Job Description

Job Summary Essential Requirements:

• Tertiary degree or equivalent diploma in a related scientific or clinical field
• Valid GCP qualification
• 1 - 2 years clinical research essential
• Knowledge of TB and scientific vocabulary advantageous
• Computer Literacy (MS Office - Outlook, Word, Excel, PowerPoint including database competency - RAVE, EDC, REDCAP)
• An understanding of publication processes and procedures
• Excellent administrative, organizational and logistical skills
• Excellent report writing skills
• Excellent communication skills (verbal and written)
• Information monitoring and managing
• Research support skills
• Technical knowledge and skill
• Resource management
• Accuracy and attention to detail is essential
• Problem-solving
• Ability to self-motivate and take initiative for tasks
• Excellent interpersonal skills and ability to work well in a multi-disciplinary study team

Responsibilities include (but not limited to):

• Prepare and submit all Ethics Committee documentation and correspondence on behalf of the Principal Investigator.
• Track submission deadlines, follow up on responses, and maintain accurate Investigator Site Files with updated study documents.
• Assist with SOP updates and ensure proper archiving of completed clinical trial files in line with GCP standards.
• Ensure investigators and pharmacist staff have valid malpractice insurance and registration certificates.
• Make sure all staff read and sign SOPs and Work Practice Guidelines.
• Track SOP review dates and ensure new staff complete required training.
• Keep signature and delegation logs updated and assist the team in preparing for new studies.
• Review and update site SOPs to align with operational systems, site processes, and regulatory requirements.
• Develop new SOPs as needed and ensure they comply with ICH GCP, SAGCP, and other guidelines.
• Circulate drafts to stakeholders for input, obtain Principal Investigator approval, and distribute final versions to staff for training and tracking.
• Liaise with Principal Investigators, team managers, and sponsor or CRO representatives.
• Attend unit meetings and perform other research-related duties as assigned.

Additional Information:

• Position will be based in Mowbray
• 6 to 12-month Fixed Term Contract
• 40 hours per week, Monday to Friday (Additional Hours as required)

Closing Date: 17 October 2025
Only shortlisted candidates will be contacted. Should you not receive a response within 30 days of the closing date, please consider your application unsuccessful.
EMPLOYMENT EQUITY STATEMENT
The University of Cape Town Lung Institute is committed to equity in our employment practices and reserves the right not to appoint.
The selection process will be guided by the Employment Equity Plan and Targets of the University of Cape Town Lung Institute (Pty) Ltd.
POPIA STATEMENT
Please note that when applying for any position, reference checks will be completed, and personal information defined in the protection of personal information Act 4 of 2013 will be processed. In applying for this position, applicants will be deemed to have consented to such processing as defined in the policy statement.
*Please Note: This Position is not on UCT Conditions of Service.
University of Cape Town Lung Institute (Pty) Ltd
Company

Skills Required