At a Glance
- Tasks: Lead clinical studies, manage data, and ensure high-quality deliverables.
- Company: Fortrea Drug Development, a respected global company with a diverse culture.
- Benefits: Competitive pay, health insurance, remote work options, and a solid work-life balance.
- Other info: Enjoy flexibility in hours and a thorough onboarding process with mentorship.
- Why this job: Make a real impact in clinical trials while developing your career in a supportive environment.
- Qualifications: Degree in life sciences or related field; experience in clinical data management preferred.
The predicted salary is between 46000 - 52000 £ per year.
Responsibilities
- Lead studies including a combination of healthy volunteer and patient populations, multi-site, client management required or reduced timelines.
- Organize and effectively prioritize workload and deliverables.
- Be accountable for all DM deliverables per the established timeline; providing instruction to DM study team(s) and reviewing their output to ensure the highest quality while adjusting resource allocations as needed.
- Develop and maintain client relationships and review client satisfaction surveys.
- Track scope changes and work with the Project Manager to ensure that Sponsor approval is received and the scope change processed.
- Provide leadership, mentorship, and coaching in DM related clinical trial processes to the internal study team.
- Be accountable for learning new DM technologies and applied processes, keeping up to date with industry‑wide technology and feasibility for process improvement at Fortrea.
Qualifications
- University/college degree (life science, pharmacy or related subject preferred), or certification in a related allied health profession from an appropriately accredited institution (e.g., nursing certification, medical or laboratory technology). Additional relevant work experience will be considered in lieu of formal qualifications.
- Experience in clinical data management as a Lead DM or Senior CDA or similar within early phase trials at CRO/pharma level.
- Excellent oral and written communication and presentation skills.
- In depth knowledge of clinical trial process and data management, clinical operations, biometrics, quality management, and systems applications to support operations.
- Working knowledge of the relationship and regulatory obligation of the CRO industry with pharmaceutical/biotechnological companies.
Benefits
- Office based or home based anywhere in the listed countries.
- Rewarding and meaningful work in an established, diverse, highly profitable and respected global company.
- Highly competitive compensation packages, including various local benefits such as pension contributions, complimentary health insurance plans, remote working allowances etc.
- A genuine work life balance.
- Flexibility in working hours.
- A thorough onboarding with support from your personal mentor.
- A permanent employment contract with Fortrea Drug Development and a rewarding career progression.
EEO Statement
Learn more about our EEO & Accommodations request here.
Clinical Data Manager - Early Phase in Leeds employer: FTLEE Fortrea Clinical Research Unit Ltd
Fortrea Drug Development is an exceptional employer, offering a dynamic work environment where clinical data managers can thrive. With a commitment to employee growth, competitive compensation packages, and a focus on work-life balance, Fortrea fosters a culture of mentorship and support, ensuring that every team member has the resources they need to succeed in their role. Located in a global setting, employees benefit from flexible working arrangements and a diverse, inclusive atmosphere that values meaningful contributions to the field of clinical research.
Contact Details:
FTLEE Fortrea Clinical Research Unit Ltd Recruitment Team
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We think this is how you could land Clinical Data Manager - Early Phase in Leeds
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