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Director, Head of Program Management

Tessera Therapeutics - Somerville, Massachusetts, United States

Posted Jun 1, 2026

Benefits

Parental leave
Not verified
Non-birth-parent leave
Not verified
Family-building benefits
  • Fertility benefits: Not verified
  • Adoption assistance: Not verified
  • Surrogacy assistance: Not verified
Mental health support
Not verified
Relocation assistance
Not verified
Childcare support
Not verified
Learning budget
Offered From the posting source checked Jun 20, 2026
Verification
Not verified checked Jun 7, 2026
Salary
$186K-$239K From the posting source checked Jun 20, 2026
401(k) match
Reported from DOL Form 5500 industry filing (not employer-specific)

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Market context

U.S. role benchmark (BLS OEWS)
$61,842 U.S. median for this role
Projected growth (BLS Employment Projections)
+1.9% - Slower

244% above the BLS role benchmark for operations aggregate.

Posted salary is far from this role benchmark; treat it as low confidence.

Matched to SOC 11-1021 - Operations aggregate by role bucket.

Source: U.S. Bureau of Labor Statistics, OEWS, May 2024 and Employment Projections, 2024-2034.

Role

Role function
Operations From the posting source checked Jun 20, 2026
Seniority
Director Plus From the posting source checked Jun 20, 2026

Schedule

Shift type
Not verified
Weekend work
Not verified

Company

Company stage
Public-company From the posting source checked Jun 20, 2026
Equity
Offered From the posting source checked Jun 20, 2026

Application

Cover letter
Not verified
Assessment
Not verified
Deadline
Not stated

Where they hire

State eligibility is not yet verified.

About this role

Director, Head of Program Management Somerville, Massachusetts, United States Your experience includes… - Bachelor's in life sciences, engineering, business, or a related field with 15 years related experience or Masters with 13 years related experience or PhD with 10 years of related experience - Significant experience in program management, program operations, or cross-functional development teams in a dynamic biotech or pharmaceutical environment - Strong understanding of drug development from research through preclinical development, IND-enabling activities, regulatory submissions, and clinical development. It's a bonus if you have commercial experience. - Demonstrated ability to bridge science and business interests - Excellent written and verbal communication skills - Being well-versed in program management principles, practices, and tools (including Office Timeline, Think-Cell, and Smartsheet/Microsoft Project) - Thriving in a dynamic and rigorous work environment, coaching and mentoring - It's a bonus if you have your Project Management Professional (PMP®) certification or experience in genetic medicines You are interested in… - Building and leading a fit-for-purpose Program Management function that enables strong execution, transparent communication, and effective decision-making across the organization - Guiding and empowering Program Managers to drive the development and management of integrated program plans (including timelines, assumptions, scenarios, risks, critical path, decision maps, goals, and budget drivers) - Establishing and continuously improving program management capabilities, tools, and practices - Partnering with Finance and Corporate Development to prepare for Portfolio Reviews - Facilitating and contributing to the Programs/Portfolio goal setting & tracking, in line with enterprise goals - Systematically monitoring program risks and

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