PURPOSE OF THE POSITION

To lead and execute preclinical in vivo studies involving rodent models (mice and rats) in support of internal and client sponsored research projects. The Temporary Senior Researcher will be responsible for designing studies, conducting experiments, analyzing data, and ensuring regulatory compliance. A key part of this role involves liaising directly with external clients to provide scientific guidance, manage expectations, and deliver high-quality research outcomes in a CRO-like environment.

KEY RESPONSIBILITIES:

Study Direction and Project Management

• Serve as GLP Study Director where applicable.
• Manage project timelines, scope, and resources.
• Coordinate cross-functional teams (vet, QA, tech staff, analysts).
• Ensure timely and successful completion of milestones.

Study Design and Scientific Execution

• Develop ethical, regulatory-compliant protocols.
• Design and implement pharmacology/toxicology/PK-PD studies.
• Ensure data quality and adherence to SOPs.

Data Analysis, Reporting, and Client Delivery

• Analyze and interpret study results using appropriate tools.
• Prepare accurate internal reports and client-ready documentation.
• Present findings clearly to clients and stakeholders.
• Respond to client feedback and follow-ups professionally.

Regulatory and Quality Compliance

• Ensure GLP, AAALAC, NDoH, and SANS 10386 compliance.
• Support internal and external audits and inspections.
• Contribute to SOP development and deviation management.
• Uphold animal welfare and ethical standards throughout.

Capacity Building and Continuous Improvement

• Mentor and support junior researchers and technical staff.
• Contribute to onboarding and capability uplift during the contract period.
• Identify and implement operational improvements.
• Participate in lessons-learned sessions or debriefs.

• PhD in Pharmacology, Pharmaceutical Sciences, Biomedical Sciences, Para-veterinary sciences, or related discipline (NQF level 10).
• A minimum of two (2) years’ laboratory experience in animal research.
• A minimum of one (1) year experience in regulatory and quality compliance.

ADDED ADVANTAGES & PREFERENCES:

• A minimum of one (1) year project and study management experience.
• A minimum of one (1) year client-facing / external liaison experience.

KEY FUNCTIONAL/ TECHNICAL COMPETENCIES:

• In Vivo Study Design and Execution.
• Scientific communication.
• Regulatory knowledge.
• Data Analysis and Scientific Reporting.
• Project and Study Coordination.
• Study documentation and reporting.

KEY BEHAVIOURAL COMPETENCIES:

• Attention to detail.
• Integrity and ethical conduct.
• Problem-solving and critical thinking.
• Effective communication.
• Accountability and ownership.

REMUNERATION

The annual total remuneration package will be commensurate with the level of appointment as advertised and in line with the NWU policy guidelines.

ENQUIRIES REGARDING JOB CONTENT MAY BE DIRECTED TO:                  Prof. Rose Hayeshi on 018 285 2606

ENQUIRIES REGARDING RECRUITMENT PROCESS MAY BE DIRECTED TO: Ms. Janine Da Gama on 016 910 3451

CLOSING DATE:                                                                                                  25 July 2025

PLANNED COMMENCEMENT OF DUTIES:                                                       As soon as possible

Kindly take note: applications must be submitted online through the official nwu vacancy website. Incomplete applications and those submitted through any other platform will not be considered.

The University subscribes to and applies the principles of Employment Equity (EE) Act and is committed to transformation. Preference will be given to candidates from the designated groups, in accordance with the principles of the EE Act and NWU Employment Equity Plan.

The University reserves the right not to make an appointment. Communication will be limited to shortlisted candidates only.

If you are not contacted within two months from the closing date of this advertisement, please accept that your application was unsuccessful.

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