Clinical Trials Research Associate
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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
$125k - $145k
...Senior Clinical Research Associate (Pain/Oncology/CNS Therapeutic Areas) Key Accountabilities Interact with personnel from study Sponsors, investigational... ...to enable quality and on-time execution of clinical trials in compliance with ICH‑GCP and relevant local regulations....SuggestedContract workTemporary workInterim roleLocal areaRemote work$110.52k - $138.15k
...Sr. Clinical Research Associate ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an... ...Senior CRA at ICON Plc, you will oversee and manage clinical trial activities to ensure they are conducted according to protocol...SuggestedFlexible hours$38 - $40 per hour
...the job poster from Baim Institute for Clinical Research Director, Human Resources at Baim Institute... ...Research The Sr. Clinical Research Associate/Field Monitor Contractor performs remote... ...Lead and/or in-house CRA Comply with Trial Master File (TMF) document submission timelines...SuggestedPart timeFor contractorsInterim roleRemote workWork from home10 hours per week$120k - $135k
...Immatics-US in Houston is looking for a Senior Clinical Research Associate to oversee clinical trial management. The successful candidate will manage monitoring activities to ensure compliance with regulations and protocols. This is a fully remote position offering a competitive...SuggestedRemote work$110.52k - $138.15k
...Senior Clinical Research Associate – Oncology – New York ICON plc is a world‑leading healthcare intelligence and clinical research organization.... ...facilitate efficient communications between the client's clinical trial team and the sites Perform remote and on‑site monitoring/co...SuggestedWork experience placementInterim roleLocal areaRemote workFlexible hours- ...The Clinical Research Associate (CRA) 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 laws, Good Clinical...Local areaRemote work
$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... ...such as protocol, electronic data capture (EDC), electronic trial master file (eTMF) systems, and CTMS (BSI). Ensure data completeness...Contract workWork at officeRemote workNight shift- ...Syneos Health is looking for an Experienced Clinical Research Associate (CRA) to join their team in Idaho. The CRA will be responsible for site qualification, monitoring compliance, and ensuring regulatory adherence while managing site-level activities. Candidates should...Remote work
- ...ICON is looking for a Senior Clinical Research Associate (CRA) to join their team in the United States. This remote position involves overseeing clinical trial activities to ensure compliance and participant safety throughout the study lifecycle. The ideal candidate has...Remote work
$105k - $117k
...A leading clinical outsourcing company seeks an Experienced Ophthalmology & Gen Med CRA 2 to join their Full Service Outsourcing team. This role involves extensive site monitoring, collaboration with study teams, and ensuring patient protocol compliance. Candidates should...Remote work- ...Senior Clinical Research Associate job at PSI CRO. Remote. We are the company that cares – for our staff, for our clients, for our partners and... ...as a Senior Monitor Experience monitoring complex Oncology trials required; experience with radiopharmaceuticals and/or breast...Remote workWork from homeWork visa
$108.5k - $201.5k
...data collection) and timely completion of Phase I-IV Pharma clinical trials within the country. The Senior CRA is responsible for delivering... ...of the drug development process specifically clinical trial/research Knowledge of international standards (GCP/ICH, FDA, EMEA)...Local areaRemote workRelocation- ...Our Client is a rapidly growing international Clinical Research Organisation offering an experienced( Senior ) CRA opportunity to work from... ...monitoring visits Maintaining study files, writing clinical trial reports and liaising with vendors Reviewing progress of projects...Work from home
- ...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 - $189k
...accordance with contracted scope of work and Good Clinical Practice. • Work with sites to adapt,... ...are available for filing in the Trial Master File (TMF) and verify that the Investigator... ...skill in applying, applicable clinical research regulatory requirements. • i.e., Good...Full timePart timeLocal areaImmediate startWorldwide- ...Clinical Research Associate - Oncology - GA, FL or NC ICON plc is a world-leading healthcare intelligence and clinical research organization. We... ...industry Experienced monitoring hematology oncology clinical trials Proficient in ICH-GCP, local regulatory requirements, and...Local areaVisa sponsorshipFlexible hours
$100k - $135k
...Piper Companies is seeking a Clinical Research Associate specializing in Cardiology or Neurology. This role involves monitoring clinical trials, ensuring compliance, and collaborating with clinical teams. The ideal candidate should have a Bachelor’s degree, 2+ years of...$91.34k - $114.17k
...world-leading healthcare intelligence and clinical research organization. We’re proud to foster an... ...currently seeking a Clinical Research Associate to join our diverse and dynamic team.... ...role in designing and analyzing clinical trials, interpreting complex medical data, and...Work experience placementFlexible 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...Hourly payTemporary workLocal areaRemote work
$71.9k - $169.3k
...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 will be responsible for monitoring and managing...Full timePart timeImmediate startWorldwide$97k - $193k
...Worldwide Clinical Trials is seeking a Senior Clinical Research Associate for a remote role focusing on CNS/Psychiatry. The ideal candidate will manage clinical research activities at sites and ensure compliance with regulations while collaborating with diverse teams....Remote workWorldwide$100k - $110k
...Piper Companies is seeking a Clinical Research Associate II to join a global organization within the clinical research and life sciences industry... ...partnering closely with investigative sites to ensure high-quality trial execution. Responsibilities Perform routine and close-out...Permanent employmentRemote work$60k - $80k
...The Department of Medicine, Division of Behavioral Medicine is seeking a Clinical Research Associate I. In this role the Clinical Research Associate I will manage and coordinate a large-scale research study on temporomandibular disorders and chronic overlapping pain conditions...- ...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
- ...Overview Experienced 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
$91.5k - $137.3k
...implementation, on-site monitoring of clinical research studies as well as on-going site management... ..., tracks and maintains study specific trial management tools/systems, and status... ...the protocol. Verifies issues or risks associated with blinded or randomized information...Contract workLocal areaRemote workNight shift- ...system built to understand and assess clinical characteristics in EMRs. Synapsis AI is... ...characteristics with complex clinical trial criteria during the exact window of time... ...member of our diverse team, our Clinical Research Associates (CRA) will collaborate closely with the...Local areaFlexible hoursShift 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...Work at office
- ...Clinical Research Associate – Full-Service Syneos Health is a fully integrated biopharmaceutical solutions organization focused on accelerating customer... ..., timeliness and completeness, reconcile it with the Trial Master File (TMF), and ensure sites are aware of archiving...Interim roleLocal areaImmediate startRemote workFlexible hours
- ...Clinical Research Associate (CRA) – Cardiovascular Medical Device MiRus is an innovative healthcare company with a growing portfolio of cardiovascular... ...from start through study closure. Engage in new study trial design with cross functional teams, including clinical and...Remote workRelocation packageMonday to FridayFlexible hours
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