Clinical Study Specialist - Trial Management & Analytics
Regeneron Pharmaceuticals, Inc
Regeneron Pharmaceuticals, Inc. is seeking a Clinical Study Specialist to join our Clinical Trial Management team. You will provide technical and administrative support to clinical study teams, helping keep studies on track from site activation through close‑out, and collaborate with study leads, managers, CROs, and sites. The role requires a Bachelor's degree with 2+ years in a clinical setting, familiarity with trial management systems and MS Office, and knowledge of ICH/GCP. #J-18808-Ljbffr Regeneron Pharmaceuticals, Inc
- Psi-Cro is looking for a dedicated Lead Monitor to oversee clinical trial operations in the United States. This role involves managing site feasibility, monitoring project timelines, and ensuring compliance with US regulations. The ideal candidate will have a minimum of...Suggested
- ...Parexel Clinical Trial Management When our values align, theres no limit to what we can achieve. At... ...assess and ensure overall integrity of study implementation and adherence to study... ...project timelines; utilizing strong analytical skills to make decision autonomously...SuggestedLocal areaImmediate startRemote workFlexible hours
- ...within the United States. The RA will support patients and sites with virtual study activities, data management, and study administration under PI delegation. Early-to-mid level experience in clinical research is preferred. Responsibilities include patient recruitment/pre-...SuggestedRemote job
$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... ...and research protocols. The Specialist collaborates closely with clinical...SuggestedWork at office- ...Overview Piper Companies is seeking a Clinical Research Associate (CRA) to support oncology-focused clinical trials for a leading organization within the life... ...monitor with a strong background in oncology studies, site management, and ensuring regulatory and protocol...SuggestedRemote work
$71.9k - $189k
...Perform monitoring and site management work to ensure that sites are conducting the study(ies) and reporting study data as... ...contracted scope of work and Good Clinical Practice. • Work with sites to... ...are available for filing in the Trial Master File (TMF) and verify that...Full timePart timeLocal areaImmediate startWorldwide$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$101.6k - $169.3k
...IQVIA is hiring Senior Clinical Research Associate 1 with experience in... ...Overview Perform monitoring and site management work to ensure that sites are conducting the study(ies) and reporting study data as... ...are available for filing in the Trial Master File (TMF) and verify...Full timePart timeLocal area$108.7k - $139.8k
...All Jobs Senior Clinical Research Associate The Senior Clinical Research... ...full lifecycle of a clinical study. The Senior CRA brings... ...Class III cardiovascular rhythm management (CRM) devices or equivalent... ...data capture (EDC), electronic trial master file (eTMF) systems,...Contract workWork at officeRemote workNight shift$103k - $130k
...from hospital labs to mobile clinics. By helping providers, patients... ...IVD and medical device clinical trials at external clinical research... ...to independently train and manage external clinical research sites... ...to: Oversee clinical study protocol execution at external...Hourly payContract workRemote workWork from homeWorldwideFlexible hoursNight shift$38 - $40 per hour
...from Baim Institute for Clinical Research Director,... ...Interim Monitoring and Study Close-out Visits, in accordance... .... Query generation and manage to resolution. Identify... ...-house CRA Comply with Trial Master File (TMF)... ...Clinical Trial Support Specialist, MedTech United States...Part timeFor contractorsInterim roleRemote workWork from home10 hours per week- ...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 monitoring...Remote job
- Freenome is seeking a Contract Clinical Research Associate to join its Clinical Development team, working remotely with occasional... ...travel to California. The ideal candidate will manage all aspects of clinical trial monitoring and is expected to deliver excellence in compliance...Remote jobContract work
$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...Remote job- Remote Jobs is seeking a Clinical Research Site Manager responsible for performance and regulatory compliance across assigned protocols and sites in... ..., patient safety, and data integrity throughout all trial phases. The role requires deep knowledge of ICH‑GCP, country...Remote work
- A leading clinical research organization in New York is seeking a Cancer Clinical Trials CRC I to support clinical trial operations under... ...collection, patient recruitment, and managing informed consent processes.... ...and ensuring the accuracy of study data. #J-18808-Ljbffr...
- ...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...
- ViziRecruiter,LLC. is seeking a Clinical Research Coordinator I to assist in the conduct of clinical trials. This role involves collecting and managing patient clinical data, obtaining informed... ...screening, and coordination of study activities. #J-18808-Ljbffr ViziRecruiter...
- ...seeking a Senior Research Associate in New York, NY to support clinical trials by ensuring timely data collection and mentoring junior... ...within 18 months. Responsibilities include obtaining consent, managing study information, and assisting in recruitment efforts. #J-1880...
- ...company is looking for a Senior Clinical Research Associate to oversee clinical trials in the United States. The position... ...responsibilities including site management, regulatory compliance, and data... ...to the success of clinical studies. #J-18808-Ljbffr CellCentric LimitedRemote job
- Regional Clinical Research Associate II BIOTRONIK is... ...catheters for cardiac rhythm management, electrophysiology and... ...II to our Clinical Studies team. Conduct on-site,... ...medical device IDE trials is preferred. Strong clinical... ...organizational, analytical, and problem-solving...Work at officeRemote workHome office
- ...Job Purpose: The Clinical Research Associate (CRA... ...for the delivery of the studies at allocated sites and... ...: Site Management Responsibilities Contributes... ...delivering quality clinical trials with reduced budget and in less time. Good analytical and problem-solving...Local areaRemote workFlexible hoursShift work
- ...Clinical Research Associate II Remote, Poland... ...average of one to two studies setting you up to be a... ...support from direct line management. About You: You... ...combining novel clinical trial designs, industry-... ...advanced biomarker and data analytics solutions, and an...Local areaRemote workWork from homeNight shift
$93.9k - $153.3k
...science and innovation to develop life‑changing medicines for people with serious diseases. We are seeking a Clinical Study Specialist to join our Clinical Trial Management team. In this role, you will provide technical and administrative support to clinical study teams...Work experience placementWorldwide- ...Kelly Science and Clinical FSP is currently seeking a Regional Clinical Research... ...Service Provider) division, a managed solution provider and business... ...plan for communication with the study teams and sites. Well-versed in clinical trial management. They are rigorous, detail...Full time
- Montefiore in New York seeks a Cancer Clinical Trials Senior Research Associate to support the research team in conducting clinical trials under... ..., data submission, recruitment support, and helping develop study protocols while auditing data quality and ensuring timely data...
- A healthcare organization based in New York seeks a Senior Research Associate to lead clinical trial activities. The role involves mentoring junior associates, ensuring timely data collection, and contributing to research protocol development. Ideal candidates will possess...
- NYU Grossman School of Medicine invites applications for a Research Associate (Per Diem) in CSTAR. You will support clinical and translational studies, recruit participants, collect data, and handle specimens while maintaining documentation and coordinating with study...Daily paidDay shiftAfternoon shiftEarly shift
- Overview Clinical Research Associate (II - Sr) - Sponsor... ...of clinical research studies to ensure compliance... ...and training materials Manage defined components of... ...teams to support clinical trial operations, including... ...to detail and strong analytical skills Problem-solving...Work at officeRemote workWork from homeFlexible hours
$80k - $125k
...Job Description Join Us as a Clinical Research Associate (Level II)... ...biotechs, spanning 2,700 clinical trials across 100+ countries in the... ...clinical monitoring and site management process. As a Clinical... .... Acting as a site processes specialist, you will ensure that the trial...Temporary workWork at officeRemote workHome officeNight shift
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