Clinical Research Associate, Experienced

🔥 2 minutes ago

🇦🇹 Austria – Remote

⏰ Full Time

🟢 Junior

🟡 Mid-level

🧪 Clinical Research

👻 Ghost score 12%

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Medpace

WebsiteLinkedInAll Job Openings

5001 - 10000 employees

Founded 1992

🏥 Healthcare

💼 Consulting

📦 Logistics

Healthcare • Consulting • Logistics

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 • Communicate with medical site staff, including coordinators, clinical research physicians, and site staff • Verify investigator qualifications, training, resources, facilities, laboratories, equipment, and staff • Verify medical records and research source documentation against case report form data • Inform site staff of entry errors and ensure good documentation practices • Communicate protocol deviations according to SOPs, GCP, and applicable regulatory requirements • Verify that investigators enroll only eligible subjects • Review regulatory documents • Manage medical device and/or investigational product/drug accountability and inventory • Verify and review adverse events, serious adverse events, concomitant medications, and corresponding illnesses • Assess site patient recruitment and retention and offer improvement suggestions • Complete monitoring reports and follow-up letters, summarizing findings, deviations, deficiencies, and recommended corrective actions

🎯 Requirements

• Must have a minimum of a university degree in a health or life science related field • Minimum 1.5 years of previous experience as a CRA • Approximately 60-80% travel in Germany, Austria and Switzerland • Proficient knowledge of Microsoft® Office and general computer literacy • Outstanding communication and presentation skills • Must be detail-oriented and efficient in time management • Excellent verbal and written communication skills in English and German • Proven experience in clinical patient management, protocol, CRF, preparing ISF, and documentation to be submitted to competent authorities • Application must be submitted in English

🏖️ Benefits

• Competitive compensation programs that recognize and reward performance • Comprehensive health, wellness, retirement, and PTO benefits • Office based environment with on-site mentors • Defined career paths with clear advancement opportunities • Industry renowned onboarding and training programs designed to accelerate professional development • Ongoing training and continuous learning opportunities throughout your career • An environment that encourages employees to influence change, contribute ideas, and grow quickly • Company-sponsored social events • Occasional WFH that provides flexibility for eligible positions after training

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