Clinical Research Associate I: Study Ops & Compliance
Icahn School of Medicine at Mount Sinai
The Icahn School of Medicine at Mount Sinai is seeking a Clinical Research Associate I to monitor all aspects of clinical trial lifecycle across sites. You will prepare and finalize essential study documents, ensure regulatory compliance, and coordinate with investigators to maintain study files and budgets. Responsibilities include site coordination, preparing materials for study conduct, tracking adverse events, and assisting during CTM meetings. #J-18808-Ljbffr Icahn School of Medicine at Mount Sinai
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...Senior Clinical Research Associate position focusing on central nervous system and psychiatry studies. Manage research activities across multiple study sites in the Northeast and... ..., overseeing site selection, regulatory compliance, training, and study closeout activities....SuggestedContract workWork at office- ...A prestigious educational institution is searching for a Research Assistant within the Department of Neurology. This role involves overseeing clinical research studies, ensuring regulatory compliance, and supporting principal investigators with administrative tasks. Candidates...SuggestedWork at office
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- ...on-site monitor to coordinate timelines and standards across clinical sites in the Netherlands. You will build relationships with investigators... ...and conduct monitoring visits, ensuring high-quality data and compliance. The role requires independent on-site monitoring experience,...Work from home
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- ...fully integrated platform in terms of research and development, clinical development, manufacturing and... ...and close-out visits per ICH-GCP and study-specific monitoring plans. Perform... ..., protocol deviations, and escalate compliance issues as needed. Prepare and finalize...Worldwide
$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... ...assures all documentation is maintained in compliance with all applicable guidelines and...TraineeshipLocal area- ...to support and strengthen our Clinical Operations team. Job... ...Profound knowledge of clinical research processes and medical terminology... ...of patients involved in a study are protected Performing and... ...assess protocol and regulatory compliance and managing required...Part timeFreelanceLocal areaRemote work
$103k - $130k
...biopharma and translational research. We’re bringing the... ...labs to mobile clinics. By helping providers,... ...Sr. Clinical Research Associate (Sr. CRA) is responsible... ...opportunity to:Oversee clinical study protocol execution at... ...data collection and compliance with FDA standards and...Hourly payFull timeContract workRemote workWork from homeWorldwideFlexible hoursNight shift$25.84 - $34.94 per hour
Research --> Support StaffNew York • ID: 1166974_RR... ...our team as a Research Associate.This role involves clinical research data collection,... ...variable hours based on study needs, operational priorities... ...and publications.Ensures compliance with Good Clinical...Hourly payDaily paidFull timeCasual workRemote workDay shiftAfternoon shiftEarly shift$74.5k - $197.5k
...to ensure that sites are conducting the study(ies) and reporting study data as... ...with contracted scope of work and Good Clinical Practice.• Work with sites to adapt, drive... ...site monitoring experience as a Clinical Research Associate (CRA) in a CRO, sponsor, or similar setting...Full timePart timeLocal areaImmediate startWorldwide- Clinical Research Systems Study Build Specialist Department: Operations Employment Type: Full Time Location... ...or related field preferred (associate degree required) AND 2+ years of clinical... ...and professional manner, and in compliance with privacy and company guidelines....Full timeContract workTemporary work
- ...ensuring the accuracy and integrity of clinical data. Your work will directly impact the... ...the Pfizer Trial Master File (PTMF) in compliance with ICH-GCP and SOPs, and ensure team members... ...(ICD) to global Project Managers and Study Managers, assisting with activities...Work at officeLocal areaWorldwide
- ...Latin America. Are you an experienced Clinical Research Associate (CRA) looking for an exciting... ...a key role in ensuring that clinical studies are conducted according to the highest... ...Ensuring clinical trial sites operate in compliance with study protocols, ICH-GCP guidelines...Full timeFor contractorsInterim roleWork at officeRemote work
- ...sets us apart is the way we integrate clinical trial execution with deep scientific knowledge... .... We are now recruiting Clinical Research Associate II to join our team in the Netherlands.... ...eye for detail. You identify potential study risks and propose solutions on how to mitigate...Local areaRemote workNight shiftDay shift
- ...Job Title 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 and...
- ...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... ...of quality, scientific rigor, regulatory compliance, and patient safety, while supporting sites throughout...Work at officeRemote work
- ...recognized laboratory services, clinical trials, and reimbursement... ...for real-time data and study transparency. Hiring Timeline... ...Job Summary: The Clinical Research Associate II (CRA II) participates in... ...resolving any issues to ensure compliance with site file audits in...Work experience placementInterim roleWork at officeRemote work
- ...Clinical Research AssociateThe Clinical Research Associate is responsible for the site management, site monitoring and close... ...patient safety and quality study execution in accordance with applicable... ...safety, site quality and compliance with GCP), to maintain investigator...Local areaRemote workWeekend work
- ...POSITION TITLE: Clinical Research Associate II DEPARTMENT: Monitoring Ora Values the Daily Practice of... ...and is accountable for performance and compliance with assigned protocols at our sites.... ...you will ensure Ora’s compliance of study conduct by monitoring the site...Daily paidFull timeInterim roleLocal areaRemote workFlexible hours
$155k - $175k
...Piper Companies is seeking a Clinical Research Associate (CRA) to support oncology-focused clinical trials for... ...monitor with a strong background in oncology studies, site management, and ensuring regulatory and protocol compliance across multi-site trials. This role is...Interim roleRemote work$75k - $95k
...biopharma and translational research. We’re bringing the... ...labs to mobile clinics. By helping providers,... ...The Clinical Research Associate II is responsible for... ...Responsibilities Lead clinical study execution across... ...out, ensuring protocol compliance, timely data collection...Hourly payContract workWork experience placementRemote workWork from homeWorldwideNight shift- ...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 work
$85k - $95k
...biopharma and translational research. We're bringing the... ...labs to mobile clinics. By helping providers,... ...The Clinical Research Associate (CRA) is responsible for... ...to: Oversee clinical study protocol execution at... ...timely data collection and compliance with FDA standards and...Hourly payRemote workWork from homeWorldwideFlexible hoursNight shift
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