Cancer Clinical Trials Regulatory Affairs Specialist
Anna Jaques Hospital
The Cancer Clinical Trials Office (CCTO) at Beth Israel Deaconess Medical Center (BIDMC) supports clinical research and provides infrastructure to 12 cancer disease programs, enabling regulatory compliance and efficient trial activation. Required is a Life Science degree with 1–3 years of related regulatory experience; strong knowledge of FDA, NIH, and OHRP guidelines is essential. A hybrid of independent and collaborative work is common for this role. #J-18808-Ljbffr Anna Jaques Hospital
- 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...SuggestedWork at office
- 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
- ...Beth Israel Lahey Health in Boston is seeking a regulatory affairs professional to support the Cancer Clinical Trials Office (CCTO) across multiple disease programs, including IND submissions and regulatory compliance for oncology trials. The role involves preparing regulatory...SuggestedWork at office
$60.01k - $88.01k
...Department Description This position is in the Cancer Clinical Trials Office (CCTO), supporting multiple... ...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- ...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...Temporary workWork at office2 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...Temporary workWork at office2 days per week
$90.32k
...Clinical Research Compliance Specialist Job Number: 25366 Functional Area: Administration Department:... ...familiarity with IRB processes and regulatory requirements. PREFERRED: Master of... ...experience with FDA-regulatory and industry-sponsored trials. Revised 2/26/2026...Part timeLocal areaVisa sponsorship$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- ...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
$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$74.4k - $111.6k
...Regulatory Affairs Specialist Medtronic is seeking a Regulatory Affairs Specialist to support the Wound... ..., manufacturing, marketing, and clinical protocol for regulatory compliance.... ...earliest possible approvals of clinical trials applications. To be considered for...H1bWork at officeLocal areaImmediate startFlexible hours- ...Job Description This individual will be part of the Global Regulatory Affairs team and assists with planning, writing, compilation, and editing... ...regulatory strategy documents (for products in phase 1-3 clinical development), labeling updates for marketed products,...
- ...Regulatory Affairs Specialist This is a full-time on-site role for a Regulatory Affairs Specialist located in Torrance, CA. The Regulatory Affairs Specialist will be responsible for regulatory documentation, compliance, requirements, submissions, and overall regulatory...Full time
$100k - $130k
...The Principal Specialist of Regulatory Affairs & Compliance provides regulatory expertise on labeling, claims, legal matters, recalls, audits, and quality compliance for the company’s product integrity and consumers’ safety. Leads cross‑functional teams, manages complex...- ...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...
- ...Foundation Medicine in Boston seeks a Senior Specialist, Regulatory Affairs (CDx) to lead regulatory submissions, shape strategy, and guide cross-functional teams through FDA pathways for companion diagnostics. You will prepare packages, respond to agency inquiries, review...
- ...Regulatory Affairs Specialist Medtronic is seeking a Regulatory Affairs Specialist to support the Wound... ..., manufacturing, marketing, and clinical protocol for regulatory compliance.... ...earliest possible approvals of clinical trials applications. To be considered for...Flexible hours
$74.4k - $111.6k
...in the Life Medtronic is seeking a Regulatory Affairs Specialist to support the Wound Management... ...labeling, manufacturing, marketing, and clinical protocol for regulatory compliance.... ...earliest possible approvals of clinical trials applications. To be considered for...Full timeH1bWork at officeLocal areaImmediate startFlexible hours- 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
$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$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- ...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
$101.44k - $126.8k
About the Job: The Senior Specialist, Regulatory Affairs (CDx) performs activities to support the regulatory submissions process through development... ...companion diagnostic regulatory strategy (analytical and clinical validation) and regulatory filings. Review validation...Work experience placementWork at office$124.8k - $176.8k
...Collaborates with outside counsel on patent, freedom‑to‑operate, and regulatory considerations for digital technologies. Monitors emerging... ...to detail, and ability to maintain confidentiality of IP affairs. Strong written and verbal communication skills; proficient with...Full timeWork at officeDay shift$125k - $175k
...Collaborates with outside counsel on patent, freedom-to-operate and regulatory considerations for digital technologies.* Monitors emerging... ...to detail and the ability to maintain confidentiality of IP affairs.Strong writing and verbal skills and experience with Word,...Work at officeImmediate start- ..., 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
$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- ...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
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