At a Glance
- Tasks: Lead clinical data management and oversee vendor contracts for oncology studies.
- Company: FTMAI Fortrea Development Ltd, a leader in clinical research.
- Benefits: Flexible working hours, remote allowances, and competitive compensation with health insurance.
- Other info: Join a dynamic team dedicated to advancing clinical research.
- Why this job: Make a significant impact in oncology while enjoying work-life balance.
- Qualifications: 8+ years of data management experience, including 2 years in sponsor management.
The predicted salary is between 60000 - 84000 £ per year.
FTMAI Fortrea Development Ltd is looking for a Senior Clinical Data Manager based in the UK. In this role, you will provide full cycle Clinical Data Management, overseeing vendor contracts and leading studies with patient populations.
The ideal candidate will have at least 8 years of DM experience, including 2 years in sponsor management.
The company offers flexibility in working hours, remote allowances, and competitive compensation packages including health insurance.
Lead Clinical Data Manager – Oncology (FSP) Remote in Maidenhead employer: FTMAI Fortrea Development Ltd
FTMAI Fortrea Development Ltd is an exceptional employer that prioritises employee well-being and professional growth. With a flexible work culture, competitive compensation packages, and opportunities for advancement in the dynamic field of oncology, employees are empowered to thrive in their roles while making a meaningful impact on patient care.
Contact Details:
FTMAI Fortrea Development Ltd Recruitment Team
StudySmarter Expert Advice🤫
We think this is how you could land Lead Clinical Data Manager – Oncology (FSP) Remote in Maidenhead
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We think you need these skills to ace Lead Clinical Data Manager – Oncology (FSP) Remote in Maidenhead
Some tips for your application 🫡
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Make sure you brush up on key pharmaceutical concepts and recent developments in the industry. You might get asked some technical questions during the interview at FTMAI Fortrea Development Ltd that show your grasp of drug development processes or regulatory requirements, so be ready to discuss them clearly.
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In a full-time pharmaceutical role, understanding the regulatory landscape is crucial. Prepare for situational questions that may test your problem-solving skills concerning compliance and safety standards. You could be asked how you'd handle a hypothetical issue regarding a drug’s market release, so think through your approach.
