158 Results for

Regulatory Affairs Jobs in Brookline, MA

Jobs

New!

Boston, MA4 days ago

$350,000–$400,000 Per Year

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Marlborough, MA22 days ago

$50–$70 Per Hour

The projects will vary in size and Product but may include supporting Quality/Regulation driven projects, supporting material or supplier changes, executing product extensions, executing value improvement projects or product design enhancements. Additionally, you will engage with functional managers to manage the portfolio of sustaining projects for your business unit and align projects priorities and resources needs to execute successfully the sustaining strategy.

Boston, MA30+ days ago

Comfortable working directly for regulatory agencies, including the Food and Drug Administration (FDA), DEA, and Boards of Pharmacies. The Regulatory Affairs Specialist will be responsible for regulatory documentation, compliance, requirements, submissions, and overall regulatory affairs activities.

Boston, Massachusetts30+ days ago

Overview: Monte Rosa Therapeutics is seeking an experienced and strategic Director of Regulatory Affairs to lead and support global regulatory efforts across our development programs, with a focus on immunology. Lead the preparation, submission, and maintenance of regulatory applications, including INDs, CTAs, marketing applications, Annual Reports, Orphan Drug Designation, Requests for Fast Track, and other regulatory documents.

Watertown, MA30+ days ago

$160,000–$275,000 Per Year

Having advanced the first degrader into the clinic for immunological diseases, Kymera is focused on building an industry-leading pipeline of oral small molecule degraders to provide a new generation of convenient, highly effective therapies for patients with these conditions. As a critical member of a growing RA organization, this role will leverage their recent and relevant hands-on experiences developing immunology treatments to help rapidly advance Kymera's I/I portfolio of targeted protein degraders.

Cambridge, MA30+ days ago

Built on unparalleled insights into protein motion and how this dynamic behavior relates to protein function, we aim to effectively drug protein targets that have previously been intractable, with an initial focus on enhancing small molecule therapeutic discovery in targeted oncology. You will work side by side with your regulatory and research and development colleagues to develop and execute innovative regulatory strategies for our fast-paced programs, including the implementation of non-clinical and clinical regualtory strategy for relevant products.

Boston, MA30+ days ago

$163,000–$182,000 Per Year

This is a critical role for a highly motivated regulatory leader with experience in rare disease drug development, combination products, and a proven track record of advancing programs from early stages through late-phase clinical development. Avalyn is reimagining the future of pulmonary fibrosis treatment with a pipeline of new inhaled formulations of approved medicines designed to reduce systemic exposure and deliver medication directly to the site of disease.

Woburn, MA30+ days ago

Development and implementation of clinical regulatory strategies and tactics,including but not limited to, Modeling Informed Drug Development (MIDD), real- world data (RWD)/real-world evidence (RWE), and meta-analysis, for pipeline and commercial assets,while considering FDA and other health authority clinical and regulatory requirements. As a part of the Regulatory Affairs team at Azurity, the Regulatory Affairs Director – Clinical Strategy will conduct in depth analysis of regulatory and clinical information to develop complex strategies supporting potential drug products for development and commercial drug products for expansion of the Azurity portfolio of medications.

Somerville, Massachusetts30+ days ago

$120,000–$165,000 Per Year

Regulatory Affairs Specialist, this position will: · Represent Regulatory Affairs on cross functional project teams and provide strategic input and technical guidance on product lifecycle planning and regulatory requirements for non-medical devices, and medical devices. · Create and ensure maintenance of technical documentation (such as clinical evaluation reports, risk management reports, 510(k) notification) as required for obtaining and/or maintaining regulatory approval/clearance for DeepHealth products.

Somerville, Massachusetts30+ days ago

$133,000–$165,000 Per Year

Lead and manage regulatory submissions, including FDA Q-submission, US 510(k)s submissions, Premarket Approvals (PMA) submissions, supplements, and reports, including Regulatory Body interactions. Regulatory Affairs Principal is responsible for developing and executing regulatory strategies, ensuring compliance with global regulations and leading the process to obtain and maintain market approval for DeepHealth’s high risk products, including AI technologies.

Bedford, Massachusetts30+ days ago

$105,000–$130,000 Per Year

Working independently, with guidance from management or senior regulatory staff, the position will participate in cross‑functional software development meetings; prepare software‑specific submission and registration documentation; assess and document software changes, cybersecurity impacts, and algorithm updates. This role is technically focused and requires advanced skills in analyzing software medical device products and regulations, reviewing verification/validation protocols and reports, evaluating risk management documentation, authoring regulatory documents for agile/iterative development environments, and promoting compliance with global digital health requirements.

Evansville, IN30+ days ago

Our Mission is to excel at constructing complex infrastructure safer, better, and faster by engaging the entrepreneurial and innovative spirit of our team members and providing limitless opportunity for personal and professional growth in a close-knit and collaborative organization. Inc. (TBI) National Heavy Civil division provides comprehensive, cutting-edge heavy civil/underground construction services through traditional and non-traditional delivery methods.

Boston, MA30+ days ago

$226,495–$258,817 Per Year

Enrollment in a Phase 2 registration-directed trial of ziftomenib in R/R NPM1-mutant AML has been completed, and in the second quarter of 2025, the companies announced the FDA's acceptance of a New Drug Application for ziftomenib for the treatment of adult patients with R/R NPM1-mutant AML and assignment of a Prescription Drug User Fee Act target action date of November 30, 2025. Ziftomenib, a once-daily, oral menin inhibitor, is the first and only investigational therapy to receive Breakthrough Therapy Designation from the U.S. Food and Drug Administration ("FDA") for the treatment of relapsed/refractory ("R/R") NPM1-mutant acute myeloid leukemia ("AML").

Waltham, MA22 days ago

$210,000–$270,000 Per Year

Oversees and leads the Regulatory Affairs function to ensure global regulatory requirements are met for Nova products including but not limited to: U.S. FDA 21 CFR Part 820 (Quality Management System Regulation (QMSR), ISO 13485:2016, EU Regulation (EU) 2017/746 (IVDR); UK Medical Devices Regulations 2002 (UK MDR 2002); Australian Therapeutic Goods (Medical Devices) Regulations 2002 (incl. Own post-market regulatory obligations, including vigilance/adverse event reporting, Field Safety Corrective Actions/recalls (as applicable), regulatory reporting, and support for post-market performance follow-up and performance evaluation report updates under IVDR, as well as post-market surveillance and vigilance requirements under UK MDR 2002.

Boston, MA30+ days ago

The Executive Director, Global Regulatory Affairs will provide strategic and operational leadership for global regulatory activities across the company’s oncology portfolio and will be accountable for the development and execution of integrated global regulatory strategies across the full product lifecycle, from early clinical development through registration, commercialization, and post‑approval lifecycle management. Ensure the preparation, review, and approval of high‑quality regulatory submissions and related documentation, including but not limited to INDs/CTAs, scientific advice packages, orphan drug applications, PIPs/PSPs, BLAs/MAAs, labeling strategy and negotiations, responses to regulatory questions, and post‑approval commitments.

Bedford, Massachusetts30+ days ago

Lead field corrections and removal for on-market products, determining classification and regulatory agency reportability based on assessed risk, preparing comprehensive regulatory strategy, authoring field communication, leading cross-functional team to ensure timely customer notification, reporting and interfacing with regulatory agencies (as required), and supervising the regulatory team that assembles and maintains the necessary support records. This leadership role owns all elements related to post-market regulatory compliance to meet worldwide regulatory requirements, including vigilance reporting, recall (product correction and removal) management, on-market product change assessment, and the post-market surveillance (PMS) program.

Cambridge, MA30+ days ago

$130,000–$190,000 Per Year

Beam's suite of gene editing technologies is anchored by base editing, a proprietary technology that is designed to enable precise, predictable and efficient single base changes, at targeted genomic sequences, without making double-stranded breaks in the DNA. Serve as Regulatory lead for PRC/MLR review of promotional, disease awareness, scientific exchange, HCP, and patient-directed materials for certain products, under the supervision of the Director of Regulatory Labelling.

Boston, Massachusetts19 days ago

Researches and analyzes regulatory information and determines acceptability of data, procedures, and other product-related documentation presented in support of product registration. Under supervision, compiles regulatory submissions, license renewal and annual registrations to the US Food and Drug Administration (FDA) and other regulatory agencies.

Cambridge, MA30+ days ago

$155,000–$190,000 Per Year

Beam's suite of gene editing technologies is anchored by base editing, a proprietary technology that is designed to enable precise, predictable and efficient single base changes, at targeted genomic sequences, without making double-stranded breaks in the DNA. In partnership and under guidance from the Regulatory Lead, drive the development of global regulatory strategy for Beam's portfolio of advanced genetic medicines and ensure integration of regulatory tactics that support the broader corporate strategy.

Cambridge, MA30+ days ago

$130,000–$160,000 Per Year

Participate in regulatory intelligence activities, monitor regulatory guidelines and trends as they pertain to global regulations and guidance, and provide regulatory advice to project teams regarding the applicability/impact on internal programs; anticipate and communicate possible regulatory paradigm shifts. Beam's suite of gene editing technologies is anchored by base editing, a proprietary technology that is designed to enable precise, predictable and efficient single base changes, at targeted genomic sequences, without making double-stranded breaks in the DNA.

Somerville, Massachusetts30+ days ago

$130,000–$160,000 Per Year

Watertown, MA30+ days ago

$235,000–$330,000 Per Year

Responsibilities include building strong collaborative partnerships with asthma key opinion leaders (KOLs) and scientific organizations, providing medical and scientific expertise for portfolio indications, and supporting data generation and dissemination, scientific publications, and advisory boards. Having advanced the first degrader into the clinic for immunological diseases, Kymera is focused on building an industry-leading pipeline of oral small molecule degraders to provide a new generation of convenient, highly effective therapies for patients with these conditions.

Needham, MA30+ days ago

Remote

Full-time

Beyond research execution, you will contribute to business strategy by identifying high-value grant opportunities that align with company growth priorities, and by engaging with strategic partners, academic institutions, and key opinion leaders to expand XRHealth’s reach and credibility. Query and analyze data from XRHealth’s centralized cloud-based Data Lake to evaluate treatment efficacy, utilization trends, and clinical outcomes across therapeutic areas (depression, anxiety, chronic pain, physical and neurorehabilitation).

Boston, MA30+ days ago

$110,070–$176,112 Per Year

In addition to the specific requirements listed below, the Senior Manager should be highly motivated, enjoy working in a fast-paced and often changing environment, have the ability to learn quickly, and be adept at setting priorities and anticipating needs. You will be a representative of Axon and lead meetings with state, city and county government officials to advance Axon's position with relevant government and law enforcement stakeholders, as well as to drive broader awareness and support for Axon's mission.

Danvers, MA30+ days ago

Description/Comment: The Medical and Scientific Affairs function provides leadership and direction on medical, scientific and clinical decisions related to the overall Leica Biosystems business strategy. Partner with internal and external resources to deliver MSL and Medical Director effectiveness, Medical insights generation, and reporting on key projects.

New!

Boston, MA3 days ago

$95,000–$105,000 Per Year

Support cross-functional teams by providing legal operational guidance, enhancing process efficiency, managing transactional documentation and stakeholder coordination, and contributing to corporate governance functions such as drafting resolutions, preparing board materials, and overseeing quarterly and annual obligations. Today, our partnership approach enables us to pursue strategic growth, build enduring relationships with a robust external network, and collaborate across our integrated platform to connect the deep and diverse expertise that unlocks breakthrough insights.

Boston, MA12 days ago

Remote

10 years’ experience as a Medical Physicist, Scientist, or MD in a clinical hospital or clinical research setting or 3 years of experience as a Medical Physicist, Scientist, or MD in a clinical hospital or clinical research setting plus 7 years of experience in healthcare industry as imaging scientist or research manager. Analyze and communicate technical and clinical product specification requirements from luminaries, market research teams, and via Medical Advisory Boards (MABs) to global business team.

Boston, MA29 days ago

Remote

$190,000–$240,000

Develop a territory profile including Centers of Excellence, key expertise, newborn screening approaches and leaders, and market access pathways to inform medical strategy and tactical planning in collaboration with our Commercial, Diagnostic, and Patient Advocacy partners. As a field-based member of the medical affairs team, the Sr MSL will be responsible for developing and enhancing professional relationships with external thought leaders involved in all phases of the clinical development process through a fair-balanced and high-value exchange of clinical and scientific information.

Cambridge, MA30+ days ago

$23–$29 Per Hour

Designed to make only the right edit at the right position within a gene while minimizing unwanted DNA modifications, Prime Editors have the potential to repair almost all types of genetic mutations and work in many different tissues, organs and cell types. The Company is leveraging its proprietary Prime Editing platform, a versatile, precise and efficient gene editing technology, to develop a new class of differentiated, one-time, potentially curative genetic therapies.

New!

Boston, MA6 days ago

$79,560–$115,720.80 Per Year

Summary: Responsible for overseeing and managing all aspects of environmental, health, and safety programs within an organization including developing and implementing policies, procedures, and initiatives to ensure compliance with regulations, preventing workplace accidents, protecting employee health, and mitigating environmental impact. The framework is comprised of ten competencies (half People-Focused, half Performance-Focused) and are defined by observable and measurable skills and behaviors that contribute to workplace effectiveness and career success.

Malden, MS30+ days ago

Manage regulatory operations activities, including preparation of eCTD submission-ready documents, coordination across functions, and adherence to regulatory guidelines and processes. This role involves managing the preparation of eCTD submission-ready documents, coordinating across functions, and ensuring quality, accuracy, and adherence to regulatory guidelines.

Boston, MA30+ days ago

Full-time

At Rhythm we are dedicated to transforming the lives of patients living with rare neuroendocrine diseases by rapidly advancing care and precision medicines that address the root cause. This role involves managing the preparation of eCTD submission-ready documents, coordinating across functions, and ensuring quality, accuracy, and adherence to regulatory guidelines.

New!

Marlborough, MA6 days ago

The anticipated compensation listed above and the value of core and optional employee benefits offered by Boston Scientific (BSC) - see www.bscbenefitsconnect.com-will vary based on actual location of the position and other pertinent factors considered in determining actual compensation for the role. The Legal Director, Global Regulatory serves in a dual-capacity global role, providing strategic legal leadership across medical device regulatory and quality matters, as well as real-world data (RWD) and real-world evidence (RWE) initiatives.

NA, MA9 days ago

Remote

Responsibilities: Lead and provide expert guidance on Chemistry, Manufacturing, and Controls (CMC) regulatory strategy and submissions for biologic products, including monoclonal antibodies, recombinant proteins, vaccines, and cell therapies. Collaborate with cross-functional teams, including manufacturing, process development, quality assurance, and regulatory affairs, to develop and execute CMC regulatory strategies aligned with product development objectives.

Boston, MA30+ days ago

You will oversee the preparation and submission of regulatory documents, manage relationships with regulatory agencies, and lead cross-functional teams to support regulatory activities across a variety of projects and therapeutic areas. Oversee and coordinate cross-functional project teams to compile data for regulatory submissions and manage timelines for all regulatory deliverables.

BOSTON, Massachusetts25 days ago

This senior leadership role is responsible for the strategic oversight, development, and execution of all regulatory compliance programs within Facilities Management. Sodexo is seeking a Director of Regulatory Compliance - Facilities Management to support operations at Tufts Medical Center, a complex, urban academic medical center.

Cambridge, MA23 days ago

Contractor

Board Certification (or equivalent) or specialist training is highly desirable; drug development experience in neurology (Huntington’s Disease) would be a great advantage, but not essential 10+ years industry experience or equivalent clinical academic experience Sound scientific and clinical judgment Successful track record of leading Phase 2/3 clinical programs (preferably in Huntington’s drug development), including major interactions with Health Authorities Familiarity with concepts of clinical research and clinical trial design, including biostatistics, regulatory agency organization, guidelines, and practices Ability to effectively present ideas and document complex medical/clinical concepts in both written and oral communication History of solving problems while exhibiting superior judgment and a balanced, realistic understanding of issues Outstanding leadership and collaboration skills working within a matrix environment. Collaborate closely with Preclinical, Regulatory Affairs, Medical Affairs and Commercial to ensure tight strategic integration of product development plans Be accountable via Clinical Research and Operations for all relevant timelines and deliverables Drive/supervise all major written deliverables (regulatory submissions, original articles, abstracts), and presentation materials Be responsible (as appropriate in line with SOPs) for final review and sign off with respect to all controlled documents including protocols, IBs, informed consent forms Influence internal and external audiences in a high impact, highly visible fashion Qualifications MD with strong research background or MD PhD, with a track record of successful research support and peer review publications.

Boston, MA30+ days ago

$129,870–$207,792 Per Year

Demonstrated leadership in partnering with Engineering, Product Management, Supply Chain, Manufacturing, Legal, and commercial teams to influence decisions, drive alignment, and support successful product launches and lifecycle compliance. Project leadership, communication, and mentorship skills, including the ability to manage multiple high-impact certification efforts, balance priorities and dependencies, guide others through ambiguity, and represent the function credibly across internal and external stakeholders.

Cambridge, MA30+ days ago

$228,000–$245,000 Per Year

This role combines scientific depth, regulatory rigor, and operational execution to ensure the design, analysis, and interpretation of clinical trials support efficient development and high-quality regulatory submissions. The Director serves as a key partner to Clinical Development, Clinical Operations Data Management, Regulatory Affairs, Medical Affairs and while building scalable biostatistics capabilities appropriate for a growing organization.

Cambridge, MA30+ days ago

The Associate Director, Global Scientific Communications Lead is a key strategic partner of the TA Medical Affairs team responsible for dynamically driving the strategic planning and tactical execution of the comprehensive scientific communications plan across publications and medical communications as a central component of the global medical strategy for the asset program and will support the Medical Communications efforts of the TA Scientific Communications team. Lead the planning and execution of the integrated congress plans including oversight of content for and design of the Medical Affairs booth, creation of FAQs, collection and generation of scientific insights, scientific symposia as well as pre-con, post-con and daily debrief meetings and communications.

Boston, Massachusetts25 days ago

The ideal candidate combines strong communications expertise with scientific literacy and a solid understanding of the biopharmaceutical sector, allowing this person to translate complex scientific and clinical data into clear and engaging narratives for investors, media, and other key stakeholders. Collaborate with internal stakeholders and external partners, including investor relations advisors, public relations firms, and media contacts, to coordinate consistent and effective corporate messaging.

Cambridge, MA30+ days ago

Graduate degree in health sciences, nursing, pharmacy, public health, epidemiology, or other relevant health-related field (MD, PhD, PharmD, NP, PA, pharmacy, or nursing degree) with at least 5 years of experience in clinical, pharmacological, or related fields of expertise. Technically fully competent to develop, review, evaluate and maintain the signal detection and management processes in line with regulations and in close liaison with the business units, including Data Sciences as well as internal PSPV stakeholders.

NA, MA9 days ago

Remote

Collaborate with cross-functional teams, including regulatory affairs, clinical development, quality assurance, and market access, to ensure alignment on regulatory strategy and objectives for EU markets. Provide regulatory guidance and support for product development, registration, and commercialization activities in EU member states, including preparation and submission of regulatory applications (e.g., MAAs, variations, notifications).

Boston, MA30+ days ago

$165,000–$230,000 Per Year

It will require collaboration across cross-functional teams, including but not limited to Medical Affairs, Patient Advocacy, Sales, Market Access and Patient Services, Communications, Regulatory, Compliance, Market Research, Commercial Operations, Legal, and commercial leadership. Lead patient strategy, messaging, and tactical plan development/execution for key disease education and branded activities, including campaign development, while determining budgets, timelines and metrics for program success.

Cambridge, MA30+ days ago

$185,000–$225,000 Per Year

Reporting to the Director of Contracts & Compliance, this role provides pragmatic, risk-balanced legal support, partners closely with cross-functional stakeholders, and helps strengthen contracting infrastructure as the company advances toward commercial-stage operations. Beam's suite of gene editing technologies is anchored by base editing, a proprietary technology that is designed to enable precise, predictable and efficient single base changes, at targeted genomic sequences, without making double-stranded breaks in the DNA.

Boston, Massachusetts30+ days ago

This role is responsible for establishing and executing global safety strategy across early‑ and mid‑stage clinical programs, with particular focus on immune‑mediated toxicities, oncology risk management, and complex benefit–risk assessment. Overview: The Director of Drug Safety & Pharmacovigilance provides strategic and hands‑on leadership for pharmacovigilance activities supporting a clinical‑stage biotech pipeline in inflammatory and oncology diseases.

Cambridge, MA16 days ago

Role SummaryThe Associate Director, Scientific Communications Lead is responsible for dynamically driving the strategic planning, development, operationalization, and execution of the Medical Affairs scientific and medical congress strategy for priority Dermatology/Immunology assets, with particular focus on US congresses. Minimum 5 years of experience (for candidates with doctoral degrees) or 7 years of experience (for candidates with master s degrees) experience in biopharma Medical Affairs, Medical Communications, Scientific Communications, Medical Education, or congress strategy/execution.

Boston, MA30+ days ago

$97,000–$105,000

Requires lifting and carrying equipment and supplies weighing up to 35 pounds; requires pushing and pulling equipment and supplies weighing up to 35 pounds; requires walking and standing; requires frequent sitting more than 75% of the workday; requires the ability to negotiate stairs; requires visual acuity and manual dexterity to operate equipment. Through innovative home- and community-based services, Vitra supports aging adults, people with disabilities, and individuals with complex care needs— supported by a Nurse, and Case Manager, Vitra ensures clients receive compassionate, personalized, and dignified care.

Cambridge, MA30+ days ago

$245,987–$332,806

The Senior Director will serve as a key member of the Technical Operations leadership team and a strategic partner to R&D, Supply Chain, Quality, Regulatory, and Commercial leadership. This CMC leader will be responsible for building and executing a comprehensive biologics manufacturing strategy, including process and analytical development, formulation development, external manufacturing, and regulatory CMC strategy.

NA, MA9 days ago

Remote

Collaborate with cross-functional teams, including manufacturing, process development, quality assurance, and regulatory affairs, to ensure efficient and compliant manufacturing operations. Conduct risk assessments and develop risk mitigation strategies for manufacturing processes, equipment, and facilities to ensure product quality and compliance with regulatory requirements.

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Regulatory Affairs Jobs in Brookline, MA

Vice President Clinical Development Ophthalmology Jobot

Associate Project Manager Careers Integrated Resources Inc

Regulatory Affairs Specialist CEDENT

Director, Regulatory Affairs – Global Regulatory Strategy Monte Rosa Therapeutics, Inc

Director, Regulatory Affairs Kymera Therapeutics

Associate Director, Regulatory Affairs Relay Therapeutics

Senior Manager / Associate Director, Regulatory Affairs Avalyn Pharma

Director, Regulatory Affairs – Clinical Strategy Azurity Pharmaceuticals - US

Sr. Regulatory Affairs Spclst Deephealth

Sr Regulatory Affairs Principal Autonomous Deephealth

Senior Principal Regulatory Affairs Specialis Werfen

Project Engineer Traylor Bros. Inc.

Director, Regulatory Affairs Kura Oncology

Director, Regulatory Affairs Nova Biomedical

Executive Director, Regulatory Affairs AVEO Oncology

Regulatory Affairs Manager II Post Market Werfen

Manager/Senior Manager Regulatory Affairs – Advertising, Labeling, and Promotion Beam Therapeutics

Manager, Regulatory Affairs Monte Rosa Therapeutics, Inc

Senior Manager, Regulatory Affairs Beam Therapeutics

Specialist I/II, Regulatory Affairs Beam Therapeutics

Sr Regulatory Affair Principal Deephealth

Senior Director, Medical Affairs, Respiratory Kymera Therapeutics

Director of Scientific Affairs XRHealth

Senior Manager, Government Affairs, Northeast Axon

Project Manager (Medical & Scientific Affairs) TechDigital Corporation

Senior Legal Affairs Associate Bain Capital

Leader Medical Affairs Canon USA & Affiliates

Senior Medical Science Liaison - Gene Therapy US Medical Affairs Orchard Therapeutics

Co-op: Clinical Development - Patient Advocacy and Medical Affairs Prime Medicine

Manager - Environmental Affairs & Safety Mass General Brigham

Associate Director, Regulatory Operations The Steely Group

Associate Director, Regulatory Operations Rhythm Pharmaceuticals

Legal Director, Global Regulatory Boston Scientific

Regulatory CMC Expert in Biologics Pharmavise Corporation

Regulatory Manager CEDENT

Director of Regulatory Compliance, FM Sodexo

Senior Medical Director Clinical Research - Neurodegeneration Integrated Resources, Inc

Manager, Global Product Compliance Axon

Director, Biostatistics Avalyn Pharma

Associate Director, Global Scientific Communications Lead Contractor Lancesoft

Associate Director, Corporate Communications Monte Rosa Therapeutics, Inc

Director, Signal Management and Innovation Lancesoft

EU Generalist Pharmavise Corporation

Director, US Rare Tumor Patient Marketing, Desmoid Tumor (DT) SpringWorks Therapeutics

Associate Director, Contracts Beam Therapeutics

Director, Drug Safety & Pharmacovigilance (Inflammation & Oncology) Monte Rosa Therapeutics, Inc

Associate Director, Global Scientific Communications & Congress Lead Lancesoft

Clinical Compliance Specialist (RN) VITRA Health

Senior Director, Technical Operations - Biologics Akebia Therapeutics

Pharmaceutical Manufacturing Specialists with Engineering Background Pharmavise Corporation

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