We’re a proud bunch of science nerds who love tackling big challenges together. Whether you’re a data wizard, analytical genius, 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 chance 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 Finland for circa. In this role, you will have the opportunity to manage all aspects of study site management including site selection, initiation, routine monitoring, close‑out and maintenance of study files.

You’ll also ensure the quality and integrity of data, compliance with relevant SOPs and regulatory requirements and study completion on time and within budget. Site administration and site monitoring responsibility for assigned clinical studies according to Dokumeds and Sponsor Standard Operating Procedures, legal requirements and ICH‑GCP Guidelines Conduct of country and site feasibility Site initiation,



routine monitoring and close‑out visits Preparation and submissions to Ethics Committees/Regulatory Authorities Assistance in site contract management 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 will be considered as an advantage; previous experience in preparation and submissions to Ethics Committees / Regulatory Authorities.

Robust Communicator: Demonstrate written, verbal and presentation skills to help showcase the successes of your work and Rho’s. Fluency in both English and local languages.

Committed to Quality: Every job at Rho requires an attention to detail, a deep understanding of our high‑quality scientific standards, and an ability to care about every outcome. Draw on your native ingenuity, sharpened and enhanced by our intellect, training, and experience.

Agile and Adaptable: Rho values the ability to change quickly. We embrace risk but manage it by planning, accepting, and learning from both failures and successes. Driver license and ability to travel Please submit your CV in English. A job with daily exciting challenges in a highly qualified and international team Competitive salary Opportunity to learn and grow professionally in Clinical Research field #

📌 Freelance Clinical Research Associate (Finland) (Ontario)
🏢 RHO
📍 Ontario