Clinical Research Associate

Randstad Belgium; Berlin; Hybrid; EUR 83.000 - 124.000; Vollzeit

Zusammenfassung

Randstad Professional is seeking a Freelance Clinical Research Associate (CRA) Consultant to support a medical device trial in Germany. The role offers hybrid work with on-site hospital visits and flexible engagement ranging from 50% to 100% of a full-time position.

The successful candidate will manage investigator sites, conduct full-cycle monitoring visits, and travel regionally across central, northern, and western Germany, while coordinating with a dedicated CRA Resource Manager and Clinical

Qualifikationen

• 3–5 years of clinical monitoring experience in pharma or medical devices.
• Bachelor’s degree in Life Sciences or related field.
• Experience monitoring medical device studies is highly preferred.

Aufgaben

• Oversee and manage investigator sites with proactive sponsor communication.
• Independently conduct and manage key monitoring visits (site qualification, initiation, interim, close-out).
• Perform on-site monitoring across central, northern, and western Germany.
• Ensure compliance with protocols, regulatory requirements, and quality standards.
• Provide regular updates to Clinical Trial Leaders via email, calls, and meetings.

Kenntnisse

Clinical monitoring

Independent work

Travel

Ausbildung

Bachelor’s degree in Life Sciences

Jobbeschreibung

Freelance Clinical Research Associate (CRA) Germany – Medical Devices

Are you an experienced Clinical Research Associate looking for your next high-impact freelance project in the medical device sector? Do you thrive in a hybrid role that combines the comfort of working from home with the energy of on-site hospital visits?

Randstad Professional is seeking an autonomous Freelance Clinical Research Associate (CRA) Consultant to support our client in executing vital clinical monitoring activities. If you are a seasoned clinical research professional who excels at independent site management, this freelance assignment offers the opportunity to partner with a global healthcare leader and make a tangible impact on patient care.

Job Content

As a Freelance CRA, you will play a pivotal role in driving the success of clinical trials within the medical device sector. You will serve as the primary link between the sponsor and various investigator sites. This is a highly flexible freelance project with an average monthly resource requirement ranging from 50% to 100% of a full-time position. We welcome applicants with differing availabilities, as we may onboard two freelancers to share the project scope.

Your day-to-day operations will be fully supported by a dedicated CRA Resource Manager for onboarding, while project-specific milestones will be coordinated via regular, scheduled collaboration with Clinical Trial Leaders.

Job Qualifications

• Experience: Minimum of 3-5 years of clinical monitoring experience, with a proven track record of handling the main monitoring visit types (Site Qualification, Site Initiation, Interim Monitoring, and Close-Out).
• Education: Minimum of a Bachelor’s degree within a Life Science field.
• Industry Expertise: Previous experience monitoring medical device studies is highly preferred.

Responsibilities

• Comprehensive Site Management: Oversee and manage investigator sites, maintaining clear and proactive communication with site staff and the sponsor.
• Full-Cycle Monitoring Visits: Independently conduct and manage all key monitoring visit types, including Site Initiation Visits, Interim Monitoring Visits, and Close-out Visits.
• Regional Travel & On-Site Presence: Execute required on-site monitoring activities and hospital visits, which are primarily situated across central, northern, and western Germany.
• Compliance & Training: Actively participate in sponsor training and ensure all clinical trial activities strictly adhere to protocols, regulatory guidelines, and quality standards.
• Reporting: Deliver clear, ad-hoc, and scheduled updates via email, telephone calls, and meetings to Clinical Trial Leaders.