FDA Regulatory Investigator
FDA
FDA in the United States seeks an Associate Investigator in the 0696 occupational series, working under streamlined Title 21 authority, and paid under the Band W pay table. The role involves inspections of FDA-regulated industries and preparation of evidentiary reports to support regulatory actions. Ideal candidates will have a bachelor's degree or higher in a relevant field or at least 2 years of related experience, with transcripts submitted. #J-18808-Ljbffr FDA
- ...Qualifications In order to qualify for the Associate Investigator position which falls under the 0696... ...positions that conduct inspections in FDA regulated industries and prepare and... ...The Food and Drug Administration is the regulatory, scientific, public health, and consumer...RegulatoryWork at office
- ...Manufacturing Technical Operations (MTO) Quality Investigations Specialist is responsible for the end‑to... ...all quality records meet internal and regulatory expectations for completeness, accuracy,... .... ~ Working knowledge of cGMP , FDA/EMA regulations, and quality systems....RegulatoryContract workShift work
$30 - $35 per hour
...experienced, self-determined, and highly motivated Part-Time SIU INVESTIGATORS that would like to join our team of professionals in our... ...coordinates with law enforcement and / or the state fraud bureaus for regulatory compliance and criminal prosecutions. The successful...RegulatoryBi-weekly payHourly payFull timePart timeWork at officeWork from home- ...Corporation in Burlington, MA is seeking an Associate Director, Regulatory Affairs to coordinate regulatory review and approval of... ...represent Regulatory on MRC and PRC, and lead interactions with FDA OPDP for respective products. The role oversees regulatory operations...Regulatory
$170.9k - $231.3k
OverviewThe Associate Director of Regulatory Affairs Strategy will work on assigned programs... ...submission of data packages to the US FDA and other international health agencies... ..., Briefing Documents for HA meetings, Investigational New Drug (IND) applications, new...RegulatoryFull timeTemporary workLocal areaWorldwideFlexible hours2 days per week$250k - $273k
...advancing a growing portfolio of approved and investigational medicines, anchored by its lead product, ARCALYST, the first and only FDA‑approved therapy for recurrent... ...compliance programs, ensuring alignment with regulatory requirements and industry best practices....RegulatoryWork at office- ...analytical and research activities in concise reports or memoranda.Essential Functions-Responsible for conducting confidential investigations of suspected fraud, waste & abuse (FWA) involving medical providers, plan members, or other entities or individuals.-Investigative...Full timeContract workWork at officeLocal areaMonday to FridayFlexible hours
$79.56k - $115.72k
...analytical and research activities in concise reports or memoranda. Essential Functions -Responsible for conducting confidential investigations of suspected fraud, waste & abuse (FWA) involving medical providers, plan members, or other entities or individuals. -...Full timeContract workWork at officeLocal areaRemote workMonday to FridayFlexible hoursShift work- ...candidates with clinically validated targets, established endpoints for regulatory approval, and strong market potential. Our pipeline includes... ..., quality standards, and regulatory expectations (eg, ICH, FDA, EMA). Manage CROs and contractors to ensure compliance,...RegulatoryFor contractorsWork at officeLocal area
- ...Align and Veeva PromoMats implementations as needed. Ensure all configurations and solutions align with industry best practices and regulatory compliance standards. Requirements: Senior-level hands-on experience configuring and implementing Veeva CRM in a Pharma/Life...RegulatoryRemote work
$200k - $400k
...seeking a highly skilled and experienced virtual Principal Investigator to join our team. As the Principal Investigator, you will be... ...on Harmonization – Good Clinical Practice) and all applicable regulatory requirements Participate in monitoring visits and sponsor...RegulatoryFull timeTemporary workPart timeWork at officeLocal areaRemote workWorldwideVisa sponsorshipWork visaFlexible hours$130k - $165k
...Care Access, visit How This Role Makes a Difference The Sub-Investigator will be responsible for travel mixed with remote tele-... ...maintain a safe clinical environment. Protocol Compliance & Regulatory Oversight Ensure compliance with study protocols, GCP, SOPs...RegulatoryFull timeTemporary workWork experience placementLive inLocal areaRemote workWorldwideFlexible hours- ...Our client is looking to appoint a Paralegal to their Legal & Compliance team, supporting transactional, contractual and regulatory work across the group's funding products. The successful candidate will provide hands‑on support to legal counsel, from contract drafting...RegulatoryContract work
- ...MA is seeking an Asset Protection Coordinator to execute safety and shortage reduction strategies in stores. The role involves investigating theft, training store teams, and collaborating with law enforcement to maintain a secure environment. The candidate should possess...
$315k - $325k
...advancing a growing portfolio of approved and investigational medicines, anchored by its lead product, ARCALYST, the first and only FDA‑approved therapy for recurrent... ...dose selection, clinical trial design, and regulatory strategy for biologic therapies from pre-clinical...RegulatoryWork at office- ...Chief Medical OfficerPosition SummaryThis individual will lead regulatory strategy and execution for growing clinical-stage oncology pipeline... ...regulatory submissions. Lead and coordinate interactions with FDA and international health authorities. Support clinical...Regulatory2 days per week3 days per week
- ...process simulations. Conduct microbial testing, deviation investigations, and CAPA processes to resolve quality issues. Monitor... ...within sterile manufacturing. Knowledge of regulatory guidance (FDA, EU, JP) and experience with aseptic processing, bioburden...RegulatoryFull timePart timeRemote work
- Mass General Brigham Health Plan Holding Company, Inc. seeks a Data Analyst focused on fraud, waste and abuse investigations. The role conducts confidential investigations, data analysis, and public records research to identify improper claim submissions. The position...
- Mass General Brigham Health Plan is seeking a Data Analyst to create, refine, and perform analytic reporting aimed at identifying potential fraudulent, wasteful, or abusive claim submissions. The role includes preliminary research of providers or members, using public records...Full time
$215k - $235k
...sounds like you then please read on!About the Role:The Director of Regulatory Affairs is responsible for leading regulatory strategy and... ...program teams and as the primary regulatory point of contact with FDA and other global health authorities.The Director provides...Regulatory$143k - $233k
...this position will play a key role in regulatory strategy development and execution of assigned... ...the execution of regulatory CMC investigational, registration and/or post-approval strategies... ...requirements and guidelines (e.g. FDA, EMA, ICH).Positive attitude, energetic...Regulatory$186.23k - $279.35k
..., and curious about what science can do, then you’re our kind of person.In this role, you will:Provide strategic and operational regulatory leadership to the development, commercialization and life cycle management of the assigned products in product teams. Apply knowledge...RegulatoryFull timeTemporary workWork at officeLocal areaWorldwideFlexible hours3 days per week- ...Regulatory Affairs ManagerA Few Words About Us Integrated Resources, Inc is a premier staffing... ...project teams on compliance matters, FDA requirements, clinical study design... ...other health authorities for assigned Investigational New Drug (IND) and New Drug Applications...Regulatory
- ...Safety Schedule: Full TimePOSITION SUMMARY:Under direction of the Sergeant, the Detective will perform comprehensive criminal investigations, non-criminal investigations, law enforcement and crime prevention work, conduct interview and interrogations and prepare cases...Full timeFixed term contractLocal areaFlexible hours
$2,280 per week
...Communicate with physicians, nurses, caregivers, and other healthcare professionals Ensure compliance with clinical, safety, and regulatory standards Support patients in improving strength, range of motion, balance, mobility, and independence Qualifications...RegulatoryFull timeContract workImmediate startShift work- ...organization.Brief team/department description:As a part of the Regulatory Affairs team at Azurity, the Regulatory Affairs Manager will be... ...development activities.Serve as primary interface with FDA and Health Canada for assigned products. Prepare and author portions...RegulatoryLive in
- ...ongoing basis (actual‑to‑expected actuarial dashboard). Help implement product changes or revisions to ensure timely response to regulatory and market requirements. Support periodic analysis and update of pricing assumptions. Analyze competitor product offerings and market...RegulatoryFull timeInternshipWork at officeRemote work
$286k - $316k
...advancing a growing portfolio of approved and investigational medicines, anchored by its lead product, ARCALYST, the first and only FDA‑approved therapy for recurrent... ...Committees (DMC)Partner with Biometrics and Regulatory Affairs to ensure clinical data support statistical...RegulatoryInterim roleWork at office- ...Solutions is seeking a skilled and self-motivated Senior/Principal Regulatory Affairs Specialist to support the BrioVAD® Left Ventricular... ...submission activities. You will prepare, review, and maintain FDA submissions, provide regulatory guidance, and monitor changes in...Regulatory
$161k - $186k
...advancing a growing portfolio of approved and investigational medicines, anchored by its lead product, ARCALYST, the first and only FDA‑approved therapy for recurrent... ...Development and Operations, Clinical Pharmacology, Regulatory, Biostatistics.Contribute as a SME to...RegulatoryWork at office
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