Sr. Clinical Research Associate
ICON
divh2Senior CRA - Ophthalmology/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./ppAs a Senior CRA at ICON Plc, you will oversee and manage clinical trial activities to ensure they are conducted according to protocol, regulatory requirements, and industry standards./ppWhat You Will Do:/ppYou will lead on clinical trial monitoring tasks requiring technical depth, with a focus on quality and continuous improvement. Key responsibilities include:/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:/ppYou will have a strong foundation in clinical trial monitoring, with the experience to work independently and guide others. Required qualifications and experience:/pulliBachelors degree in a relevant scientific discipline or healthcare-related field/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./liliOphthalmology experience required/liliWillingness to travel as required (approximately 60%)/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
ICON- ...company is seeking an experienced CRA II or Senior CRA to support clinical trials. This role involves site qualification, monitoring, and... ...benefits aimed at work-life balance in an inclusive environment. A passion for high-quality research is essential. #J-18808-Ljbffr...SeniorRemote work
- ...A global clinical research organization is looking for a Clinical Research Associate to conduct site evaluations and ensure compliance during clinical trials. This role requires a Bachelor's degree in a relevant field and experience in independent monitoring. Successful...SeniorRemote work
- ...ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment... ...of GCP, local laws and regulations, assigned protocols and associated protocol specific procedures including monitoring guidelines...SuggestedLocal areaFlexible hoursNight shift
$91.34k - $114.17k
...Clinical Research Associate, Sponsor Dedicated ICON plc is a world-leading healthcare intelligence and clinical research organization. We're proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape...SuggestedWork experience placementFlexible hours- Senior Clinical Research Associate - Oncology ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape...SuggestedFlexible hours
- ...Clinical Research Associate job at ICON. Blue Bell, PA. CRA II OR Senior CRA (home-based in the U.S.) What you will be doing Conducting site qualification, initiation, monitoring, and close-out visits for clinical trials. Ensuring protocol compliance, data integrity, and...Work from homeFlexible hours
- ...divh2Clinical Research Associate/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...
- Clinical Research Associate - Baltimore, MD/Philadelphia, PA ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our...Flexible hours
- ...Clinical Research Associate Responsible for providing Clinical Research support for all clinical trials. Under the direction of supervisor or designee, this position will serve as support for the clinical study team. Essential Duties And Responsibilities Participate...
$71.9k - $169.3k
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