Senior Clinical Research Associate

divh2Senior Clinical Research Associate - Home Based - France/h2pICON plc is a world-leading healthcare intelligence and clinical research organization. Were proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development./ppWe are currently seeking a Senior Clinical Research Associate (CRA) to join our diverse and dynamic team. As a Senior CRA at ICON Plc, you will play a critical role in overseeing and managing clinical trial activities to ensure they are conducted according to protocol, regulatory requirements, and industry standards. You will contribute to the success of clinical trials by ensuring data integrity, participant safety, and compliance throughout the study lifecycle./ppWhat You Will Be Doing:/pulliMonitoring clinical trial sites to ensure adherence to study protocols, regulatory requirements, and Good Clinical Practice (GCP) standards./liliConducting site visits to assess site performance, resolve issues, and provide support to ensure successful trial execution./liliCollaborating with cross-functional teams to ensure timely and accurate data collection and reporting./liliProviding training and guidance to site staff and other CRAs to maintain high standards of clinical trial conduct./liliBuilding and maintaining effective relationships with site personnel and stakeholders to facilitate smooth trial operations./li/ulpYour Profile:/pulliAdvanced degree in a relevant field such as life sciences, nursing, or medicine./liliExtensive experience as a Clinical Research Associate, with a strong understanding of clinical trial processes and regulatory requirements./liliProven ability to manage multiple sites and projects simultaneously, with strong organizational and problem-solving skills./liliExpertise in monitoring practices, data integrity, and site management, with proficiency in relevant clinical trial software and tools./liliExcellent communication, interpersonal, and stakeholder management skills, with the ability to influence and drive compliance within a complex environment./liliAbility to travel at least 60% of the time (international and domestic - fly and drive) and should possess a valid drivers license./li/ulpRequired Skills:/pulliPhase I Oncology Expertise: Strong background in early-phase oncology trials, including safety, PK/PD, and dose-escalation studies./liliIndication-Specific Knowledge: Experience with breast, ovarian, prostate, and pancreatic cancer clinical trials./liliInvestigational Product Familiarity: Prior exposure to PARP inhibitors (a plus but not mandatory)./liliTraditional Monitoring Model: Solid skills and proficiency in on-site monitoring, full source data verification, IP accountability and regulatory compliance./liliTrip Report Writing: Proven ability to produce detailed, accurate, and timely monitoring visit reports. Extensive experience working with a CTMS platform (Siebel CTMS, Veeva Vault CTMS, Medidata CTMS, Oracle Clinical/Clinical One, or others)./li/ulpWhat ICON can offer you:/ppOur success depends on the quality of our people. Thats why weve made it a priority to build a diverse culture that rewards high performance and nurtures talent./ppIn addition to your competitive salary, ICON offers a range of additional benefits. Our benefits are designed to be competitive within each country and are focused on well-being and work life balance opportunities for you and your family./ppOur benefits examples include:/pulliVarious annual leave entitlements/liliA range of health insurance offerings to suit you and your familys needs./liliCompetitive retirement planning offerings to maximize savings and plan with confidence for the years ahead./liliGlobal Employee Assistance Programme, TELUS Health, offering 24-hour access to a global network of over 80,000 independent specialized professionals who are there to support you and your familys well-being./liliLife assurance/liliFlexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidized travel passes, health assessments, among others./li/ulpAt ICON, inclusion belonging are fundamental to our culture and values. Were dedicated to providing an inclusive and accessible environment for all candidates. ICON is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status./ppIf, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know or submit a request here./ppInterested in the role, but unsure if you meet all of the requirements? We would encourage you to apply regardless theres every chance youre exactly what were looking for here at ICON whether it is for this or other roles./p/div