Clinical Research Associate
$91.34k - $114.17kICON
Clinical Research Associate - Early Development Multi Therapeutic Area - Midwest ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster. As a values-driven organisation, integrity, collaboration, agility, and inclusion are at the heart of how we work and interact with each other, customers, patients, and suppliers. What you will be doing: Serve as the primary point of contact between investigation sites and the sponsor Conduct all types of site visits, including selection, initiation, routine monitoring, and close-out Ensure site compliance with ICH-GCP, SOPs, and regulations Maintain up-to-date documentation in CTMS and eTMF systems Support and track site staff training and maintain compliance records Monitor patient safety, ensuring timely and accurate AE/SAE/PQC reporting Support subject recruitment and retention efforts at the site level Oversee drug accountability and ensure proper storage, return, or destruction Resolve data queries and drive timely, high-quality data entry Document site progress and escalate risks or issues to the clinical team Assist in tracking site budgets and ensuring timely site payments (as applicable) Collaborate with cross-functional partners including CTAs, LTMs, and CTMs You are: A graduate with a Bachelor's degree in Life Sciences or equivalent, or a qualified RN Eligible to work in United States without visa sponsorship A clinical research professional with 2+ years of on-site monitoring experience in the pharmaceutical or CRO industry Experienced monitoring early development Phase I/II clinical studies, across multiple therapeutic areas Proficient in ICH-GCP, local regulatory requirements, and clinical systems like CTMS and eTMF A clear communicator, problem-solver, and collaborative team player Willing and able to travel up to 60% for on-site monitoring visits across the Midwest region; preference given to candidates residing in Midwest region near major HUB airports to support efficient regional travel Employment with ICON is contingent upon having the legal right to work in the country where the role is based. Rewards & Benefits ICON offers a competitive and comprehensive total rewards package designed to support your health, wellbeing, and career development. Benefits may include: Competitive base salary and performance related incentives Health and wellbeing programmes including medical, dental, and vision coverage where applicable Retirement and pension plans Life assurance and disability coverage Employee assistance programmes and wellbeing resources Learning and development opportunities through structured training and career pathways Benefits may vary depending on role and location. Inclusion and Accessibility ICON is an equal opportunity employer. We are committed to building an inclusive and accessible workplace where everyone feels valued and supported. If you require reasonable accommodations during the recruitment process, please let us know or submit a request here. Salary Range $91,336.00-$114,170.00 ICON
- ...out visits) in accordance with contracted scope of work and Good Clinical Practice. Work with sites to adapt, drive, and track subject... ...Good knowledge of, and skill in applying, applicable clinical research regulatory requirements. i.e., Good Clinical Practice (GCP) and...SuggestedLocal area
- ...Job Description 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
$110.52k - $138.15k
...Senior Clinical Research Associate - Northeast 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$110.52k - $138.15k
...Senior Clinical Research Associate - Oncology - New York 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...SuggestedWork experience placementInterim roleLocal areaRemote workFlexible hours$103k - $130k
...players in biopharma and translational research. We're bringing the best minds together... ...it happen, from hospital labs to mobile clinics. By helping providers, patients, and families... ...possible. The Sr. Clinical Research Associate (Sr. CRA) is responsible for?set-up,...SuggestedHourly payContract workRemote workWork from homeWorldwideFlexible hoursNight shift- ...institutions and leading players in biopharma and translational research. We’re bringing the best minds together to accelerate... ...proven playbook to make it happen, from hospital labs to mobile clinics. By helping providers, patients, and families get faster, more...Worldwide
- ...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
- ...mostly on-site data monitoring is a flag; covering all visit types evenly is needed. Experience in creating (not just reviewing) clinical documents such as training materials for SIVs, protocols, CRFs, ICFs, and brochures. Experience participating in Data Management activities...Remote workFlexible 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
$120k - $135k
...in more than 50 cancers. Our cutting-edge science and robust clinical pipeline form the broadest PRAME franchise with the most... ...patients globally.Role Overview:We are seeking a Senior Clinical Research Associate (CRA) to support our Clinical Operations team. The Senior...Temporary workWork at officeImmediate startVisa sponsorship$71.9k - $169.3k
...trusted partnerships that help bring breakthrough treatments to patients faster. Job Overview We are seeking a dedicated Clinical Research Associate (CRA) to join our team and play a key role in ensuring the successful execution of clinical trials. In this position, you...Full timePart timeImmediate startWorldwide$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$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$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$101.6k - $169.3k
...IQVIA is hiring Senior Clinical Research Associate 1 with experience in either oncology, cardiovascular, renal, metabolic, CNS, Obesity (GLP-1), diabetes, GI, MASH/NASH, dermatology, or respiratory: Job Overview Perform monitoring and site management work to ensure that...Full timePart timeLocal area$120k - $140k
...and resolves site performance, quality, or compliance problems and escalates per protocol to upper management Work with in-house Clinical Trial Assistant to collect, review, and monitor required regulatory documentation for study start-up, study maintenance, and study...Interim roleLocal areaRemote workFlexible hours$58.66k - $81.68k
...Job Description The Clinical Research Associate I monitors all aspects of clinical research trial(s) Clinical study life-cycle responsibilities including site management, ongoing maintenance and closure of pre-clinical, Phase I through Phase IV, and post-marketing studies...TraineeshipLocal area- ...autoimmune disease, with unmet medical needs worldwide. InnoCare has built up a fully integrated platform in terms of research and development, clinical development, manufacturing and commercialization. To date, the Company has developed a robust product pipeline...Worldwide
- Overview Piper Companies is seeking a Clinical Research Associate (CRA) to support oncology-focused clinical trials for a leading organization within the life sciences and pharmaceutical research industry. The Clinical Research Associate (CRA) role is ideal for an experienced...Remote work
- Objective As a Clinical Research Associate II (CRA II) specializing in oncology, you will play a crucial role in the execution and management of Phase 1, Phase 2, and Phase 3 clinical trials. You will collaborate closely with cross‑functional teams to ensure adherence to...Interim roleLive inLocal areaRemote work
- A clinical research organization is seeking Clinical Research support in Pennsylvania. The role involves assisting with clinical trials, including protocol design, regulatory document management, and site evaluations. Candidates should have a BA or equivalent, basic knowledge...
- 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...
$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- A clinical research organization is seeking a Clinical Research support professional in New York, NY. The role involves assisting in the design of protocols, managing regulatory documents, and conducting ongoing study monitoring. Candidates should possess a degree in a...
- 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, evaluate...RelocationVisa sponsorship
- 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
- 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...
$53.36k - $67.81k
...Clinical Research Associate I - Clinical Trial Charge Monitoring We are seeking a detail-oriented and analytical team member to ensure accurate, compliant, and timely billing of clinical trial related services. This role supports the integrity of our research billing...Work at office- Experienced Clinical Research Associate - Sponsor Dedicated Syneos Health is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique clinical, medical affairs and commercial insights into outcomes to...Contract workInterim roleLocal areaImmediate startRemote workFlexible hours
- Mount Sinai Morningside in New York is seeking a Clinical Research Associate I to monitor clinical trials from site management through maintenance and closure across Phase I-IV and post‑marketing studies. You will prepare and edit key study documents, maintain the clinical...
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