Remote Regulatory Affairs Manager - Clinical Trials & IRB
$90k - $105kThe Geneva Foundation
THE GENEVA FOUNDATION is seeking a Regulatory Affairs Manager to oversee regulatory compliance for the MIRROR Program. The role involves managing a team, guiding submissions to institutional review boards, and ensuring adherence to regulatory standards for clinical research. This fully remote position supports projects across the United States, offering a salary range of $90,000 - $105,000 annually based on qualifications. Candidates should have substantial experience in regulatory affairs and clinical research. J-18808-Ljbffr
$90k - $120k
...Regulatory & Clinical Affairs Manager (Remote) Position Summary The Regulatory & Clinical Affairs Manager is responsible for overseeing regulatory compliance... ...Affairs Manage administrative aspects of clinical trial and clinical affairs activities, serving as a liaison...Remote workWorldwide- ...Manager of Regulatory Affairs and Quality Assurance Founded in 1965,... ...The UCI Center for Clinical Research (CCR) is driven... ...life-saving clinical trials designed to strengthen... ...Review Board [IRB]), and the Quality Assurance... ...locations. Remote work will only be approved...Remote workWork experience placementWork at officeLocal areaFlexible hours
- Job Summary: The Clinical Compliance Manager will provide GCP compliance support to... ...and guidance regarding regulatory requirements, GCP guidelines... ...risk assessment of clinical trial activity to identify priority... ...conflicts. #LI-CF1 #LI-REMOTE EEO Disclaimer Parexel is an...Remote workContract work
- ...Director, Clinical Research Regulatory Support Services (Remote) Join the transformative team at City of Hope... ...clinical research across the COH system. Manage a team of regulatory coordinators... ...submissions to committees such as IRB, CPRMC, DSMB, and IBC, while...Remote workWork experience placement
$265k - $300k
...A clinical-stage biotechnology company is seeking an Executive Director of Clinical Quality Assurance to oversee quality assurance for clinical trials. This remote role requires expertise in GCP, GPvP, and GLP, ensuring compliance with regulations. Responsibilities include...Remote work$195k - $314.6k
...understanding and management of disease, and give... ...- Counsel, Clinical Development will be part of the Regulatory Legal Team (RLT),... ...modernization of clinical trials through AI,... ...Global Regulatory Affairs, Policy, and Legal... ...trial sites and, for remote roles located outside...Remote workFull timeH1bVisa sponsorshipWork visaFlexible hours- - Clinical Strategy & Protocol Development o Lead the development of IRB and clinical study protocols in alignment... .... o Submit and manage regulatory applications (FDA... ...regulatory, and medical affairs to ensure alignment... ...of clinical trial design, including randomized...Remote work
$95k
Johns Hopkins University seeks a JH-ACH IRB Program Manager to oversee the operations of the IRB Program. This role involves working with various... ...medical setting. This is a full-time position with a remote designation, requiring some travel for in-person meetings. The...Remote jobFull time$125k - $145k
...biotechnology firm focused on bladder cancer treatment seeks a Manager of Regulatory Affairs. This remote role requires overseeing regulatory strategies and... ...of regulatory experience, and knowledge of CMC and clinical requirements. The position offers a competitive salary...Remote workFlexible hours$213k - $350k
...will help advance our clinical pipeline from IND to... ...clinical strategy, clinical trial design, and execution... ...clinical project management, regulatory affairs, clinical operations,... .... We are open to remote employees About... ...regulatory authorities, IRBs, and ethics...Remote workImmediate start- ...Clinical Study Manager-Remote(Job Id- 3908-1) ~ Contract Artech is the 10th Largest... ...issues (monitoring and/or regulatory) with appropriate escalation... ...and site documentation for the Trial Master File and site file Supports local IRB workflow, submission through...Remote workContract workLocal areaImmediate start
$44.15 - $66.25 per hour
...Health Sciences - Clinical Trial Methods Center of... ...coordination of Regulatory Services for NCCT... ...with institutional, IRB, federal and... ...training, performance management, coaching, and... ...development; supports remote training and... ...compliance and regulatory affairs. Assists...Remote workDaily paidFull timeTemporary workPart timeFlexible hoursShift work$135 - $175 per hour
...learning to extract clinically meaningful EEG... ...As the Clinical Affairs Manager (Part-Time) , you... ...practice, supporting regulatory approval, and... ...per month) and is remote within the U.S.,... ...preparation and clinical trial protocols Oversee... ...Support hospital IRB processes and...Remote workPart time- ...and interpretation of clinical trials and the data... ...with sites including IRBs and interaction with operations teams Manages program development,... ..., quality assurance, regulatory, medical affairs, marketing, legal, biostatistics... ...accommodation. #LI-remote Seniority level Seniority...Remote workFull time
$131.56k - $164.45k
...days) The Senior Manager, Clinical Trials is the end-to-end owner... ..., budget, and regulatory readiness across FDA... ...Evaluation, Medical Affairs, and the Clinical Development... ...and international EC/IRB processes ~ Proficiency... ...to support any remote/hybrid employee functionality...Remote workTemporary workLocal areaFlexible hours$160k - $170k
...Senior Manager, Clinical Compliance Fully Remote • Irvine, CA 92618 Overview Salary Range $160,000.00 -... ...Supervisor/Manager Title: VP, Clinical Affairs Job Location & Environment:... ..., department procedure lifecycle, regulatory intelligence, and internal training...Remote workFull timeContract workWork at officeHome office- ...Clinical Trials Data Coordinator - Remote Join the transformative team at City of Hope , where we're changing lives and making a real difference... ...trials, Federal, State, and Local Regulations, and IRB requirements. City of Hope is an equal opportunity...Remote workFull timeLocal area
- ...’s client is a clinical‑stage biopharmaceutical... ...Location: Remote – USA... ...and/or clinical trial in partnership... ...development of regulatory documents in support... ...Ethics Committees/IRBs, and other... ...development strategy. Manage engagements... ...Regulatory, Medical Affairs) to ensure an...Remote workInterim role
$31.51 - $62.64 per hour
...Angeles, CA, USA Onsite or Remote Fully On-Site Work... ...direct supervision of the Clinical Trials Administrator, The Regulatory Coordinator is responsible for submitting and managing all regulatory... ...applications to the FDA, IRB, ISPRC, DSMB, ancillary departments...Remote workHourly payLocal areaMonday to Friday$55k - $70k
...points for wellness screenings, clinical trials, and patient navigation. We... ...execution aligns with IRB-approved materials, HIPAA standards... ...Organized, proactive, and able to manage multiple priorities in a fast... ...systems, dashboards, and remote coordination tools....Remote workFlexible hours$68k - $70k
Saybrook University is seeking an IRB Associate Director (Remote) responsible for assisting the IRB Director with administrative activities associated with IRB applications. The role requires strong knowledge of OHRP regulations, excellent communication skills, and experience...Remote work$44.15 - $66.25 per hour
...Medical Center - LC: Clinical Trials: Morehead Status:... ...position is primarily remote with some onsite/offsite... ...Essential Functions Manages multiple projects and... ...matters as well as regulatory management of trials in... ...Institutional Review Boards (IRB), and Human Subjects...Remote workFull timeContract workTemporary workWork at officeFlexible hoursShift work- ...Senior Clinical Trial Coordinator Join Us as a Senior Clinical Trial... ...risks to project leads and line manager as appropriate. Supports... ...Reviews and tracks local regulatory documents. Transmits documents... ...documents to client and centralized IRB/IEC. Analyzes and...Remote workLocal areaHome office
- ...Clinical Trial Coordinator Black Canyon Consulting (BCC... ...in Bethesda, MD and/or remote work. The National... ...researchers, designers, product managers, scientists, security... ...required reporting to regulatory bodies and intramural... ...with FDA and IRB requirements for IND protocol...Remote workFull timeWork at officeFlexible hours
- ...edge science and robust clinical pipeline form the... ...an Associate Director Regulatory Affairs – Clinical Lead* to strengthen... ...in Tübingen, Munich or remote (Germany) in a highly... ...Drive initial clinical trial application and its lifecycle management, including major Substantial...Remote workSummer workRelocation package
$170 - $190 per hour
...Medical Director, Clinical Development Location: Remote - USA ONLY Pay Rate:... ...hematologic oncology trials, including multiple... ...safety, contribute to regulatory submissions, and collaborate... ...Ops, and Medical Affairs to deliver high-... ..., annual reports, IRB/EC responses. Drive...Remote work- ...through a model that combines clinical excellence with a hospitality... ...a dedicated, senior owner on regulatory and clinical compliance for... ...history. The role The Sr. Manager, Clinical Compliance is the... ...sheet. This role is also remote but could include travel....Remote jobTemporary work
- ...and execution of clinical studies. This Lead Clinical Study Manager-4 (CSM IV) / Senior... ...-market clinical trials to support regulatory approvals and key... ...of the Clinical Affairs team, this role... ...reports); organize IRB/EC submissions... ...Perform on-site and remote site...Remote workWorldwideShift work
- ...Future of Eye Care iuvo Clinical is a full-service... ...complex ocular device trial, we provide the expertise... ...career! Clinical Study Manager We currently have an opportunity... .../GCP/GDP, HIPAA, and IRB requirements/... ...ENVIRONMENT Office setting / remote home office. iuvo Clinical...Remote workContract workWork at officeLocal areaHome office
- ...and execution of clinical studies. The Clinical Study Manager-4 (CSM IV) role... ...to help regulatory approvals and key... ...of the Clinical Affairs team, this role... ...CRAs), clinical trial assistants (CTAs... ...reports), organizing IRB/EC submissions... ...on-site and remote site...Remote workInterim roleLocal areaFlexible hoursShift work
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