Senior Clinical Research Associate

Precision Medicine Group

. Monitor and own the progress of clinical studies at investigative sites .

Posted 9/21/2026full-timeRemote • Germany, Poland, Hungary, United Kingdom, FranceSeniorWebsite

Core Competencies

Role fit

Core 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 and mentoring junior staff. Proficient in regulatory submissions and financial management within clinical trial environments.

Highest-signal resume keywords

CRA CertificationClinical Trial MonitoringRegulatory SubmissionsStudy Start-Up ActivitiesFluency in English

ATS Keywords

Tailor your resume

Applicant Tracking System Keywords

Tip: use these terms in your resume and cover letter to boost ATS matches.

Hard Skills

Clinical Study ManagementProtocol ComplianceICH-GCP StandardsTherapeutic Area ExperienceFinancial Management

Soft Skills

Client InteractionTeam CollaborationMentoring

Certifications & Qualifications

CRA Certificate

Industry Keywords

CROPharmaceuticalBiotechnologyMedical DeviceClinical Trials

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, applicable regulations, and standards
Coordinate activities required to set up and monitor studies
Identify investigators
Help prepare regulatory submissions
Conduct pre-study and initiation visits
Handle appropriately sized clinical trials
Support clinical study teams on larger-scope trials
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
Experience monitoring clinical trials across a variety of therapeutic areas
Availability for domestic travel including overnight stays, 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 language(s) considered an asset
Graduate or postgraduate degree with a concentration in a scientific or healthcare discipline preferred
Study start-up activities experience preferred
Understanding of financial management preferred for Senior CRAs

Benefits

Comp & perks

Employees are empowered to make an impact
Meaningful client relationships
Career growth opportunities
Professional development
Highly collaborative and quality-focused environment
Fully home-based work within Germany