The role includes advancing programs from target identification through preclinical development toward early clinical translation, ensuring decisions are guided by robust, decision-enabling data. The ...
The role includes advancing programs from target identification through preclinical development toward early clinical translation, ensuring decisions are guided by robust, decision-enabling data. The ...
Biologist
Cambridge, MA · On-site
$149 - $215/hr
Support the discovery and preclinical development of innovative cancer therapeutics using diverse modalities, including small‑molecule inhibitors, targeted degraders, and biologics. * Provide ...
New
Biologist
Cambridge, MA · On-site
$149 - $215/hr
Support the discovery and preclinical development of innovative cancer therapeutics using diverse modalities, including small‑molecule inhibitors, targeted degraders, and biologics. * Provide ...
New
This role will set and execute imaging strategy from preclinical through late clinical development, predominantly in oncology across solid tumors and hematologic malignancies and across therapy ...
This role will set and execute imaging strategy from preclinical through late clinical development, predominantly in oncology across solid tumors and hematologic malignancies and across therapy ...
This role will set and execute imaging strategy from preclinical through late clinical development, predominantly in oncology across solid tumors and hematologic malignancies and across therapy ...
This role will set and execute imaging strategy from preclinical through late clinical development, predominantly in oncology across solid tumors and hematologic malignancies and across therapy ...
Associate Director, Biomarker & Assay Development
Cambridge, MA · On-site
$165K - $185K/yr
Design, oversee, and interpret translational and preclinical studies, including studies evaluating ... Lead assay development, vendor selection, qualification, validation, transfer, and troubleshooting ...
Associate Director, Biomarker & Assay Development
Cambridge, MA · On-site
$165K - $185K/yr
Design, oversee, and interpret translational and preclinical studies, including studies evaluating ... Lead assay development, vendor selection, qualification, validation, transfer, and troubleshooting ...
Associate Director, Biomarker & Assay Development
Cambridge, MA · On-site
$180 - $230/hr
Design, oversee, and interpret translational and preclinical studies, including studies evaluating ... Lead assay development, vendor selection, qualification, validation, transfer, and troubleshooting ...
Associate Director, Biomarker & Assay Development
Cambridge, MA · On-site
$180 - $230/hr
Design, oversee, and interpret translational and preclinical studies, including studies evaluating ... Lead assay development, vendor selection, qualification, validation, transfer, and troubleshooting ...
Clinical Program Lead (CPL) - RLT Focus
Cambridge, MA · Hybrid
$248K - $461K/yr
Provides strategic medical guidance and leads the development of experimental oncology agents in the TCO portfolio, beginning with PE / DC (Portfolio Entry / Drug Candidate) of preclinical ...
Clinical Program Lead (CPL) - RLT Focus
Cambridge, MA · Hybrid
$248K - $461K/yr
Provides strategic medical guidance and leads the development of experimental oncology agents in the TCO portfolio, beginning with PE / DC (Portfolio Entry / Drug Candidate) of preclinical ...
Clinical Program Lead (CPL) - RLT Focus
Cambridge, MA · On-site
$248K - $461K/yr
Provides strategic medical guidance and leads the development of experimental oncology agents in the TCO portfolio, beginning with PE / DC (Portfolio Entry / Drug Candidate) of preclinical ...
Clinical Program Lead (CPL) - RLT Focus
Cambridge, MA · On-site
$248K - $461K/yr
Provides strategic medical guidance and leads the development of experimental oncology agents in the TCO portfolio, beginning with PE / DC (Portfolio Entry / Drug Candidate) of preclinical ...
Senior Preclinical Data Engineer
Boston, MA · On-site +1
$90K - $140K/yr
We are seeking a Senior Preclinical Data Engineer to support preclinical research and development activities across multiple global sites. This is a hands-on data role focused on managing ...
Senior Preclinical Data Engineer
Boston, MA · On-site +1
$90K - $140K/yr
We are seeking a Senior Preclinical Data Engineer to support preclinical research and development activities across multiple global sites. This is a hands-on data role focused on managing ...
Senior Director, Biologics Analytical Development and Quality Control
Boston, MA · On-site
$250 - $280/hr
Senior Director, Biologics Analytical Development and Quality Control About this position About Us ... The incumbent will collaborate with other functions to deliver quality products for preclinical ...
Senior Director, Biologics Analytical Development and Quality Control
Boston, MA · On-site
$250 - $280/hr
Senior Director, Biologics Analytical Development and Quality Control About this position About Us ... The incumbent will collaborate with other functions to deliver quality products for preclinical ...
Senior Director, Biologics Drug Substance Development and Manufacturing
Boston, MA · On-site
$250 - $280/hr
Senior Director, Biologics Drug Substance Development and Manufacturing Position Overview The ... The incumbent will collaborate with other functions to deliver quality products for preclinical ...
Senior Director, Biologics Drug Substance Development and Manufacturing
Boston, MA · On-site
$250 - $280/hr
Senior Director, Biologics Drug Substance Development and Manufacturing Position Overview The ... The incumbent will collaborate with other functions to deliver quality products for preclinical ...
Technical Associate I
Cambridge, MA · On-site
MECHANICAL ENGINEERING , Traverso Laboratory , to join a multidisciplinary team developing clinically relevant solutions to human disease; and support the preclinical development and in vivo ...
Technical Associate I
Cambridge, MA · On-site
MECHANICAL ENGINEERING , Traverso Laboratory , to join a multidisciplinary team developing clinically relevant solutions to human disease; and support the preclinical development and in vivo ...
Senior Director, Biologics Analytical Development and Quality Control
Boston, MA · On-site
$250K - $280K/yr
Position Overview The Senior Director, Biologics Analytical Development and Quality Control, will ... The incumbent will collaborate with other functions to deliver quality products for preclinical ...
Senior Director, Biologics Analytical Development and Quality Control
Boston, MA · On-site
$250K - $280K/yr
Position Overview The Senior Director, Biologics Analytical Development and Quality Control, will ... The incumbent will collaborate with other functions to deliver quality products for preclinical ...
Senior Director, Biologics Analytical Development and Quality Control
Boston, MA · On-site
$250 - $280/hr
Senior Director, Biologics Analytical Development and Quality Control Position Overview The Senior ... The incumbent will collaborate with other functions to deliver quality products for preclinical ...
Senior Director, Biologics Analytical Development and Quality Control
Boston, MA · On-site
$250 - $280/hr
Senior Director, Biologics Analytical Development and Quality Control Position Overview The Senior ... The incumbent will collaborate with other functions to deliver quality products for preclinical ...
$55K/yr
S. research facility in Lexington, Massachusetts supports clients across a range of preclinical pharmacology and drug development programs. Position Summary Medicilon USA is seeking a Research ...
$55K/yr
S. research facility in Lexington, Massachusetts supports clients across a range of preclinical pharmacology and drug development programs. Position Summary Medicilon USA is seeking a Research ...
Senior Director, Biologics Drug Substance Development and Manufacturing
Boston, MA · On-site
$250K - $280K/yr
Position Overview The Senior Director, Biologics Drug Substance Development and Manufacturing, will ... The incumbent will collaborate with other functions to deliver quality products for preclinical ...
Senior Director, Biologics Drug Substance Development and Manufacturing
Boston, MA · On-site
$250K - $280K/yr
Position Overview The Senior Director, Biologics Drug Substance Development and Manufacturing, will ... The incumbent will collaborate with other functions to deliver quality products for preclinical ...
Director, Clinical Development
Lexington, MA · On-site
$89K - $122K/yr
... preclinical programs utilizing our versatile RNA medicines platform. Driven by the calling to ... The Director, Clinical Development will collaborate closely with cross-functional partners ...
Director, Clinical Development
Lexington, MA · On-site
$89K - $122K/yr
... preclinical programs utilizing our versatile RNA medicines platform. Driven by the calling to ... The Director, Clinical Development will collaborate closely with cross-functional partners ...
Scientist - RNA Sciences & Preclinical Manufacturing
Cambridge, MA · On-site
$128K - $155K/yr
This role sits at the interface of RNA/DNA research, process development, and preclinical material production in support of in vivo studies, platform development, and technology maturation. The ...
Scientist - RNA Sciences & Preclinical Manufacturing
Cambridge, MA · On-site
$128K - $155K/yr
This role sits at the interface of RNA/DNA research, process development, and preclinical material production in support of in vivo studies, platform development, and technology maturation. The ...
Research Associate II
Lexington, MA · On-site
Individual will be responsible for the conception and implementation of enzymatic and cell based assays for the characterization of a small molecule therapeutic currently in preclinical development.
Research Associate II
Lexington, MA · On-site
Individual will be responsible for the conception and implementation of enzymatic and cell based assays for the characterization of a small molecule therapeutic currently in preclinical development.
Senior Director, Biologics Drug Substance Development and Manufacturing
Boston, MA · On-site
$250 - $280/hr
Senior Director, Biologics Drug Substance Development and Manufacturing About this position About ... The incumbent will collaborate with other functions to deliver quality products for preclinical ...
Senior Director, Biologics Drug Substance Development and Manufacturing
Boston, MA · On-site
$250 - $280/hr
Senior Director, Biologics Drug Substance Development and Manufacturing About this position About ... The incumbent will collaborate with other functions to deliver quality products for preclinical ...
Preclinical Development information
See Massachusetts salary details
$36K - $45.6K
7% of jobs
$45.6K - $55.1K
0% of jobs
$55.1K - $64.6K
3% of jobs
$64.6K - $74.2K
6% of jobs
$82.4K is the 25th percentile. Wages below this are outliers.
$74.2K - $83.7K
9% of jobs
The median wage is $92.6K / yr.
$83.7K - $93.2K
25% of jobs
$100.1K is the 75th percentile. Wages above this are outliers.
$93.2K - $102.8K
33% of jobs
$102.8K - $112.3K
2% of jobs
$112.3K - $121.8K
8% of jobs
$121.8K - $131.4K
3% of jobs
$131.4K - $140.9K
2% of jobs
$36K
$92.9K
$140.9K
How much do preclinical development jobs pay per year?
What is preclinical development?
A Preclinical Development job involves overseeing the research and testing of drug candidates before they enter clinical trials. Professionals in this role design and conduct studies to assess a drug’s safety, efficacy, and pharmacokinetics using laboratory and animal models. They collaborate with scientists, regulatory experts, and project managers to generate data required for regulatory approval. Their work helps identify potential risks and optimize drug formulations before human testing begins.
What are the typical responsibilities of someone working in preclinical development?
Professionals in Preclinical Development are responsible for designing, conducting, and analyzing laboratory and animal studies to evaluate the safety and efficacy of new drug candidates before clinical trials. They often collaborate closely with research scientists, regulatory teams, and project managers to ensure studies meet compliance standards and scientific objectives. Daily tasks may include developing protocols, interpreting data, preparing regulatory documentation, and troubleshooting experimental issues. This role offers opportunities to gain broad exposure to the drug discovery process and can lead to advancement into project leadership or regulatory affairs positions.
What are the key skills and qualifications needed to thrive in preclinical development, and why are they important?
To excel in Preclinical Development, you need a solid background in biology, pharmacology, or related life science fields, often supported by an advanced degree and experience with laboratory research. Familiarity with Good Laboratory Practice (GLP) regulations, data analysis software, and animal study management systems is expected. Strong attention to detail, effective problem-solving skills, and the ability to communicate complex findings clearly are valuable soft skills. These competencies are essential to ensure the successful and compliant progression of drug candidates toward clinical trials.
What are the most commonly searched types of Preclinical Development jobs in Massachusetts?
The most popular types of Preclinical Development jobs in Massachusetts are:
What are popular job titles related to Preclinical Development jobs in Massachusetts?
For Preclinical Development jobs in Massachusetts, the most frequently searched job titles are:
What job categories do people searching Preclinical Development jobs in Massachusetts look for?
The top searched job categories for Preclinical Development jobs in Massachusetts are:
- Director International Business Development
- Director Of Development Operations
- Adme Dmpk
- Vice President Bark Air
- Business Product Manager
- Director Preclinical Development
- Non Profit Business Development
- Vice President International Industrial Designer
- Vice President Global Business Development
- Vice President Preclinical Development

Full-time
Medical, Dental, Vision, Life, Retirement, PTO
Re-posted 24 days ago
Eli Lilly and Company rating
8.9
Based on 64 frontline employees who took The Breakroom Quiz
9th of 86 rated pharmaceutical
Job description
At Lilly, the work is demanding because patients are waiting. We unite caring with discovery to help make life better for people around the world, knowing that every decision, every detail, and every day matters. Headquartered in Indianapolis, Indiana, our over 50,000 employees around the globe take on complex challenges to discover and deliver life-changing medicines, strengthen how health is understood and managed, and support the communities we serve. This is hard, urgent, selfless work-but it's work worth doing. If you're driven by purpose and ready to bring your best to work that truly matters for patients, we invite you to join us.
Position: Senior Director - Osteoporosis, Women's Health
Location: Boston, MA or Indianapolis, IN
About Lilly
At Lilly, we unite caring with discovery to make life better for people worldwide. As a global healthcare leader headquartered in Indianapolis, Indiana, we are committed to advancing innovation in areas of high unmet medical need. With a proven track record in obesity research and a growing focus on women's health, we seek an experienced discovery leader to help build a portfolio of transformative therapies to improve outcomes for women everywhere and arrest age-related functional decline across genders. This role offers the opportunity to shape strategy, drive impactful drug discovery and development programs, and contribute to Lilly's mission of scientific excellence and patient-centered care.
Position Summary
The Director / Senior Director will serve as the scientific and strategic leader for osteoporosis preclinical discovery, responsible for defining, implementing, and continuously evolving Lilly's preclinical discovery strategy in osteoporosis. This leader will drive the integration of human biology, translational science, and preclinical models to establish a differentiated and execution-focused discovery framework. The role includes advancing programs from target identification through preclinical development toward early clinical translation, ensuring decisions are guided by robust, decision-enabling data.
The successful candidate will play a central role in shaping the osteoporosis pipeline, building critical capabilities, and establishing best-in-class approaches to target prioritization and validation within the Women's Health portfolio.
Key Responsibilities
Strategy Leadership
- Build and lead an innovative lab focused on novel approaches to identify and validate targets/pathways for osteoporosis. Bring novel, high potential targets into the pipeline for therapeutic approaches for the treatment of osteoporosis.
- Define and implement the preclinical discovery strategy for osteoporosis, including target discovery, validation and prioritization frameworks, experimental approaches, and decision criteria
- Drive portfolio prioritization, articulating differentiation, risk, and alignment with clinical and regulatory expectations
- Build and evolve preclinical and translational capabilities (internal and external) to support execution of the strategy
- Identify and shape external opportunities, including academic collaborations, CRO partnerships, and business development opportunities
- Ensure alignment of osteoporosis strategy with broader Women's Health and musculoskeletal portfolio objectives
Scientific & Project Leadership
- Lead osteoporosis discovery programs, driving target identification, validation, and progression of therapeutic candidates
- Design and implement end-to-end experimental strategies across in vitro, ex vivo, and in vivo systems
- Generate decision-enabling data to support program advancement and portfolio decisions
Translational Strategy
- Define and implement translational approaches linking mechanisms to clinical outcomes, including biomarker strategies and PK/PD relationships
- Ensure preclinical programs are designed to enable clear clinical differentiation, incorporating relevant endpoints such as bone density, bone strength, and microarchitecture
Cross-functional Leadership
- Serve as biology lead on cross-functional teams, partnering closely with colleagues across function
- Influence decision-making and problem-solving to accelerate program progression
External Engagement
- Lead and manage strategic collaborations with CROs and academic partners
- Maintain scientific leadership through publications, presentations, and external engagement in osteoporosis and skeletal biology
People Leadership
- Directly recruit and supervise scientists and provide mentoring, performance management and career development.
Basic Qualifications
- Ph.D. in a relevant subject area
- Minimum of 10 years of relevant experience in academia, industry or related field
Additional Preferences
- Deep expertise in osteoporosis and skeletal biology, including bone remodeling
- 10 years' experience after post doc training
- Demonstrated success in drug discovery, from target identification through preclinical development
- Proven track record of shaping discovery strategy and influencing portfolio decisions
- Strong experience with preclinical in vitro, ex vivo, and in vivo models for osteoporosis
- Experience building new capabilities, platforms, or external collaborations
- Strong cross-functional leadership and scientific communication skills
- Passion for advancing innovative therapies addressing unmet needs in women's health
Lilly is dedicated to helping individuals with disabilities to actively engage in the workforce, ensuring equal opportunities when vying for positions. If you require accommodation to submit a resume for a position at Lilly, please complete the accommodation request form (https://careers.lilly.com/us/en/workplace-accommodation) for further assistance. Please note this is for individuals to request an accommodation as part of the application process and any other correspondence will not receive a response.
Lilly is proud to be an EEO Employer and does not discriminate on the basis of age, race, color, religion, gender identity, sex, gender expression, sexual orientation, genetic information, ancestry, national origin, protected veteran status, disability, or any other legally protected status.
Our employee resource groups (ERGs) offer strong support networks for their members and are open to all employees. Our current groups include: Africa, Middle East, Central Asia (AMECA), Black Employees at Lilly (BE@Lilly), Chinese Culture Network (CCN), EnAble, Evolve, Lilly Indian Network (LIN), Organization of Latinx at Lilly (OLA), Pride (LGBTQ+ Allies), Veterans Leadership Network (VLN) and Women's Initiative for Leading at Lilly (WILL).
Actual compensation will depend on a candidate's education, experience, skills, and geographic location. The anticipated wage for this position is
$163,500 - $281,600Full-time equivalent employees also will be eligible for a company bonus (depending, in part, on company and individual performance). In addition, Lilly offers a comprehensive benefit program to eligible employees, including eligibility to participate in a company-sponsored 401(k); pension; vacation benefits; eligibility for medical, dental, vision and prescription drug benefits; flexible benefits (e.g., healthcare and/or dependent day care flexible spending accounts); life insurance and death benefits; certain time off and leave of absence benefits; and well-being benefits (e.g., employee assistance program, fitness benefits, and employee clubs and activities).Lilly reserves the right to amend, modify, or terminate its compensation and benefit programs in its sole discretion and Lilly's compensation practices and guidelines will apply regarding the details of any promotion or transfer of Lilly employees.
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About Eli Lilly
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Eli Lilly, based in Indianapolis, IN, US, is one of the pioneers in the pharmaceutical industry with a rich history dating back to 1876. This global pharmaceutical company focuses on discovering, developing, manufacturing and selling pharmaceutical products in approximately 120 countries. The company's product categories include endocrinology, oncology, cardiovascular, neuroscience, and immunology. Having invested over $9 billion in research and development in the past decade, Eli Lilly is also committed to creating high-quality medicines that meet real needs. As a recipient of several awards and recognitions, Eli Lilly is known for its focus on life-saving research and drug development. Their mission is to make medicines that help people live longer, healthier, and more active lives.
Industry
Pharmaceutical product wholesalers
Company size
10,000+ Employees
Headquarters location
Indianapolis, IN, US
Year founded
1876