Medpace
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.
Entry-Level Clinical Research Associate – Clinical Study Coordinator Experience Required
🔥 24 minutes ago
🗣️🇩🇪 German Required
📊 Check your resume score for this job
Improve your chances of getting an interview by checking your resume score before you apply.
Medpace
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 at research sites in compliance with the approved protocol • Communicate with medical site staff including coordinators, clinical research physicians, and their site teams • Verify investigator qualifications, training, and resources, including facilities, laboratories, equipment, and staff • Verify medical records and research source documentation against case report form data; inform site staff of entry errors, ensure good documentation practices, and communicate protocol deviations per SOPs, GCP, and applicable regulatory requirements • Perform on-site and virtual/remote monitoring using a risk-based monitoring approach (including centralized data review) through the integrated Clinical Trial Management System to identify site deviations/deficiencies and implement corrective/preventive actions to restore compliance and mitigate future risks • Confirm investigators enroll only eligible subjects • Review regulatory documentation • Manage medical device and/or investigational product/drug accountability and inventory • Review and verify adverse events, serious adverse events, concomitant medications, and related illnesses to ensure accurate reporting per the protocol • Assess clinical site patient recruitment and retention performance and recommend improvements • Complete monitoring reports and follow-up letters, including summaries of significant findings, deviations, deficiencies, and recommended actions to achieve compliance
🎯 Requirements
• Bachelor’s degree in a health- or science-related field (minimum) • Experience as a Clinical Research Coordinator • Ability to travel 60–70% within the DACH region • Proficient with Microsoft® Office • Detail-oriented with strong time-management skills • Excellent verbal, written, and presentation skills in German and English
🏖️ Benefits
• Dynamic work environment with varied day-to-day responsibilities • Broad experience across multiple therapeutic areas • Work within a team of therapeutic and regulatory experts • Clear CRA career progression with opportunities for mentoring and management roles • Competitive compensation with potential for a substantial travel bonus • Flexible work hours across different days of the week • In-house travel agents • Ongoing therapeutic training provided by in-house physicians who are medical and regulatory experts
Apply Now
