
Freelance Clinical Research Associate, Germany
Posted 6 days ago

Posted 6 days ago
This is a fully remote position, open to applicants in Germany.
• Responsible for the administration and monitoring of assigned clinical studies in accordance with Dokumeds, Sponsor Standard Operating Procedures, legal obligations, and ICH-GCP Guidelines.
• Conduct feasibility assessments for countries and sites.
• Perform site initiation, routine monitoring, and close-out visits.
• Prepare and submit documentation to Ethics Committees and Regulatory Authorities.
• Provide assistance in managing site contracts.
• A university degree in medicine, pharmacy, nursing, or life sciences, along with a minimum of 2 years of prior on-site monitoring experience in a CRO or pharmaceutical company; freelancing experience is considered a plus; familiarity with preparation and submissions to Ethics Committees/Regulatory Authorities is essential.
• Strong communication skills: Ability to demonstrate written, verbal, and presentation skills that effectively highlight the achievements of your work and those of Rho. Fluency in both English and local languages is required.
• Commitment to quality: Every position at Rho necessitates attention to detail, a thorough understanding of our high-quality scientific standards, and a genuine concern for all outcomes.
• High character: Contribute positively to our collaborative culture through honesty and integrity. At Rho, we appreciate a strong team spirit characterized by loyalty, accountability, and mutual trust. We collaborate effectively, work diligently, and share laughter. We take responsibility for our actions, forgive honest mistakes, and respect each other.
• Critical thinking: Rho values thoughtful analysis. Utilize your natural creativity, enhanced through our intellect, training, and experience. We assess situations and opportunities objectively and incisively, crafting innovative, practical solutions.
• Agility and adaptability: Rho values the ability to swiftly adapt. We proactively anticipate, respond to, and capitalize on changes in our environment. We embrace risk while managing it through planning and learning from both failures and successes. The capacity to adapt and evolve is invigorating.
• A valid driver's license and the willingness to travel.
• A role that offers daily exciting challenges within a highly qualified and international team.
• An employee-friendly work environment.
• Competitive salary.
• Opportunities for professional learning and growth in the field of Clinical Research.
Parexel
ICON plc
Precision Medicine Group
Worldwide Clinical Trials
Get handpicked remote jobs straight to your inbox weekly.