Clinical Research Associate
ICON
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 of clinical development./ppAs a CRA II at ICON, you will design and analyze clinical trials, interpreting complex medical data, and contribute to the advancement of innovative treatments and therapies. This is a sponsor dedicated position looking for a candidate located in Central or Miami, FL./ppWhat You Will Do:/ppYou will contribute to clinical trial monitoring activities, taking responsibility for your deliverables and working collaboratively. Key responsibilities include:/pulliConducting site qualification, initiation, monitoring, and close-out visits for clinical trials./liliEnsuring protocol compliance, data integrity, and patient safety throughout the trial process./liliCollaborating with investigators and site staff to facilitate smooth study conduct./liliPerforming data review and resolution of queries to maintain high-quality clinical data./liliContributing to the preparation and review of study documentation, including protocols and clinical study reports./li/ulpYour Profile:/ppYou will bring relevant clinical trial monitoring experience, along with the following qualifications and skills. Required qualifications and experience:/pulliBachelors degree in a scientific or healthcare-related field./liliMinimum of 2 years of experience as a Clinical Research Associate./liliIn-depth knowledge of clinical trial processes, regulations, and ICH-GCP guidelines./liliStrong organizational and communication skills, with attention to detail./liliAbility to work independently and collaboratively in a fast-paced environment./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
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- ...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
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- ...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...Remote work
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- ...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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$19.47 - $22 per hour
...Clinical Research Assistant B The clinical research assistant will work with the Penn Center for Quantitative Echo and the Penn Cardio-Oncology clinical research program to support ongoing research projects. The research assistant will be responsible for logging and...Hourly payWork at officeLocal areaFlexible hours$22 - $25 per hour
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