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
- Beth Israel Deaconess Medical Center (BIDMC) is seeking a Regulatory Affairs professional to support cancer center trials and regulatory submissions within the Cancer Clinical Trials Office (CCTO). The role involves preparing IRB submissions, amendments, INDs, and safety...SuggestedWork at office
$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$190k - $210k
Olema Oncology is a clinical-stage biopharmaceutical company committed... ...patients living with breast cancer and beyond. It’s an exciting... ...pivotal Phase 3 clinical trials. We expect top‑line data... ...Associate Director, Global Regulatory Affairs, Compliance As the Global Associate...SuggestedWork at officeFlexible hours2 days per week- ...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...SuggestedTemporary workWork at office2 days per week
- ...powering the acceleration of clinical research to transform... ...By combining deep clinical trial expertise with cutting-edge... ...employees world-wide.As a Clinical Regulatory Specialist at Iterative Health, you will... ...clinical research, regulatory affairs, clinical operations, or a...SuggestedTemporary workWork at office2 days per week
- ...execution phases, and provide budgeting/financial flexibility by offering contingent labor as a variable cost.Job Description• The Regulatory Affairs Operations (RA Ops) submission group is organized to provide submission development support to project teams and the...Immediate start
- ...Clinical Research Compliance Specialist Vice President for Research, to ensure compliance with federal, state... ...familiarity with IRB processes and regulatory requirements. PREFERRED: Master of... ...with FDA-regulatory and industry-sponsored trials. Revised 2/26/2026...Local area
$94k - $150k
Job TitleSenior Regulatory Affairs SpecialistJob DescriptionSenior Regulatory Affairs Specialist, UltrasoundThe Senior Regulatory Affairs Specialist for Ultrasound collaborates... ...ANVISA, and offering strategic guidance on clinical studies and evaluations.Your role:Act as an...Full timeWork at officeImmediate startWork visaRelocation package3 days per week$120k - $160k
...members to perform at a higher level through a deep understanding of their bodies and daily lives.WHOOP is looking for a Regulatory Affairs Specialist II, Expansion to be a core member of the Digital Health team.As the Regulatory Affairs Specialist II, Expansion, you...Full timeWork at officeRelocation- Tufts Medical Center in Boston seeks a Regulatory Project Manager to oversee regulatory requirements of clinical research projects under PI supervision. You will coordinate protocol submissions, prepare documents, and maintain study records to ensure compliance with Tufts...
- CLINICAL RESEARCH COMPLIANCE SPECIALIST , Vice President for Research, to ensure compliance with federal, state, and local policies, and guidelines related to research protocols involving human subjects at MIT on behalf of the Committee on the Use of Humans as Experimental...Local area
- ...Regulatory Affairs Associate Integrated Resources, Inc is a premier staffing firm recognized... ...specialty areas: Information Technology (IT), Clinical Research, Rehabilitation Therapy and... ...CRO to file initial CTAs (clinical trial applications) and amendments Tracking...
$147.4k
Posting Description SENIOR LICENSING AND BUSINESS DEVELOPMENT OFFICER, Technology Licensing Office, is responsible for the commercialization of MIT’s IP portfolio arising from research and activities on MIT’s campus; managing a large portfolio of cases, including, technology...Full timeWork at officeVisa sponsorship$120.44k
Posting Description LICENSING AND BUSINESS DEVELOPMENT OFFICER, Technology Licensing Office, is responsible for the commercialization of MIT’s intellectual property (IP) portfolio arising from research and other activities on MIT’s campus. The Licensing Officer manages ...Permanent employmentFull timeWork at officeVisa sponsorship- ...regions. Position Summary The position of Senior Regulatory Affairs Specialist is responsible for preparing regulatory submissions (e.g... ...functional collaboration with Manufacturing, Quality, R&D, Clinical and Marketing departments. · Computer proficiency in MS...For subcontractorRemote workFlexible hours
- ...Description Our client, a growing biopharma company, is seeking a Regulatory Affairs Specialist to support regulatory strategy and submission activities as the company advances its pipeline through clinical development. Key Responsibilities Support preparation,...Shift work
- ...multiple openings for Life Science Quality Assurance Analysts, Regulatory Affairs Specialist, and Quality Control Analysts. All of these roles will... ...industry with a focus on information technology, clinical research, quality, regulatory affairs, manufacturing, or...H1bRelocationRelocation package
- Olympus Corporation is hiring for a Regulatory Affairs role based in Massachusetts. The successful candidate will assist in obtaining marketing approvals and provide regulatory input for new product developments. Candidates should have at least 3 years of regulatory affairs...
$175.35k - $219.2k
...the Job: The Associate Director, Regulatory Affairs is responsible for supporting the regulatory... ...to guide treatment options for cancer patients. The incumbent functions as the... ...implement regulatory strategy for non-clinical product development and clinical development...- ..., focuses on implementing and maintaining governance frameworks, managing risk remediation activities, and ensuring adherence to regulatory and internal security standards. The incumbent oversees requirements gathering and documentation for the Identity and Access Management...Work experience placementWork at officeLocal area
$130k - $150k
...to help you reach your potential, but also to contribute to our clients’ success.About the DepartmentFranklin Templeton’s Global Regulatory Compliance department provides oversight, guidance and monitoring of the various teams who market Franklin Templeton’s products and...Full timeWork at officeLocal area- ...Job Overview: We are seeking a detail-oriented Regulatory Associate to join our Regulatory Affairs team. In this role, you will play a vital part in... ...standards, and facilitating the approval process for clinical trials and product launches. This position offers the...Contract workWork at office
$80k - $150k
...registered reps•Assisting with Compliance testing related to broker-dealer and marketing procedures and practices•Assisting with regulatory training of client-facing personnel•Staying informed of regulatory changes and industry trends and business•Assisting in responding...Full timeRemote workFlexible hours1 day per week$98.18k - $115.5k
...individual will be primarily responsible for reviewing and monitoring elements of Adviser compliance programs in an ever-changing regulatory environment, a variety of internal and external documentation and reporting and preparing for and conducting annual due diligence...Full timeWork at officeLocal areaRemote workFlexible hours3 days per week- ...Development, the Office of the General Counsel) to ensure timely service delivery, risk management, and compliance with all applicable regulatory, funder, and university requirements.Position Summary:Reporting to the Senior Director of the Office of Research and Academic...Work at office
- ...Security to oversee all duties related to Metro Boston Security Team Specialist Department and Metro Boston Transportation services, and... ...time, experience in investigatory or law enforcement work, or regulatory administration work (B) and equivalent combination of the...Full timePart timeWork experience placementWork at officeLocal areaMonday to FridayWeekend work
$86.7k - $170.9k
Position Summary Consultant - Regulatory & Compliance - Enterprise Operations & Risk Our Deloitte Regulatory, Risk & Forensic team helps client leaders translate multifaceted risk and an evolving regulatory environment into defensible actions that strengthen, protect...Local areaVisa sponsorship$150k - $200k
...program across registered private equity funds, private debt funds, and exchange-traded funds (ETFs), ensuring adherence to applicable regulatory requirements and internal policies. This role will work closely with investment, operations, legal, product, and distribution...Full timeLocal area3 days per week- ...must have at least (A) four years of full-time, or equivalent part-time, experience in investigatory or law enforcement work, or regulatory administration work (B) and equivalent combination of the required experience and the substitutions below.Substitutions:A Bachelor...Full timeContract workTemporary workPart timeWork experience placementWork at officeRemote work1 day per week
- ...an Agency within the Office of Consumer Affairs and Business Regulation (OCABR), is responsible... ...the standards for accuracy of clinical glass thermometers, tests and approves coin... ...evidence; prepare reports; and communicate regulatory requirements.Ability and willingness to...Full timePart timeWork experience placementWork at officeLocal area
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