Medpace
Biotechnology • Healthcare Insurance • Pharmaceuticals
Medpace is a full-service contract research organization (CRO) that accelerates the development of safe and effective medical therapeutics. The company offers a comprehensive range of services to biopharmaceutical companies, including clinical trial management, regulatory affairs, and integrated laboratory services. With expertise across various therapeutic areas, Medpace facilitates collaboration among medical professionals to optimize the clinical development process and enhance trial efficiency.
Clinical Research Associate, Entry and Experienced Level
September 4
🗣️🇸🇪 Swedish Required
Medpace
Biotechnology • Healthcare Insurance • Pharmaceuticals
Medpace is a full-service contract research organization (CRO) that accelerates the development of safe and effective medical therapeutics. The company offers a comprehensive range of services to biopharmaceutical companies, including clinical trial management, regulatory affairs, and integrated laboratory services. With expertise across various therapeutic areas, Medpace facilitates collaboration among medical professionals to optimize the clinical development process and enhance trial efficiency.
📋 Description
• Conduct qualification, initiation, monitoring, and closeout visits for research sites in compliance with the approved protocol • Communication with the medical site staff including coordinators, clinical research physicians and their site staff • Verifying adequate investigator qualifications, training and resources, including facilities, laboratories, equipment, and staff • Medical record and research source documentation verification against case report form data, including informing the site staff of any entry errors, ensuring good documentation practices are being adhered to and communicating protocol deviations appropriately per SOPs, GCP and applicable regulatory requirements • Verification that the investigator is enrolling only eligible subjects • Regulatory document review • Medical device and/or investigational product/drug accountability and inventory • Verification and review of adverse events, serious adverse events, concomitant medications and corresponding illnesses to confirm accurate data reporting in accordance with the protocol • Assessing the clinical research site’s patient recruitment and retention success and offering suggestions for improvement • Completion of monitoring reports and follow-up letters, which includes providing summaries of the significant findings, deviations, deficiencies, and recommended actions to secure compliance.
🎯 Requirements
• Applicants must be fluent in Swedish and English • Minimum of a bachelor’s degree; Health or life science related field • 1 year clinical research experience minimum for Entry level • 1+ year direct and independent monitoring experience for any level above Entry CRA • Willing to travel approximately 40-60% in Sweden • Familiarity with Microsoft® Office • Strong communication and presentation skills a plus
🏖️ Benefits
• Flexible work environment • Competitive compensation and benefits package • Competitive PTO packages • Structured career paths with opportunities for professional growth • Company-sponsored employee appreciation events • Employee health and wellness initiatives • Awards Recognized by Forbes as one of America's Most Successful Midsize Companies in 2021, 2022, 2023 and 2024 • Continually recognized with CRO Leadership Awards from Life Science Leader magazine based on expertise, quality, capabilities, reliability, and compatibility
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