies. The role involves acting as either an Investigator or Assistant Study Investigator as appointed by Test Facility Management. Primary responsibilities include the development of study protocols and budgets, ensuring regulatory compliance, monitoring animal welfare, and managing study reporting.
Key Responsibilities
Investigator Duties
Serve as the Investigator on studies as appointed by Test Facility Management.
Lead the drafting of study protocols and budget development, including writing, editing, and reviewing documents.
Draft and submit research approval applications to the IACUC and IBC, addressing any subsequent queries.
Obtain all necessary approvals from national and international regulatory authorities, including NBA, NACOSTI, DVS, and NEMA.
Ensure the health and welfare of study personnel and animals by monitoring adherence to the Biosafety Manual and animal welfare policies.
Oversee the receipt, dispensing, and disposal of investigational veterinary products and imported biological materials in accordance with SOPs and legal permits.
Manage and oversee study phases outsourced to external laboratories, consultants, or vendors.
Provide technical guidance and training to research staff.
Maintain effective communication with study sponsors and monitors regarding progress and results.
Coordinate daily research activities such as dose preparation, administration, observations, and sample collection.
Assistant Study Investigator Duties
Provide lead support to Investigators on assigned studies.
Manage the study master file, including preparation, close-out, raw data reviews, and data management.
Assist in drafting study proposals, protocols, reports, and ethics applications.
Coordinate study setup, including facility logs, animal selection, and acclimation.
Report study progress and adverse events to the Investigator and Sponsor.
General Management
Perform Team Lead duties including resource scheduling and updating departmental worksheets.
Coordinate responses to Quality Assurance (QA) and regulatory audits.
Develop and execute novel study models and implement preventative measures for suspected serious diseases.
Requirements
Education: Master’s degree in Natural or Biological Sciences.
Experience: A minimum of 7 years of relevant professional experience.
Expertise: Deep knowledge of animal health, welfare, biosecurity, bio-safety, and the 3Rs (Refine, Replace, Reduce) concept.
Standards: Familiarity with VICH GL9 (GCP) guidelines.
Technical Skills: Experience with qPCR and immune assays (ELISA, IFN-y ELISpot, and VINT) is an added advantage.
Soft Skills: Ability to work in multi-cultural environments, take initiative, and work with limited supervision.
How to Apply
Interested and qualified candidates should apply online via the ILRI recruitment portal. To apply, please visit: https://www.myjobmag.co.ke/apply-now/1215137. This link will direct you to the official application page on the International Livestock Research Institute (ILRI) website (www.ilri.org).
How to Apply
Interested and qualified candidates should apply via the International Livestock Research Institute (ILRI) recruitment portal. To access the application form, visit: https://www.myjobmag.co.ke/apply-now/1215137. This will redirect you to the official career site at www.ilri.org.
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