Clinical Data Manager - Early Phase Leeds

Meeveem Limited; Leeds; On-site; GBP 50,000 - 70,000; Full time

Benefits offered by this job

Competitive compensation package

Health insurance

Remote working allowances

Pension contributions

Work-life balance

Job summary

Meeveem Limited in the United Kingdom is seeking a Clinical Data Manager to lead data management activities for early phase studies. This role offers flexibility in remote or hybrid work environments and supports professional growth with mentorship.

The ideal candidate will have a strong background in clinical data management with key responsibilities including leading studies, managing deliverables, and nurturing client relationships. Join a respected and profitable global company that values work-life balance and career development.

Qualifications

• University degree in life sciences or pharmacy preferred.
• Experience as a Lead DM or Senior CDA in early phase trials.
• Excellent written and oral communication skills.

Responsibilities

• Lead data management studies across multi-site timelines.
• Accountable for all DM deliverables and quality.
• Develop client relationships and process scope changes.

Skills

Leadership in data management

Communication skills

Clinical trial knowledge

Familiarity with DM technologies

Education

Degree in life science or related field

Certification in health profession

Job description

Clinical Data Manager - Early Phase

full remote or hybrid

Do you have experience leading data management activities across early phase studies? Are you looking for a new challenge in an environment where you will be closely supported by your Manager, peers and Senior Leaders in your team? Perhaps you are seeking to gain further experience in new therapeutic areas.

Join our growing team and discover your extraordinary potential by working as a Clinical Data Manager within our Early Phase team.

What you can expect from us

• 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

Your responsibilities

• Lead studies including (but not limited to) a combination of healthy volunteer and patient populations, multi-site, client management required or reduced timelines. Ability to organize and effectively prioritize workload and deliverables.
• Be accountable for all DM deliverables as assigned per the established timeline; providing instruction to their DM study team(s) and review of their study team’s output to ensure the highest quality, while adjusting resource allocations accordingly.
• 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.
• Provides leadership, mentorship, and coaching in DM related clinical trial processes to the internal study team.
• Accountable for learning new DM technologies and applied processes, keeping up to date with industry wide technology and feasibility for process improvement at Fortrea.

Your profile

• 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.

Learn more about our EEO & Accommodations request here.