Lead and manage the Biometrics and Medical Writing teams, ensuring they are engaged, high‑performing and aligned with CDD objectives
Job Summary
Lead and manage the Biometrics and Medical Writing teams, ensuring they are engaged, high‑performing and aligned with CDD objectives.
Ensure all Data Management, Medical Writing and Statistical Sciences activities comply with ICH GCP and all relevant UK/EU regulatory requirements.
We create a working environment that supports your wellbeing and provide a generous benefits package, a wide range of career and personal development opportunities and high-quality tools.
Matching Summary
Lead and manage the Biometrics and Medical Writing teams, ensuring they are engaged, high‑performing and aligned with CDD objectives.
Skills & Requirements
Must-have
Clinical trial data management
ICH GCP compliance
Regulatory requirements UK/EU
Statistical expertise for trial design
Computer system validation (CSV)
External service provider management
Nice-to-have
Oncology experience
Early phase trials experience
Act with ambition, courage and determination
Act with rigour and professionalism
Act to have a positive impact on people
Act inclusively and collaboratively
Key Requirements
Science graduate or PhD (or equivalent relevant experience)
Extensive clinical trials and drug development experience
Extensive clinical trial data experience
Proven team management experience
Working knowledge of UK/EU early clinical trial regulations
Working knowledge of UK/EU GDPR and data privacy legislation