Key Responsibilities:
- Coordinate the collection, processing,
compilation, verification and storage of study data or samples and ensure
all processes are conducted in line with Good Clinical Laboratory Practice
(GCLP) and the study protocols.
- Conduct Data analysis and interpretation of
study data or samples to identify insights and synthesize the same through
statistical summaries and other data visualization techniques.
- Lead and support in troubleshooting of new
laboratory assays and ensure laboratory experiments (DNA/RNA extraction,
qPCR and sequencing) within the team are conducted as per the SOPs
- Contribute to report writing, dissemination and
publishing of study research work by authoring in various reputable
scientific journals, preparing policy briefs and disseminating at various
internal and external meetings, conferences, workshops and other relevant
Scientific forums
- Network, collaborate and partner with the other
Departments, research groups and other internal and external stakeholders
and support in the Study Project Management to ensure quality of outputs
and timely completion of the Project.
- Conduct training and Mentorships to other
Researchers by designing, implementing and reviewing mentorship plans,
developing user-friendly learning aids and reference materials as well as
delivering virtual or physical training sessions to the assigned researchers,
students and interns.
- Supervise the Study team by providing day to day
supervision and coordinating both the Study research and operations teams
and participate in other study HR Management issues as assigned
- Contribute to the Study full compliance with all
relevant internal ethical and Research Governance protocols, policies and
procedures as well as all external legal, ethical and regulatory
requirements by ensuring proper documentation and adherence at all
Research Phases.
- Provide inputs and necessary technical support
to the Principal Investigator and other Programme Researchers in
identifying sustainable funding opportunities and developing proposals to
secure Research Grants and funding.
Qualifications
- Minimum Master’s Degree in Biological Sciences,
Bioinformatics, or any other relevant field from a recognized university
Mandatory
- Minimum Three (3) Years experience in Genomics
and Bioinformatics at a reputable Research institution Mandatory
- Demonstrated experience in capacity building and
the use of current technology in Health Research, specifically R and other
bioinformatics software. Mandatory
- Demonstrated high levels of integrity and
confidentiality Mandatory
- Excellent interpersonal, verbal and written
communication skills Mandatory
- Ability to work with diverse, multidisciplinary
teams and build strong relationships with internal and external
collaborators Mandatory
- Excellent analytical skills and ability to
deliver quality outputs within strict timelines. Mandatory
- Strong team coordination and decision-making
skills Mandatory
How to
Apply
