Freelance Clinical Research Associate (Germany)

TN Germany; Deutschland; Vor Ort; EUR 45.000 - 70.000; Vollzeit

Zusammenfassung

Join a forward-thinking company redefining the role of Clinical Research Organizations. As a Freelance Clinical Research Associate, you'll manage all aspects of study site management while ensuring data quality and compliance with regulations. This role offers a supportive community and opportunities for professional growth in an exciting and dynamic environment. Embrace challenges and contribute to impactful projects that shape the future of clinical research. If you're passionate about making a difference and thrive in a collaborative atmosphere, this is the perfect opportunity for you.

Leistungen

Employee-friendly work environment

Opportunities for professional growth

Daily exciting challenges in a highly qualified team

Qualifikationen

• At least 2 years of on-site monitoring experience in CRO or Pharma.
• Experience with ethics and regulatory submissions is a plus.

Aufgaben

• Manage site administration and monitoring for clinical studies.
• Conduct feasibility assessments and site initiation visits.
• Ensure compliance with SOPs and regulatory requirements.

Kenntnisse

On-site monitoring experience

Strong communication skills

Critical thinking

Attention to detail

Adaptability

Ausbildung

University degree in medicine

University degree in pharmacy

University degree in nursing

University degree in life sciences

Jobbeschreibung

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Freelance Clinical Research Associate (Germany), de

Client: Rho Inc

Location: de, Germany

Job Category: Other

EU work permit required: Yes

Job Reference: a18f2b9f623b

Job Views: 2

Posted: 05.05.2025

Expiry Date: 19.06.2025

Job Description:

Join us in redefining what it means to work for a CRO.

When you work at Rho, it’s more than just a job—you become part of the Rho Factor. We’re a proud bunch of science nerds who love tackling big challenges together. We’re not your typical CRO, and we’re not trying to be. Here, curiosity is encouraged, fresh approaches are welcome, and collaboration is at the heart of everything we do.

Whether you’re a data wizard, analytical genius, healthcare advocate, project mastermind, or any other role, you’ll fit right into the equation of the Rho Factor. Expect plenty of geeky jokes, eccentric personalities, spontaneous brainstorms, and a supportive community where people genuinely care about their work—and each other.

You’ll have the opportunity to experience a thriving company with real stability - financial, workforce, and corporate, which has created a safe environment to innovate and develop over a long and rewarding career.

We are currently hiring a Freelance Clinical Research Associate in Germany to join our team! In this role, you will manage all aspects of study site management including site selection, initiation, routine monitoring, close-out, and maintenance of study files. You’ll also ensure data quality and integrity, compliance with SOPs and regulatory requirements, and timely, within-budget study completion.

Our Clinical Operations team reports that joining Rho has been one of their best career moves in terms of contentment, financial rewards, and growth, contributing to our stability.

What You Will Be Doing:

• Site administration and monitoring for assigned clinical studies according to Dokumeds, Sponsor SOPs, legal requirements, and ICH-GCP guidelines
• Conducting country and site feasibility assessments
• Site initiation, routine monitoring, and close-out visits
• Preparing and submitting documents to Ethics Committees/Regulatory Authorities
• Assisting in site contract management

Requirements

• University degree in medicine, pharmacy, nursing, or life sciences and at least 2 years of on-site monitoring experience in CRO or Pharma; freelancing experience is a plus; experience with ethics and regulatory submissions.
• Strong communication skills: written, verbal, and presentation skills; fluency in English and local languages.
• Attention to detail and commitment to high-quality scientific standards.
• High character: honesty, integrity, teamwork, loyalty, accountability, mutual trust, and respect.
• Critical thinking: ability to evaluate situations objectively and craft practical solutions.
• Adaptability: willingness to respond to and embrace change, managing risks effectively.
• Driver's license and ability to travel.

Please submit your CV in English. We look forward to hearing from you!

We offer:

• Daily exciting challenges in a highly qualified, international team
• Employee-friendly work environment
• Opportunities for professional growth in Clinical Research