Clinical Research Associate
ICON
Clinical Research Associate - St Louis/Kansas City/Ohio 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. We are currently seeking a Clinical Research Associate to join our diverse and dynamic team. As a Clinical Research Associate at ICON, you will play a pivotal role in designing and analyzing clinical trials, interpreting complex medical data, and contributing to the advancement of innovative treatments and therapies. What you will be doing Conducting site qualification, initiation, monitoring, and close-out visits for clinical trials. Ensuring protocol compliance, data integrity, and patient safety throughout the trial process. Collaborating with investigators and site staff to facilitate smooth study conduct. Performing data review and resolution of queries to maintain high-quality clinical data. Contributing to the preparation and review of study documentation, including protocols and clinical study reports. Your profile Bachelor's degree in a scientific or healthcare-related field. Minimum of 9 months onsite monitoring experience as a Clinical Research Associate; level (CRA I, CRA II, or Senior CRA) determined by total years of experience. In-depth knowledge of clinical trial processes, regulations, and ICH-GCP guidelines. Strong organizational and communication skills, with attention to detail. Ability to work independently and collaboratively in a fast-paced environment. Ability to travel at least 60% of the time (international and domestic - fly and drive) and should possess a valid driver’s license. 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. 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. 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. 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. 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. #J-18808-Ljbffr
- ...language model-based system built to understand and assess clinical characteristics in EMRs. Synapsis AI is designed for installation... .... As a vital member of our diverse team, our Clinical Research Associates (CRA) will collaborate closely with the AI Research and software...SuggestedLocal areaFlexible hoursShift work
$71.9k - $189k
...out visits) in accordance with contracted scope of work and Good Clinical Practice. • Work with sites to adapt, drive, and track... ...Good knowledge of, and skill in applying, applicable clinical research regulatory requirements. • i.e., Good Clinical Practice (GCP)...SuggestedFull timePart timeLocal areaImmediate startWorldwide- ...Job Description As a Clinical Research Associate at PSI you will enjoy a variety of monitoring tasks and work on clinical studies in different therapeutic indications, maintaining the highest quality standards in the industry. You will: Act as the main line of communication...SuggestedWork visa
- ...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...Suggested
$91.5k - $137.3k
...involving start-up and study implementation, on-site monitoring of clinical research studies as well as on-going site management. Incumbents work... ...according to the protocol. Verifies issues or risks associated with blinded or randomized information related to IP. Applies...SuggestedContract workLocal areaRemote workNight shift- ...Overview As a clinical research associate (CRA), you are responsible for completing clinical research and administrative tasks for clients. You facilitate documentation for clinical research. As a CRA, you monitor clinical tasks for correct functioning and completion,...RelocationVisa sponsorship
$84.5k - $162k
...AbbVie, please visit us at . Job Description Covering the NJ/PA Area Advance AbbVie's pipeline by striving for excellence in clinical research, turning science into medicine for our patients and leveraging new advanced capabilities to drive industry leading performance...Contract workTemporary workLocal area$115k - $125k
...Piper Companies is seeking a Clinical Research Associate (CRA) to join a global leader in clinical research and healthcare analysis for a remote permanent position located based out of CST . The Clinical Research Associate (CRA) will travel to sites 8-10 days out of the...Permanent employmentWork at officeRemote work- ...Summary In this Clinical Research Associate role (may be contract or full‑time employee), you will be responsible for monitoring the progress of clinical studies, either at investigative sites or remotely, and ensure clinical trials are conducted, recorded, and reported...Full timeContract workInterim roleLocal areaRemote work
- ...Clinical Research Associate I Required Qualifications Bachelor's degree (foreign equivalent or higher). In lieu of a Bachelor's degree, a combination of clinical/healthcare, medical type industry setting and/or human research experience totaling four (4) years full-time...Daily paidFull timeWork at officeLocal areaVisa sponsorshipWork visaShift work
$91.34k - $114.17k
...ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment... ...Advert Posting We are currently seeking a Clinical Research Associate to join our diverse and dynamic team. As a Clinical Research...Work experience placementFlexible hours- ...Summary The Breast Center at Baylor College of Medicine is seeking a skilled Clinical Research Associate. The ideal candidate will facilitate communication between requestors and providers of breast cancer-related human biospecimens. The Coordinator executes the decisions...
$91.34k - $114.17k
...Clinical Research Associate - Oncology - Connecticut 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...Work experience placementLocal areaVisa sponsorshipFlexible hours$100k - $110k
...Piper Companies is seeking a Clinical Research Associate II to join a global organization within the clinical research and life sciences industry for a remote permanent role with 60-75% travel across the United States. This CRA II will support cardiovascular, CNS, and...Permanent employmentRemote work$100k - $125k
...Yoh is seeking a passionate and motivated clinical research professional to join our team of specialized clinical talent. We work with industry... ...want to connect with you! Position Title Clinical Research Associate Opportunity Details Opportunity Type: Direct Full Time...Full timeRemote work- ...Clinical Research Associate I/II Benefits include: Medical, Dental, and Vision Insurance, 401(k), Stock Options NOTE: You must have a minimum of 3-5 years prior experience combined in-house and field monitoring to be considered for this position (medical device experience...Local areaRemote workWorldwide
$125k - $145k
...work, Alira Health SOPs and regulatory requirements, i.e. Good Clinical Practice (GCP) and International Conference on Harmonization (ICH... ...utilizing the filing index and medidata as necessary. Supports research sites with local Institutional Review Board (IRB)/Ethics...Contract workLocal areaRemote workFlexible hours- ...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...Flexible hours
- ...Kelly Science and Clinical FSP is currently seeking a Regional Clinical Research Associate for a long-term engagement in the US with one of our Global Medical Device clients. This person will join our Kelly FSP (Functional Service Provider) division, a managed solution...Full time
$108.7k - $139.8k
...All Jobs Senior Clinical Research Associate The Senior Clinical Research Associate is a senior individual contributor and leader within the EBR Clinical organization, accountable for monitoring excellence, data integrity, and site engagement across the full lifecycle...Contract workWork at officeRemote workNight shift- ...Senior Clinical Research Associate - Cardio (Smartpulse A-fib) - All Regions 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...Flexible hours
- ...for a CRA/Sr CRA in the US. Oncology Experience required. Cell therapy experience is strongly preferred. Job Purpose The Clinical Research Associate (CRA) has local responsibility for the delivery of the studies at allocated sites and is an active participant in the local...Local areaRemote workFlexible hoursShift work
$38 - $40 per hour
...exclusive features. Direct message the job poster from Baim Institute for Clinical Research Director, Human Resources at Baim Institute for Clinical Research The Sr. Clinical Research Associate/Field Monitor Contractor performs remote and on-site visits, such as, Qualification...Part timeFor contractorsInterim roleRemote workWork from home10 hours per week- ...We are working with a fast growing organization who is seeking to bring on experienced Clinical Research Associates located nationwide. The role requires limited to no travel and offers a tremendous opportunity to partner with a growing, high-quality and innovative team...Interim role
$102k - $162k
...Job TitleSenior Clinical Research AssociateJob DescriptionThe Senior Clinical Research Associate is responsible for developing comprehensive study plans/protocols, ensuring adherence to ISO/FDA regulatory requirements, Good Clinical Practice (GCP) guidelines, and study...Full timeWork at officeImmediate startRemote workWork visa3 days per week- ...management activities to ensure compliance with regulatory standards. The successful candidate will leverage their knowledge of Good Clinical Practice and manage site-related activities while supporting patient recruitment. Join a passionate team dedicated to making a...
- ...requirements Prepare, organize and submit IRB documentation for clinical trials Process and submit IND safety reports as delegated by... ...clinical trial operations What you’ll bring 2–6 years of clinical research experience, including at least 2 years in regulatory affairs or...Local areaWork from homeFlexible hours
$4,000 - $9,000 per month
...Clinical Research Associate DotLab is transforming the diagnosis and management of endometriosis, a disease that affects 1 in 10 women worldwide and currently requires surgery to diagnose. The disease is the cause of over half of unexplained infertility, and is a primary...Work experience placementWork at officeRemote workWorldwideFlexible hours- A leading clinical research organization in New York is seeking a Cancer Clinical Trials CRC I to support clinical trial operations under supervision. Responsibilities include data collection, patient recruitment, and managing informed consent processes. Applicants should...
- A leading healthcare organization in New York is seeking a Research Associate to oversee clinical trials. The role requires strong clinical research skills, a Bachelor's degree, and GCP training. Responsibilities include managing daily trial activities, ensuring compliance...
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