Senior Clinical Research Associate I

PSI CRO AG; München; Vor Ort; EUR 50.000 - 70.000; Vollzeit

Zusammenfassung

PSI CRO AG is seeking a Senior Clinical Research Associate I to enhance patient lives through clinical studies. This role involves conducting monitoring visits, managing site communications, and training junior CRAs. The position offers excellent working conditions and a commitment to professional development.

Leistungen

Excellent and flexible working conditions

Unique combination of team collaboration and independent work

Competitive salary and benefits package

Qualifikationen

• Independent on-site monitoring experience in Germany.
• Experience in monitoring visits in AMG studies, Phases II and/or III.
• Full working proficiency in German and English.

Aufgaben

• Conduct and report onsite and remote monitoring visits.
• Perform CRF review, source document verification, and query resolution.
• Assist in training of less expert CRAs.

Kenntnisse

Communication

Collaboration

Problem-solving

Planning

Multitasking

Ausbildung

College/University degree in Life Sciences

Tools

MS Office

Jobbeschreibung

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.

Job Description

As a Senior Clinical Research Associate I 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 inOncology, Hematology, Infectious / Rare / Gastro-intestinal Diseasesis 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.

Additional Information

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.