Senior Clinical Trial Monitor & Site Leadership
ICON Strategic Solutions
Sr. Clinical Research Associate - South East 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 the future of clinical development. As 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. What You Will Do: You will lead on clinical trial monitoring tasks requiring technical depth, with a focus on quality and continuous improvement. Key responsibilities include: 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. Your Profile: You will have a strong foundation in clinical trial monitoring, with the experience to work independently and guide others. Required qualifications and experience: Bachelor's degree in a relevant scientific discipline or healthcare-related field Extensive experience as a Clinical Research Associate, with a strong understanding of clinical trial processes and regulatory requirements. Proven ability to manage multiple sites and projects simultaneously, with strong organizational and problem-solving skills. Expertise in monitoring practices, data integrity, and site management, with proficiency in relevant clinical trial software and tools. Excellent communication, interpersonal, and stakeholder management skills, with the ability to influence and drive compliance within a complex environment. Willingness to travel as required (approximately 60%) What ICON can offer you: Our success depends on the quality of our people. That’s why we’ve made it a priority to build a diverse culture that rewards high performance and nurtures talent. In 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. Our benefits examples include: Various annual leave entitlements A range of health insurance offerings to suit you and your family’s needs. Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead. Global Employee Assistance Programme, LifeWorks, offering 24-hour access to a global network of over 80,000 independent specialized professionals who are there to support you and your family’s well-being. Life assurance Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidized travel passes, health assessments, among others. Visit our careers site to read more about the benefits ICON offers. At ICON, inclusion & belonging are fundamental to our culture and values. We’re 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. If, 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 Interested in the role, but unsure if you meet all of the requirements? We would encourage you to apply regardless - there’s every chance you’re exactly what we’re looking for here at ICON whether it is for this or other roles. Are you a current ICON Employee? Please click here to apply #J-18808-Ljbffr ICON Strategic Solutions
$240k - $275k
...Job Description Senior Director, Medical Monitor, Hematology-Oncology... ...Hybrid) Department: Clinical Development -... ...key contributor to trial design, safety evaluation... ...Provide senior clinical leadership from trial startup... .... Participate in site feasibility,...SeniorWebsite$114k - $210.9k
...Health Commercial LLC is seeking an experienced Clinical Trial Manager to oversee site management and ensure compliance in... ...should possess a Bachelor's degree or RN, leadership skills, and expertise in clinical monitoring. The position offers a competitive salary range...SeniorWebsite$114k - $210.9k
Syneos Health/inVentiv Health Commercial LLC is seeking an experienced Clinical Trial Manager to oversee site management and clinical monitoring. The role requires strong leadership skills, a background in site management, and a solid understanding of regulatory compliance...SeniorWebsite- ...A leading organization in clinical research is seeking a Clinical Research Associate... ...role involves significant travel, monitoring clinical sites, and maintaining robust documentation... ...background in clinical research with leadership skills and a keen attention to detail...SeniorWebsiteRemote work
- ...ICON Strategic Solutions is looking for a Clinical Research Associate who will lead clinical trial monitoring with a focus on quality and continuous improvement. The... ...individual will ensure adherence to protocols and conduct site visits to support successful trial execution. The...SeniorWebsite
- ...A leading clinical research organization is seeking a CRA II to manage study sites and ensure compliance with protocols. Responsibilities... ...site visits, and preparing monitoring reports. The ideal candidate... ..., particularly in oncology trials. A 4-year degree in a life...SeniorWebsiteNight shift
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$79.72k - $119.58k
...Description The Senior Clinical Research Monitor is responsible for performing ongoing internal reviews... ...product compliance) for IRB approved trials conducted by Tisch Cancer Institute.... ...and/or Clinical Research Support Unit Leadership, audits of clinical trials. Assists...SeniorTraineeshipRemote work$95.17k - $156.36k
...Senior Analyst – Cyber Risk & Control Monitoring Do you want to be part of a collaborative Cybersecurity Governance... ...goals. Through skill-building, leadership development and philanthropic opportunities... ..., refer to the Guardian Careers site. Visa Sponsorship Guardian...SeniorWebsiteFull timeWork at officeVisa sponsorshipWork visaFlexible hours3 days per week$95.17k - $156.36k
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$140k - $165k
...Summit-Therapeutics is seeking a Senior Manager, Clinical Site Partner (CSP) to lead operational aspects of clinical trials across the United States. This remote position demands... ...The ideal candidate will have exceptional leadership and organizational skills, with a proven...SeniorWebsiteRemote work- ...Corgan is looking for a Senior Healthcare Planner to join their Healthcare team in the United States. This role emphasizes leading healthcare... ..., extensive experience in healthcare planning, and strong leadership skills. This full-time role requires presence in the office...SeniorWebsiteFull timeWork at officeMonday to Friday
- ...Services. This role entails overseeing clinical project teams, driving efficiencies,... ...or equivalent, 10+ years in clinical trials, and strong leadership skills. The opportunity offers a... ...Eastern U.S., and the possibility of travel for site meetings. #J-18808-Ljbffr...SeniorWebsiteRemote work
$134.4k - $219.2k
Initial Therapeutics, Inc. is seeking a Senior Manager, Global Site Start-Up Lead to drive site activation for high-profile clinical trials. The role requires extensive experience... ...drug development process and strong leadership skills. In addition to overseeing CRO performance...SeniorWebsite- ...architecture firm in New York is seeking a Senior Project Manager to join their Data Centers team. In this full-time on-site position, you'll lead project initiatives, manage... ...at least 12 years of experience, and strong leadership abilities. Join a firm committed to...SeniorWebsiteFull time
$114k - $210.9k
...Commercial LLC is looking for an Experienced Clinical Trial Manager to oversee site management and ensure compliance with trial protocols. This role requires strong leadership skills, expertise in clinical trial monitoring, and the ability to resolve conflicts effectively...SeniorWebsite$175k - $200k
...advisory-focused investment bank. Our team of senior professionals delivers a wide array of... ...professional to serve as Head of Monitoring & Assurance. This individual will be responsible... ...framework (SEC and FINRA) ~ Prior leadership experience managing a monitoring team...SeniorWebsiteWork at office$115k - $125k
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...A clinical research organization is seeking a Clinical Research Associate II to oversee study site management in a remote capacity. Ideal candidates will have a degree in a scientific... ...CRA experience, especially in oncology trials. The role requires excellent...WebsiteRemote work- ...Alira Health Boston, LLC is seeking a dedicated Site Monitor to ensure compliance and the quality of clinical trials. This role involves performing site monitoring visits, providing training, and collaborating across teams to maintain high standards of clinical trial...Website
- ...GForce Life Sciences to source a skilled Clinical Site Lead (CSL). The CSL will oversee... ...maintenance, data collection, and field monitoring to ensure compliance with protocols, regulations... ...academic field. 10+ years of clinical trial monitoring experience required....WebsiteLocal areaRemote workWork from home
$30 - $40 per hour
Join Us in Shaping the Future of Clinical Research Adams Clinical is a leading clinical trial site network committed to accelerating the development of life-changing... ...seeking a Per Diem Assistant Psychedelic Dosing Monitor to support clinical trials focused on...WebsiteHourly payDaily paid3 days per week$160 - $180 per hour
...Contract Description The Medical Monitor tasks include: Provide clinical development support including Phase... ...and reporting of clinical trials and related regulatory deliverables... ...assessments Promptly engage with site staff if/when an SAE arises to ensure...WebsiteHourly payContract workFor contractorsRemote work
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