Global Data Manager - homebased (FSP)
Durban, KwaZulu-Natal, South Africa · Full Time
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- Experience
- 5+ yrs
- Salary
- —
- Openings
- 1
- Posted
- 4 hours ago
- Work mode
- In office
- Education
- BS/BA degree or higher
- Eligibility
- Applicants should hold a BS/BA degree or higher, preferably in Health Sciences, or an equivalent degree with professional clinical exposure. Candidates must have at least 5 years of data management experience, 3 years of lead/co-lead experience, vendor management experience, and RAVE experience. Th…
- Resume
- Required to apply
Where you'll work
Job description
Role overview
This position is focused on providing data management support, oversight, and/or accountability across one or more clinical trials. The role works closely with trial customers and internal/external stakeholders to align expectations, manage deliverables, and ensure high-quality clinical data management throughout the study lifecycle.
Key responsibilities
- Act as the main contact with the trial customer and relevant partners to define, align, and confirm data management expectations.
- Plan, monitor, and coordinate the content, format, quality, and timing of key data management outputs such as CRFs, data review plans, QC plans, oversight plans, database release plans, final datasets, submission plans, and archival activities.
- Work with the customer and other functional teams to collect content requirements and integration needs for eCRFs and other data capture tools.
- Set standards for clinical data conventions and quality expectations.
- Define expected dataset structure and content.
- Build timelines and follow up to keep all data management milestones on track.
- Carry out study-level oversight activities in line with the oversight plan, QC procedures, and work instructions with limited direction.
- Prepare clinical data management documentation, including submission packages, while maintaining quality, scientific accuracy, organization, clarity, compliance, and consistency.
- Maintain inspection readiness for all study data management deliverables and support regulatory inspections and audits where needed.
- Support the planning, creation, and tracking of study deliverables to ensure deadlines are met.
- Take part in assigned clinical working groups to ensure data management and therapeutic area needs are addressed.
- Capture and share lessons learned, best practices, and frequently asked questions at the study level.
- Present and provide training during investigator and monitor meetings.
Experience and qualifications
- A BS/BA degree or higher is required, preferably in Health Sciences.
- Alternatively, a BS/BA degree or higher with professional exposure or experience in clinical settings is acceptable.
- At least 5 years of experience in data management.
- At least 3 years of lead or co-lead experience.
- Experience in vendor management.
- Hands-on experience with RAVE.
Important notice
This position is not eligible for UK visa sponsorship.
About the employer
The hiring organization is a global leader in clinical research services, commercial insights, and healthcare intelligence for the life sciences and healthcare industries. The company supports the development and commercialization of innovative medical treatments aimed at improving patient outcomes and population health worldwide.
Hiring integrity
The employer follows a zero-tolerance approach to candidate fraud. All information and credentials submitted during the recruitment process must be accurate and complete. Any false statement, misrepresentation, or omission may lead to immediate rejection of the application, or termination of employment if discovered later, subject to applicable law.