Clinical Research Associate

4w1 month ago

Rho

DE · Contract · €55,000 – €75,000

About this role

Join Rho as a Freelance Clinical Research Associate in Germany. You will be part of a team redefining what it means to work for a CRO. Rho is not your typical CRO; curiosity is encouraged and collaboration is at the heart.

Site administration and monitoring responsibilities include conducting country and site feasibility, site initiation, routine monitoring, and close-out visits. You will also prepare submissions to Ethics Committees/Regulatory Authorities and assist in site contract management.

At Rho, you become part of the Rho Factor—a community of science nerds who love tackling big challenges together. Expect geeky jokes, spontaneous brainstorms, and a supportive environment where people genuinely care about their work and each other.

This role offers the opportunity to thrive in a stable company with financial and workforce stability. Join a group where many have made their best career moves in terms of contentment, financial rewards, and career growth.

Requirements

University degree in medicine, pharmacy, nursing or life science and at least 2 years of previous on-site monitoring experience in CRO or Pharma company; previous freelancing experience considered an advantage; experience in preparation and submissions to Ethics Committees/Regulatory Authorities.
Strong communicator with written, verbal, and presentation skills; fluency in both English and local languages.
Committed to quality with attention to detail and deep understanding of high-quality scientific standards.
High-character with honesty, integrity, team spirit, loyalty, accountability, and mutual trust.
Critical thinker with native ingenuity and ability to evaluate situations objectively and craft novel solutions.
Agile and adaptable with ability to change quickly, embrace risk, plan, and learn from failures.
Valid driver license and ability to travel.

Responsibilities

Take responsibility for site administration and monitoring for assigned clinical studies, following Dokumeds and Sponsor SOPs, legal requirements, and ICH-GCP Guidelines.
Conduct country and site feasibility assessments.
Perform site initiation, routine monitoring, and close-out visits.
Prepare and submit documents to Ethics Committees and Regulatory Authorities.
Assist in site contract management.

Benefits

A job with daily exciting challenges in a highly qualified and international team.
Employee-friendly work environment.
Opportunity to learn and grow professionally in the Clinical Research field.