Clinical Research Associate (Germany)

Allucent; München; Vor Ort; EUR 60.000 - 80.000; Vollzeit

Benefits dieser Stelle

Comprehensive benefits package

Competitive salaries

Flexible Working hours

Training budget

Remote working opportunities

Leadership and mentoring opportunities

Buddy Program

Career progression opportunities

Employee referral program

Online training access

Spot Bonus Award Program

Loyalty Award Program

Zusammenfassung

Allucent is seeking a Clinical Research Associate (CRA) in Munich, Germany. The CRA will manage monitoring activities, ensuring compliance with trial protocols and regulatory standards. The candidate should have at least 5 years of experience in clinical research, particularly in oncology or rare diseases, with strong communication skills in both English and German. Benefits include flexible working hours, competitive salaries, and opportunities for internal growth and professional development.

Qualifikationen

• Minimum of 5 years’ experience in clinical research, ideally in oncology or rare diseases.
• Strong understanding of GCP and regulatory guidelines.
• Ability to manage priorities and work independently.

Aufgaben

• Independently manage all aspects of monitoring for assigned clinical trials.
• Ensure compliance with protocols, GCP, ICH, SOPs, and regulatory requirements.
• Build strong site relationships as the primary contact.
• Identify and resolve site issues to maintain trial integrity.

Kenntnisse

Monitoring activities in complex trials

Communication in English

Communication in German

Understanding of ICH-GCP

Regulatory guidelines knowledge

Independent working

Jobbeschreibung

The role

Bring your monitoring expertise to the forefront of innovation. We are looking for a Clinical Research Associate (CRA) to join our A-team. As a CRA at Allucent, you will independently control and monitor investigational sites, proactively detect issues, and provide solutions to ensure clinical studies are performed according to the trial protocol and in compliance with SOPs, applicable regulations, and the principles of Good Clinical Practice.

As a CRA, you will take the lead on monitoring activities, owning your sites and relationships with investigators. You’ll be the bridge between sponsor and site, ensuring trial integrity while being supported by a collaborative, experienced team. This includes work related to regulatory affairs, site activation processes—including contracting and start‑up activities—to ensure smooth and compliant study execution. You will travel throughout Germany.

Main responsibilities

• Independently manage all aspects of monitoring for assigned clinical trials across study phases, including site initiation, routine monitoring, and close‑out visits.
• Ensure compliance with protocols, GCP, ICH, SOPs, and applicable regulatory requirements.
• Build strong site relationships, acting as a primary point of contact and ensuring high‑quality data collection.
• Identify and resolve site issues, escalating as needed to maintain trial integrity and patient safety.
• Activities around regulatory affairs, site activation and study‑startup.

To be successful you will possess:

You’re an experienced CRA ready to take the next step with a company that truly values your expertise and independence. You thrive in an agile, collaborative environment and want to be part of a team making a real impact.

• Experience leading monitoring activities in complex trials, ideally in oncology or rare disease with a minimum of at least 5 years’ experience.
• Strong understanding of ICH‑GCP and regulatory guidelines.
• Clear and confident communicator in English and German.
• Comfortable working independently and managing priorities.
• Willingness to travel, as required (8 days out of residence per month).

Benefits of working at Allucent™ include:

• Comprehensive benefits package per location
• Competitive salaries per location
• Departmental Study/Training Budget for furthering professional development
• Flexible Working hours (within reason)
• Opportunity for remote/office‑based working depending on location
• Leadership and mentoring opportunities
• Participation in our enriching Buddy Program as a new or existing employee
• Internal growth opportunities and career progression
• Financially rewarding internal employee referral program
• Access to online soft‑skills and technical training via GoodHabitz and internal platforms
• Eligibility for our Spot Bonus Award Program in recognition of going above and beyond on projects
• Eligibility for our Loyalty Award Program in recognition of loyalty and commitment of longstanding employees

Disclaimers:

*Office‑based employees are required to work in‑office no less than two (2) days per each work week. There are certain positions for which employees are required to work in‑office no less than three (3) days per each work week for employees within reasonable distance from one of our global offices.