Cambridge, Massachusetts, United States · On-site
$177k–$278k/yr
By clicking the “Apply” button, I understand that my employment application process with Takeda will commence and that the information I provide in my application will be processed in line with Takeda’s Privacy Notice an…
Skills: Risk-Based Quality Management, GCP Regulations, Clinical Program Oversight, Inspection Readiness, Root Cause Analysis
Cambridge, Massachusetts, United States · On-site
$144k–$178k/yr
Project/division: SecureBio Detection Team: Laboratory Science Start date: ASAP Status: full-time SecureBio employee Starting compensation: $144,000 to $178,000, depending on experience Visa sponsorship: not available Wo…
Skills: LIMS Platform Management, Laboratory Science, Project Leadership
Cambridge, Massachusetts, United States · On-site
$38/hr–$50/hr
HealthFitness, a Trustmark company, is a proven leader in providing fitness solutions that engage and connect people both on-site and online, to create a strong community of health. Our work focuses on creating meaningfu…
Skills: Swim Instruction, Program Design, CPR/AED Certification, First Aid, Stroke Proficiency
Cambridge, Massachusetts, United States · Hybrid
$139k–$238k/yr
At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less in…
Skills: Clinical Operations, Developing Others, Drug Discovery Development, Hybrid Project Management, Inclusive Leadership
Cambridge, Massachusetts, United States · On-site
$35/hr–$50/hr
HealthFitness, a Trustmark company, is a proven leader in providing fitness solutions that engage and connect people both on-site and online, to create a strong community of health. Our work focuses on creating meaningfu…
Skills: Personal Training, Fitness Assessment, Workout Program Design, Strength Training, Cardiovascular Training
Cambridge, Massachusetts, United States · On-site
$137k–$215k/yr
By clicking the “Apply” button, I understand that my employment application process with Takeda will commence and that the information I provide in my application will be processed in line with Takeda’s Privacy Notice an…
Skills: Pharmacovigilance, Risk Management, Signal Detection, Safety Reporting, Regulatory Compliance
Cambridge, Massachusetts, United States · On-site
$18/hr–$20/hr
HealthFitness, a Trustmark company, is a proven leader in providing fitness solutions that engage and connect people both on-site and online, to create a strong community of health. Our work focuses on creating meaningfu…
Skills: Lifeguarding, CPR/AED, First Aid, Water Safety, Chemical Testing
Cambridge, Massachusetts, United States · Hybrid
$131k–$209k/yr
The Role: Joining Moderna offers the unique opportunity to be part of a pioneering team that's revolutionizing medicine through mRNA technology, with a diverse pipeline of development programs across various diseases. As…
Skills: Python, SQL, ETL/ELT Pipelines, Data Modeling, Security Data Engineering
Cambridge, Massachusetts, United States · On-site
$137k–$180k/yr
At Eisai, satisfying unmet medical needs and increasing the benefits healthcare provides to patients, their families, and caregivers is Eisai’s human health care (hhc) mission. We’re a growing pharmaceutical company that…
Skills: Alliance Management, Search & Evaluation, Neurology Expertise, Strategic Planning, Stakeholder Engagement
Cambridge, Massachusetts, United States · On-site
$88k–$144k/yr
Your Impact at LILA Lila Sciences is seeking an Associate Scientist/Scientist I specializing in high-throughput protein purification and analytics to join the Protein Sciences team within the Autonomous Science Platform.…
Skills: Protein Purification, AKTA Chromatography, Mass Spectrometry, Bioassay Development, LC-MS
Cambridge, Massachusetts, United States · On-site
$110k–$166k/yr
Overview Alnylam’s Translational Research group is seeking a highly motivated Metabolomics Scientist to join our team. We use untargeted and targeted liquid chromatography-tandem mass spectrometry (LC-MS/MS)-based omics …
Skills: LC-MS/MS, Metabolomics, Lipidomics, Sample Preparation, Bioinformatics
Cambridge, Massachusetts, United States · Hybrid
$211k–$237k/yr
Amylyx has an audacious mission to usher in a new era for treating diseases with high unmet needs. Where others see challenges, we see opportunities that we pursue with urgency, rigorous science, and unwavering commitmen…
Skills: Medical Information Strategy, Inquiry Management, Vendor Management, Content Strategy, Launch Readiness
Cambridge, Massachusetts, United States · On-site
$145k–$170k/yr
About the Role: The Senior Clinical Trial Manager will be at the forefront of our early phase studies. The role will report into the Senior Director of Clinical Operations and will be in a highly visible role for a novel…
Skills: Clinical Trial Management, CRO Management, GCP/ICH Guidelines, Study Start-up, Trial Master File
Cambridge, Massachusetts, United States · On-site
Your Impact at LILA We are seeking a Senior Principal Scientist, Small Molecule Therapeutics to lead the protein science and structural biology strategy supporting small molecule therapeutics across Lila’s discovery plat…
Skills: Protein Expression, Protein Purification, Structural Biology, X-ray Crystallography, Cryo-EM
Cambridge, Massachusetts, United States · On-site
Your Impact at LILA Science only creates impact when the right people understand it. At Lila Science, our Government sector team sits at the interface between world-class researchers and the government clients and intern…
Skills: Technical Writing, Grant Writing, Life Sciences Translation, AI Prompting, LLM Workflow Automation
Cambridge, Massachusetts, United States · On-site
$184k–$294k/yr
Your Impact at LILA The Distinguished Scientist, Small Molecule Therapeutics will play a key role in building a world-class small molecule screening organization across Lila’s discovery platform. The qualified candidate …
Skills: DNA-encoded Libraries (DEL), Biophysical Assay Development, Biochemical Assay Development, High-throughput Screening (HTS), Protein Construct Design
Cambridge, Massachusetts, United States · On-site
$121k–$147k/yr
Company Overview: Prime Medicine is a leading biotechnology company dedicated to creating and delivering the next generation of gene editing therapies to patients. The Company is leveraging its proprietary Prime Editing …
Skills: Genome Editing, Prime Editing, pegRNA Design, Molecular Biology, Cell Culture
Cambridge, Massachusetts, United States · Hybrid
Live Your Best Life at Lap of Love Veterinary Hospice! Join Lap of Love as an In-Home, Associate Veterinarian in Boston, MA and surrounding areas. Imagine a veterinary role that honors your time, supports your well-being…
Skills: Hospice Care, Euthanasia, Veterinary Medicine, Compassionate Care, Mobile Veterinary Practice
Cambridge, Massachusetts, United States · Hybrid
Live Your Best Life at Lap of Love Veterinary Hospice! Join Lap of Love as an In-Home, Associate Veterinarian in Boston, MA and surrounding areas. Imagine a veterinary role that honors your time, supports your well-being…
Skills: Hospice Care, Euthanasia, Veterinary Medicine, Compassionate Care, Mobile Veterinary Practice
Cambridge, Massachusetts, United States · On-site
$58k–$78k/yr
When you join the growing BILH team, you're not just taking a job, you’re making a difference in people’s lives. Job Description: The Medical Education Coordinator is responsible for overseeing and coordinating all hospi…
Skills: CME Coordination, Accreditation Compliance, Event Planning, Administrative Support, Microsoft Office
Cambridge, Massachusetts, United States • On-site
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Lead risk-based quality management and inspection readiness for oncology clinical programs to reduce compliance risks and accelerate time to market. Serve as a strategic quality leader within governance bodies to safeguard asset value and ensure patient safety and data integrity.
Requires a scientific or medical degree with at least 10 years of pharmaceutical industry experience, including 5 years in Quality or Compliance. Must possess deep expertise in GCP regulations and a proven track record of leading global regulatory inspections and complex investigations.
By clicking the “Apply” button, I understand that my employment application process with Takeda will commence and that the information I provide in my application will be processed in line with Takeda’s Privacy Notice and Terms of Use. I further attest that all information I submit in my employment application is true to the best of my knowledge.
Are you looking for a patient-focused, innovation-driven company to inspire you and empower you to shine? Join us as a Director, Clinical Program Quality & Excellence (CPQE), Oncology based in Cambridge, MA reporting to the Head, Clinical Program Quality Oncology.
At Takeda, we are transforming the pharmaceutical industry through our R&D-driven market leadership and being a values-led company. To do this, we empower our people to work towards their potential through life-changing work. Certified as a Global Top Employer, we offer stimulating careers, and work toward excellence in everything we do. We foster an inclusive, collaborative workplace, in which our global teams are united by an unwavering commitment to provide Better Health and a Brighter Future to people around the world.
Here, you will be a necessary contributor to our inspiring, bold mission.
Shape, at the asset-level, a risk based quality management model that elevates clinical program performance, strengthens regulatory confidence, and accelerates time to market by proactively reducing systemic compliance risks.
Serve as a strategic quality leader at asset-level key governance bodies (e.g. Global Program Team, Clinical Sub-Team, Clinical Review Board), shaping portfolio decision making by providing objective insights on emerging risks, critical quality issues, and mitigation strategies that safeguard program continuity and asset value.
Lead real time inspection readiness at the asset-level, across all Study Execution Teams, driving operational discipline, cross functional issue resolution, and sustained adherence to global GCP and regulatory expectations throughout end to end clinical trial delivery.
Champion a culture of accountability, scientific rigor, and quality by design at the asset-level, influencing senior stakeholders and partners to adopt robust quality practices that protect patient safety, uphold data integrity, and support successful regulatory submissions worldwide.
Responsible for quality management for assigned asset-level clinical programs, developing and implementing proactive, risk-based quality management strategies to drive compliance and de-risk clinical programs.
Lead escalation of quality issues, risks and mitigations to enable data-driven, quality and patient-centric decision-making at relevant governance levels (e.g. Global Program Team, Clinical Sub-Team, Clinical Review Board)
Lead investigations into Serious Breaches (GCP), Scientific Misconduct, and other significant quality events and deviations, applying robust root cause analysis to ensure effective resolution and prevention of recurrence.
Drive inspection readiness for assigned asset-level clinical programs in TAU, providing oversight to drive sustainable compliance embedded end to end in clinical programs.
Lead global GCP inspection strategy for assigned asset-level clinical programs, leading the planning for submission‑related inspections, representing Takeda as a Subject Matter Expert (SME) in clinical program quality oversight during regulatory interactions.
Develop and implement robust, risk-based audit strategy for assigned asset-level clinical development programs that enables early detection of potential quality issues with appropriate mitigations to reduce clinical program risks.
Support and mentor the CPQ team for assigned Study Execution Teams (SETs) in the development, implementation and refinement of a proactive quality oversight model, embedding real-time inspection readiness by driving proactive compliance, documentation quality and the framework for proactive investigation and cross‑functional resolution of quality events.
Contribute to the R&D Quality GxP Center of Continuous Improvement and Performance in CTD and PV through comprehensive approach in sharing insights and learnings throughout clinical program delivery.
Scientific or allied health/medical degree (BSc required; MSc or PhD preferred).
10 or more years of progressive experience in the global pharmaceutical industry, including at least 5 years in Quality and/or Compliance supporting clinical development programs.
Advanced expertise across the clinical development lifecycle, from R&D through commercialization and lifecycle management, with deep, hands‑on knowledge of GCP regulations and guidelines.
Experience in quality leadership roles, including quality systems oversight, clinical portfolio governance, audit programs, global regulatory inspection management, and complex investigation and remediation activities.
Dynamic and adaptable leadership style, combining a strong sense of urgency with the flexibility to operate effectively in fast‑changing, complex environments.
Strategic, creative, and resourceful, with an entrepreneurial mindset and a willingness to be hands‑on to drive impact and results.
Strong interpersonal skills and executive presence, with the ability to influence, align, and lead stakeholders at all organizational levels.
Strong communication skills, with experience representing teams and organizations in diverse, global, and high‑stakes settings.
Decisive, proactive, and well‑organized, with the ability to prioritize effectively and manage competing demands.
Open‑minded and appropriately risk‑tolerant, demonstrating humility, resilience, and comfort with challenge and constructive debate.
Unwavering integrity and ethical standards, with a strong commitment to patient safety, scientific rigor, and regulatory compliance.
Takeda Compensation and Benefits Summary
We understand compensation is an important factor as you consider the next step in your career. We are committed to equitable pay for all employees, and we strive to be more transparent with our pay practices.
U.S. Base Salary Range:
$177,000.00 - $278,080.00
The estimated salary range reflects an anticipated range for this position. The actual base salary offered may depend on a variety of factors, including the qualifications of the individual applicant for the position, years of relevant experience, specific and unique skills, level of education attained, certifications or other professional licenses held, and the location in which the applicant lives and/or from which they will be performing the job. The actual base salary offered will be in accordance with state or local minimum wage requirements for the job location.
U.S. based employees may be eligible for short-term and/ or long-term incentives. U.S. based employees may be eligible to participate in medical, dental, vision insurance, a 401(k) plan and company match, short-term and long-term disability coverage, basic life insurance, a tuition reimbursement program, paid volunteer time off, company holidays, and well-being benefits, among others. U.S. based employees are also eligible to receive, per calendar year, up to 80 hours of sick time, and new hires are eligible to accrue up to 120 hours of paid vacation.
Takeda is proud in its commitment to creating a diverse workforce and providing equal employment opportunities to all employees and applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, gender expression, parental status, national origin, age, disability, citizenship status, genetic information or characteristics, marital status, status as a Vietnam era veteran, special disabled veteran, or other protected veteran in accordance with applicable federal, state and local laws, and any other characteristic protected by law.
Better Health, Brighter Future
We strive to transform lives. While the science we advance is constantly evolving, our core purpose is enduring. For more than two centuries, our values have guided us to do what’s right for patients and for society. We know that changing lives requires us to do things differently. We start by listening to and addressing what really matters to patients, the people who love them, and those in the healthcare system who provide care. And that’s what inspires us all to be bold, push boundaries and set new standards that open up greater opportunities. Read our community guidelines: https://takeda.info/communityguidelines
Offices: Tokyo, JP · 1 Takeda Parkway, Deerfield, Illinois 60015, US · 40 Landsdowne St, Cambridge, Massachusetts 02139, US · Avenida das Nações Unidas, 14.401, Torre Jequitibá - 10°, 11° e 12° andares, São Paulo, 04794-000, BR · 43 Old Oak Rd, Bellville, Western Cape 7550, ZA
Based on 895 listings with disclosed salaries, most healthcare jobs in Cambridge, MA pay between $65k–$258k per year. Individual offers vary with seniority, company size, and specialization.
There are currently 1,030 open healthcare positions in Cambridge, MA listed on Clera. New openings are added daily as companies post roles.
Companies currently hiring include Sanofi, Novartis, Anna Jaques Hospital, Takeda, Biogen, among others. Browse the listings above to see every active employer.
Yes — 419 of the 1030 open healthcare positions offer remote or hybrid work (47 remote, 372 hybrid).
Each listing links directly to the employer's application page. Apply early — fresh listings get the most recruiter attention in the first two weeks.
