KCR Placement is a full-service functional sourcing and recruitment provider. We specialize in high-speed and high-quality talent sourcing for the CRO, Pharmaceutical, Biotech and Medical Device industries across Europe.
Our employees are KCR Placement's most crucial asset. We commit to placing our candidates at the center of all we do and prepare them for long-term career development and success with competitive benefits and vibrant work environment.
The KCR Placement team is supported by a specialized referral network of expert professionals and is dedicated to providing sourcing services and client support from job requisition to job offer.

On behalf of our partner, one of the global leaders in clinical research, we are seeking an experienced CRA to join their innovative and collaborative team.

As a CRA, you will collaborate with one of the world's leading pharmaceutical companies. With a diverse portfolio of medicines, this company has established a long-standing tradition of pioneering innovative treatments and preventive solutions worldwide.

Clinical Research Associate I, II/ Senior CRA

Location: Germany (home-based)

Main Responsibilities:

• Conducting site qualification, initiation, monitoring, and close-out visits for clinical trials;
• Ensuring protocol compliance, data integrity, and patient safety throughout the trial process;
• Collaborating with investigators and site staff to facilitate smooth study conduct;
• Performing data review and resolution of queries to maintain high-quality clinical data;
• Contributing to the preparation and review of study documentation, including protocols and clinical study reports.

Qualifications, Skills & Experience:

• Degree in medicine, science, or equivalent;
• Min. 1 year of direct monitoring experience;
• Fluent in Local Languages and English (verbal and written) and excellent communication skills, including the ability to understand and present technical information effectively;
• Excellent understanding and working knowledge of clinical research, phases of clinical trials, current GCP/ICH & country clinical research law & guidelines;
• Excellent understanding of Global, Country/Regional Clinical Research Guidelines and ability to work within these guidelines;
• Driver's license;
• Hands on knowledge of Good Documentation Practices;
• Demonstrated high level of monitoring skill with independent professional judgment.

Benefits:

• Various annual leave entitlements;
• A range of health insurance offerings to suit you and your family’s needs;
• Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead;
• Global Employee Assistance Program;
  
• Country-specific flexible benefits.

Our Privacy Policy

As KCR became part of the ICON group, your personal data will be shared with ICON and processed in accordance with privacy notice: https://www.iconplc.com/privacy/job-applicants

If you want your candidacy to be considered also for future recruitments, please send us an additional consent: “I agree to the processing of my personal data for any future recruitments conducted by ICON”. Such consent may be placed in your CV or electronic correspondence addressed to us. You can withdraw your consent at any time. Withdrawal of consent does not affect the legality of the processing carried out prior to its withdrawal.

KCR is an equal opportunity employer. In line with our motto, ‘We see human behind every number,’ KCR is committed to fostering an inclusive culture and maintaining a diverse, safe, and respectful working environment with equitable treatment for all.

We are committed to non-discriminatory practices and provide an equal opportunity for all qualified employees and job applicants within all employment sectors. We believe that in developing a desirable culture of belonging in which diverse perspectives and voices are welcomed and heard, the full potential of employees can be achieved.