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Precision Medicine Group

Senior Clinical Research Associate

Precision Medicine Group

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

Posted 9/21/2026full-timeRemote • Hungary, Poland, United Kingdom, France, GermanySeniorWebsite

Core Competencies

Role fit
Core Competencies

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Demonstrates expertise in monitoring and managing clinical studies, ensuring compliance with protocols and regulations, and effectively training and mentoring junior staff. Proficient in coordinating study activities and engaging with clients while managing travel commitments.

Highest-signal resume keywords
CRA CertificationClinical Trial MonitoringRegulatory SubmissionsStudy Start-Up ActivitiesFluency in English

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills
Clinical Study ManagementICH-GCP ComplianceSOP AdherenceTherapeutic 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, and applicable regulations and standards
  • Coordinate activities required to set up and monitor studies, including identifying investigators, helping prepare regulatory submissions, and conducting 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

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, up to 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
  • Fully home-based within Hungary
  • Professional development opportunities
  • Opportunity to train and mentor junior staff members
  • Equal opportunity employment
  • Reasonable accommodation support for applicants with disabilities