At a Glance
- Tasks: Lead strategic data management for key clinical development programmes in biotech.
- Company: Innovative biotechnology organisation with a focus on growth and collaboration.
- Benefits: Competitive salary, bonus, share options, and fully remote work.
- Other info: Join a dynamic team with opportunities for professional growth.
- Why this job: Make a real impact in regulatory submissions and inspection readiness.
- Qualifications: Extensive experience in Clinical Data Management and leadership roles.
The predicted salary is between 63000 - 77000 £ per year.
We're partnering with an innovative biotechnology organisation to appoint an experienced Director, Data Management to provide strategic leadership and SME oversight across key clinical development programmes. This is a high-impact leadership position for an experienced Clinical Data Management professional who combines strong technical expertise with exceptional attention to detail and proven experience managing CRO partnerships.
You'll play a critical role in ensuring high-quality data management deliverables, maintaining vendor accountability, supporting regulatory submissions, and leading inspection readiness activities ahead of significant development milestones.
What you'll be doing:
- Provide strategic leadership and Subject Matter Expert oversight across Clinical Data Management activities
- Review study documentation, plans, deliverables, and processes to ensure quality and compliance
- Identify risks, gaps, and process improvements proactively across ongoing programmes
- Manage CRO performance, ensuring accountability for timelines, quality standards, and deliverables
- Oversee database build activities in partnership with external vendors
- Lead inspection readiness planning, preparation, and execution activities
- Support regulatory submissions and health authority interactions
- Collaborate with cross-functional stakeholders across Clinical Operations, Biostatistics, Regulatory Affairs, and Medical teams
What we're looking for:
- Extensive Clinical Data Management experience within biotech, pharma, or CRO environments
- Previous Director-level or equivalent leadership experience
- Strong Subject Matter Expertise in Clinical Data Management
- Significant experience overseeing and managing CRO partnerships
- Experience supporting regulatory submissions and inspection readiness activities
- Proven ability to identify risks, resolve issues proactively, and drive high-quality outcomes
- Excellent stakeholder management and communication skills
- Strong understanding of clinical development processes and regulatory requirements
Why this opportunity?
- Lead Data Management activities for a late-stage Phase III programme approaching regulatory submission
- Play a pivotal role in inspection readiness and strategic regulatory milestones
- Join a growing and innovative biotechnology organisation
- Work closely with senior leadership and key decision-makers
- Fully remote working arrangement with minimal travel requirements
- Competitive salary, bonus, and share option scheme
Interested or know someone who could be a fit? Feel free to reach out directly or apply confidentially!
Director Data Management employer: Meet Life Sciences
As a Market Access Consultant with our client, you will be part of a dynamic team that values innovation and collaboration in the evolving healthcare landscape. The company offers a supportive work culture with opportunities for professional growth, including mentoring junior team members and leading impactful projects. With competitive compensation, hybrid working options, and comprehensive benefits, this role provides a meaningful opportunity to contribute to the expansion of European Value & Access capabilities while enjoying a fulfilling work-life balance.
