Director Data Management
Meet Life Sciences ·
p strong Job Title: /strong Director, Data Management /p p strong Location: /strong Remote (UK) /p p strong Employment Type: /strong Full-time, Permanent /p p br /p p Were partnering with an innovative biotechnology organisation to appoint an experienced strong Director, Data Management /strong to provide strategic leadership and SME oversight across key clinical development programmes. /p p br /p p 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. /p p br /p p Youll 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. /p p br /p p strong
What youll be doing
/strong /p ul li Provide strategic leadership and Subject Matter Expert oversight across Clinical Data Management activities /li li Review study documentation, plans, deliverables, and processes to ensure quality and compliance /li li Identify risks, gaps, and process improvements proactively across ongoing programmes /li li Manage CRO performance, ensuring accountability for timelines, quality standards, and deliverables /li li Oversee database build activities in partnership with external vendors /li li Lead inspection readiness planning, preparation, and execution activities /li li Support regulatory submissions and health authority interactions /li li Collaborate with cross-functional stakeholders across Clinical Operations, Biostatistics, Regulatory Affairs, and Medical teams /li /ul p br /p p strong
What were looking for
/strong /p ul li Extensive Clinical Data Management experience within biotech, pharma, or CRO environments /li li Previous Director-level or equivalent leadership experience /li li Strong Subject Matter Expertise in Clinical Data Management /li li Significant experience overseeing and managing CRO partnerships /li li Experience supporting regulatory submissions and inspection readiness activities /li li Proven ability to identify risks, resolve issues proactively, and drive high-quality outcomes /li li Excellent stakeholder management and communication skills /li li Strong understanding of clinical development processes and regulatory requirements /li /ul p br /p p strong Why this opportunity? /strong /p ul li Lead Data Management activities for a late-stage Phase III programme approaching regulatory submission /li li Play a pivotal role in inspection readiness and strategic regulatory milestones /li li Join a growing and innovative biotechnology organisation /li li Work closely with senior leadership and key decision-makers /li li Fully remote working arrangement with minimal travel requirements /li li Competitive salary, bonus, and share option scheme /li /ul p br /p p Interested or know someone who could be a fit? Feel free to reach out directly or apply confidentially! /p p /p