Clinical Safety Specialist

The Clinical Safety Specialist will collaborate with the clinical safety team to oversee the implementation of InterSystems' Clinical Safety Management Framework, enhancing the development and execution of our innovative healthcare products.Key ResponsibilitiesDeliver clinical safety assurance services across all InterSystems products.Modify and enhance Inte…

At InterSystems, we are proud to power some of the most critical applications in the healthcare industry, managing over a billion patient records worldwide. With a legacy spanning more than 40 years, we have partnered with the U.S. Department of Veterans Affairs (VA) to enhance the delivery of essential services, including healthcare, for Veterans and their families. We are currently looking for a dedicated Clinical Specialist to enhance the utilization of our software solutions within VA medical centers and associated clinics. This pivotal role serves as a clinical subject-matter expert, facilitating communication between frontline VA clinicians and our internal teams in sales, marketing, product development, and implementation.

Join Natera, Inc. as a Clinical Oncology Specialist, where you will play a pivotal role in advancing cancer diagnostics and treatment solutions. You will engage with healthcare professionals to provide expert knowledge on our innovative products and services, contributing to improved patient outcomes.

The Alliance for Clinical Trials in Oncology Foundation is dedicated to advancing cancer clinical research by expanding the capabilities of the Alliance for Clinical Trials in Oncology. Our mission is to address significant treatment challenges through large-scale clinical trials aimed at discovering innovative methods for the prevention, treatment, and cure of various cancers, including leukemia, lymphoma, and solid tumors such as breast, prostate, lung, and gastrointestinal cancers. We also strive to educate the medical community on effective cancer diagnosis, treatment, and prevention strategies.In 2014, we established the Alliance Foundation Trials, LLC (AFT), a wholly-owned subsidiary focused on conducting impactful cancer clinical research in collaboration with industry partners.We are currently seeking a Clinical Research Associate (CRA) to play a crucial role in the management and execution of clinical trial operations across AFT studies. The CRA will be responsible for site management and study start-up activities, including conducting feasibility assessments, supporting site selection, maintaining trial master files (eTMF), and overseeing clinical trial management systems (CTMS). The ideal candidate will work closely with CROs, vendors, and investigative sites to ensure compliance with ICH GCP guidelines and organizational standards throughout the study lifecycle. Join our team of dedicated professionals passionate about transforming cancer care.

Role Overview Ramboll is seeking a Consultant in Occupational Health & Safety to join the Boston, Massachusetts team. This role focuses on improving workplace safety standards and supporting a strong health culture across client organizations. What You Will Do Collaborate with clients to design and deliver customized safety solutions Conduct risk assessments for various workplace environments Implement and maintain safety management systems Support clients in meeting regulatory compliance requirements Promote safe work practices across diverse industries About Ramboll Ramboll works with clients across multiple sectors to create safer, healthier workplaces. The team values practical expertise and a collaborative approach to occupational health and safety challenges.

About Merlin: At Merlin Labs, we are an innovative aerospace startup focused on revolutionizing aviation with our cutting-edge non-human pilot technology. Supported by top-tier investors, our mission is to advance the future of flight by promoting both crew-reduced and uncrewed aviation solutions. We are dedicated to tackling some of the most pressing challenges in the aviation industry through autonomy and innovation.About You: We are seeking a dynamic and strategic leader who excels in the implementation and management of Safety Management Systems (SMS) and Quality Management Systems (QMS) within the realm of advanced aviation technologies. You bring a robust project management background in highly regulated sectors and possess in-depth expertise in aviation regulations and certification processes from agencies like the FAA and EASA. Your exceptional organizational skills and innovative mindset empower you to lead intricate technical programs and foster groundbreaking advancements in aviation.

Ramboll seeks a Senior Manager of Health & Safety to oversee programs across the Americas region from its Boston, Massachusetts office. This leadership role shapes health and safety efforts for all operational sites in the area. Key responsibilities Direct health and safety initiatives throughout the Americas Ensure compliance with safety regulations and standards Promote a strong culture of safety within the organization Implement effective safety practices across diverse locations Requirements Significant experience managing health and safety programs Demonstrated ability to lead and influence safety culture and practices

Join our dynamic team at Alimentiv as a Senior Clinical Operations Lead, where you will play a pivotal role in shaping the future of clinical trials. We are looking for a strategic thinker with extensive experience in clinical operations to lead our initiatives and ensure the successful execution of clinical studies.

About Merlin: Merlin Labs is an innovative aerospace startup with venture backing, dedicated to developing autonomous flying technology. We are creating a non-human pilot system that facilitates both crew-reduced and uncrewed flights. Supported by some of the most prominent investors in the field, we are accelerating our growth alongside our clientele to implement autonomy today, addressing significant challenges in aviation.About You: Are you passionate about aviation safety and certification? Are you an accomplished system safety engineer seeking a unique opportunity not found in traditional aerospace environments? If you envision making a substantial contribution to the future of safe aviation systems in a startup with a certification-driven ethos, then the System Safety Engineer position at Merlin could be your next career move.

Company Overview Avalyn Pharma is innovating the landscape of pulmonary fibrosis treatment through a groundbreaking pipeline of inhaled formulations. These approved medications are expertly designed to minimize systemic exposure and deliver targeted therapy directly to the affected areas. Pulmonary fibrosis, characterized by lung tissue scarring, diminishes lung function and quality of life, contributing to increased mortality rates. Conventional therapeutic options may slow disease progression but often come with significant toxicities that limit their application. Avalyn’s inhaled approach directly addresses the underlying causes of pulmonary fibrosis, aiming to enhance patient outcomes with reduced systemic side effects. Currently, Avalyn’s AP01, an optimized inhaled formulation of pirfenidone, is under investigation in the MIST Phase 2b study for progressive pulmonary fibrosis (PPF). This formulation has demonstrated clinical proof-of-concept with better efficacy and safety profiles compared to existing treatments, having been evaluated in over 150 patients with various forms of pulmonary fibrosis. Furthermore, Avalyn has completed two Phase 1 studies for AP02, an inhaled formulation of nintedanib for idiopathic pulmonary fibrosis (IPF), with plans for a Phase 2 clinical trial in the works. For more details, please visit avalynpharma.com and follow us on LinkedIn.

Welcome to knownwell, a pioneer in weight-inclusive healthcare solutions. Join our innovative team that is transforming obesity care delivery through a comprehensive approach that includes weight management, primary care, nutrition counseling, and health coaching. Our unique care model integrates both in-clinic and virtual services to ensure that patients receive the support they need, exactly when they need it.With $50 million in funding—including a $25 million round led by CVS Health Ventures and supported by a16z Bio + Health, Flare Capital, MassMutual, and Intermountain Ventures—we are rapidly expanding access to evidence-based obesity care across the nation. As the Clinical Research Coordinator (CRC), you will oversee and synchronize all facets of our clinical trials. Your role is vital in ensuring compliance with regulatory requirements, sponsor expectations, and Good Clinical Practice (GCP) guidelines. You will serve as the primary point of contact between the clinical research team, patients, and external stakeholders, facilitating the efficient and timely execution of clinical research initiatives.

Join Ramboll as a Senior Manager of Health & Safety for the Americas, where you will lead initiatives to develop and implement safety protocols across various projects. You will work closely with cross-functional teams to ensure compliance with health and safety regulations while fostering a culture of safety within the organization.

At Olema Oncology, we are committed to pioneering innovative therapies for breast cancer and beyond. Our flagship program, palazestrant (OP-1250), represents a groundbreaking complete estrogen receptor antagonist (CERAN) currently under development for metastatic breast cancer. This treatment holds the promise of being a game changer both as a standalone therapy and in combination with other treatments for ER+/HER2- metastatic breast cancer. Additionally, we are advancing our follow-on candidate, OP-3136, a powerful KAT6 inhibitor that has the potential to set new standards in treatment.Our success is propelled by a culture that encourages fearless support, motivation, and constructive challenge among team members. At Olema, we believe that prioritizing our people leads to exceptional outcomes. If you are eager to contribute to an unstoppable mission, we invite you to join us in making a significant impact for our patients, your career, and beyond.View our latest corporate presentations here.About the Role: Director of Clinical Monitoring OversightAs the Director of Clinical Monitoring Oversight, you will report directly to the Senior Director of Clinical Operations and will play a pivotal role in providing strategic and operational leadership for global clinical site monitoring across Olema’s clinical programs. You will ensure that all clinical monitoring activities—whether conducted by internal teams, Functional Service Providers (FSPs), or Clinical Research Organizations (CROs)—are executed with utmost quality, consistency, and compliance with Good Clinical Practice (GCP) regulations.Your responsibilities will include overseeing Olema’s Clinical Monitoring Oversight Leads, regional monitoring teams, and overall site performance. You will also develop and implement monitoring oversight strategies and standards that drive operational excellence, data integrity, and inspection readiness across all clinical trials, focusing on risk-based and data-driven methodologies.This position is based in either our Boston, MA or San Francisco, CA office and will require approximately 15% travel.

At Veeva Systems, we are driven by our mission to revolutionize the life sciences sector, facilitating the swift delivery of therapies to patients. As one of the most rapidly expanding SaaS companies in history, we achieved over $3 billion in revenue last fiscal year and are poised for even greater growth. Our core values—Do the Right Thing, Customer Success, Employee Success, and Speed—define who we are. In 2021, we made history by becoming a public benefit corporation, committed to balancing the needs of our customers, employees, society, and investors. As a Work Anywhere company, we offer the flexibility to work from home or from our offices, allowing you to thrive in an environment that suits you best. Join us in transforming the life sciences industry and making a positive impact on the communities we serve.The RoleAs a Solution Consultant, you will serve as the essential link between intricate pharmacovigilance challenges and Veeva’s top-tier cloud solutions. In this role, you will act as a trusted advisor to the most innovative Life Sciences companies, guiding Safety/Pharmacovigilance teams in transitioning from outdated legacy systems to our unified Vault Safety platform.We are looking for a candidate with a robust background in Life Sciences, a natural curiosity for technology, outstanding presentation and communication skills, and a collaborative mindset.

Key ResponsibilitiesLead and oversee the implementation of EHS standards across our US operations.Develop and maintain a comprehensive compliance management system that proactively addresses EHS challenges to fulfill our commitments and responsibilities.Provide expert guidance to management and various business units on EHS issues, participating in regular discussions with the Leadership team, regional managers, and department heads.Support the establishment of effective EHS frameworks within the US, ensuring rigorous health and safety compliance management.Contribute to the continuous evolution and execution of corporate EHS policies and objectives on an organization-wide basis.Foster strong collaborative relationships with executive leaders and senior management across the retail team, group EHS team, and other stakeholders including construction, facilities management, HR, and legal services.Deliver strategic recommendations to senior management regarding necessary programs, systems, and resources; monitor regional EHS KPI's aligned with group objectives.Address urgent environmental, health, and safety matters swiftly to safeguard employees, customers, and stakeholders and mitigate business risks.Act as a role model for the EHS team in the US, enhancing team capabilities and contributing to performance evaluations as necessary.Build constructive relationships with key figures in regulatory enforcement agencies.Promote and advise on consultative arrangements within the region, ensuring retail and HR teams understand and support these obligations.Collaborate with EHS Country Managers in other regions to establish uniform best practices across Primark.Champion a culture of safety awareness and lead by example to integrate safety into everyday operations.Conduct workplace risk assessments and reviews in accordance with legal requirements, determining necessary actions and priorities.Investigate incidents and accidents thoroughly, maintaining accurate records and ensuring actionable recommendations are implemented to prevent recurrence.Perform EHS inspections as mandated by legislation and company policy, identifying potential hazards and suggesting appropriate corrective measures.

Anthropic seeks a Director of Resilience Operations to join its Global Safety, Intelligence & Security team. This leader will focus on developing and implementing strategies that help protect Anthropic’s worldwide operations from various risks. Role overview This position involves shaping the company’s approach to resilience. The Director will guide efforts to strengthen safety and security across multiple locations, ensuring that the organization can respond effectively to challenges and disruptions. Locations Boston, MA San Francisco, CA New York City, NY Seattle, WA Washington, DC

Join our dynamic team as a Clinical Investigator specializing in Breast Oncology or Hematology. In this role, you will conduct groundbreaking research and clinical trials, contributing to the advancement of cancer treatment. You will collaborate with top researchers and healthcare professionals to drive innovative solutions in patient care.

Become a Pioneer in the Sleep Fitness RevolutionJoin Eight Sleep, where our mission is to enhance human potential through exceptional sleep quality. As the world's first sleep fitness company, we are transforming the concept of well-being and creating cutting-edge hardware, software, and AI technology to facilitate optimal sleep. Our innovative products are designed to maximize mental, physical, and emotional performance, turning each night into a personalized, data-driven recovery session. Trusted by elite athletes and health-conscious individuals across over 30 countries, we are at the forefront of the sleep revolution.Featured as one of Fast Company's Most Innovative Companies in multiple years, we are committed to building a high-performance team that prioritizes speed, focus, and impactful results. Our culture is characterized by an obsession with detail and continuous improvement to ensure our members achieve better sleep and stronger mornings.Unwavering Standards and CommitmentOur intensity reflects the demands of our mission at Eight Sleep. We strive for excellence, inspired by the dedication of top performers worldwide. We are a team that operates with focus and tenacity, constantly pushing to excel in our craft. This is not a conventional 9-to-5 job. Our team is deeply engaged, often going above and beyond because we are passionate about our work.If you thrive under pressure and seek to make a significant impact in your career, you will find your place here. However, if you prefer an easy-going environment, this may not be the role for you.Your RoleWe are in search of a Senior Clinical Trial Manager to oversee the comprehensive execution of our clinical studies, including regulatory trials. This operationally intensive role requires a hands-on approach and expertise in initiating studies from the ground up, managing third-party clinical sites, drafting IRB and informed consent documents, overseeing data management, and ensuring timely and budget-compliant study completion.You will serve as a vital link between our internal teams and external clinical sites, investigators, IRBs, CROs, and, when needed, study participants. A strong understanding of regulatory requirements for medical devices and a proven track record of successful clinical study delivery supporting regulatory submissions are essential.

Join our dynamic team at Precede as a Senior Clinical Laboratory Associate, where your expertise will play a pivotal role in advancing our clinical testing capabilities. You will lead laboratory operations, ensuring the highest standards of quality and accuracy in all testing procedures.Your responsibilities will include overseeing clinical trials, managing laboratory staff, and collaborating with cross-functional teams to interpret complex data. We are looking for a detail-oriented professional who thrives in a fast-paced environment and is passionate about contributing to innovative health solutions.

Role Overview Syska Hennessy Group seeks a Senior Fire Protection and Life Safety Engineer in Boston, MA. This role focuses on designing and implementing fire protection systems that support occupant safety across a range of building projects. What You Will Do Lead the design and execution of fire protection systems for diverse projects. Apply advanced engineering principles to develop effective, practical solutions. Work closely with architects, contractors, and clients to build comprehensive fire safety strategies. Ensure all designs and recommendations meet local codes and industry standards. Assess fire and life safety risks, then develop mitigation plans based on analysis. Collaboration and Impact This position requires frequent collaboration with project teams and clients. Strong analytical skills and a commitment to safety will guide decisions and help shape safer environments for building occupants.