Clinical Research Associate I
Myana
Required Qualifications Bachelor's degree (foreign equivalent or higher) in biology, or related field. Two (2) years of full-time clinical research experience. Experience with IRB submissions. Experience with clinical trials. Experience with Microsoft Excel, Word, and/or PowerPoint. Preferred Qualifications One (1) or more years of full-time experience working on clinical trials in a coordinator role. Experience with grant finances. Brief Description of Duties The Department of Neurology at Stony Brook Medicine runs over 25 sponsored clinical studies in the disease areas of stroke, neuromuscular disorders, movement disorders, multiple sclerosis, and epilepsy. Department faculty also conduct investigator-initiated clinical studies. We seek a highly motivated and skilled study coordinator to manage the Department's studies in several disease areas, with a focus on neuromuscular diseases (muscular dystrophy, amyotrophic lateral sclerosis (ALS), and spinal motor atrophy (SMA)). The study coordinator will report to the Neurology Department Administrator and will work closely with several principal investigators of the studies and other research staff in the Neurology Department. Must have excellent organizational skills and attention to detail, ability to work effectively in a team environment, strong verbal and written communication skills, willingness to learn new research techniques, and ability to multitask and manage multiple projects at once. Must have a general interest in neurological diseases and the ability to stay on track with deadlines. Duties Submit necessary paperwork to the sponsor and for IRB approval for new and ongoing studies. Recruit and screen patients for eligibility in clinical studies. Review medical records and follow up with phone calls for interested patients. Consent patients prior to the study according to protocol. Schedule and conduct study visits and patient follow ups as needed. Handle paperwork related to research activities. Collect and analyze patient data. Maintain data for both sponsor and investigator use and ensure compliance with study protocol and regulatory agencies. Attend meetings. Submit data forms to the sponsor. Other duties as assigned. Special Notes The Research Foundation of SUNY is a private educational corporation. Employment is subject to the Research Foundation policies and procedures, sponsor guidelines and the availability of funding. FLSA Exempt position, not eligible for the overtime provisions of the FLSA. Minimum salary threshold must be met to maintain FLSA exemption. For this position, we are unable to sponsor candidates for work visas. EEO Statement Stony Brook University is committed to excellence in diversity and the creation of an inclusive learning, and working environment. All qualified applicants will receive consideration for employment without regard to race, color, national origin, religion, sex, pregnancy, familial status, sexual orientation, gender identity or expression, age, disability, genetic information, veteran status and all other protected classes under federal or state laws. Salary The starting salary range (or hiring range) to be offered for this position is noted below, it represents SBU's good faith and reasonable estimate of the range of possible compensation at the time of posting. #J-18808-Ljbffr
$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...SuggestedPermanent employmentWork at officeRemote work- ...Bright Uro is seeking a Clinical Research Associate I (CRA I) to join their dynamic team. This entry-level role offers exposure to the full lifecycle of clinical studies, including oversight at investigational sites and data collection. Candidates must be detail-oriented...SuggestedWork 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...SuggestedContract workInterim roleLocal areaImmediate startRemote workFlexible 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...Suggested
- ...Bright-Uro, based in the U.S., is seeking a Clinical Research Associate I to provide support for clinical studies. This role involves significant travel, requiring on-site visits throughout the Midwest, contributing to the quality and integrity of various research projects...Suggested
$71.9k - $189k
...Clinical Research Associate, Sponsor Dedicated Location: Gloucester, United States of America | Full time | Field-based | R1541733 To be eligible for this position, you must reside in the same country where the job is located. Essential Functions Perform site monitoring...Full timePart timeLocal areaImmediate start$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...Contract 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
- ...The Position The Position (Phase 1 healthy volunteer studies): CRA/Sr. CRA drives quality clinical research and delivery of monitoring and site management activities, ensuring patient safety/rights and wellbeing, data reliability, scientific integrity, and regulatory/process...Local areaRemote workNight shiftWeekend work
- ...Philadelphia, United States | Posted on 01/22/2025 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. Participate and assist in design...
- ...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...Local areaFlexible hoursShift work
- ...CRA Clinical Research Associate When our values align, there's no limit to what we can achieve. At Parexel, we all share the same goal - to improve the world's health. From clinical trials to regulatory, consulting, and market access, every clinical development solution...Remote workFlexible hours
- ...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...Flexible hours
- ...Title: Clinical Research Associate This role is located in either New York or New Jersey 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 study team(s). The CRA works...Hourly payTemporary workLocal areaRemote work
- ...Clinical Research Associate - Oncology - GA, FL or NC 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...Local areaVisa sponsorshipFlexible hours
- ...innovation, and we’re building a collaborative, dynamic team to bring transformative solutions to life. About the Role: The Clinical Research Associate I (CRA I) is an exciting entry point into the world of clinical research at Bright Uro, offering hands‑on exposure across...Work experience placementInterim roleWork at office
- ...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...
$62.6k - $97.1k
...patients of all ages. Informed by basic research done at our Sloan Kettering Institute, scientists... ...to conduct innovative translational and clinical research that is driving a revolution in... ...: Join our team as a Clinical Research Associate ! This position offers the opportunity...Work at office2 days per week3 days per week$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,...Hourly payContract workRemote workWork from homeWorldwideFlexible hoursNight shift$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...Work experience placementInterim roleLocal areaRemote workFlexible hours$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...Work experience placementFlexible hours$103k - $130k
...Sr. Clinical Research Associate (Sr. CRA) The Sr. Clinical Research Associate (Sr. CRA) is responsible for the set‑up, initiation, execution, monitoring and close‑out of IVD and medical device clinical trials at external clinical research sites and/or laboratories. The...Contract workRemote workNight shift$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- ...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$110.52k - $138.15k
...Senior Clinical Research Associate - Oncology - East Coast 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...Work experience placementFlexible hours- ...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
$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- ...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
- ...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
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