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Senior Clinical Research Associate
Precision For Medicine. Monitor and own the progress of clinical studies at investigative sites .
Core Competencies
Role fitCore Competencies
Use this summary to align your resume positioning with the role.
Demonstrates expertise in monitoring and managing clinical studies, ensuring compliance with protocols and regulations, and effectively training junior staff. Proficient in conducting pre-study activities and interacting with clients while managing financial aspects of clinical trials.
Highest-signal resume keywords
CRA Certification5+ Years CRA/SCRA ExperienceIVD ExperienceFluency in Spanish and EnglishStudy Start-Up Activities Experience
ATS Keywords
Tailor your resumeApplicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard Skills
Clinical Study MonitoringRegulatory SubmissionsProtocol ComplianceSOPs AdherenceICH-GCP KnowledgeClinical Trial ManagementFinancial ManagementStudy Initiation VisitsInvestigator IdentificationClinical Trial Coordination
Soft Skills
Client InteractionTraining and MentoringTeam Collaboration
Certifications & Qualifications
CRA Certificate
Industry Keywords
CROPharmaceuticalBiotechnologyMedical DeviceOncologyInfectious DiseasesGastrointestinal StudiesEuropean Clinical TrialsDomestic TravelInternational Travel
About the role
Key responsibilities & impact- Monitor and own the progress of clinical studies at investigative sites
- Ensure clinical studies are conducted, recorded, and reported according to protocol, SOPs, ICH-GCP, and applicable regulations and standards
- Coordinate activities required to set up and monitor studies
- Identify investigators and help prepare regulatory submissions
- Conduct pre-study and initiation visits
- Handle appropriately sized clinical trials
- Support larger clinical trials with clinical study teams
- Train and mentor junior staff members
- Interact directly with clients
- Initiate payments
- Participate in proposal activities, including development and client presentations
Requirements
What you’ll need- 4-year college degree or equivalent experience
- Holder of CRA certificate
- Minimum 5 years of CRA/SCRA experience within a CRO, pharmaceutical, biotechnology, or medical device environment
- Extensive experience in IVD (In Vitro Diagnostics), oncology, infectious diseases and gastrointestinal studies
- Proven experience monitoring studies across multiple European countries
- Availability for domestic travel including overnight stays, up to approximately 50–60% travel commitment
- International travel may be required for some senior level positions
- Fluency in Spanish and English is required
- Additional language(s) considered an asset
- Study start-up activities experience preferred
- Understanding of financial management preferred for Senior CRAs
Benefits
Comp & perks- Fully home-based within Spain
- Professional development
- Career growth opportunities
- Empowerment to make an impact
- Meaningful client relationships
- Equal opportunity employment
- Reasonable accommodation during the application process