Waltham, Massachusetts, United States · Hybrid
$204k–$306k/yr
Job Title: Global Development Scientist, Director Waltham, MA / Boston, MA Introduction to role: Are you ready to steer global hematology trials that turn bold science into life-changing medicines? As Global Development …
Skills: Clinical Strategy Translation, Protocol Leadership, Trial Design, Data Integrity, Regulatory Submissions
Waltham, Massachusetts, United States · On-site
$246k–$369k/yr
At AstraZeneca, we are committed to advancing the science of oncology to deliver life-changing medicines to patients most in need. With a combination-focused pipeline that exploits the power of six scientific platforms (…
Skills: Drug Development, Hematology Oncology, Strategic Leadership, Project Management, Regulatory Submissions
Waltham, Massachusetts, United States · On-site
Position Purpose Partnering closely with global and regional Global Regulatory Affairs colleagues, as well as Global Operations stakeholders, to address regulatory strategy challenges and deliver innovative, timely regul…
Skills: Regulatory CMC Strategy, Global Regulatory Affairs, Digital Innovation, AI/ML Applications, Vendor Management
Waltham, Massachusetts, United States · On-site
$42/hr–$57/hr
Site: The General Hospital Corporation Mass General Brigham relies on a wide range of professionals, including doctors, nurses, business people, tech experts, researchers, and systems analysts to advance our mission. As …
Skills: Magnetic Resonance Imaging, Patient Positioning, Imaging Parameters, Quality Assurance Scans, IV Catheter Insertion
Waltham, Massachusetts, United States · Hybrid
$118k–$196k/yr
PURPOSE AND SCOPE: Leads epidemiologic data analysis in support of therapies and marketed products within the Fresenius Medical Care (FME) nephrology portfolio in the Renal Research Institute (RRI). Real world evidence (…
Skills: Epidemiologic Data Analysis, Real World Evidence, Observational Study Design, SAS Programming, Biostatistics
Waltham, Massachusetts, United States · Remote OK
$185k–$250k/yr
Director of Marketing – Retina Reports to: Head of Retina Business Department: Retina Marketing Location: Hybrid in Waltham, MA or 100% Remote with business travel requirements including frequent visits to Waltham office…
Skills: Pharmaceutical Marketing, Buy-and-Bill Mechanics, Retina Therapeutic Area, Brand Architecture, Omnichannel Tactics
Waltham, Massachusetts, United States · Hybrid
$160k–$185k/yr
The Associate Director, Market Access Analytics, is responsible for collaborating, partnering, and developing analytics to support LUMRYZ and the Rare Disease – Sleep Medicine Business Unit at Alkermes. This position wil…
Skills: Market Access Analytics, SQL Programming, Tableau, Excel, PowerPoint
Waltham, Massachusetts, United States · On-site
The Department of Developmental Services (DDS) is seeking a full-time or part-time Intake and Eligibility Psychologist to join our Metro Regional Office. This role will provide clinical assessment and evaluation at the r…
Skills: Clinical Assessment, Eligibility Determination, Psychological Testing, Motivational Interviewing, Trauma Informed Care
Waltham, Massachusetts, United States · On-site
The Department of Developmental Services (DDS) is seeking a full-time or part-time Intake and Eligibility Psychologist to join our Metro Regional Office. This role will provide clinical assessment and evaluation at the r…
Skills: Clinical Assessment, Psychological Evaluation, Eligibility Determination, Adaptive Functioning Assessment, Psychological Testing
Waltham, Massachusetts, United States · Hybrid
$227k–$284k/yr
Zenas is a clinical-stage global biopharmaceutical company committed to becoming a leader in the development and commercialization of transformative therapies for patients with autoimmune diseases. Our core business stra…
Skills: Biomarker Strategy, Assay Development, Translational Science, Clinical Development, Vendor Management
Waltham, Massachusetts, United States · On-site
$97k–$184k/yr
Company Description About AbbVie AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a r…
Skills: Conjugation Process Development, Tangential Flow Filtration, HPLC/UPLC, Organic Chemistry, Drug-Conjugate Chemistry
Waltham, Massachusetts, United States · On-site
$140k/yr
We're committed to bringing passion and customer focus to the business. Position Summary Trinity Life Sciences is seeking ambitious and intellectually curious individuals who are passionate about the life sciences to joi…
Skills: Commercial Strategy, Data Analysis, Project Management, Client Presentation, Mentorship
Waltham, Massachusetts, United States · On-site
$60k–$70k/yr
Work Schedule Standard (Mon-Fri) Environmental Conditions Adherence to all Good Manufacturing Practices (GMP) Safety Standards, Laboratory Setting, Office, Some degree of PPE (Personal Protective Equipment) required (saf…
Skills: Asset Management, Customer Service, CMMS, Microsoft Office, Inventory Management
Waltham, Massachusetts, United States · On-site
$115k–$160k/yr
We are looking for a Senior Staff Gear Train Engineer to develop the gearboxes and drivetrains inside our next-generation humanoid robots. This role spans the full gear lifecycle — concept design, analysis, and manufactu…
Skills: Gear System Design, CAD, GD&T, Gear Simulation, Planetary Gear Design
Waltham, Massachusetts, United States · Remote OK
$157k–$215k/yr
Job Description We are seeking a highly experienced Senior Clinical Risk Manager to lead the execution of our Risk-Based Quality Management (RBQM) strategy across a portfolio of complex clinical trials. In this role, you…
Skills: Risk-Based Quality Management, Clinical Operations, Risk Assessment Categorization Tools, Quality Risk Management Plans, Key Risk Indicators
Waltham, Massachusetts, United States · On-site
$210k–$230k/yr
Company Overview: Innoviva Specialty Therapeutics, Inc., a subsidiary of Innoviva, Inc., is a biopharmaceutical company focused on developing innovative solutions for patients and healthcare providers in the fields of Cr…
Skills: Strategic Sourcing, Procurement Operations, Supplier Management, Contract Negotiation, Spend Analytics
Waltham, Massachusetts, United States · Remote OK
$120k–$180k/yr
Work Schedule Standard (Mon-Fri) Environmental Conditions Office Job Description At Thermo Fisher Scientific, you’ll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringin…
Skills: Biostatistics, Pharmacovigilance, R, SAS, Observational Study Design
Waltham, Massachusetts, United States · On-site
$20/hr–$22/hr
Ophthalmic Consultants of Boston (OCB) was established in 1969 to offer patients the highest quality eye care and laser/surgical treatment. OCB is the premier eye care provider in the region with nineteen practice locati…
Skills: Visual acuity testing, Visual field testing, Lensometry, Auto refractometry, Refractometry
Framingham, Massachusetts, United States · Hybrid
$86k–$124k/yr
Job title: Data System Analyst Location: Framingham, MA About the job This position resides within the Operations group, which is part of the Global CMC Development organization and is responsible for supporting equipmen…
Skills: Data Management, Computer System Validation, GxP Compliance, Laboratory Automation, Enterprise Content Management
Waltham, Massachusetts, United States · On-site
$177k–$225k/yr
As a Spatial AI Research Scientist on the Atlas VLA Research team, you will build the perception and geometric reasoning systems that give Atlas a grounded 3D understanding of the world. Your work spans the full spectrum…
Skills: SLAM, 3D Reconstruction, State Estimation, C++, Python
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Lead the clinical and scientific strategy for global hematology trials, converting disease strategy into protocols and study documents. Oversee data integrity, regulatory submissions, and collaboration with cross-functional teams to move therapies from hypothesis to registration.
Requires a BS degree with a PhD, PharmD, or MD strongly preferred, and at least 5 years of drug development experience. Candidates should have technical knowledge of haemato-oncology and a strong understanding of FDA and GCP regulations.
Waltham, MA / Boston, MA
Introduction to role:
Are you ready to steer global hematology trials that turn bold science into life-changing medicines? As Global Development Scientist, Director, you will shape the clinical evidence that moves transformative therapies from hypothesis to registration and into the hands of physicians and patients who need them most.
You will join a global, cross-functional team pushing the boundaries of cancer research, leveraging multiple scientific platforms including immuno-oncology, tumor drivers and resistance, DNA damage response, antibody-drug conjugates, cell therapy and epigenetic approaches. Empowered to act on smart risks, you will translate strategy into decisive studies, accelerate promising assets across early and late development, and help define standards of care.
Can you see yourself leading pivotal protocols and turning complex data into clear, compelling conclusions for regulators and the medical community?
Clinical Strategy Translation: Convert disease strategy and target product profiles into study concepts, protocols and key study documents in partnership with the Clinical Project Team and Global Study Team.
Protocol Leadership and Governance: Provide the clinical and scientific leadership and integrity for protocols and clinical plans; own the final protocol and governance approvals, ensuring alignment with GCP, ICH and AstraZeneca quality standards.
Trial Design and Delivery: Provide clinical/scientific input into early and late phase trials, including studies involving immunotherapy and cell therapy; partner with Clinical Operations to plan, recruit and deliver at pace, ensuring high-quality execution.
Data Integrity and Interpretation: Lead clinical data review and medical data cleaning; synthesize efficacy and safety signals with the Global Development Medical Director; draw clear conclusions that inform go/no-go decisions and publications; deliver high-quality clinical study reports on time.
Regulatory Evidence and Submissions: Prepare and contribute clinical content for global submissions (e.g., NDA/BLA) and lifecycle documents including Investigator’s Brochure, DSUR, PSUR and regulatory responses to enable worldwide registration.
Stakeholder Collaboration: Build strong internal networks across clinical, operations and quality, and form effective relationships with regulatory bodies and external service providers to maintain momentum and resolve issues quickly.
Site and Investigator Engagement: Provide timely responses to investigational sites on ICF changes and protocol questions; plan and deliver effective investigator meetings and training to drive consistency and quality.
Cross-Program Leadership and Improvement: Lead or contribute to cross-asset or cross-tumor initiatives, evaluate new opportunities and externally sponsored research, and drive process improvements that raise performance across the portfolio.
Ethical and Compliance Leadership: Operate to the highest ethical standards in accordance with internal SOPs, local regulations and Good Clinical Practice.
BS required; PhD in a scientific field, PharmD or MD is strongly preferred
Minimum of 5 years of relevant experience
Industry or Academic experience in drug development required with experience in malignant haematology clinical trials strongly preferred
Sufficient technical knowledge (haemato-oncology background preferred) to be able to interact with confidence with internal and external partner
Possesses sound foundational knowledge of FDA and other major country regulations and detailed knowledge of Good Clinical Practice other regulations governing clinical research
Possesses general knowledge of 1) medical monitoring 2) Regulatory approval process in relevant countries; 3) pharmaceutical industry/R&D operations; 4) marketing and commercial fundamentals
Drug Development/Clinical Development Planning: Demonstrates a consistent track record to both independently complete, and lead peers in completion in components of sophisticated plans, related documents, appropriate methodologies, measures, analytical plans and evaluation tools
Ability to drive/contribute to protocol design, writing and implementation
Experience contributing to or leading clinical components of NDA/BLA submissions and interactions with regulatory authorities
Hands-on experience with immunotherapy, cell therapy and combination trial design in haematologic malignancies
Proven leadership of cross-functional initiatives and process improvement projects across assets or tumor areas
Track record of collaboration with external service providers and oversight of global studies across regions
Experience planning and delivering investigator meetings and training; strong communication that influences diverse stakeholders
More than 7–10 years of total clinical development experience is a plus
When we put unexpected teams in the same room, we unleash bold thinking with the power to inspire life-changing medicines. In-person working gives us the platform we need to connect, work at pace and challenge perceptions. That's why we work, on average, a minimum of three days per week from the office. But that doesn't mean we're not flexible. We balance the expectation of being in the office while respecting individual flexibility. Join us in our unique and ambitious world.
Why AstraZeneca:
Here, science and courage go hand-in-hand. You will work on one of the most dynamic pipelines in cancer, with access to unparalleled data, novel biomarkers, innovative endpoints and cutting-edge trial designs that span from early to late development. We bring unexpected teams together, empower people to speak up and make fast, evidence-led decisions, and value kindness alongside ambition. Your expertise will directly shape how new medicines are discovered, tested and delivered to patients worldwide, supported by a collaborative network of global experts and the resources to move quickly when the science is clear.
Ready to lead pivotal hematology development and turn bold science into decisive evidence for patients—send your CV to start a conversation about what you can achieve here.
The annual base pay (or hourly rate of compensation) for this position ranges from $203,709.60 -$305,564.40 USD Annual. Our positions offer eligibility for various incentives—an opportunity to receive short-term incentive bonuses, equity-based awards for salaried roles and commissions for sales roles. Benefits offered include qualified retirement programs, paid time off (i.e., vacation, holiday, and leaves), as well as health, dental, and vision coverage in accordance with the terms of the applicable plans.
Our mission is to build an inclusive environment where equal employment opportunities are available to all applicants and employees. In furtherance of that mission, we welcome and consider applications from all qualified candidates, regardless of their protected characteristics. If you have a disability or special need that requires accommodation, please complete the corresponding section in the application form.
We're transforming the future of healthcare by unlocking the power of what science can do for people, society and the planet. For more information, visit www.astrazeneca.com. Community Guidelines: bit.ly/2MgAcio
Offices: 1 Francis Crick Avenue, Cambridge Biomedical Campus, Cambridge, Cambridgeshire CB2 0AA, GB · Astraallen, Sodertalje, Stockholm County 152 57, SE
Based on 278 listings with disclosed salaries, most science & research jobs in Waltham, MA pay between $106k–$258k per year. Individual offers vary with seniority, company size, and specialization.
There are currently 313 open science & research positions in Waltham, MA listed on Clera. New openings are added daily as companies post roles.
Companies currently hiring include Allergan, Thermo Fisher Scientific, Dyne Therapeutics, Alkermes, mouhamedzz, among others. Browse the listings above to see every active employer.
Yes — 116 of the 313 open science & research positions offer remote or hybrid work (37 remote, 79 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.
