Senior CRA

Parexel

. Conduct qualification visits, site initiation visits, monitoring visits, and termination visits at assigned clinical sites .

Posted 11/6/2026full-timeRemote • NorwaySeniorWebsite

Core Competencies

Role fit

Core Competencies

Use this summary to align your resume positioning with the role.

Demonstrates expertise in conducting clinical site visits, ensuring compliance with GCP and regulatory requirements, and developing patient recruitment strategies. Strong communication skills in multiple languages enhance relationship-building with clinical sites and staff.

Highest-signal resume keywords

Clinical Research Associate ExperienceGCP CompliancePatient Recruitment StrategiesInterpersonal Communication SkillsFluency in Norwegian

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Clinical Research KnowledgeSite MonitoringData Quality EvaluationRegulatory Documentation ManagementSite Document Verification

Soft Skills

Excellent Verbal CommunicationExcellent Written Communication

Industry Keywords

SOP ComplianceHuman Subjects ProtectionClinical Trial PerformanceSite Integrity OversightBiological Science Degree

Tech Stack

Tools & technologies

Google Cloud Platform

About the role

Key responsibilities & impact

Conduct qualification visits, site initiation visits, monitoring visits, and termination visits at assigned clinical sites
Generate visit and contact reports
Build and maintain relationships with clinical sites and staff
Address and resolve site issues and questions as the site's sole point of contact
Oversee study integrity and promote rapport with sites
Review trial performance and safeguard human subjects' rights and well-being
Develop patient recruitment strategies with clinical sites to meet enrollment timelines
Ensure compliance with SOPs, protocols/amendments, GCP, and applicable regulatory requirements
Evaluate reported data quality and integrity, site efficacy, and drug accountability
Monitor completeness and quality of regulatory documentation
Perform site document verification
Manage site quality and delivery from site identification through close-out

Requirements

What you’ll need

Experienced Clinical Research Associate
Excellent interpersonal, verbal, and written communication skills
Fluent in Norwegian
Good level of Swedish and Danish
Educated to degree level in biological science, pharmacy, or another health-related discipline, or equivalent nursing qualification or other equivalent experience
Knowledge of clinical research
Compliance with GCP, applicable regulatory requirements, protocols/amendments, and standard operating procedures

Benefits

Comp & perks

World class technology and training catered to individual experience
Less travel and a lower protocol load compared to industry peers
Bonus incentive program
Opportunity to work within multiple therapeutic areas
Career advancement opportunities in clinical research
Flexible work arrangement