Clinical Data Manager

Carrot Recruitment are acting as a recruitment agency on the sourcing of a Clinical Data Manager for a clinical-stage biotechnology company at the forefront of cancer drug development. Our client combines cutting-edge science with a patient-centric approach, offering a dynamic and mission-driven work environment. With recent strategic investments from major pharmaceutical partners, the company is well-funded and poised for significant growth.

This is a unique opportunity to contribute to the development of transformational therapies that aim to improve the lives of people with difficult-to-treat cancers.

Everything you need to know about the role:

• As the Clinical Data Manager, you’ll have significant recent experience of managing all activities related to clinical data, and at all stages of process.
• You will be responsible for all elements of the clinical data management and be able to showcase your ability to work in an agile and fast-paced environment, with integrity and accuracy.
• Serve as the lead Data Manager on a study level and contribute to the design of the eCRF, collection of data and review of data for accuracy and completeness.
• Interact with members of the multidisciplinary project teams to provide ongoing data management support for clinical trials.
• Familiarity with risk-based data management process.
• Oversee database builds, including UAT, ensuring data integrity and security.
• Participate in the development and implementation of the standard processes and guidelines for the DM function.
• Management of data management tasks, on a study level performed by the vendor, in adherence with established standards including third party vendor data reconciliation, protocol deviation collection, SAE reconciliation and data issue resolution.
• Coordinate internal cross-functional review of data management documents, as required.
• Stay abreast of new and/or evolving local regulations, guidelines and policies related to clinical development.

Experience and qualities that make you a strong fit:

• Bachelor’s degree in computer science, life sciences or equivalent.
• Recent relevant experience in a Clinical Data role.
• Current and up-to-date GCP training.
• Experience in setting up EDC systems is essential, and vendor management experience preferred.
• Experience in oncology essential, multiple myeloma preferred.
• In-depth understanding of clinical trial processes and involved functional stakeholders.
• Knowledge of FDA, EMA and ICH regulations/guidelines and the drug development process is preferred but not essential.
• Proficient in Excel.

What’s on offer?

• A competitive salary.
• Comprehensive benefits package, including medical insurance, pension, bonus and share scheme.
• Hybrid working model (Manchester location preferred, although commuting distance from Cambridge/London would also be possible).
• Opportunities to be part of a fast-growing biotech at a significant part of their development.

Could this be the role for you?

If you’re ready to take on this exciting opportunity and bring your expertise to a company that’s listed as one to watch, we’d love to hear from you. Please apply with your most recent CV, to be considered.