Regulatory Specialist
Beth Israel Lahey Health
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 documents, liaising with IRBs, and implementing SOPs to ensure high-quality, compliant trial activities. A Life Science background and 1–3 years of experience are required, with Master’s preferred. #J-18808-Ljbffr
- ...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...SuggestedImmediate 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...SuggestedFull timeWork at officeRelocation$74.4k - $111.6k
...Regulatory Affairs SpecialistMedtronic is seeking a Regulatory Affairs Specialist to support the Wound Management Regulatory Affairs team. The selected candidate will provide regulatory support on a range of medical devices focusing on a diverse line of Sutures (absorbable...SuggestedH1bWork at officeLocal areaImmediate startFlexible hours$74.4k - $111.6k
...Regulatory Affairs Specialist Medtronic is seeking a Regulatory Affairs Specialist to support the Wound Management Regulatory Affairs team. The selected candidate will provide regulatory support on a range of medical devices focusing on a diverse line of Sutures (absorbable...SuggestedH1bWork at officeLocal areaImmediate startFlexible hours$100k - $130k
...Principal Regulatory Specialist 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-...Suggested- ...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
- ...Environmental Health Regulatory Specialist Our client is looking for an Environmental Health Regulatory Specialist to ensure strict compliance with the state's environmental protection regulations for air quality, facility-wide emission restrictions, and reporting requirements...Contract work
- ...enables us to be a powerful contributor and connector of right Talent. Job Description This individual will be part of the Global Regulatory Affairs team and assists with planning, writing, compilation, and editing of periodic regulatory reports (i.e. DSURs, orphan...
- ...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...
- ...Regulatory Affairs Specialist Medtronic is seeking a Regulatory Affairs Specialist to support the Wound Management Regulatory Affairs team. The selected candidate will provide regulatory support on a range of medical devices focusing on a diverse line of Sutures (absorbable...Flexible hours
$74.4k - $111.6k
...healthcare while building a career grounded in purpose, growth, and impact. A Day in the Life Medtronic is seeking a Regulatory Affairs Specialist to support the Wound Management Regulatory Affairs team. The selected candidate will provide regulatory support on a...Full timeH1bWork at officeLocal areaImmediate startFlexible hours$94k - $150k
Job TitleSenior Regulatory Affairs SpecialistJob DescriptionSenior Regulatory Affairs Specialist, UltrasoundThe Senior Regulatory Affairs Specialist for Ultrasound collaborates with regulatory teams and authorities to secure timely product clearances. Responsibilities...Full timeWork at officeImmediate startWork visaRelocation package3 days per week- BNY is seeking an Associate for the Regulatory Reporting team in Boston, MA. The role entails preparing regulatory filings for the Commodity Futures Trading Commission and National Futures Association. The ideal candidate will have a Bachelor’s degree in accounting and...
$80.9k - $127.05k
...US-Nationwide-FIELD Full time 20186058 What Regulatory Affairs contributes to Cardinal Health Regulatory provides regulatory... ...Mansfield, MA. Job Summary The Principal Regulatory Affairs Specialist supports the Medical Solutions Regulatory Affairs team by...Full timeTemporary workWork experience placementLocal areaImmediate startRemote workFlexible hours$70k - $90k
...rapidly growing company that invests in its people and their ability to drive real progress.Licensing and Regulatory SpecialistThe Licensing and Regulatory Specialist supports the Legal & Regulatory compliance team. This role will primarily be responsible for obtaining,...Contract workWorldwide- ...Regulatory Affairs Nonclinical / Clinical Associate DirectorThe Global Regulatory Affairs (GRA) is responsible for obtaining approval for new products and ensuring that approval is maintained throughout the product lifecycle.GRA serves as the interface between the regulatory...
$120k - $202.5k
Role SummaryThe Regulatory Remediation Specialist is a Vice President-level individual contributor within the Risk & Governance organization. This role has end-to-end responsibility over high-visibility documentation, including design and closure memos, that support risk...Full timeTemporary workFlexible hoursShift work- ...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...
- ...Health is headquartered in Cambridge, Massachusetts, and New York City with 250+ employees world-wide.As a Senior Clinical Regulatory Specialist at Iterative Health, you will play a key role in supporting the compliant execution of Phase 2-4 industry-sponsored clinical...Temporary workWork at office2 days per week
- ...Iterative Health is headquartered in Cambridge, Massachusetts, and New York City with 250+ employees world-wide.As a Clinical Regulatory Specialist at Iterative Health, you will play an important role in supporting the compliant and efficient execution of Phase 2-4...Temporary workWork at office2 days per week
$101.44k - $126.8k
About the Job: The Senior Specialist, Regulatory Affairs (CDx) performs activities to support the regulatory submissions process through development of regulatory strategy and submission of materials to health authorities such as FDA for approval of novel platforms. This...Work experience placementWork at office- BNY Mellon, in Boston, MA, seeks an Associate, Regulatory Reporting to join the Fund Reporting team. You will prepare and coordinate regulatory filings for funds and ensure timely submissions to regulators. The role requires 3+ years in regulatory/financial reporting for...
- 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...Work at office
$60.01k - $88.01k
...protocols. Oversee reporting of AEs, SAEs, IND safety data, violations, deviations and submission of other study documents to support regulatory compliance, and troubleshoots processes and procedures when issues are identified. Assist investigators and study teams in...Work experience placementWork at officeLocal areaImmediate start$85k - $95k
...Regulatory And Clinical SpecialistAs a global medtech company, we are driven by our Vision of changing the trajectory of lives for a new... ...to alter the course of lives.The Regulatory and Clinical Specialist will support the clinical evaluation activities, review promotional...Remote workWorldwide$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- Foundation Medicine in Boston, MA is seeking a TheRight to Operate Specialist to support regulatory compliance across CLIA, CAP, MA/NY state requirements and internal policies. You will collaborate cross-functionally to prepare documentation and respond to audits, ensuring...
- ...reports and documents; verify facts; conduct interviews and on-site inspections; collect evidence; prepare reports; and communicate regulatory requirements.Ability and willingness to pursue weights and measures certification.Multilingual skills are preferred.License and/...Full timePart timeWork experience placementWork at officeLocal area
$196k - $270k
...Biogen's US business. Your expertise will ensure that our business operations adhere to the highest standards of compliance and regulatory conduct. By developing and delivering comprehensive training programs, you'll be an educational pillar for both new and established...Full timeTemporary workWork at officeLocal area
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