Senior Clinical Research Associate

Precision For Medicine

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

Posted 9/21/2026full-timeRemote • United KingdomSeniorWebsite

Core Competencies

Role fit

Core Competencies

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Demonstrates expertise in monitoring and managing clinical studies, ensuring compliance with protocols, SOPs, and regulations. Proficient in training and mentoring staff while effectively interacting with clients and managing study-related activities.

Highest-signal resume keywords

CRA CertificationClinical Trial MonitoringRegulatory SubmissionsStudy Start-Up ActivitiesFinancial Management

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Clinical Study ManagementProtocol ComplianceICH-GCP StandardsTherapeutic Area ExperienceRegulatory KnowledgeData ReportingInvestigator IdentificationTrial CoordinationPre-Study VisitsInitiation Visits

Soft Skills

Client InteractionTeam CollaborationMentoringCommunicationProblem Solving

Certifications & Qualifications

CRA Certificate

Industry Keywords

CROPharmaceuticalBiotechnologyMedical DeviceClinical TrialsSOPsScientific DisciplineHealthcare Discipline

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 and helping 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, with approximately 50–60% travel commitment
International travel may be required for some senior-level positions
Fluency in English and the local language
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, build meaningful client relationships, and grow their careers
Professional development opportunities
Fully home-based work within the United Kingdom
Equal opportunity employment
Reasonable accommodation support during the application process