Clinical Research Associate / Senior Clinical Research Associate

PSI CRO

1d • Hybrid

About The Position

Join a highly motivated, international team as a Clinical Research Associate or Senior Clinical Research Associate. This role is hybrid in Munich/Planegg or home-based in Germany. You will conduct and report onsite and remote monitoring visits, review case report forms (CRFs), perform source document verification, resolve queries, and manage site communications. You may also contribute to site identification and, depending on experience, help train less experienced CRAs.

The position offers ownership of assigned studies, including responsibility for site strategy, performance, and delivery. You will work across multiple sponsors and therapeutic areas, with a focus on fewer protocols, deeper study involvement, strong site relationships across Germany and, where applicable, Switzerland, and complex, scientifically engaging trials. The role emphasizes autonomy, quality, collaboration, and opportunities to develop broader project leadership skills.

The company is a privately owned, mid-sized CRO founded in 1995, with more than 3,000 employees. It offers structured onboarding, continuous mentoring, internal career progression, technologically integrated systems, flexible working conditions, and a supportive international team focused on quality delivery and long-term development.

Requirements

• College or university degree in Life Sciences, or an equivalent combination of education, training, and experience.
• Independent on-site monitoring experience in Germany.
• Independent experience conducting all types of monitoring visits in AMG studies, Phase II and/or Phase III.
• Full professional proficiency in German and English.
• Advanced proficiency in MS Office applications.
• Ability to plan, multitask, and work in a dynamic team environment.
• Communication, collaboration, and problem-solving skills.
• Ability to travel and a valid driver’s license.

Nice To Haves

• Experience in Switzerland.
• Experience in Oncology, Hematology, Infectious Diseases, Rare Diseases, or Gastro-intestinal Diseases.
• French or Italian language skills.

Responsibilities

• Conduct and report all types of onsite monitoring visits and remote visits.
• Perform CRF review, source document verification, and query resolution.
• Manage site communication and site management.
• Participate in the site identification process.
• Depending on experience, assist in training less experienced CRAs.
• Take the lead for assigned studies, including site strategy, performance, and delivery.
• Build and maintain strong site relationships across Germany and, where applicable, Switzerland.

Benefits

• Excellent and flexible working conditions that support work-life balance.
• Competitive salary and comprehensive benefits package.
• Structured onboarding with hands-on mentoring and continuous support.
• Clear career development opportunities and visible internal growth paths.
• Supportive international team and a culture of trust, visibility, and recognition.
• Technologically integrated work environment with in-house systems designed to reduce administrative burden.
• Stable environment where long tenures are common and career building is encouraged.

What This Job Offers

• Job Type: Full-time
• Career Level: Mid Level