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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, SOPs, and ICH-GCP standards. Proficient in training and mentoring staff while effectively interacting with clients and managing regulatory submissions.
Highest-signal resume keywords
CRA CertificateClinical Trial MonitoringRegulatory SubmissionsTherapeutic Area ExperienceFinancial Management
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 ManagementProtocol ComplianceSOP AdherenceStudy Setup CoordinationPre-Study VisitsInitiation VisitsClinical Trial HandlingProposal DevelopmentClient PresentationsTravel Availability
Soft Skills
MentoringClient InteractionTeam Support
Certifications & Qualifications
CRA Certificate
Industry Keywords
CROPharmaceuticalBiotechnologyMedical DeviceICH-GCPClinical ResearchStudy Start-Up Activities
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 study setup and monitoring activities
- Identify investigators
- Help prepare regulatory submissions
- Conduct pre-study and initiation visits
- Handle appropriately sized clinical trials
- Support larger clinical study teams
- Train and mentor junior staff members
- Interact directly with clients
- Initiate payments
- Participate in proposal activities, including development and client presentations
- Build the company’s network of experienced clinical research professionals for future project requirements
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
- Experience monitoring clinical trials across a variety of therapeutic areas
- Availability for domestic travel including overnight stays, with approximately 50–60% travel commitment
- International travel may be required for some senior-level positions
- Fluency in English and the local language is required
- Additional languages considered an asset
- Preferred: graduate or postgraduate degree in a scientific or healthcare discipline
- Preferred: study start-up activities experience
- Preferred for Senior CRAs: understanding of financial management
- Please apply in English
Benefits
Comp & perks- Employees are empowered to make an impact
- Build meaningful client relationships
- Career growth opportunities
- Professional development
- Collaborative environment
- Quality-focused environment
- Accountability-focused environment
- Fully home-based work within Hungary
- Equal Opportunity Employer