Clinical Trials Research Associate
Montefiore New Rochelle
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 with protocols, and coordinating between various departments. Candidates must demonstrate exemplary communication and leadership potential, with a proven track record in research. The position offers an opportunity to become specialized in clinical projects after thorough training. #J-18808-Ljbffr
- ...InnoCare has built up a fully integrated platform in terms of research and development, clinical development, manufacturing and commercialization. To... ..., or biotech. Minimum 2 years of direct oncology trial monitoring experience (Phase I–III/IV) – non-negotiable....SuggestedWorldwide
- ...East Coast to support and strengthen our Clinical Operations team. Job Requirements:... ...activities Profound knowledge of clinical research processes and medical terminology... ...primarily responsible for monitoring clinical trials and Ensuring that clinical trial is...SuggestedPart timeFreelanceLocal areaRemote work
$58.66k - $81.68k
...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...SuggestedTraineeshipLocal area$103k - $130k
...biopharma and translational research. We’re bringing the best minds... ...from hospital labs to mobile clinics. By helping providers, patients... ....The Sr. Clinical Research Associate (Sr. CRA) is responsible for... ...and medical device clinical trials at external clinical research...SuggestedHourly payFull timeContract workRemote workWork from homeWorldwideFlexible hoursNight shift$74.5k - $197.5k
...with contracted scope of work and Good Clinical Practice.• Work with sites to adapt, drive... ...are available for filing in the Trial Master File (TMF) and verify that the Investigator... ...monitoring experience as a Clinical Research Associate (CRA) in a CRO, sponsor, or similar...SuggestedFull timePart timeLocal areaImmediate startWorldwide$25.84 - $34.94 per hour
Research --> Support StaffNew York • ID: 1166974_RR00124855 • Full-Time... ...opportunity to join our team as a Research Associate.This role involves clinical research data collection,... ...participants who are enrolled in clinical trials and cohort studies.Conducts chart...Hourly payDaily paidFull timeCasual workRemote workDay shiftAfternoon shiftEarly shift- ...improving patients’ lives by ensuring the accuracy and integrity of clinical data. Your work will directly impact the development of new... ...In this role, you will: Coordinate and support clinical trial activities, assisting managers in their execution. Contribute to...Work at officeLocal areaWorldwide
- ...advanced and interventional oncology for breast cancer clinical studies is hiring a Remote Clinical Research Associate to work in the United States. As a Clinical... ...resolution of missing or inconsistent data. Maintain the Trial Master File, regulatory site files, and clinical...Work at officeRemote work
- ...Clinical Research AssociateThe Clinical Research Associate is responsible for the site management, site monitoring and close-out of assigned clinical trials investigator sites to ensure patient safety and quality study execution in accordance with applicable prevailing...Local areaRemote workWeekend work
- ...Role: Clinical Research Associate (CRA) responsible for site performance and compliance in a specified country, managing all phases of clinical trial conduct at assigned sites. Objectives: ensure adherence to ICH-GCP, local regulations, and company policies, while fostering...Work experience placementLocal areaRemote work2 days per week3 days per week
- ...EPM Scientific is currently partnering with a leading Cardiovascular Medical Device company that is seeking an experienced Clinical Research Associate Contractor on a remote basis. Key Requirements Proven experience as a CRA within the cardiovascular medical device field....Contract workFor contractorsFreelanceImmediate startRemote work
$85k - $95k
...biopharma and translational research. We're bringing the best minds... ...from hospital labs to mobile clinics. By helping providers, patients... .... The Clinical Research Associate (CRA) is responsible for set-... ...and medical device clinical trials at external clinical research...Hourly payRemote workWork from homeWorldwideFlexible hoursNight shift- ...personalized neuroscience-based therapeutics. Primary Role The Clinical Research Associate (CRA) is responsible for the oversight of assigned... ...initiation through site close out. The CRA assists the Clinical Trial Manager and/or Clinical Project Manager by managing their assigned...Interim roleRemote work
$75k - $95k
...biopharma and translational research. We’re bringing the best minds... ...from hospital labs to mobile clinics. By helping providers, patients... ...The Clinical Research Associate II is responsible for set-up,... ...and medical device clinical trials at external clinical research...Hourly payContract workWork experience placementRemote workWork from homeWorldwideNight shift- ...POSITION TITLE: Clinical Research Associate II DEPARTMENT: Monitoring Ora Values the Daily Practice of … Prioritizing Kindness * Operational Excellence... ...continuity of site relationships through all phases of the trial. Performs, with oversight, clinical study site management/...Daily paidFull timeInterim roleLocal areaRemote workFlexible hours
- A medical device company focused on cervical spine conditions is seeking a Clinical Research Associate. Responsibilities include managing clinical trials, ensuring compliance, and coordinating operations with study sites. The ideal candidate will have 3-5 years of clinical...Remote work
$155k - $175k
...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 monitor...Interim roleRemote work- ...PSI is a leading Contract Research Organization with more than 30 years in the industry... ...indications. Job Description As a Clinical Research Associate at PSI you will enjoy a variety of... ...accurate and timely information flow with trial sites on Adverse Events and protocol/...Contract workWork visa
- ...Parexel is seeking a Clinical Research Associate with Ophthalmology monitoring experience to manage clinical sites from identification through closeout, ensuring study quality, patient safety, regulatory compliance, and accurate clinical data. You will conduct onsite monitoring...Remote work
- ...Job TitleResponsible 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 and assist in design and...
- ...therapies to patients. What sets us apart is the way we integrate clinical trial execution with deep scientific knowledge, laboratory... ...from direct line management. We are now recruiting Clinical Research Associate II to join our team in the Netherlands. This is a remote...Remote workNight shiftDay shift
- ...Clinical Research Associate II (FSP - Sponsor Dedicated) At ICON Strategic Solutions, you will work in a sponsor-dedicated model, supported by... ...As a CRA II at ICON, you will design and analyse clinical trials, interpreting complex medical data, and contribute to the...Remote workWorldwideFlexible hours
- ...professionals located in Latin America. Are you an experienced Clinical Research Associate (CRA) looking for an exciting opportunity to contribute to... .... Experience supporting global or multinational clinical trials. Experience working with US-based clients or stakeholders....Full timeFor contractorsInterim roleWork at officeRemote work
- ...The Clinical Research Associate is responsible for managing and monitoring clinical trials to ensure they are conducted in compliance with study protocols, ICH-GCP, and applicable regulations. This includes site selection, initiation, monitoring, and close-out activities...Work at office
- ...Description Clinical Research Associate - Full-Service Syneos Health® is a leading fully integrated biopharmaceutical solutions organization... ...and completeness. Reconciles contents of the ISF with the Trial Master File (TMF). Ensures the investigator/physician site...Contract workInterim roleLocal areaImmediate startRemote workFlexible hours
$97k - $193k
...Senior Clinical Research Associate position focusing on central nervous system and psychiatry studies. Manage research activities across multiple... ...Responsibilities Manage research activities at clinical trial sites, including site identification and selection Conduct...Contract workWork at office- ...Position Summary The Clinical Research Associate (CRA) is responsible for monitoring clinical trial sites to ensure studies are conducted, recorded, and reported in accordance with the protocol, Standard Operating Procedures (SOPs), Good Clinical Practice (GCP), and...Work at officeLocal areaFlexible hoursAfternoon shift
- Precision for Medicine is recruiting Clinical Research Associate I/II for a remote-based role with travel to sites in France, ideally based in Paris or the Paris area. You will monitor studies, ensure protocol compliance, and support regulatory activities. The position...Remote job
- Syneos Health is seeking a Part Time CRA (0.5 FTE) to be homebased in Lithuania under a Single Sponsor (FSP). This role supports site qualification, monitoring, and data integrity across studies, with up to 75% travel. The candidate will ensure compliance with GCP/ICH and...Remote jobPart time
- Overview As a clinical research associate (CRA), you are responsible for completing clinical research and administrative tasks for clients. You facilitate... ...based on findings. Responsibilities Develop and write trial protocols (outlining purpose and methodology) Present trial...RelocationVisa sponsorship
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