Senior Clinical Research Associate - Medical Device

Senior Clinical Research Associate - Surgical Device - Central Region At ICON Strategic Solutions, you will work in a sponsor-dedicated model, supported by ICON’s global expertise. As the world’s largest FSP organisation, with over 90 sponsor partnerships, we offer stability, career development and a collaborative environment where your work contributes to the development of treatments that benefit patients worldwide. You will lead on clinical trial monitoring tasks requiring technical depth, with a focus on quality and continuous improvement. Monitoring clinical trial sites to ensure adherence to study protocols, regulatory requirements, and Good Clinical Practice (GCP) standards. Conducting site visits to assess site performance, resolve issues, and provide support to ensure successful trial execution. Collaborating with cross-functional teams to ensure timely and accurate data collection and reporting. Providing training and guidance to site staff and other CRAs to maintain high standards of clinical trial conduct. Building and maintaining effective relationships with site personnel and stakeholders to facilitate smooth trial operations. You will have a strong foundation in clinical trial monitoring, with the experience of working independently and guide others. A bachelor’s degree is required, preferably a Bachelor of Science Degree in Life Science, Physical Science, Nursing or Biological Science.

• 3-5 years of CRA monitoring experience in CRO/pharma environments
• Strong preference for at least 1 year of medical device monitoring experience- however, complex pharma monitoring experience will be considered.
• Strong problem-solving skills to mitigate risks and identify issues at sites and implement effective solutions promptly.
• Strong interpersonal skills to establish and maintain effective working relationships with site personnel, investigators, and internal teams.
• A well-executed plan for communication with the study teams and sites.
• Well-versed in clinical trial management. Willingness to travel as required (approximately 60%)

Employment with ICON is contingent upon having the legal right to work in the country where the role is based. ICON offers a competitive and comprehensive total rewards package designed to support your health, wellbeing, and career development. Competitive base salary and performance related incentives Health and wellbeing programmes including medical, dental, and vision coverage where applicable Retirement and pension plans Life assurance and disability coverage Employee assistance programmes and wellbeing resources Learning and development opportunities through structured training and career pathways Visit our careers site to read more about the benefits ICON offers. Inclusion and Accessibility We are committed to building an inclusive and accessible workplace where everyone feels valued and supported.