Clinical Research Associate (Germany)

Allucent; Deutschland; Hybrid; EUR 52.000 - 70.000; Vollzeit

Benefits dieser Stelle

Comprehensive benefits per location

Competitive salaries per location

Flexible working hours

Opportunity for remote/office-based*"

Leadership and mentoring opportunities

Buddy Program

Career progression

Employee referral program

Zusammenfassung

Allucent is seeking a Clinical Research Associate (CRA) to join our team in Germany. You will independently monitor investigational sites, manage relationships with investigators, and ensure trial execution aligns with protocol, SOPs, and GCP.

You will travel across Germany, support regulatory affairs and site activation, and uphold trial integrity while collaborating with a mature team dedicated to advancing therapies.

Qualifikationen

• Experience leading monitoring activities in complex trials.
• Strong understanding of ICH-GCP and regulatory guidelines.
• Clear and confident communicator in English and German.
• Willingness to travel, as required (8 DOS per month).

Aufgaben

• Independently monitor investigational sites across study phases and ensure data quality.
• Build and maintain strong site relationships with investigators.
• Support regulatory affairs, site activation, and startup activities.
• Escalate site issues to maintain trial integrity and patient safety.

Kenntnisse

CRA experience

GCP/ICH knowledge

English/German bilingual

Travel readiness

Jobbeschreibung

About Allucent™

At Allucent™, our mission is to shine a light on new therapies that improve lives. When you join our team, you’ll use your unique skills, expertise, and knowledge to forge meaningful partnerships with clients while helping them turn groundbreaking ideas into life-changing treatments.

If you’re passionate about advancing pharmaceuticals and biologics, fueled by an entrepreneurial spirit, and eager to collaborate with top minds across science, business, and operations, we’d love to connect. Together we can accelerate innovation and grow side by side, making a last impact on patients worldwide.

Together we SHINE. Find more information about our values.

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, pro-actively detect issues, 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 aspectsof monitoring for assigned clinical trials across study phases, including site initiation, routine monitoring, and close-out visits.
• Ensure compliancewith 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 aroundregulatory affairs, site activationandstudy-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 ofICH-GCPandregulatory guidelines.
• Clear and confident communicator inEnglish and German.
• Comfortable working independently and managing priorities.
• Willingness to travel, as required (8 DOS 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.