48 open listings · Page 2 of 2
Roles posted by organizations here, alongside roles we found on employers’ own careers sites. Crawled roles say so on the card and send you to the employer to apply. Only show organizations on Career App
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Medical Patient Language Writing Specialist
Cohere Health
Full-time · United States · $85,000 – $92,000
This role involves translating complex medical policies and coverage decisions into clear, patient-friendly communications that meet regulatory standards. It suits experienced medical writers or healthcare communicators who want to improve how patients understand their care options and coverage determinations.
Listed on Cohere Health’s careers site · Apply there ↗
General Counsel, Moody's Analytics
Moody's Corporation
Full-time · New York, NY · $280,500 – $406,650
This is a senior legal leadership role directing all legal matters for Moody's Analytics, a data and analytics business segment, with responsibility for commercial contracts, M&A, regulatory compliance, and managing a global legal team. The position suits an experienced in-house counsel with deep expertise in software and SaaS licensing who can balance legal risk with business growth at the executive level.
Listed on Moody's Corporation’s careers site · Apply there ↗
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Senior Recovery Certification and Operations Engineer
Relativity Space
Full-time · Cape Canaveral, FL · $116,500 – $175,000
This role leads regulatory certification and compliance efforts for Relativity Space's offshore recovery vessels that land and recover rockets, coordinating with agencies like the Coast Guard and working across design, construction, and operational phases. It suits someone with marine vessel certification experience and regulatory coordination skills who thrives in a fast-paced aerospace environment.
Listed on Relativity Space’s careers site · Apply there ↗
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Partner Manager, Global Health
Menlo Ventures Portfolio
Full-time · New York, NY · $215,000 – $300,000
This role leads clinical research and validation work for deploying Claude in global health settings, particularly in low-resource countries. It suits clinicians with deep experience in LMIC care delivery who want to shape how AI tools are rigorously tested and improved for real-world clinical use.
Listed on Menlo Ventures Portfolio’s careers site · Apply there ↗
Pharmacy Operations Lead
Cigna
Full-time · Newark, DE · $21 – $31 / hour
A supervisory role overseeing daily receiving and inventory operations at a pharmaceutical distribution center, managing staff and ensuring accurate, compliant handling of products. Suits someone comfortable with hands-on leadership, operational metrics, and pharmaceutical supply chain standards.
Listed on Cigna’s careers site · Apply there ↗
Associate Director, US Omnichannel/Digital Engagement
Biogen
Full-time · Cambridge, MA · $164,000 – $226,000
Lead omnichannel and digital engagement strategy for assigned pharmaceutical brands at Biogen, orchestrating personalized customer journeys across channels using AI-powered tools. This role suits strategists with healthcare marketing experience who can translate brand objectives into measurable campaign execution while partnering closely with brand, media, and analytics teams.
Listed on Biogen’s careers site · Apply there ↗
Principal Scientist, Biostatistics, Late-Stage Clinical Development
Merck
Full-time · 2 locations · $190,800 – $300,300
A leadership role in biostatistics within a pharmaceutical R&D department, responsible for designing and analyzing clinical trials, managing statistical programming teams, and ensuring regulatory compliance for drug and vaccine development. This suits experienced statisticians who want to advance into senior scientific leadership while driving the statistical strategy behind clinical research programs.
Listed on Merck’s careers site · Apply there ↗
Choose a location to apply
Distribution Quality Lead - Korea, India and South East Asia
Medtronic
Lead quality assurance for Medtronic's medical device distribution operations across Korea, India, and Southeast Asia, managing a team of five QA professionals and ensuring compliance with regulatory and internal standards. This role suits experienced quality professionals in regulated industries who can oversee complex supply chain compliance and drive process improvements across multiple regions.
Listed on Medtronic’s careers site · Apply there ↗
EHS&S Sr. Manager
Moderna
$130,800 – $209,400
This senior manager role oversees environmental health and safety operations at Moderna's Norwood manufacturing facility, leading complex EHS programs, investigations, and compliance initiatives across R&D and production environments. The position suits experienced EHS professionals with strong expertise in regulated biopharmaceutical operations who can drive culture change and manage high-risk work activities across cross-functional teams.
ISO 45001Root Cause AnalysisISO 14001Risk AssessmentCorrective And Preventive Action (CAPA)Regulatory Compliance
Listed on Moderna’s careers site · Apply there ↗
Senior Director, Managed Access Programs, Medical Evidence Generation (Worldwide Medical Affairs)
Bristol Myers Squibb
Full-time · $229,380 – $277,956
This role oversees the global strategy and implementation of managed access programs across multiple therapeutic areas, ensuring patients with unmet medical needs can access Bristol Myers Squibb's medicines in compliant and ethical ways. The position requires extensive pharmaceutical industry experience with deep knowledge of regulations, and involves leading cross-functional teams to standardize processes, capture evidence, and optimize program performance worldwide.
Listed on Bristol Myers Squibb’s careers site · Apply there ↗
Senior Director, Opinion Leader Programming HIV Treatment
Gilead Sciences
Full-time · United States - California - Foster City · $261,375 – $338,250
This senior leadership role oversees opinion leader strategy and relationship management across Gilead's HIV treatment business, including speaker programs, advisory boards, and KOL engagement. The position suits experienced pharmaceutical marketing executives with strong leadership skills and the ability to manage complex cross-functional initiatives in specialty care settings.
Listed on Gilead Sciences’s careers site · Apply there ↗
Senior Process Engineer, Technical Operations - Small Molecule Drug Substance
Merck
Full-time · Elkton, VA · $117,000 – $184,200
A senior technical role leading small molecule drug substance manufacturing at a new U.S. facility, responsible for process ownership from design through commercial production. Suits experienced process engineers ready to drive technical excellence and guide technology transfers in a fast-paced biopharmaceutical setting.
Associate Director, Clinical Operations – Therapeutics/Oncology
Moderna
Full-time · $142,500 – $256,500
This role oversees clinical trial operations for cancer and immunotherapy programs at a biopharmaceutical company, managing budgets, timelines, and cross-functional teams through all phases of drug development. It suits experienced clinical operations professionals with a background in oncology who can lead complex studies and vendor relationships independently.
Listed on Moderna’s careers site · Apply there ↗
Director, Oncology Medical Engagement Excellence
Bristol Myers Squibb
Full-time · $204,200 – $247,437
This role leads medical engagement strategy and execution for Bristol Myers Squibb's oncology portfolio, ensuring field medical teams effectively educate healthcare professionals on appropriate medicine use. It suits experienced medical affairs professionals with oncology expertise who can influence across complex, matrixed organizations and translate global medical strategy into coordinated field execution.
Listed on Bristol Myers Squibb’s careers site · Apply there ↗
Director, Patient Safety (MD)
Gilead Sciences
Full-time · United States - California - Foster City · $243,100 – $314,600
Gilead is seeking a physician leader to oversee the medical review of safety reports for both experimental and marketed drugs, ensuring rigorous case assessments that protect patients and meet regulatory standards. This role combines clinical expertise with management responsibility, requiring someone who can drive quality improvements in safety processes while mentoring junior reviewers.
Listed on Gilead Sciences’s careers site · Apply there ↗
Associate Director, Technical Operations - Small Molecule Drug Substance
Merck
Full-time · Elkton, VA · $142,400 – $224,100
Lead technical operations for small molecule drug manufacturing at a newly built U.S. site, overseeing process scale-up, technology transfer, and commercial production of active pharmaceutical ingredients. Suited to experienced pharmaceutical process engineers seeking to drive operational excellence and build manufacturing capability from startup through commercialization.
Associate Director, Aseptic & Sterile Process Engineering
Bristol Myers Squibb
Full-time · Devens, MA · $170,650 – $206,793
This role leads technical strategy for aseptic and sterile processing in an advanced automated cell therapy manufacturing environment, requiring deep expertise in contamination control, regulatory readiness, and process simulation. It suits experienced pharmaceutical or biotech engineers who can influence cross-functional teams and translate complex aseptic principles into automated manufacturing systems.
Listed on Bristol Myers Squibb’s careers site · Apply there ↗
Clinical Trials Manager
Gilead Sciences
United States - California - Foster City · $133,195 – $189,640
This role oversees the operational execution of clinical trials across assigned geographic regions or study components, managing budgets, timelines, vendor relationships, and regulatory compliance. It suits experienced life sciences professionals with project management skills and knowledge of clinical trial processes who want to drive the advancement of therapeutic development.
Listed on Gilead Sciences’s careers site · Apply there ↗
Sr. Principal Scientist (Sr. Director) - Regulatory Liaison
Merck
Full-time · $190,800 – $300,300
A senior regulatory leadership role managing global approval strategies for cardiovascular and metabolic drugs from development through market launch. This suits experienced regulatory scientists who have led complex submissions with multiple indications and want to shape product strategy while working directly with FDA and international health authorities.
Listed on Merck’s careers site · Apply there ↗
Bouwkundige Vakspecialist
Merck
Full-time
This role leads technical and execution aspects of complex construction and engineering projects at pharmaceutical manufacturing sites, managing engineers while ensuring quality, safety, and compliance standards. It suits experienced construction specialists who combine technical expertise with coaching skills and want to work on diverse, mission-critical projects in a large, growing organization.
Listed on Merck’s careers site · Apply there ↗
Director, Operations - Pharm Ops
Merck
Full-time · Elkton, VA · $173,200 – $272,600
This director-level role leads pharmaceutical operations and team development at a new small-molecule manufacturing site, balancing site ramp-up and long-term operational excellence. The position suits experienced operations leaders with strong regulatory and manufacturing backgrounds who can build organizational culture and drive continuous improvement.
Listed on Merck’s careers site · Apply there ↗
Director, Operations - API
Merck
Full-time · Elkton, VA · $173,200 – $272,600
Lead the operational and technical strategy for a new small molecule pharmaceutical manufacturing facility's API production, overseeing site ramp-up, team development, and the establishment of operating systems from the ground up. This role suits experienced manufacturing leaders with deep expertise in regulated environments who are energized by building high-performing organizations and driving operational excellence during critical growth phases.
Principal Scientist, Regulatory Liaison
Merck
Full-time · $173,200 – $272,600
This role leads global regulatory strategy for vaccine and infectious disease products, serving as the primary regulatory contact between the company, FDA, and international agencies throughout drug development and commercialization. It suits experienced scientists with strong command of pharmaceutical regulation and the ability to work independently on complex, multi-indication programs.
Listed on Merck’s careers site · Apply there ↗