Senior CRA

🔥 1 minute ago

🇳🇴 Norway – Remote

⏰ Full Time

🟠 Senior

🧪 Clinical Research

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Parexel

WebsiteLinkedInAll Job Openings

10,000+ employees

Founded 1983

💼 Consulting

🏥 Healthcare

📦 Logistics

💰 Venture Round on 1990-01

Consulting • Healthcare • Logistics

Parexel is one of the world's largest clinical research organizations (CROs), providing comprehensive services for the clinical development process from Phase I to IV. The company specializes in portfolio management, clinical trial management, regulatory strategy, market access, and lifecycle management for biopharmaceuticals. Parexel aims to speed life-changing medicines to market by leveraging its clinical, regulatory, and therapeutic expertise. With a global team of over 21,000 professionals, Parexel works to integrate patient insights and innovative trial designs to develop treatments across therapeutic areas such as oncology, neuroscience, rare diseases, and more. It focuses on delivering patient-centric and efficient clinical trials.

📋 Description

• 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

• 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

• 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

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