Clinical Research Associate / Senior Clinical Research Associate

PSI CRO; München; Hybrid; EUR 55.000 - 75.000; Vollzeit

Zusammenfassung

A clinical research organization in Munich is seeking a Clinical Research Associate / Senior Clinical Research Associate to conduct monitoring visits and ensure quality standards in clinical studies. The ideal candidate will possess a degree in Life Sciences, independent monitoring experience, and fluency in German and English. This role offers competitive salary, flexible working conditions, and opportunities for professional growth.

Leistungen

Excellent working conditions

Flexible work schedule

Competitive salary and benefits package

Qualifikationen

• Full working proficiency in German and English is required.
• Experience in Oncology, Hematology, and Rare Diseases is a plus.
• Ability to travel with a valid driver's license.

Aufgaben

• Conduct onsite and remote monitoring visits.
• Perform CRF review and source document verification.
• Manage site communication and identification process.

Kenntnisse

Independent monitoring experience

Communication skills

Collaboration

Problem-solving skills

Ausbildung

College/University degree in Life Sciences

Tools

MS Office

Jobbeschreibung

Clinical Research Associate / Senior Clinical Research Associate

• Full-time

We are the company that cares – for our staff, for our clients, for our partners and for the quality of the work we do. A dynamic, global, mid-size company founded in 1995, we bring together more than 2,800 driven, dedicated and passionate individuals. We work on the frontline of medical science, changing lives, and bringing new medicines to those who need them.

As a Senior / Clinical Research Associate at PSI you will be involved in improving patients' lives while enjoying a variety of monitoring tasks and working on clinical studies in different therapeutic indications, maintaining the highest quality standards in the industry.

Office-based in Munich/Planegg or Home-based in Germany

You will:

• Conduct and report all types of onsite monitoring visits as well as remote visits.
• Perform CRF review, source document verification and query resolution.
• Be responsible for site communication and management.
• Be involved in site identification process.
• Assist in training of less expert CRAs, depending on your level of experience.

Qualifications

• College/University degree in Life Sciences or an equivalent combination of education, training & experience.
• Independent on-site monitoring experience in Germany.
• Independent experience in all types of monitoring visits in AMG studies, Phases II and/or III.
• Experience in Oncology, Hematology, Infectious / Rare / Gastro-intestinal Diseases is a plus.
• Full working proficiency in German, English and MS Office applications.
• Ability to plan, multitask and work in a dynamic team environment.
• Communication, collaboration, and problem-solving skills.
• Ability to travel and valid driver’s license.

As a privately owned mid-size CRO, we are constantly growing, offering plenty of opportunities for personal and professional growth. With no investors to please, our management focuses on company culture and operational delivery over quarter-to-quarter profitability.

Make the right call and take your career to a whole new level. Join a company that focuses on its people and invests in their professional development and success.

Our extensive onboarding and mentorship program will prepare you to fulfil your tasks with the highest standards, offering you:

• Excellent and flexible working conditions.
• A unique combination of team collaboration and independent work.
• Competitive salary and benefits package.

If you'd like to hear more about PSI, our organic growth and company culture, and learn more about the studies that we run and our high repeat and referral business rates, please apply for this vacancy.