Clinical Research Associate, Virtual Event

Medpace

Clinical Research Associate role at Medpace with a focus on drug and medical device development. Engaging in comprehensive monitoring and training to ensure compliance and efficiency.

Posted 6/7/2026full-timeRemote • 🇩🇪 GermanyJuniorWebsite

Tech Stack

Tools & technologies

Google Cloud Platform

About the role

Key responsibilities & impact

Travelling to study sites (Germany-wide) to conduct qualification, initiation, monitoring, and closeout visits 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

What you’ll need

Must have a minimum of a Bachelor’s degree in a health or science related field
Experience as a Clinical Research Coordinator (1 year)
Ability to travel 60-70% to locations in the DACH region is required; some visits may be conducted remotely
Proficient knowledge of Microsoft® Office
Strong communication and presentation skills
Must be detail-oriented and efficient in time management
Excellent verbal and written communication skills in German and English.

Benefits

Comp & perks

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

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills & Tools

clinical researchdata verificationprotocol complianceadverse event reportingmedical record verificationinvestigator qualificationspatient recruitmentmonitoring reportsdocumentation practicesregulatory document review

Soft Skills

communication skillspresentation skillsdetail-orientedtime managementinterpersonal skills

Certifications

Bachelor's degree in health or science related field