Clinical Research Associate

🔥 14 hours ago

🇫🇮 Finland – Remote

⏰ Full Time

🟢 Junior

🟡 Mid-level

🧪 Clinical Research

👻 Ghost score 10%

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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, site initiation, monitoring, 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 apply problem-solving skills • Review trial performance and safeguard the rights and well-being of human subjects • 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 the completeness and quality of regulatory documentation • Perform site document verification • Manage site quality and delivery from site identification through close-out

🎯 Requirements

• Site Management experience or equivalent experience in clinical research • Understanding of clinical trials methodology and terminology • Excellent interpersonal, verbal, and written communication skills • Fluency in Finnish • Good/conversational level of Swedish • Educated to degree level, preferably in biological science, pharmacy, or another health-related discipline, or equivalent nursing qualification or other equivalent experience • Ability to conduct clinical site visits and manage site relationships • Knowledge of SOPs, protocols/amendments, GCP, and applicable regulatory requirements • Experience or ability to evaluate clinical data quality, site efficacy, and drug accountability • Experience or ability to monitor regulatory documentation and perform site document verification

🏖️ 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 • Consistent performance discussions and evaluations • Management support for career growth • Opportunities to progress into senior CRA roles, line management, Quality, Project Leadership, or other positions • Open team environment with regular clinical research team discussions and knowledge sharing