Sr. Manager/Director, Clinical Trial Site Engagement
San Francisco
Permanent
USD135000 - USD200000
Clinical Development
PR/511195_1745367397
Sr. Manager/Director, Clinical Trial Site Engagement
Sr. Manager/Director, Clinical Trial Site Engagement
San Francisco, CA - On-site
$135,000 - $200,000
I am working with a Bay area Neurology Biotech looking for a seasoned Clinical Trial Site Engagement Director to spearhead patient recruitment and enrollment strategies for their growing clinical trial pipeline. My client is a growing, patient focused biotech with indications in CNS. The ideal candidate will have a proven track record of meeting and exceeding enrollment timelines while upholding quality and compliance standards, and have worked extensively with CNS patient populations.
Responsibilities
- Formulate detailed, data-driven enrollment strategies for CNS clinical trials
- Set realistic site-level enrollment targets based on historical data and current landscape analysis
- Deploy innovative recruitment methods tailored to specific patient groups
- Conduct root cause analysis for enrollment issues and develop targeted intervention plans
- Work with cross-functional teams to align enrollment strategies with overall program timelines
- Perform regular site performance reviews using established metrics and KPIs
- Lead productive, solution-focused meetings with sites to tackle enrollment barriers
- Develop and implement site-specific enrollment acceleration plans for underperforming sites
- Provide specialized training and resources to enhance site recruitment capabilities
- Make data-driven decisions regarding site additions or closures based on enrollment performance
- Collaborate with medical, regulatory, and operational teams to implement protocol amendments that could enhance enrollment feasibility
- Work with data management teams to monitor and analyze enrollment metrics
- Partner with finance to optimize resource allocation for recruitment initiatives
- Coordinate with CROs and vendors to ensure alignment on enrollment strategies and performance expectations
- Present enrollment status and forecasts to senior leadership and stakeholders
Qualifications
- Advanced degree required (PhD, PharmD, or MD) in life sciences, healthcare, or related field
- Additional certifications in clinical research or project management (PMP, CCRA) highly desirable
- Minimum 7-10 years of clinical research experience with at least 5 years focused on enrollment management
- Demonstrated expertise in CNS trials, particularly in ADHD, depression, and/or Alzheimer's disease
- Proven success in accelerating enrollment in complex, competitive clinical trial environments
- Experience managing adolescent/pediatric recruitment challenges
- Track record of developing and implementing innovative recruitment strategies
- Experience with global trials preferred
- In-depth understanding of CNS disorder patient pathways and treatment landscapes
- Familiarity with diagnostic criteria and assessment tools for ADHD, depression, and cognitive disorders
- Knowledge of age-specific recruitment challenges and solutions (adolescent, geriatric populations)
- Understanding of regulatory considerations for recruitment in vulnerable populations
- Expertise in analyzing enrollment metrics and forecasting models
If you feel you are a good fit for the role, please don't hesitate to apply!