Clinical Engagement Lead - Western Europe
$88,000–$107,900 year
On-site · Barcelona, Catalonia, Spain
Job Summary
Clinical Engagement Lead, field-based senior clinical development professional responsible for building and managing investigator and site relationships across Western Europe (Spain, France, United Kingdom, and other Western European countries) to support Beeline Medicines’ clinical trial portfolio. Acts as primary site-facing liaison with investigators, academic medical centers, and research sites; leads site identification, feasibility, activation, enrollment optimization, and ongoing engagement; provides region-wide scientific engagement and field intelligence to Clinical Development, Medical Affairs, and Commercial teams; collaborates with MSLs and supports patient recruitment and study execution; requires strong immunology/inflammation knowledge, GCP/ICh/FDA compliance, driver’s license, 50%+ travel, and ability to work evenings/weekends as needed. Offers flexible/hybrid work arrangements and significant travel within assigned geography.
Required Qualifications
- Bachelor's degree in scientific or related discipline required
- Advanced degree preferred—MS or MPH in a relevant clinical, biomedical, or pharmaceutical sciences discipline
- 8+ years of experience in clinical development, clinical research, clinical operations, or a field-based clinical engagement role within the pharmaceutical or biotech industry
- Demonstrated experience managing investigator relationships and supporting clinical trial site activation and enrollment
- Experience in immunology, inflammation, or a related therapeutic area strongly preferred
- Experience collaborating with CROs, investigative sites, and field medical teams, including MSL partnerships
- Strong scientific and clinical knowledge of immunology and inflammation — including disease biology, standard of care, clinical trial design considerations, and the competitive clinical research landscape across relevant I&I indications
- Expertise in clinical trial site management and investigator engagement — including site feasibility assessment, investigator identification and qualification, site initiation support, and enrollment optimization strategies
- Working knowledge of GCP requirements, ICH guidelines, and FDA regulations governing investigator interactions, clinical site oversight, and field-based clinical development activities
- Highly self-directed field professional — manages a complex investigator portfolio independently, prioritizes site engagement activities strategically, and operates with minimal supervision across a broad geography
- Relationship-driven and trusted clinical trial resource — builds genuine, long-term partnerships with investigators and site staff based on scientific credibility, reliability, and authentic commitment to supporting research excellence
- Proactive field intelligence contributor — consistently translates field observations into actionable insights that improve program strategy, site selection, and enrollment performance
- Professional fluency in English (written and verbal) required
- Ability to safely and successfully operate a motor vehicle is required. Valid Driver’s License and a driving record in compliance with company standards
- Position may require ability to travel 50%+ as needed of time or more including occasional overnight stay driven by business need
- Must be able to work evenings and weekends, as needed, for physician or patient events (both in person and virtual)
- Depending on geography, must have the ability to manage a multi-state territory with diverse customer base
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