Clinical Research Associate (m/w/d)

About the Opportunity

You will join an internationally active CRO with a strong focus on oncology. The role is being filled directly and is offered as a permanent full-time position.

The hiring partner is a specialized personnel services provider operating across Germany, connecting professionals and managers in IT and life sciences. The firm uses long-standing industry expertise to create tailored staffing solutions and help clients attract strong talent.

Key Responsibilities

• Prepare for, carry out, and follow up on pre-study, initiation, monitoring, and close-out visits in line with the trial monitoring plan.
• Track site performance and support trial sites with recruitment activities and study-related queries.
• Work closely with medical, project management, quality management, and data management teams to keep the study running smoothly.
• Support sites with audit and inspection preparation and accompany them through audits and inspections.

Candidate Profile

Applicants should bring a completed degree in a scientific or medical field, or a vocational background in a medical profession, ideally supplemented by additional training as a CTA, CRA, or in a similar qualification path.

Experience in clinical research and familiarity with GCP and ICH guidelines are expected. The position also calls for careful, precise handling of study data and regulatory requirements.

You should enjoy working across disciplines, communicating with international partners, and be willing to travel within Germany. Excellent written and spoken German and English are required.

Additional Information

All positions are offered through direct placement and as permanent employment contracts.