Senior Clinical Research Associate I

PSI CRO; Deutschland; Vor Ort; EUR 50.000 - 90.000; Vollzeit

Zusammenfassung

An established industry player is seeking a Senior Clinical Research Associate I to join their dynamic team. This role offers the opportunity to improve patients' lives through a variety of monitoring tasks across clinical studies. You will be responsible for conducting onsite and remote visits, managing site communication, and training less experienced colleagues. With a focus on company culture and professional growth, this position provides excellent working conditions and a competitive salary package. If you're ready to elevate your career in a supportive environment, this opportunity is perfect for you.

Leistungen

Flexible working conditions

Team collaboration

Independent work

Competitive salary and benefits package

Qualifikationen

• Independent on-site monitoring experience in Germany.
• Full working proficiency in German and English.

Aufgaben

• Conduct and report all types of onsite and remote monitoring visits.
• Responsible for site communication and management.

Kenntnisse

Monitoring Skills

Communication Skills

Problem-solving Skills

Multitasking

Team Collaboration

Ausbildung

College/University degree in Life Sciences

Tools

MS Office

Jobbeschreibung

Company Description

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

You will:

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

Qualifications

1. College/University degree in Life Sciences or an equivalent combination of education, training & experience.
2. Independent on-site monitoring experience in Germany.
3. Independent experience in all types of monitoring visits in AMG studies, Phases II and/or III.
4. Experience in Oncology, Hematology, Infectious / Rare / Gastro-intestinal Diseases is a plus.
5. Full working proficiency in German, English and MS Office applications.
6. Ability to plan, multitask and work in a dynamic team environment.
7. Communication, collaboration, and problem-solving skills.
8. 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:

1. Excellent and flexible working conditions.
2. A unique combination of team collaboration and independent work.
3. 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.