1,460 Results for

Safety Director Jobs in Boston, MA

Jobs

Hingham, MA

$120,000–$150,000 / year

Location: Linden Ponds by Erickson Senior LivingLinden Ponds, a 5-star CMS-rated community, is seeking an Assistant Director of Nursing, RNto help lead our CCRC—a role ideal for a clinical leader who is passionate about person-centered care and developing strong, cohesive teams. Linden Ponds helps people live better lives by fulfilling our promises of a vibrant lifestyle, financial stability, and focused health and well-being services for those who live and work with us.

Today

Boston, MA

$125,000–$150,000 / year

Information collected and processed as part of your Jobot candidate profile, and any job applications, resumes, or other information you choose to submit is subject to Jobot's Privacy Policy, as well as the Jobot California Worker Privacy Notice and Jobot Notice Regarding Automated Employment Decision Tools which are available at jobot.com/legal. The Safety Manager oversees safety programs across multiple multifamily construction sites, working closely with site leadership to maintain a proactive safety culture.

1 day ago

Nashua, NH

Full time

Corresponds directly with overseas freight forwarders (which is most often after hours) this direct correspondence helps to ensure that product shipped is not delayed in customs in foreign countries. Create warehouse procedures with Warehouse Manager for the proper handling storage, workflow of product through warehouse operations.

30+ days ago

Lowell, MA

Ensures and documents that residents/families have input into the care planning process; Acts as liaison between residents, families, outside agencies, and the Center Administrator to ensure that the resident's rights are maintained; Takes responsibility for conducting family meetings as needed; Functions in a management capacity and adheres to all policies and procedures of the Center as a representative of CareOne Administration; Performs administrative requirements such as completing necessary forms and reports under the direction of the Administrator and submitting such reports to the Administrator and/or consultants as required; Facilitates discharge planning including the development of an organized discharge plan for all customers; Concerns self with the safety of all Center residents in order to minimize the potential for fire and accidents. Also ensures that the Center adheres to legal, safety, health, fire, and sanitation codes by being familiar with his/her in carrying out the Center's fire, safety and disaster plans and by being familiar with current MSDS; Puts customer service first and adheres to the CareOne Culture of Excellence Pledge.

1 day ago

Concord, MA

$75,000–$85,000 / year

Social Service functions include but are not limited to: supervising social service staff, direct services, advocacy, counseling, service coordination, education, in-servicing, policy and program development and community relations. The Assistant Director of Social Services will abide by and practice according to the company's Social Service Policies and Procedures Manual, State and Federal guidelines and the National Association of Social Workers' "Code of Ethics".

Today

Hingham, MA

$120,000–$150,000 / year

1 day ago

Andover, MA

$100,000–$130,000 / year
Full time

This privately held construction management firm focuses exclusively on life science, lab, and clean room environments, supporting pharmaceutical and research clients across greater Boston. The Safety Manager will oversee and implement comprehensive safety programs to ensure compliance with regulations and promote a safe working environment for all construction projects.

18 days ago

Lepage, ME

Strong organizational and time management skills with the ability to handle multiple priorities simultaneouslySolid understanding of budgeting, inventory control, and cost managementEffective communication, leadership, and team-building abilities. Supervisory or team lead experience in a fast-paced manufacturing environmentStrong working knowledge of food safety systems (HACCP, GMP, SSOPs, SQF).

29 days ago

Boston, MA

Comprehensive knowledge of construction safety principles, techniques, and methods Comprehensive knowledge of OSHA laws, regulations, and policies Capable of identifying known potential exposures and recommending corrective action Strong computer skills and familiarity with the Microsoft Office suite. • Works in real-time with Gilbane Insurance Group, Senior Management, Corporate and Division Safety Directors to identify loss leaders and effectively create safety procedures to reduce the number and severity of claims on all projects.

30+ days ago

Boston, Massachusetts

$185,000–$245,000 / year
Full time

Works in real time with Gilbane Insurance Group, Senior Management, Corporate and Division Safety Directors to identify loss leaders and effectively create safety procedures to reduce the number and severity of claims on all projects. • Regularly visit key projects within area of responsibility with Division Safety Directors to mentor, support development and ensure consistent application of safety program; organize minimum field presence and coaching expectations.

30+ days ago

Key Responsibilities: Manage the site Safety and Training Department including but not limited to: all aspects of site safety training; classroom and behind-the-wheel training schedules, logistics and documentation; and personnel and qualification files pertaining to training, safety and loss matters. This position is responsible for employee and passenger safety; the development and deliverance of safety training programs; serving as the corporate liaison to external agencies; and assisting with safety-related components with other internal departments.

30+ days ago

Beverly, MA

$187,200–$228,800 / year

Team Leadership and Management: • Manage and mentor a team of professionals, including the Performance Improvement project managers, Quality/Safety site leaders, the Patient Experience Manager and the Regulatory and Patient Safety Manager. Over-Arching Goals: The Executive Director will oversee and ensure that the Hospitals follow the overarching goals of quality and safety to provide high quality, patient-centered care while ensuring the safety and well-being of patients, healthcare providers, and staff.

30+ days ago

North Andover, Massachusetts

We are seeking an experienced Director of Safety & Training to lead instructional operations for a CDL training program focused on developing the next generation of professional drivers. This senior-level leadership role is responsible for ensuring excellence in training delivery, safety, and regulatory compliance across all phases of instruction.

2 days ago

Cambridge, MA

$115,000–$160,000 / year

Reporting to the Executive Director of Public Safety at Beth Israel Deaconess Medical Center, the Director of Public Safety at Mount Auburn Hospital plays a critical leadership role in fostering a safe, welcoming, and secure environment for patients, staff, and visitors. Recommend and implement operational strategies related to staffing models, scheduling practices, contracted services, investigations, contingency planning, labor relations, and other departmental operations to support efficient and effective Public Safety services.

30+ days ago

Attleboro, MA

$101,120.77–$157,957.62 / year

The Director serves as the primary liaison with internal leaders and external partners (e.g., public safety, emergency management, and regulatory agencies) and ensures preparedness for all-hazards events through planning, training, exercises, response, recovery, and mitigation activities consistent with national incident management principles and healthcare best practices. The Director provides enterprise leadership for Safety, Security, Emergency Management, and Hazardous Materials programs to protect patients, visitors, employees, providers, and volunteers.

30+ days ago

$286,560–$347,244 / year

Oversee, prepare and/or review aggregate safety review documents (eg, Development Safety Update Reports [DSUR], Periodic Benefit-Risk Evaluation Reports [PBRER]) and safety sections of relevant clinical trial documents (eg, protocols, clinical study reports [CSR], investigator brochures [IB], informed consent forms [ICF]) and regulatory filings (eg, clinical trial applications [CTA], marketing authorization applications [MAA]). Based on eligibility*, additional time off for employees may include unlimited paid sick time, up to 2 paid volunteer days per year, summer hours flexibility, leaves of absence for medical, personal, parental, caregiver, bereavement, and military needs and an annual Global Shutdown between Christmas and New Years Day.

30+ days ago

Waltham, MA

$208,000–$244,000 / year

The role provides second line assurance for Gas Field Safety, ensures effective governance of the Process Safety Management System, and champions the consistent application of Human and Organizational Performance (HOP) principles to strengthen and lead incident analysis, organizational learning, and corrective action quality to reduce the likelihood and severity of high‑consequence safety events. Influence decision‑making related to high‑risk activities, non‑routine work, abnormal operations, and major projects to protect employees, contractors, customers, and the public, using analytics, insights, and technical expertise to inform prioritization and resource allocation.

30+ days ago

Boston, MA

$122,000–$177,000 / year

Participates in DoM and QPS Department meetings including Inpatient Directors meeting, Ambulatory GIM meeting, QPS Medical Chiefs meeting, M and Ms, DOM Grand Rounds, QPC and Patient Safety Steering Committee and other meetings as requested. The Director coaches, mentors, and provides educational programs for staff and residents regarding quality improvement processes, program development to improve patient outcomes, clinical efficiency and value, patient-centered care, and patient satisfaction.

30+ days ago

Cambridge, MA

$199,000–$343,275 / year

Required Skills: Preferred Skills: Clinical Operations, Clinical Research and Regulations, Clinical Trials, Collaborating, Data Governance, Data Management and Informatics, Developing Others, Drug Discovery Development, Global Market, Inclusive Leadership, Industry Analysis, Innovation, Leadership, Market Research, Program Management, Research Ethics, Scientific Evaluation, Scientific Research, Stakeholder Management The anticipated base pay range for this position is : The anticipated base pay range for this position is: $199,000-$343,275 Additional Description for Pay Transparency: The anticipated base pay range for this position is: $199,000-$343,275 The Company maintains highly competitive, performance-based compensation programs. Job Function: Discovery & Pre-Clinical/Clinical Development Job Sub Function: Clinical Development & Research - MD Job Category: People Leader All Job Posting Locations: Beerse, Antwerp, Belgium, Cambridge, Massachusetts, United States of America, San Diego, California, United States of America, Spring House, Pennsylvania, United States of America, Titusville, New Jersey, United States of America Job Description: Director, Clinical Translational Safety Lead (Within Translational Safety-TPPIT) In addition to the US based locations, this role can also be based in Belgium, which is linked to R-071725 Clinical Translational Safety Lead.

30+ days ago

Boston, MA

Remote

$196,200–$294,400 / year

This position manages the technical aspects of end-to-end safety case intake, processing, quality control, and regulatory submissions within a therapeutic area (as assigned) covering the applicable drug, biologic, medical device, and combination products, ensuring operations are consistent, compliant, and inspection-ready worldwide. The role also represents GPS in cross-functional initiatives and requires strong technical PV expertise, communication, project management, and vendor management skills.

2 days ago

Cambridge, MA

$194,000–$267,000 / year

Regular employees are eligible to receive both short term and long-term incentives, including cash bonus and equity incentive opportunities, designed to reward recent achievements and recognize your future potential based on individual, business unit and company performance. The Associate Medical Director, Global Safety Physician will be responsible for global pharmacovigilance for investigational and/or marketed products, including: • review and analysis of safety data • design of clinical trials • identification and investigation of safety signals • management of benefit-risk profile for assigned compounds and products.

30+ days ago

Cambridge, MA

$185,500–$344,500 / year

Internal Title: Director #LI-Hybrid Location: Cambridge, MA USA In this key role you will provide global, end to end nonclinical safety leadership across multiple therapeutic areas and modalities, ensuring scientifically robust, fit for purpose, and regulatory compliant safety strategies that enable successful clinical trial initiation and support registration. You will be a critical enabler of portfolio progression, providing authoritative nonclinical safety leadership, regulatory credibility with Health Authorities, and strategic integration across therapeutic areas and modalities.

30+ days ago

Duxbury, MA

$124,536–$168,124 / year

Nature of Public Contacts: Employee interacts constantly with co-workers, the public and groups or individuals who have conflicting opinions or objectives, diverse points of view or differences where skillful questioning is required; one on one relationships with a person(s) who may be under severe stress, where gaining a high degree of communication may be required to obtain the desired effect. Supervisory Responsibility: The Director exercises full managerial authority over all ROCCC personnel—including Deputy Director, Operations Supervisors, Administrative Supervisors, Public Safety Dispatchers, and support staff—and directs the work of consultants or vendors supporting center operations.

15 days ago

Boston, MA

As the clinical voice of the physician and patient, the Global Medical Director will partner with Clinical Research, Research and Development (R&D), Quality, Regulatory Affairs and Commercial teams to support innovation, clinical evidence generation, product development and patient safety. Partner with Clinical Research, Clinical Evidence, Quality, Regulatory Affairs, R&D, Marketing and Business Development teams to support product strategy and medical decision-making.

24 days ago

Chelmsford, Massachusetts

Remote

The Acute Care Technology division of ZOLL Medical Corporation develops and delivers innovative lifesaving products and software solutions to EMS, hospital, public safety, and military customers globally. The Director of NA/LATAM Public Safety Partner Marketing will be responsible for building scalable regional programs, elevating partner engagement and educating the channel on the value of ZOLL solutions.

25 days ago

$163,800–$204,400 / year

Responsible for management, execution, and continuous improvement of company safety programs including but not limited to Aviation Safety Action Program (ASAP), Internal Evaluation Program (IEP), Fatigue Risk Management Plan (FRMP), Twelve-Five Safety Security Program (TFFSP), company safety training program, and safety promotion program. The Director of Safety & Security collaborates with the Director of Operations, Chief Pilot, Chief Flight Instructor, Director of Maintenance, and Executive Vice President to develop and execute the day-to-day management and administration of company safety programs.

30+ days ago

$170,000–$200,000 / year

Data Bridging: You understand ETL/ELT pipelines, webhook-driven events, and API constraints, knowing how to query unstructured data from a 20-year-old database just as smoothly as a modern cloud feed. Cross-Platform Data Integration: Define requirements for robust data bridges, APIs, and ingestion pipelines that cleanly unify data across legacy on-premise infrastructure and modern cloud platforms.

10 days ago

Somerville, MA

This role is designed for a highly experienced safety leader who can operate with broad autonomy, influence senior cross-functional stakeholders, and drive an integrated, proactive, and scientifically rigorous approach to signal detection, aggregate safety assessment, benefit-risk evaluation, and safety governance across development programs. Oversee the preparation and strategic quality of core safety deliverables, including DSURs and other aggregate reports, Reference Safety Information, safety sections of Investigator Brochures, protocols, informed consent forms, clinical study reports, regulatory responses, and other key documents.

30+ days ago

Boston, Massachusetts

Authoring safety sections, in collaboration with team members, on regulatory responses, IBs/CCDS, protocols, ICFs, Data Monitoring Committee reports and requests, and other documents, and provide the necessary quality control to ensure alignment with core safety position. The Associate Director, Safety Scientist plays a leadership role within Global Patient Safety (GPS) to actively evaluate and manage risk in collaboration with the GPS Medical Director(s) and cross-functional team members within the global regulatory framework.

2 days ago

Cambridge, Massachusetts

PhD or DVM, or equivalent advanced degree in Toxicology, Pharmacology, Pathology, Veterinary Sciences, or a related field, with 5+ years, Masters with 7+ or a Bachelors with 10+ of relevant experience in biotech or pharmaceutical drug development, or direct experience as a Study Director at a GLP-qualified CRO. We’re seeking an Associate Director, Nonclinical Safety Evaluation (NSE) who will play a pivotal role in overseeing and critically evaluating nonclinical safety studies across City’s RNAi therapeutic programs.

22 days ago

Braintree, MA

$120,548–$156,715 / year

Undergraduate and Graduate Education: Major study -- safety or occupational health fields (safety, occupational health, industrial hygiene), or degree in other related fields that included or was supplemented by at least 24 semester hours of study from among the following (or closely related) disciplines: safety, occupational health, industrial hygiene, occupational medicine, toxicology, public health, mathematics, physics, chemistry, biological sciences, engineering, and industrial psychology. If your education was completed at a foreign college or university, you must show comparability to education received in accredited educational institutions in the United States and comparability to applicable minimum coursework requirements for this position.

30+ days ago

Andover, Massachusetts

18 days ago

Skills: Excellent leadership and line management skills Excellent knowledge of drug safety and the drug development process Excellent knowledge of and ability to interpret and apply global safety regulations Experience in data analysis, evaluation of safety data and the preparation of safety reports preferred Excellent team / project leadership and delegation skills Ability to train and mentor people Excellent presentation skills Excellent interpersonal skills Excellent time management skills Client focused approach to work Experience with Pharmacovigilance related computing systems Clinical Research or Pharmacovigilance knowledge /qualifications Computer proficiency, ability to work with web-based applications and familiarity with the Windows operating system and Microsoft Office apps Ability to comprehend various regulatory or client requests and be able to strategize a handling approach Flexible attitude with respect to work assignments and new learnings Ability to manage multiple and varied tasks with enthusiasm and prioritize workload with attention to detail Willingness to work in a matrix environment and to value the importance of teamwork Knowledge and Experience: Minimum 13+ years of pharmaceutical and/or CRO experience including but not limited to areas of focus in clinical operations, sales and decentralized clinical trials/direct to patient studies 7-10 years of management experience, including direct project management or program oversight Requires BA/BS degree or equivalent combination of education and experience or equivalent related degree and/or experience, plus significant executive and/or senior management experience, preferably in worldwide clinical research, pharmaceutical, or biotechnology company A strong background in Safety Operations execution is desirable Minimum of thirteen (13) years of related experience, including seven to ten (7-10) years of progressive management experience, including direct project management or program oversight. You will lead operational level planning with significant business oversight, drive 'positive change' throughout Parexel through continuous process improvement programs, as well as make significant contributions to the leadership of the Business Unit (BU) and the development of the strategy and direction of the BU.

30+ days ago

Boston, MA

$200,000–$300,000 / year

At Vertex, our Total Rewards offerings also include inclusive market-leading benefits to meet our employees wherever they are in their career, financial, family and wellbeing journey while providing flexibility and resources to support their growth and aspirations. This role will optimizes patient safety of Vertex products and maintenance of compliance with the Pharmacovigilance regulations of Regulatory Agencies around the globe, through the effective and timely completion of Safety activities through the product life cycle.

4 days ago

Boston, Massachusetts

Overseeing the GPS DASH/DST teams across therapeutic areas, the role will ensure consistent conduct and timely execution of Benefit-Risk activities by GPS DASH/DST teams, including pre-marketing risk assessment, planning for First-In-Human (FIH) studies, safety content of key Modules (SCS, CLO, Labelling) in regulatory authority submissions for approval, including planning, content and execution of Risk Management Plans (RMPs) and/or Risk Evaluation and Mitigation Strategies (REMS) for and post-marketing requirements. The Executive Medical Director, Patient Safety/Head Medical Safety and Risk Management will oversee all safety and benefit-risk related activities of the GPS Physician (Disease-area Safety Heads, DST Chairs) and the Aggregate Report Risk Management (ARRM) Groups within the Vertex Global Patient Safety (GPS) Department.

30+ days ago

Boston, Massachusetts

The Director, Safety Scientist plays a leadership role within Global Patient Safety organizing and mentoring safety scientists to actively evaluate, manage and strategize risk in collaboration with the GDS Medical Directors and cross-functional team members within the global regulatory framework. Responsible for authoring safety section in collaboration with team members on regulatory responses, IBs/CCDS, protocol, ICF review, Data Monitoring Committees reports and requests, and other documents, and provide the necessary quality control to ensure alignment with core safety position.

2 days ago

Boston, MA

$170,000–$220,000 / year

As a senior member of our Field Management team, you'll be the driving force behind a world‑class safety program that supports high‑density MEP environments, live electrical systems, energization activities, and the construction of cutting‑edge data centers. Base Salary Range: $170K-$220K: Placement within the listed range depends on many factors including, but not limited to geographic location, years of experience, project size capability (for Construction & Field roles) and internal company equity.

30+ days ago

Boston, Massachusetts

Leads the safety physicians and scientists to support the safety strategy and input into the program design, monitoring, and data interpretation from pre-clinical and clinical studies, communication and post-marketing surveillance, epidemiology, pre-clinical and literature, epidemiology for each asset. Is accountable for project representation for Global Patient Safety at governance and other forums where safety is involved, eg DRC, eCRC, SARB, FSIRB, and DSMB/DMC, Medical Affairs Review Committees (MARC), product teams such CPT and GPT and Advisory Board meetings in partnership with GSH.

4 days ago

Boston, MA

$280,895–$421,342 / year

30+ days ago

Boston, MA

$165,000–$210,000 / year

Analyzes leading and lagging indicators, provides direction to Business Unit leadership on focus areas and trends, and recommends corrective actions when needed. We are dedicated to building a diverse, inclusive and authentic workplace, so if you're excited about this role but your past experience doesn't align perfectly with every qualification in the job description, we encourage you to apply anyway.

30+ days ago

Boston, MA

U.S. Base Salary Range: $170,000 - $220,0000 Placement within the listed range depends on many factors including, but not limited to geographic location, years of experience, project size capability (for Construction & Field roles) and internal company equity. As a senior member of our Field Management team, you’ll be the driving force behind a world‑class safety program that supports high‑density MEP environments, live electrical systems, energization activities, and the construction of cutting‑edge data centers.

30+ days ago

Boston, Massachusetts

$165,000–$210,000 / year
Full time

Analyzes leading and lagging indicators, provides direction to Business Unit leadership on focus areas and trends, and recommends corrective actions when needed. We are dedicated to building a diverse, inclusive and authentic workplace, so if you’re excited about this role but your past experience doesn’t align perfectly with every qualification in the job description, we encourage you to apply anyway.

30+ days ago

Waltham, MA

$246,400–$308,000 / year

Zenas' earlier stage programs include ZB021, a clinical-stage, potentially best-in-class, oral, IL-17AA/AF inhibitor; ZB022, a preclinical, potentially best-in-class, oral, brain-penetrant, TYK2 inhibitor; and ZB014, a preclinical half-life extended anti-CD-19 and FcRIIb monoclonal antibody. Our core business strategy combines our experienced leadership team with a disciplined product candidate acquisition approach to identify, acquire and develop product candidates globally that we believe can provide superior clinical benefits to patients living with autoimmune diseases.

30 days ago

Cambridge, MA

$210,000–$235,000 / year

Contribute to the generation of aggregate safety reports including development safety update reports, periodic benefit risk evaluation reports, and provide medical input in review of new or existing safety documents to ensure compliance with relevant regulatory requirements, such as protocols, safety summaries and regulatory reports. The targeted salary range reflects what Nuvalent reasonably and in good faith expects to offer for this position at the time of posting, but the final salary determination may be within or outside this range based on various factors, including, but not limited to, experience, skills, education, and market factors.

30+ days ago

Cambridge, Massachusetts

This role will have specific emphasis and accountability for products in Moderna’s emerging and/or established Systemic IV portfolio (spanning Autoimmune, Immuno-Oncology, and/or Rare Disease), with additional responsibilities to partner with Platform Science teams to support the safety evaluation and optimization of novel and existing technologies, as well as in other therapeutic areas as needed based on evolving business needs. Accountable for the design, execution, critical analysis, and reporting of GLP/non-GLP nonclinical safety in vitro and/or in vivo studies conducted in multiple species under the nonclinical safety assessment umbrella for the assigned therapeutic area(s) via collaborative partnerships with study monitors and program team representatives (e.g., DMPK, bioanalytical, operations, etc.).

30+ days ago

Boston, Massachusetts

Evaluating aggregate safety data and providing contributions to core regulatory documents i.e. Periodic Safety Update Reports, Drug Safety Update Reports, Risk Management Plans, and other routine and non-routine safety and risk/benefit evaluations for internal or regulatory purposes as required. Representing Alexion GPS at internal strategic and/or advisory/governance committees, other project/product team(s) or subteam(s) as a key cross functional member and subject matter expert, and/or act as an external technical resource at DSMB or Regulatory Authority meetings.

7 days ago

Boston, MA

$249,827.20–$374,740.80 / year

We would prefer for you to have: 2-3 years safety and risk management experience in the pharmaceutical, biotech or CRO industry Rare, Ultra-Rare or Orphan Disease Area experience Strong verbal and written communication skills including making recommended courses of action to management Excellent, independent judgment based on knowledge and expertise Strong personal time-management and project-management skills Proficiency in Microsoft Word, PowerPoint and Excel. Evaluating aggregate safety data and providing contributions to core regulatory documents i.e. Periodic Safety Update Reports, Drug Safety Update Reports, Risk Management Plans, and other routine and non-routine safety and risk/benefit evaluations for internal or regulatory purposes as required.

30+ days ago

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Safety Director Jobs in Boston, MA

Assistant Director of Nursing, RN Erickson Senior Living

Safety Manager - Multifamily Construction Jobot

Director of Traffic/Warehousing Continental Resources

Director of Social Services Care-One

Assistant Director of Social Services Care One

Assistant Director of Nursing, RN Linden Ponds by Erickson Senior Living

Safety Manager - Life Science Projects Michael Page USA

Asst. Sanitation Manager Aramark

Safety Director II Gilbane Building Co

Safety Director II Next 150 Construction, LLC

Director of Safety and Training Transdev North America Inc

Executive Director, Quality and Safety Lahey Hospital and Medical Center

Director of Safety & Training Raymond Search Group

Director, Public Safety, Mount Auburn Hospital Lahey Hospital and Medical Center

Director of Safety, Security, and Emergency Management Sturdy Memorial Hospital

Director, Medical Safety Assessment Physician Bristol-Myers Squibb Co

Director - NE Process and Gas Field Safety National Grid Plc

Director, Quality & Patient Safety Boston Medical Center

Director, Clinical Translational Safety Lead Johnson & Johnson

Director, Patient Safety ICSR Vertex Pharmaceuticals Inc

Associate Medical Director, Global Drug Safety Biogen Inc

Director, Nonclinical Safety Assessment Expert (Multiple Therapeutic Areas) Novartis AG

Regional Public Safety Dispatch Director Town of Duxbury

Medical Director, EP, Medical and Patient Safety Gateway Recruiting

Director, Partner Marketing - Public Safety ZOLL Medical

Director, Aviation Safety & Security TransMedics Group Inc

Director of Product - Public Safety AI & Intelligence Solutions Motorola Solutions Inc

Director, Safety Science Generate Biomedicines Inc

Associate Director, Safety Scientist Alexion

Associate Director, Toxicology (Nonclinical Safety Evaluation) City Therapeutics

Supervisory Safety and Occupational Health Specialist (Assistant Area Director) U.S. Department of Labor

Director, Aviation Safety & Security TransMedics

Executive Director, Patient Safety Parexel International Corp

Patient Safety Associate Medical Director Vertex Pharmaceuticals Inc

Executive Medical Director, Patient Safety (Hybrid) Vertex Pharmaceuticals

Director, Safety Scientist Alexion

Director Safety Mission Critical Shawmut Design and Construction

Global Safety Program Lead/Sr Medical Director Alexion

Global Safety Program Lead/Sr Medical Director Alexion Pharmaceuticals Inc

Safety Director I Gilbane Building Co

Director- Safety- Mission Critical Shawmut

Safety Director I Next 150 Construction, LLC

Medical Director - Drug Safety & Pharmacovigilance Zenas BioPharma (USA) LLC

Associate Medical Director, Drug Safety and Pharmacovigilance PV Nuvalent Inc

Senior Director, Nonclinical Safety Evaluation ModernaTX

Medical Director, Global Patient Safety Alexion

Medical Director, Global Patient Safety Alexion Pharmaceuticals Inc

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