Clinical Data Consultant
Part-Time, approximately 3 days per week
Outside IR35
Remote (Occasional travel to Oxfordshire)
CPL Life Sciences are actively seeking an experienced Clinical Data Manager to support our growing biotech partner as they progress multiple indications from phase I-II.
This part-time contract will focus on overseeing clinical data management activities while contributing to strategic planning to support future growth.
Key Responsibilities:
* Lead and oversee clinical data management processes across ongoing and upcoming studies
* Ensure high-quality, compliant data collection, validation and reporting in line with regulatory standards
* Collaborate cross-functionally with clinical, regulatory and biostatistics teams
* Support the optimisation of data management systems and workflows
* Contribute to clinical data strategy and infrastructure planning to enable scalability and future growth
* Provide expert guidance on data standards, governance and best practice
Requirements:
* Proven experience in clinical data management within biotech, pharma or CRO settings
* Strong understanding of GCP standards and regulatory requirements
* Experience with EDC systems and data validation processes
* Strategic mindset with the ability to support organisational growth initiatives
* Excellent communication and stakeholder management skills
* Prior consulting or contract experience
* Ideally have previous experience in supporting early phase Biotech
Please apply here if this role is of interest.