Overview
Rho is an award-winning, stable, full-service Contract Research Organization (CRO) known for its collaborative and dynamic culture based in the US. We are expanding our presence in Europe to deliver global full-service clinical development services and unmatched customer support worldwide.
We are redefining what it means to work for a CRO. At Rho, you'll be part of a team that takes healthcare and clinical research personally, with shared experiences driving a passion to heal, cure, and solve humanity's biggest challenges.
We are committed to you just as you're committed to us. You'll have the opportunity to experience a thriving company with real stability – financial, workforce, and corporate – creating a safe environment to innovate and develop over a long and rewarding career. With a collaborative team of smart, talented, and positive people, you'll be celebrated and respected for your expertise and given the freedom to think creatively, challenge the norm, and problem-solve.
We are currently hiring a Freelance Clinical Research Associate in Ireland to join our amazing 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 the quality and integrity of data, compliance with relevant Standard Operating Procedures (SOPs) and regulatory requirements, and study completion on time.
We require 0.2 FTE - 0.3 FTE to start as soon as possible. The role will involve study start-up and site management activities in Ireland.
Responsibilities
* Site administration and site monitoring responsibility for assigned clinical studies according to Dokumeds and Sponsor SOPs, legal requirements, and International Council for Harmonisation Good Clinical Practice (ICH-GCP) Guidelines.
* Conduct country and site feasibility assessments.
* Perform site initiation, routine monitoring, and close-out visits.
* Prepare and submit documentation to Ethics Committees/Regulatory Authorities.
* Assist with site contract management.
Qualifications
* University degree in medicine, pharmacy, nursing, or life science, and at least 2 years of previous on-site monitoring experience in a CRO or pharmaceutical company. Previous freelancing experience is an advantage, as is experience with preparing and submitting documentation to Ethics Committees/Regulatory Authorities.
* Strong communication skills: demonstrate written, verbal, and presentation skills to showcase successes and achievements.
* Commitment to Quality: attention to detail, understanding of high-quality scientific standards, and care about every outcome.
* High-Character: contribute to a collaborative culture with honesty and integrity. Value a strong team spirit, loyalty, accountability, and mutual trust. Work smart together, work hard together, and laugh together.
* Critical Thinker: evaluate situations objectively and incisively, craft novel solutions, and adapt to changes in the environment.
* Agile and Adaptable: respond to changes, take calculated risks, plan, accept, and learn from failures and successes.
* Valid driver's license and ability to travel.
Please submit your CV in English. We look forward to hearing from you.
We offer:
* A job with daily exciting challenges in a highly qualified and international team.
* Employee-friendly work environment.
* Competitive salary.
* Opportunity to learn and grow professionally in the Clinical Research field.