Remote Clinical Research Associate: Regulatory IRB
Mass General Brigham Incorporated.
Mass General Brigham Incorporated is seeking a Clinical Research Associate in Boston. The role involves maintaining regulatory compliance, preparing IRB documentation, and managing communications with trial participants and organizations.
Applicants should have a bachelor's degree and 1-2 years of research-related experience. Strong attention to detail and effective communication skills are essential for success in this position.
#J-18808-Ljbffr- Regional Clinical Research Associate IIBIOTRONIK is one of the leading manufacturers... ...team. Conduct on-site, remote, and centralized monitoring... ...BIOTRONIK procedures, and IRB/EC policies. Supports clinical... ...subject safety through review of regulatory documents, medical records,...Remote workRegulatoryFull timeContract workWork at officeHome office
- ...the world's health. From clinical trials to regulatory, consulting, and market access... ....Job Purpose:The Clinical Research Associate (CRA) has local... ...application/documents to EC/IRB and to Regulatory Authorities... ...Performs monitoring visits (remote and onsite), as well as remote...Remote workRegulatoryLocal areaFlexible hoursShift work
$110.52k - $138.15k
Senior Clinical Research Associate - Oncology Phase I - ChicagoICON is a global healthcare... ...team and the sites Perform remote and on-site monitoring/co-... ...Review Board (IRB)/Ethics Committee (EC) submissions... ...sites and the client's regulatory inspections Contribute to site...Remote workRegulatoryFull timeInterim roleLocal area$95k - $125k
...independent oversight of clinical centers to ensure the... ...studies. The Clinical Research Associate will ensure that... ...the study protocol and regulatory standards by qualifying... ...related questions. Perform remote and on-site monitoring... ...the preparation of IRB/EC submissions. Collect...Remote workRegulatoryWork experience placementLocal areaFlexible hours$96.2k - $151.4k
...throughout all phases of a clinical research study, taking overall... ...Monitoring Plan and associated documents.Gains an in... ...activities.Performs remote and on-site... ...and monitors required regulatory documentation for study... ...externally with vendors and IRB/IECs and Regulatory...Remote workRegulatoryFull timeFor contractorsLocal areaFlexible hours2 days per week3 days per week- ...healthcare intelligence and clinical research organisation united by... ...Clinical Research Associate II (CRA II)... ...delivery. This is a fully remote role based in The Netherlands... ...with ICH-GCP and regulatory requirements Conduct... ..., and ethics/IRB approvals Collaborate...Remote workRegulatoryWork from homeWorldwide
- ...Please note that hybrid or remote work options are NOT available... ...contributor to serve as a CLINICAL RESEARCH ASSOCIATE II to Dr. Judy Tan to... ...participants, assisting in IRB submission activities, budget... ...supervising staff with regulatory submissions to the Institutional...Remote workRegulatoryLocal area
$20.16 - $29.01 per hour
...Clinical Research Regulatory Coordinator Investigator Mass General Brigham relies on a wide range of... ...clinical teams, Institutional Review Boards (IRB), clinical trial sponsors, and federal... ...and communication skills. Remote Work Location: 55 Fruit Street Pay...Remote workRegulatoryHourly payContract work$85k - $125k
...member of the Alira Health Clinical team. The CRA is highly... ...Alira Health SOPs and regulatory requirements, i.e. Good... ...necessary. Supports research sites with local Institutional Review Board (IRB)/Ethics Committee (EC)... ...in an environment of remote collaborators. EU (Italy...Remote workRegulatoryContract workWork at officeLocal areaFlexible hours$80k - $125k
.... Primary Role The Clinical Research Associate (CRA) is responsible for the... ...SOPs, GCP guidelines, and regulatory requirements from site initiation... ..., the Ethic Committees (IRB/IEC), Sponsor and the... ...goals Location Remote Salary Range $80-125...Remote workRegulatoryInterim role2 days per week1 day per week- ...LLC Position Title: Sr. Clinical Research Associate *Multiple Openings... ...Raleigh, NC 27609 *100% Remote reporting to Raleigh, NC.... ...specific documents, essential regulatory documents, and updated or amended... .... Prepare and submit IRB/IEC and MoH/RA applications...Remote workRegulatoryFull timeImmediate start
$103k - $130k
...Sr. Clinical Research Associate (Sr. CRA) The Sr. Clinical Research Associate (Sr. CRA) is... ...organization. The role is fully remote within the United States. Responsibilities... .../or outstanding queries. Manage IRB submissions and all study regulatory documentation to maintain an...Remote workRegulatoryContract workNight shift- ...years prior experience in clinical operations role to be... ...LOCATION This is a remote position. SUMMARY... ...sites, maintaining regulatory compliance, contributing... ...ICF review/approval, IRB/EC submission (including... ...the activities associated with site startup....Remote workRegulatoryContract workLocal areaWorldwide
- ...Job Purpose: The Clinical Research Associate (CRA) has local responsibility... ...accountable for study start-up and regulatory maintenance. Tasks may... .../documents to EC/IRB and to Regulatory Authorities... ...Performs monitoring visits (remote and onsite), as well as remote...Remote workRegulatoryLocal areaFlexible hoursShift work
- ...Overview Clinical Research Associate I Be Part of One Team, One Purpose.... ...at investigative sites or remotely to ensure clinical trials are... ...ICH GCP, and all applicable regulatory requirements. The CRA will... ...Institutional Review Board IRB Ethics Committee EC Regulatory...Remote workRegulatoryWork experience placementInterim roleCasual workLocal areaWork from homeFlexible hours
- ...world's health. From clinical trials to regulatory, consulting, and... ...application/documents to EC/IRB and to Regulatory... ...monitoring visits (remote and onsite), as well... ...with the activities associated with audits and... ...Provides feedback on any research related information...Remote workRegulatoryLocal areaFlexible hoursShift work
- ...Senior Clinical Research Associate (Sr. CRA) The Senior Clinical Research Associate... ...Clinical Practice (GCP), regulatory requirements, and company... ...activities (on‑site, virtual, remote). Actively participate... ...(GCP, FDA, ISO), IRB/EC requirements, and company...Remote workRegulatoryContract work
- ...Senior Clinical Research Associate Veranex's mission as an Innovation CRO is to... ...preclinical and clinical research, regulatory affairs, and market access... ...studies. Location: Remote, US What You Will Do:... ...Institutional Review Board (IRB)/Ethics Committee (EC) requirements...Remote workRegulatoryWork experience placementWork at officeShift work
$4,000 - $9,000 per month
...Clinical Research Associate DotLab is transforming the diagnosis and management... ...initially focus on conducting remote site visits including... ...protocols and all applicable regulatory frameworks. In the future,... ...applicable regulatory standards, IRB policies, and DotLab...Remote workRegulatoryWork experience placementWork at officeWorldwideFlexible hours$110.52k - $138.15k
Senior Clinical Research Associate - Oncology - Central/East (NY/NJ or TX) ICON... ...compliant with applicable local regulatory requirements and... ..., informed consent review, IRB/IEC submission support, and... ...collected, either onsite or remotely Provides regular site status...Remote workRegulatoryWork experience placementLocal areaWork visa$48k - $60k
...the Town of Mount Pleasant, NY is seeking a Clinical Research Coordinator to manage pre-clinical trial setup, ensure regulatory compliance, and oversee patient screening and... ...prioritization. Responsibilities include assisting in IRB processes, monitoring adverse events, and...Regulatory- ...Senior Clinical Research Associate - Oncology Phase I - Miami, FL ICON plc is... ...and the sites ~ Perform remote and on-site monitoring/co-monitoring... ...Review Board (IRB)/Ethics Committee (EC) submissions... ...sites and the client's regulatory inspections ~ Contribute...Remote workRegulatoryInterim roleLocal areaFlexible hours
- Alameda Health System seeks a Clinical Research Associate to coordinate all aspects of clinical trials at the Adult Immunology Clinic,... ...patients when appropriate. Responsibilities include regulatory compliance, IRB coordination, budgeting, and assisting investigators...Regulatory
$100.7k - $167.9k
...Sr. Clinical Research Associate (CRA) Dexcom Corporation (NASDAQ DXCM) is a pioneer... ...to study reports and regulatory submission deliverables.... ...Institutional Review Boards (IRBs), and key opinion leaders.... ...operations, including on-site and remote training & support,...Remote workRegulatoryWorldwideHome officeFlexible hours$110.52k - $138.15k
...Senior Clinical Research Associate - Oncology - Central/East (NY/NJ or TX) ICON... ...compliant with applicable local regulatory requirements and... ..., informed consent review, IRB/IEC submission support, and... ...collected, either onsite or remotely Provides regular site status...Remote workRegulatoryWork experience placementLocal areaWork visaFlexible hours$85k - $105k
...POSITION SUMMARY: The Clinical Research Associate II (CRA II) will be a key contributor... ...prior to submission to the IRB/EC. Collection of startup... ...SOPs, GCP, and applicable regulatory requirements to the... ...background check #LI-KN1 #REMOTE Positions in Minnesota...Remote workRegulatoryFull timeTemporary workInterim roleWork at officeLocal areaWorldwide- ...principal investigator of a clinical research study. The position... ...data, and compiling regulatory reports. This position... ...studies. May oversee remote screening locations. Monitors... ...documents such as IRB applications.... ...direct experience for an associate degree; • (b) Four years...Remote workRegulatoryFull timeContract workTemporary workWork experience placementFor subcontractor
$120k - $135k
Company & Job Overview The Clinical Research Associate (CRA) will support Clinical Operations... ...preparing and submitting regulatory and ethics documents such as IRB/EC submissions, contracts, and... ...Clinical Monitoring Perform remote monitoring activities such as source...Remote workRegulatoryContract workWork at office- Clinical Research Associate II Emmes Group is a full-service contract research organization... ...Responsibilities Schedule and conduct remote and onsite monitoring visits... ...to Institutional Review Board (IRB) / Ethics Committee (EC) / Regulatory Authority. Assist with site...Remote workRegulatoryContract workInterim role
- Clinical Research Associate I (Onsite) The Clinical Research Associate I position is... ...Los Angeles, CA. Hybrid or remote work options are not available... ...‑up patients. Assist with regulatory submissions to the Institutional Review Board (IRB) including adverse events, serious...Remote workRegulatoryLocal area
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