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 who are classified as a top biotech to watch in this space
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 the 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
- Stays 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 - 2 days per week on site (Manchester location preferred, although commuting distant Cambridge 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.
:quality(80))
:quality(80))
:quality(80))