Data Manager in Clinical Trials
Full-time
ATS Client
Company Description PSI is a leading Contract Research Organization (CRO) with 30 years of experience in the pharmaceutical industry. Originated in Switzerland, PSI is a privately owned, full-service CRO with a global reach, supporting clinical trials across multiple countries and continents. Our reputation for being highly selective about the projects we undertake highlights our commitment to delivering high-quality, timely services across a broad spectrum of therapeutic indications. At PSI, we foster an environment where a diverse range of colleagues feel welcomed and valued. Our inclusive culture is a cornerstone of our success, enabling us to attract and retain top talent globally. We are not just about conducting clinical trials; we are about building a community where every team member has the opportunity to thrive and contribute to groundbreaking advancements in the pharmaceutical industry. Job Description Clincial Data Manager plays a critical role in the clinical research project. If you are detail-oriented and committed to quality, able to work with large volume of clinical or medical data, you might be the professional we are looking for. Full-time employment in Pretoria, South Africa Responsibilities will include:
- Track database set-up, testing, maintenance and data entry
- Communicate with clients, project teams and vendors on data management matters
- Review study documents, design and develop project specific guidelines and instructions
- Design eCRF, Data Management and Data Validation Plans and test EDC databases
- Ensure data entry, follow-up and validation, including manual CRF review and SAE reconciliation
- Code medical data
- Track and report metrics leading to database lock
- Coordinate the processing, dispatch and archiving of CRFs/queries
- Maintain Clinical Data Management working files
- Perform database QC checks, prepare and attend audits
- Train site staff and project teams on CRF completion and data management topics
- College/University degree (Life Science, Pharmacy degree is a plus)
- Demonstrated experience of managing clinical or medical data
- Full working proficiency in English
- Experience with Clinical Data Management systems (e.g. Medidata Rave, Oracle InForm)
- Proficiency in MS Office applications
- Organisational and time management skills
- Ability to work independently and multi-task
Vacancy posted a month ago
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