Freelance CRA, Ireland

3 weeks ago

Dublin, Dublin City, Ireland Rho, Inc. Full time
Overview

Rho, an award-winning, stable, full-service CRO known for its collaborative, dynamic culture based in the US, is quickly expanding their presence in Europe. We will deliver global full-service clinical development services and unmatched customer support – worldwide.

Join us in redefining what it means to work for a CRO. Working at Rho, you'll be joining a team who take healthcare and clinical research personally, with shared experiences that drive a passion to heal, cure and solve some of humanity's biggest challenges.

At Rho, we're 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, which has created 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 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.

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 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.
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 Pharma company; previous freelancing experience will be considered an advantage; previous experience in preparation and submissions to Ethics Committees / Regulatory Authorities.
  • Strong 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 attention to detail, a deep understanding of our high-quality scientific standards, and an ability to care about every outcome.
  • High-Character: Contribute to our collaborative culture with honesty and integrity. At Rho, we value a strong team spirit highlighted by loyalty, accountability, and mutual trust. We work smart together, we work hard together, and we laugh together. We take responsibility for our actions, forgive honest mistakes and respect one another.
  • Critical Thinker: Rho values thinking. Draw on your native ingenuity, sharpened and enhanced by our intellect, training, and experience. We evaluate situations and opportunities objectively and incisively; we then craft novel, practical solutions.
  • Agile and Adaptable: Rho values the ability to change quickly. We eagerly anticipate, respond to, and take advantage of changes in our environment. We embrace risk but manage it by planning, accepting, and learning from both failures and successes. The opportunity to adapt and evolve energizes us.
  • Driver license and ability to travel.

Please submit your CV in English. We're excited to hear 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.
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