Junior Scientist
Job Description
Junior Scientist (E)
South African Medical Research Council
2026/05/27 Cape Town
Job Reference Number: R950A
Department: South African Cochrane Centre
Business Unit:
Industry: Academic
Job Type: Contract
Positions Available: 1
Salary: Market Related Cochrane South Africa is seeking a motivated and detail-oriented Junior Scientist (Entry-Level) to support activities under the Clinical Trial Registry Project. This ground-breaking project aims to assist in developing and linking a national clinical trial registry with the Pan African Clinical Trials Registry (PACTR), a crucial step in promoting research transparency and integrity across Africa.
Job DescriptionCochrane South Africa is seeking a motivated and detail-oriented Junior Scientist (Entry-Level) to support activities under the Clinical Trial Registry Project.
This ground-breaking project aims to assist in developing and linking a national clinical trial registry with the Pan African Clinical Trials Registry (PACTR), a crucial step in promoting research transparency and integrity across Africa.
The post provides a unique opportunity for a junior researcher to contribute to strengthening research infrastructure on the continent.
Project work- Support implementation work of the SECRET project related to setting up the registry (e.g., collecting inputs from stakeholders, assisting in documentation).
- Contribute to the development and revision of SOPs and project workflows.
- Participate in stakeholder engagement activities, including logistics coordination for stakeholder consultative workshops.
- Conduct data collection activities, ensuring adherence to SOPs and ethical standards.
- Assist in preparing reports, and updates to registry websites.
- Assist with the development and pilot testing of tools and templates for implementing the registry.
- Develop first drafts of presentations for workshops and the related training materials.
- Contribute to research reports and publications.
- Perform quality control checks on files and research documentation for accuracy and compliance.
- Transcribe meeting recordings and notes from workshops and consultations.
- Provide stakeholders and key individuals with promotional materials for the SECRET project.
- Support administrative needs such as document filing and meeting coordination.
- Support data collection, curation and documentation related to registry development and stakeholder consultation activities.
- Manage trial data information and conduct analysis to identify research topics.
- Conduct data entry, cleaning, and verification using standard templates and tools.
- Perform basic data analysis using Excel or other entry-level tools (e.g., frequency counts, summaries).
Duration: 12 months
Remuneration: R per annum (CTC)
Job RequirementsCore Requirements:
- A 4-year tertiary qualification in Life Sciences, Epidemiology, or related.
- Basic understanding of scientific research methods.
- Able to coordinate aspects of studies/projects under full guidance of supervisor.
- Understand and adhere to the scientific protocols, policies and procedures.
- Limited understanding of analysis, interpretation and reporting of research data.
- At least 1-2 years of experience in research, data collection, or health project implementation.
- Ability to follow scientific protocols, standard operating procedures, and ethical research practices.
Advantageous:
- Honours or Master's coursework advantageous.
- Familiarity with data entry, transcription, or qualitative and/or quantitative data handling.
- Strong organisational and administrative skills with attention to detail.
Closing date:
8 June 2026
About This Role
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