Regulatory Affairs Specialist, Cancer Clinical Trials
BILH Performance Network
Beth Israel Deaconess Medical Center (BIDMC) is seeking a Regulatory Affairs Specialist to support the Cancer Clinical Trials Office (CCTO). You will prepare IRB submissions, assist with INDs, and coordinate regulatory documents for oncology trials across multiple disease programs. You'll work with investigators and cross‑functional teams to ensure compliance, timely trial activations, and accurate regulatory reporting to FDA/NIH. #J-18808-Ljbffr BILH Performance Network
$82k - $131.5k
...Discover your opportunities at Yale! Overview Reporting to the Regulatory Affairs Manager, the Senior Regulatory Affairs Specialist independently leads regulatory activities for Yale Cancer Center Clinical Trials Office clinical research protocols from study activation...SuggestedFull timeInterim roleWork at officeLocal areaRemote work$60.01k - $88.01k
...people’s lives. This position is in the Cancer Clinical Trials Office (CCTO), supporting multiple... ...submission of other study documents to support regulatory compliance, and troubleshoots... ...Master's degree preferred in Regulatory Affairs 1-3 years related work experience required...SuggestedWork experience placementWork at officeLocal areaImmediate start- Tampa General Cancer Institute is seeking a Cancer Registrar I to ensure cancer data are abstracted completely and accurately in line with ACS and Florida CDS requirements. The role includes case finding, abstracting eligible cancer cases, and maintaining lifelong follow...Suggested
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$80.9k - $127.05k
...What Regulatory Affairs contributes to Cardinal Health Regulatory provides regulatory affairs... ...and regulatory submissions as well as clinical research and manufacturing process consulting... ...The Principal Regulatory Affairs Specialist supports the Medical Solutions Regulatory...SuggestedTemporary workWork experience placementLocal areaRemote workFlexible hours$65k - $101k
...Overview Reporting to the Director of Operations at the Yale Cancer Center Clinical Trials Office, the Research Billing Compliance Analyst is the... .... Advanced knowledge and experience with clinical trial regulatory documents such as protocols, informed consent documents,...Full timeWork at officeRemote work- Yale Cancer Center is seeking a Research Billing Compliance Analyst to serve as the primary liaison for centralized billing offices... ..., ensure CMS alignment, and maintain documentation within the Clinical Trial Management System. The role requires a Bachelor’s degree in Health...Remote job
$120k - $160k
Senior Regulatory Affairs Specialist Location: Remote (U.S. only, excluding Alaska and Hawaii) Job Type... ...analysis in infant brain imaging Breast cancer pathology AI with predictive and... ...use scoping, predicate analysis, and clinical study design. Deliver clear, actionable...Full timeRemote workFlexible hours- ...company powering the acceleration of clinical research to transform patient outcomes... ...cardiology. By combining deep clinical trial expertise with cutting-edge AI, we connect... ...world-wide. As a Senior Clinical Regulatory Specialist at Iterative Health, you will play a key...Temporary workWork at office2 days per week
- ...Nihon Kohden Orange Med is seeking a Regulatory Affairs Specialist to coordinate routine regulatory activities across domestic and international markets, supporting product registrations, submissions, and post-market requirements. You will manage regulatory information...
$107.2k - $160.8k
...Select how often (in days) to receive an alert: he Regulatory Affairs Specialist is responsible for day-to-day regulatory affairs tasks required... ...and approve IFU, labels and promotion material Work with Clinical and Quality to prepare post-market data for inclusion in...Work at officeImmediate startFlexible hours- ...industry in Australia and is applying this same pioneering spirit to solving future energy challenges. About the Role The Regulatory Affairs Specialist supports execution of the Louisiana LNG regulatory program throughout the full project lifecycle, from project...Part timeFor contractorsWork at officeLocal areaRelocation packageFlexible hours
$99k - $129k
## Senior Regulatory Affairs SpecialistApplyremote type: Fully Remotelocations: Remote - UStime... ...the role of **Senior Regulatory Affairs Specialist** with global regulatory expertise.... ...data from millions of heartbeats into clinically actionable information. Through a relentless...Full timeWork at officeRemote work- ...Senior Regulatory Affairs Specialist This will person will be a Regulatory liaison between product development and the regulatory agencies. This position will be responsible for regulatory submissions for new ANDAs and any changes being made to existing products. The...
- ...CrossCountry Mortgage, LLC is seeking a Regulatory Affairs Counsel to manage and support responses to federal and state regulatory examinations, audits, and inquiries. This role requires providing consistent and effective counsel during the examination lifecycle while...
$103.3k - $141k
...multiple compounds in mid- to late-phase clinical development across our core therapeutic... ...and preparation of document packages for regulatory submissions for new and mature products... ...earliest possible approvals of clinical trials applications. May act as Regulatory Strategy...Local area- ...A leading company in workforce solutions is looking for a Regulatory Support Specialist to guide product compliance and manage regulatory submissions... ...in natural sciences, substantial experience in regulatory affairs, and the ability to navigate complex compliance issues...
$186.4k - $209.7k
...scale. Modern financial infrastructure presents a similar challenge. Payment systems, banking products, compliance obligations, and regulatory frameworks all exist for a reason. The goal isn’t to eliminate complexity. It’s to build systems that allow innovation, growth,...Remote workShift work$80k - $95k
...updates as new positions become available. Job Purpose The Regulatory Affairs Specialist is responsible for coordinating and executing routine... ...Coordinates with internal departments to obtain technical, clinical, quality, labeling, and other supporting documentation necessary...Work at officeWorldwideWeekend workAfternoon shift- Rowell’s Services in New Hampshire is seeking a Licensed Septic Inspector to join a family-owned, service-focused team. You will inspect septic systems, communicate clearly with customers and the dispatch and keep the company vehicle ready for the next call. We value craftsmanship...
$56.6k - $88.44k
...inspections of manufacturing and distribution warehouse operations to identify hazards and ensure compliance with company policies and regulatory requirements Support incident investigations and root cause analyses; recommend corrective and preventive actions and verify...Work experience placementWork at officeLocal areaWorldwideFlexible hours- Key Responsibilities Author, compile, review, and submit regulatory documents in eCTD format, including NDAs, ANDAs, DMFs, and post-approval... ...discipline or equivalent experience. 2+ years of Regulatory Affairs experience within the pharmaceutical industry. Experience...Work at office
- ...Reports to: Vice President, Regulatory Affairs & Quality Assurance ABOUT SYNERGY... ...-level Regulatory Affairs Specialist to support the global... ...tissue between R&D, Quality, Clinical, and our commercial and distributor... ...and international clinical trials. Monitor evolving FDA...Full time
- Enbridge is seeking a Specialist II, Regulatory Affairs to support development of intrastate natural gas pipeline projects through regulatory filings, compliance, and permitting activities. The role requires strategic regulatory guidance and market intelligence to advance...
- Eastman seeks a Regulatory Affairs Specialist II for International Chemical Control Laws at its Kingsport corporate HQ. The role focuses on supporting registration requirements, regulatory compliance, and global submissions across markets. Responsibilities include coordinating...
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- Select how often (in days) to receive an alert: Regulatory Affairs Specialist II - International Chemical Control Laws Founded in 1920, Eastman is a global specialty materials company that produces a broad range of products found in items people use every day. With the...Night shift
- Harba Solutions Inc. is seeking a Regulatory Affairs professional to manage end-to-end eCTD submissions, maintain regulatory documentation, and support FDA activities for marketed pharmaceutical products. You will monitor FDA and international guidelines, draft labeling...
- Senior Regulatory Affairs Specialist - Medical Devices Clinical San Diego , California Contract Aug 10, 2026 Senior Regulatory Affairs Specialist - Medical Devices Position Overview Viltis is seeking an experienced Senior Regulatory Affairs Specialist to support a leading...Contract work
$36.31 - $38.22 per hour
Job Summary The Compliance Specialist ensures that the regulatory and compliance requirements are met for each property and reports to the Associate Director... ..., ancestry, citizenship, disability, medical condition (cancer or genetic characteristic), genetic information or...Hourly payFull timeWork at officeLocal area
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