Clinical Trials Regulatory Assistant IRB Submissions
BRCR Global
BRCR Global is seeking a Regulatory Assistant in Florida, NY to support daily regulatory activities and ensure compliance in clinical trials. The role involves preparing and managing regulatory documents such as protocols and consent forms, communicating with the IRB and sponsors, and assisting with audits and training. The ideal candidate has a Bachelor's degree in Science, at least one year of relevant experience, and is bilingual in English and Spanish. Strong communication skills are essential for this position. #J-18808-Ljbffr
- ...Memorial Healthcare System is seeking an IRB Coordinator in New York to manage daily activities of the IRB office. The role includes reviewing research protocols for regulatory compliance and assisting with board meetings. The ideal candidate will have a Master’s degree...RegulatoryWork at office
$71.9k - $189k
...Clinical Research Associate, Sponsor Dedicated Hollywood, United States of America |... ...progress of assigned studies by tracking regulatory submissions and approvals, recruitment and... ...documents are available for filing in the Trial Master File (TMF) and verify that the...RegulatoryFull timePart timeLocal areaImmediate start$155.68k - $202.38k
...QuidelOrtho seeks a Senior Manager of Regulatory Affairs to lead and support regulatory strategies for the Transfusion Medicine Business Unit. Ideal candidates will have over 10 years in the regulated diagnostics industry and 7 years specifically in regulatory strategy...RegulatoryRemote work- ...Clinical Research Associate - Oncology - West Palm Beach, FL ICON plc is a world‑leading... ...elevate risks or issues to the clinical team Assist in tracking site budgets and ensuring... ...studies Proficient in ICH‑GCP, local regulatory requirements, and clinical systems like...RegulatoryLocal areaVisa sponsorshipFlexible hours
- ...About Evestia Clinical Evestia Clinical is a biotech‑focused global... ...guidance through complex clinical trials in specialized areas,... ...any visit types while ensuring regulatory and protocol compliance Participate... ...Corporate Holidays Employee Assistance Program (EAP) Wellness...RegulatoryTemporary workWork at officeFlexible hours
- A research organization in New York is seeking a Regulatory Associate to manage regulatory documents for clinical trials. Responsibilities include preparing submissions to the IRB and sponsor, maintaining compliance, and coordinating with multiple teams. The ideal candidate...RegulatoryFull time
- ...Clinical Research Associate - Cross Therapeutic Area - Miami ICON plc is a world-leading... ...escalate risks or issues to the clinical team Assist in tracking site budgets and ensuring... ...preferred. Proficient in ICH-GCP, local regulatory requirements, and clinical systems like...RegulatoryLocal areaVisa sponsorshipFlexible hours
- ...The Regulatory Assistant plays a crucial role in the clinical trial process by giving support and overseeing the daily regulatory... ...all the communication with the IRB and Sponsor. Prepare each study... ..., and any other IRB-required submissions. Work with staff members to...Regulatory
- ...of the Institutional Review Board (IRB) office, including review of research protocols for regulatory compliance, protocol review management, and assistance with the meetings of the Board.... ...and facilitates revisions to the submissions. Makes final outcome determinations...RegulatoryWork experience placementWork at office
- The Regulatory Associate is responsible for the development... ...pertaining to the clinical trials conducted at K2... ...start‑up, modification submissions, ongoing reporting, and... ...Review Board (IRB) and the clinical trial... ...the need for archiving assistance of closed regulatory...RegulatoryFull timeImmediate startMonday to ThursdayShift workWeekend work
- ...Lupin Pharmaceuticals, Inc. is seeking a Senior Director of Regulatory Affairs based in New York. This role involves managing regulatory... ...for complex inhalation products, coordinating high-quality submissions to the FDA, and building effective relationships with...Regulatory
- ...Executive Search is looking for a Director of Regulatory Affairs for an immune-oncology biotech... ...emphasizes ownership across IND submissions and regulatory documentation like DSURs... ...manage agency interactions while shaping clinical development strategy. #J-18808-Ljbffr...Regulatory
- ...Manufacturing, and VP of Engineering, the Head of Licensing and Regulatory Affairs leads the implementation of AMPERA's licensing... ...communication skills. Experience in the development, review, and submission of technical documentation and government correspondence. Strong...Regulatory
- ...month contract in Town of Florida, New York. This role supports compliance with tax abatement agreements and regulatory reporting while ensuring accurate submission of documentation. Key responsibilities include preparing compliance documents, coordinating with various...RegulatoryContract work
- ...overseeing interprofessional instructional design and ensuring regulatory compliance with all accreditation bodies. They execute and... ...managing multiple accreditations. Direct experience managing data submissions, credit tracking, and compliance for JA‑PARS, MOC, CE broker,...RegulatoryWork experience placement
- ...overcoming resistance to cancer immunotherapy is seeking a Director of Regulatory Affairs, a hands‑on role with capacity for real ownership across IND submissions, DSURs, Investigator's Brochures, and clinical protocols. What we're looking for 8-12+ years of regulatory...Regulatory
$183k - $228.8k
A leading medical technology company is seeking a Senior Advisor in Regulatory and Clinical Affairs. This remote role involves guiding regulatory strategies and supporting FDA submissions for medical devices. Candidates must have a Master's degree or equivalent, extensive...RegulatoryRemote work- ...compliance with tax abatement agreements, regulatory reporting requirements, and internal... ...ensures accurate, timely preparation and submission of required documentation while collaborating... .... Perform operational SOX testing and assist with fixed asset and inventory...RegulatoryContract workLocal area
$16.3 per hour
...Description Summary Under immediate supervision, this position assists with the preparation, set up, break down, and clean‑up of the... ...waste materials properly according to established safety and regulatory protocols. Assists faculty with lab activities. Maintains laboratory...RegulatoryHourly payPart timeWork at officeImmediate startMonday to FridayWeekend work- ...Clinical Appeals Nurse (RN) Status: Exempt Location: Remote Department: Clinical... ...clinical guidelines, payer policies, and regulatory standards Draft clear, concise, and... ...documentation Timeliness of appeal submission Identification of systemic denial trends...RegulatoryRemote work
- ...Associate/ Assistant Vice President for Research Administration... ...University, including application submissions, contracting, post award... ...strict compliance with regulatory requirements and providing... ...of the research community. Clinical Trials Management : Assist in the...RegulatoryContract work
- ...performance, and compliance with legal and regulatory requirements. Essential Duties and... ...and executive summaries. Complete survey submissions for annual and ad hoc salary surveys... ...compensation and incentive initiatives. Assists in the preparation of meeting materials...RegulatoryTemporary work
$183k - $228.8k
...What's the role? The Senior Advisor,Regulatory and Clinical Affairs,USis responsible... ...strategy andsupport of a variety of FDA submissions including pre-submissions (Q-subs), pre... ...Dental ~401k Matching ~ Employee Assistance Programs ~ Paid time off including...RegulatoryLocal areaRemote work$133.3k - $183.3k
...validation activities, and ensuring our IT environment meets regulatory and internal policy requirements. The ideal candidate is a self... ...in your resume and application is accurate and authentic. Submissions found to be fraudulent or misleading will result in disqualification...RegulatoryFull timeWork at officeRemote work3 days per week- ...bank requirements, card network rules, and regulatory frameworks. We specialize in... ...Manage merchant onboarding from application submission through account activation . Collect... ...high-risk merchant cases when needed. Assist with maintaining underwriting documentation...RegulatoryRemote workVisa sponsorshipFlexible hours
- ...efficient services to clients. By streamlining regulatory processes, Florida Building Code... ...Authority Inc. plays a vital role in assisting businesses and individuals with their construction... ...and meeting deadlines for client submissions. Qualifications Valid DBPR Inspector...RegulatoryFull time
- ...people that work for us. SUMMARY OF FUNCTIONS The Safety Assistant supports the implementation and maintenance of health... ...state, and local environmental regulations and help prepare regulatory reports and submissions. Assist in emergency preparedness planning, including...RegulatoryLive inWork at officeLocal areaRelocation package
- ...regulations and payer requirements. Ensure timely and accurate submission of claims and the effective management of accounts receivable... ...possible to improve efficiency in revenue cycle processes. Monitor regulatory changes that impact revenue cycle operations and ensure...RegulatoryLocal areaRemote work
- ...Oversee billing and coding processes to ensure accurate and timely submission of claims. Ensure compliance with coding guidelines, payer requirements, and regulatory standards. Collaborate with clinical departments to resolve coding and documentation issues. Claims...RegulatoryLocal area
- ...Responsibilities The Senior Director of Regulatory Affairs is responsible for establishing... ...and HORA, reviewing ANDAs pre- or post-submission, proactively working with cross-... ...development experience required (CMC and PK/PD Clinical development). Responsible for the...RegulatoryWork at office
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