Senior Cost Manager - Infrastructure Consultancy

Join our team as a Senior Health and Safety Consultant at AECOM in Cambridge. We are looking for an experienced professional who is passionate about promoting health and safety standards across various projects. In this role, you will collaborate with stakeholders to develop and implement safety programs, conduct risk assessments, and ensure compliance with regulations. Your expertise will contribute to creating a safer working environment for all.

Join the team at Triumvirate Environmental, a leading environmental services firm in North America, as an Environmental Health & Safety Consultant in our Cambridge office.In this role, you will leverage your expertise in Environmental Health and Safety (EH&S) principles to address challenges and uncover opportunities for our diverse clientele. Your primary focus will be on client satisfaction while providing tailored consulting and staffing solutions.Triumvirate serves prestigious institutions in higher education, life sciences, healthcare, and industrial sectors, ensuring compliance and promoting sustainable practices. We are dedicated to fostering an engaging workplace culture that emphasizes growth, development, and innovation.This position is based onsite and will support clients throughout the greater Boston area while reporting directly to the Regional EHS Director.

Role Overview Lila Sciences seeks an Environmental Health and Safety (EHS) Coordinator (Contractor) to support environmental health, safety, and sustainability programs in laboratory settings. This onsite contract role is based in Cambridge, MA. The position is hands-on, with regular engagement on the lab floor to manage compliance workflows and help build ESG and ISO-compliant programs from the ground up. This role offers the chance to gain practical EHS and laboratory safety experience in a mission-driven scientific environment. The coordinator will also contribute to program development and sustainability reporting. What You Will Do Assist in developing and maintaining EHS programs and policies that meet local, state, and federal regulations, including documenting incidents and tracking corrective actions. Provide ongoing EHS oversight through lab tours, facility walkthroughs, and regular safety inspections. Support biosafety, chemical safety, and hazardous waste management processes, working closely with lab teams to ensure regulatory compliance. Help deliver EHS training and onboarding for new employees and contractors. Contribute to Lila Sciences' ESG program by collecting data, monitoring progress, and preparing sustainability reports and dashboards. Assist with compliance activities for ISO 14001 and ISO 45001, focusing on documentation and process coordination. Participate in developing EHS standards for the AISF blueprint through documentation, policy coordination, and workflow organization. Qualifications Bachelor's degree in Environmental Studies, Environmental Health and Safety, Sustainability, or a related field. 1-3 years of experience in EHS, sustainability coordination, program administration, or a similar area. Strong organizational, communication, and documentation skills. Ability to work independently, manage multiple priorities, and maintain attention to detail. Interest in lab safety, environmental compliance, and sustainability, with a desire to deepen technical EHS knowledge. Familiarity with AI tools is a plus. Preferred Experience Experience with biosafety, chemical hygiene, or hazardous waste handling (from academic, internship, or professional settings). Knowledge of ISO 14001 and/or ISO 45001 standards.

Join Integrated Resources Inc. as a Senior Drug Safety Associate and contribute to the vital field of drug safety and pharmacovigilance. In this role, you will play a key part in monitoring and ensuring the safety of pharmaceutical products, working closely with cross-functional teams to assess risk and implement safety measures.

Join our dynamic team at Harvard University as a Senior Human Resources Consultant. In this pivotal role, you will leverage your expertise to enhance our HR strategies and provide valuable guidance across various departments. Collaborate with stakeholders to optimize HR processes and contribute to a thriving organizational culture.

Scholar Rock, Inc. is a pioneering biopharmaceutical firm dedicated to the discovery, development, and delivery of transformative therapies for individuals suffering from serious diseases with significant unmet medical needs. As a recognized leader in the biology of the transforming growth factor beta (TGFβ) superfamily of proteins, Scholar Rock is committed to advancing innovative treatments where the modulation of protein growth factors is crucial. Over the last decade, we have developed a robust pipeline aimed at redefining the standard of care for neuromuscular conditions, cardiometabolic disorders, cancer, and other diseases where growth factor-targeted therapies can radically change patient outcomes. Scholar Rock is the first and only company to demonstrate clinical proof of concept for a muscle-targeted treatment in spinal muscular atrophy (SMA). Our commitment to unlocking unique therapeutic strategies is driven by our proprietary platform, which has generated novel monoclonal antibodies designed to modulate protein growth factors with remarkable precision. By leveraging cutting-edge scientific advancements in therapeutic areas that have historically been overlooked by conventional treatments, Scholar Rock tirelessly works to create new avenues for patient care. Discover more about our innovative approach at ScholarRock.com and follow us on @ScholarRock and LinkedIn.Position Overview:The Senior Medical Director of Drug Safety & Pharmacovigilance plays a critical role within the company, significantly influencing the development and lifecycle management of drug projects. This position is responsible for defining and implementing safety strategies and providing expert guidance during both pre- and post-approval phases for assigned products. The Senior Medical Director will proactively lead risk management initiatives in compliance with global regulatory standards, continuously evaluating safety data, conducting signal detection, and managing the safety profiles of compounds. Additionally, this role will involve close collaboration with cross-functional teams to achieve project objectives within established timelines and quality standards.

Join Harvard University as a Senior Human Resources Consultant, where you will play a pivotal role in shaping the HR strategies that support our diverse and dynamic community. In this full-time position, you will collaborate with various departments to enhance HR practices, drive employee engagement, and ensure compliance with federal and state regulations.

Join our innovative team at ttp1 as a PhD Ultrasound Consultant. In this pivotal role, you will leverage your expertise in ultrasound technology to drive advancements in health tech solutions. Collaborate with a dynamic group of professionals dedicated to improving healthcare outcomes through cutting-edge technology.

As a Drug Safety Associate at Integrated Resources Inc., you will play a crucial role in ensuring the safety and efficacy of pharmaceutical products. You will be responsible for monitoring and evaluating adverse events, coordinating safety reports, and contributing to the overall pharmacovigilance efforts within our organization. Your attention to detail and analytical skills will be vital in supporting our commitment to patient safety.

We are open to hiring for this role at various levels of expertise. For the right candidate, this position can be structured as a Senior Research Manager, with compensation tailored to experience and the anticipated scope of work, potentially exceeding the listed pay rate.About the Cambridge Boston Alignment InitiativeThe Cambridge Boston Alignment Initiative (CBAI) is a nonprofit research organization dedicated to promoting research and education aimed at facilitating a safe and beneficial transition to advanced AI systems. Our efforts include generating original research and accelerating AI safety initiatives through our fellowship programs.Our first summer fellowship cohort has already published significant papers at the Mechanistic Interpretability Workshop at NeurIPS and had accepted papers at ICLR. Additionally, some fellows have transitioned to roles at Goodfire and Redwood Research. Following a successful launch in 2025, we are poised for rapid expansion in 2026, with plans to host multiple fellowship cycles (Fall, Spring, and Summer), double our fellowship cohort, and quadruple our team size.Refer candidates to us and earn $5,000 if they are hired.The RoleIn this role, you will collaborate closely with research fellows and their esteemed mentors—renowned researchers from Cambridge and beyond—to support pioneering work on interpretability, AI control, formal verification for provably safe AI, evaluations, and various aspects of AI governance and policy. We are looking for research managers with experience in both technical research and governance and policy research.Research Management Responsibilities (0.7 FTE)Conduct regular one-on-one meetings with fellows to provide constructive feedback on research progress, assist in overcoming challenges, and coach them through issues such as debugging research methodologies and preparing literature scaffolds, as well as supporting data collection, analysis, and methodology development for experiments and hypothesis testing.Offer feedback on fellows' research and help cultivate an environment that encourages rigorous approaches among them.Connect fellows with relevant resources, literature, and opportunities available during and after the fellowship program.Facilitate communication between fellows and their mentors to ensure a supportive research ecosystem.

Join our team as a Clinical Safety Data Manager, where you will play a pivotal role in ensuring the safety and efficacy of our clinical trials. You will manage safety data, conduct thorough analyses, and collaborate closely with cross-functional teams to maintain the highest standards of patient safety.

AbbVie is seeking a highly skilled Associate Director to lead our Safety Operations Portfolio. This pivotal role involves overseeing safety operations while ensuring compliance with regulatory requirements. The ideal candidate will possess exceptional leadership skills and a strong background in pharmacovigilance.Join our dynamic team and contribute to advancing healthcare solutions that enhance patient safety and improve health outcomes. This is an exciting opportunity for professionals looking to make a meaningful impact in the pharmaceutical industry.

Join Steritech as a Food Safety and Compliance SpecialistLocation: Cambridge, OntarioSteritech is a leader in food safety and quality assurance, serving as a trusted partner to some of the most recognized brands across various sectors including manufacturing, food service, retail, and hospitality. Our mission is to empower clients to deliver the safest and healthiest experiences to their customers. As part of the Rentokil Terminix family, we uphold the highest standards in food safety and compliance.Your Future Starts Here! At Steritech, we are dedicated to fostering a culture of continuous learning and professional growth. With a majority of our management team having advanced from specialist roles, we believe in nurturing talent from within. Joining our team means embarking on a career path filled with opportunities for advancement. We equip you with the necessary tools, resources, and mentorship to ensure your success, as we recognize that your achievements contribute to our collective success.As a Food Safety & Compliance Specialist, you will partner with clients in the hotel, restaurant, and grocery sectors to ensure adherence to brand standards, food quality, and exceptional service.Key Responsibilities:Conduct thorough assessments to evaluate compliance with regulatory, industry, and proprietary standards.Monitor food preparation and cooking practices to uphold food safety and sanitation standards.Collaborate with clients to identify and address the root causes of discrepancies in assessments while developing corrective action plans.Educate and guide clients on creating a safer and healthier workplace for their employees and customers.Willingness to travel up to 50% of the time by car and/or plane, approximately 10 overnight stays per month.

Join Bicycle Therapeutics, a pioneering biopharmaceutical company, as the Director of Clinical Safety Science specializing in Radiopharmaceuticals. In this critical role, you will lead the evaluation and management of clinical safety data, ensuring the highest standards of patient safety and regulatory compliance. You will collaborate closely with cross-functional teams to drive innovative solutions in our clinical development programs.

Your Contribution at Lila At Lila, we are assembling a highly skilled and proactive AI safety team that will collaborate with all core departments, including science, model training, and lab integration, to effectively address risks associated with scientific superintelligence. The primary mission of this team is to develop and execute a tailored safety strategy that aligns with Lila's unique objectives and deployment methodologies. This will encompass formulating technical safety strategies, engaging with the broader ecosystem, and producing technical documentation such as risk and capability assessments and safety measures. Your Responsibilities Establish the research and development strategy for Lila’s safety framework concerning biological and physical risks. Design and implement capability evaluations to identify scientific risks (both recognized and novel) arising from state-of-the-art scientific models integrated with automated physical laboratories across biological and physical sciences. Lead and coordinate threat modeling sessions with both internal and external scientific experts, including monitoring advancements in technologies and their applications. Create and curate high-quality training and testing datasets for evaluations and safety systems. Assess risks linked to Lila’s capabilities, considering interactions with the broader ecosystem of capabilities (including general-purpose frontier models and specialized scientific tools). Contribute to extensive, high-quality research initiatives when needed for scientific capability evaluation and restriction. Engage in external communications regarding Lila’s safety initiatives. Qualifications for Success A PhD in a biological sciences field (e.g., molecular biology, virology, computational biology) or a physical sciences field (e.g., materials science, physics, chemistry, chemical or nuclear engineering) or equivalent experience. Proven track record in setting research directions for open issues surrounding dual-use risks in biological and physical sciences. Experience in scientific computing within the biological or physical sciences. Understanding of dual-use research and dissemination issues in relation to relevant safety, regulatory, and governance frameworks (e.g., export controls, biological and chemical-related conventions). Excellent communication skills, capable of articulating complex technical concepts to non-specialist audiences. Demonstrated leadership capabilities in guiding teams of internal and external collaborators in developing Lila's perspective on biological and physical risks.

Join our team as a Senior Arboricultural Consultant, where you will play a pivotal role in enhancing urban environments through effective tree management and consultancy. In this position, you will apply your expertise to provide clients with comprehensive advice on tree preservation, management, and planning. Your responsibilities will include conducting tree surveys, preparing reports, and collaborating with various stakeholders to ensure sustainable practices.

Join our dynamic team at mindlance2 as a Consultant, where you will have the opportunity to leverage your expertise to drive impactful solutions for our clients. This role requires a strategic thinker who can analyze complex problems, provide actionable insights, and collaborate effectively with diverse teams.

We are seeking a highly skilled Associate Director of Drug Safety and Pharmacovigilance to join our dynamic team at Nuvalent. This pivotal role involves overseeing drug safety operations, ensuring compliance with regulatory requirements, and enhancing the pharmacovigilance strategy. The ideal candidate will possess a deep understanding of drug safety processes and a passion for advancing patient safety in the pharmaceutical industry.

Join our dynamic team at Integrated Resources, Inc. as a Clinical Safety Data Manager. In this pivotal role, you will oversee the management and analysis of clinical safety data, ensuring compliance with regulatory standards and enhancing patient safety. Your expertise will be vital in developing safety databases and implementing data management processes that support clinical trials.