• Job Description

  Req#: 2274

  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.

  Our Clinical Team will tell you, joining Rho has been one of their best career moves in terms of contentment, financial rewards and career growth, which is why we have such stability in the group!

  Responsibilities

  Conduct Clinical study according to Sponsor requirements based on excellent knowledge of Good Clinical Practice, Protocol and applicable regulations:

  • Serve as your country’s clinical research industry subject matter expert
  • Plan and perform Site visits (SIV, SMV and SCOV) and site management activities to ensure compliance with Project Management plan and Protocol
  • Help to plan and perform Country and Site Feasibility, including assessment of potential Risks and challenges, as well as select Study sites and perform pre-study visits
  • Assist in selection of Study specific Vendors and perform Vendor assessments
  • Support in negotiation and execution of Investigator/ Institution contracts
  • May help to prepare documents submission to Ethics Committee, Competent Authorities and other bodies (as applicable), including communication with Sponsor, EC/ CA and other involved parties
  • Provide input in supportive Study specific processes, e.g., Study supplies management, patient reimbursement management etc.

  Qualifications

  • 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 study start-up experience, including but not limited to country and site feasibility, Investigator/ Institution agreement management, submissions to Ethics Committees/ Regulatory Authorities (including initial submissions) is preferred; Advanced knowledge of applicable country clinical research regulatory guidelines and ICH-GCP guidelines

  • 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 an 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!

  A few more things to know about us:

  Benefits: Rho provides a comprehensive benefits package for all benefit-eligible employees, and generous paid time off, holidays, parental leave and bereavement leave.

  Flexibility: We encourage a work-life balance that allows employees to bring their best selves to work while being passionate about their lives outside work.

  #LI-Remote

  #LI-CC1

  #ClinicalOperations

• About the company

  Our integrated team of experts ensure consistent trials that run smarter and more efficiently from development through submissions and publishing.

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