Director, Program Leader, Preclinical Development

Moderna; Cambridge (MA); On-site; USD 150,000 - 200,000; Full time

Job summary

Moderna seeks a Director for the Preclinical Program Lead role in Cambridge, focused on leading cross-functional teams and driving preclinical studies. The successful candidate will define strategies for drug candidates, ensuring their evaluation to support IND submission, contributing to the advancement of Moderna's mRNA technology.

Benefits

Best-in-class healthcare coverage

Holistic approach to well-being

Generous paid time off

Lifestyle Spending Accounts

Family planning and adoption benefits

Savings and investment opportunities

Qualifications

• 12 years of experience in drug discovery with a B.S/M.S or 9+ years with a Ph.D.
• Experience in gene editing and autoimmune diseases.
• Familiarity with disease biomarkers and IND filing.

Responsibilities

• Manage multiple preclinical projects and guide cross-functional teams.
• Lead preclinical studies to support IND submission.
• Communicate project updates and support scientific engagement with external collaborations.

Skills

Project Leadership

Communication

Strategic Thinking

Decision-Making

Problem-Solving

Education

B.S/M.S in Genetics, Biochemistry, Molecular Biology or related field

Ph.D. in a relevant field

Job description

The Role:

We seek a talented, experienced and motivated Director for the Preclinical Program Lead role supporting the Rare Disease and Immune Therapeutic Research therapeutic areas. The Preclinical Program Lead will be responsible for defining the overall strategy for the development of the preclinical program, aligning with the company’s business objectives, to support the advancement of Moderna’s mRNA technology platform and pipeline. The successful candidate will lead a cross-functional team and will be responsible for setting the strategic direction for preclinical studies, ensuring that a drug candidate is comprehensively evaluated for safety and efficacy to support IND submission and enable clinical evaluation. The Preclinical Program Lead will report progress and findings to senior management, scientific advisory boards, and cross-functional teams, providing updates on the project status, risks, and go/no-go decisions. Experience in gene editing is required, additional experience in Immunology would be a plus.

Applicants should be outstanding team members and have extensive experience in project leadership. The ability to effectively communicate across internal multi-disciplinary teams and with external partners is required. The candidate will need to manage multiple projects in a fast-moving and results-oriented environment. Experience in IND filing is required as the candidate will facilitate programs moving into Development.

Here's What You’ll Do:

• Manage multiple projects of moderate to large size and scope involving cross-functional collaboration within Research and across departments. Provide scientific expertise, guidance and strategy to successfully drive programs through Go/No Go decisions.

• Lead a cross-functional team to develop, optimize, validate and execute preclinical studies to support IND submission

• Support programs through IND filing collaborating with multiple functions within Moderna, working closely with clinical development teams to ensure a smooth transition and transfer of program data and leadership to enable Phase I clinical trials.

• Author and review regulatory documents

• Communicate effectively to discuss project progress, interpret and present data internally and externally.

• Provide expert level guidance in designing and implementing cell biology, biochemistry and biomarker related studies for rare and/or autoimmune diseases.

• Ability to manage and supervise team members to meet project timelines

• Support scientific engagement with external collaborations. Act as a scientific resource providing guidance and mentorship to colleagues.

Here’s What You’ll Bring to the Table:

• A B.S/M.S degree in Genetics, Biochemistry, Molecular Biology, Cell Biology, Immunology, or related field with 12 years of overall experience in drug discovery and development or a Ph.D. with 9+ years of experience specifically in drug discovery in pharmaceutical, biotech or CRO

• Solid background and training in Gene Editing and/or Immunology

• Experience in autoimmune diseases

• Managerial capabilities such as strategic thinking, decision-making, problem-solving, communication, and delegation, good knowledge and experience in Gene Editing research and biologics, and track record of making contributions to advance therapeutics from concept to proof-of concept in-vivo into a clinical candidate

• Familiarity with disease biomarkers

• Experience in drug discovery or translational research in a biotech setting

• Experience in IND filing required

• This role is based in our new LEED-certified HQ in Cambridge, MA and is expected to be in office 70% of the time with flexibility to work from home up to 30%.

At Moderna, we believe that when you feel your best, you can do your best work. That’s why our US benefits and global well-being resources are designed to support you—at work, at home, and everywhere in between.

• Best-in-class healthcare coverage, plus a suite of voluntary benefit programs to support your unique needs
• A holistic approach to well-being, with access to fitness, mindfulness, and mental health support
• Lifestyle Spending Accounts to personalize your well-being journey
• Family planning and adoption benefits
• Generous paid time off, including vacation, volunteer days, sabbatical, global recharge days, and a discretionary year-end shutdown
• Savings and investment opportunities
• Location-specific perks and extras

About Moderna

Since our founding in 2010, we have aspired to build the leading mRNA technology platform, the infrastructure to reimagine how medicines are created and delivered, and a world-class team. We believe in giving our people a platform to change medicine and an opportunity to change the world.

By living our mission, values, and mindsets every day, our people are the driving force behind our scientific progress and our culture. Together, we are creating a culture of belonging and building an organization that cares deeply for our patients, our employees, the environment, and our communities.

We are proud to have been recognized as a Science Magazine Top Biopharma Employer, a Fast Company Best Workplace for Innovators, and a Great Place to Work in the U.S.

If you want to make a difference and join a team that is changing the future of medicine, we invite you to visit modernatx.com/careers to learn more about our current opportunities.

Our Working Model

As we build our company, we have always believed an in-person culture is critical to our success. Moderna champions the significant benefits of in-office collaboration by embracing a 70/30 work model. This 70% in-office structure helps to foster a culture rich in innovation, teamwork, and direct mentorship. Join us in shaping a world where every interaction is an opportunity to learn, contribute, and make a meaningful impact.

Moderna is a smoke-free, alcohol-free, and drug-free work environment.

Equal Opportunities

Moderna is committed to equal employment opportunity and non-discrimination for all employees and qualified applicants without regard to a person's race, color, sex, gender identity or expression, age, religion, national origin, ancestry or citizenship, ethnicity, disability, military or protected veteran status, genetic information, sexual orientation, marital or familial status, or any other personal characteristic protected under applicable law.Moderna is a place where everyone can grow. If you meet the Basic Qualifications for the role and you would be excited to contribute to our mission every day, please apply!

Moderna is an E-Verify Employer in the United States. We consider qualified applicants regardless of criminal histories, consistent with legal requirements.

Accommodations

We’re focused on attracting, retaining, developing, and advancing our employees. By cultivating a workplace that values diverse experiences, backgrounds, and ideas, we create an environment where every employee can contribute their best.

Moderna is committed to offering reasonable accommodations to qualified job applicants with disabilities. Any applicant requiring an accommodation in connection with the hiring process and/or to perform the essential functions of the position for which the applicant has applied should contact the Accommodations team at [e-mail] .

Export Control Notice

This position may involve access to technology or data that is subject to U.S. export control laws, including the Export Administration Regulations (EAR). As such, employment is contingent upon the applicant’s ability to access export-controlled information in accordance with U.S. law. Due to the nature of the work and regulatory requirements, only individuals who qualify as U.S. persons (citizens, permanent residents, asylees, or refugees) are eligible for this position. For this role Moderna is unable to sponsor non-U.S. persons to apply for an export control license.

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