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Director/Associate Director, BioPharma Portfolio & Program Management

Natera

LocationUnited States
SeniorityDirector / Associate Director
CompanyNatera
Verified recentlyChecked today
Compensation

$185k-$231k

Salary details are shown when available from the source listing. Sign in before applying so the role can be reviewed against your resume, salary goals, seniority, timezone, and location eligibility.

Requirements and working style

Decision details from the source listing

Experience

10+ years stated

Education

Advanced degree (PhD, PharmD, or MS) in a life sciences field

Schedule

unspecified

Benefits stated
Annual performance incentive bonusLong-term equity awardsMedical, dental, and vision benefits401(k) with company matchPaid time off and company holidaysWellness and work-life benefits

These fields are normalized from the employer's text. Confirm details on the employer site before applying.

WFH.team analysis

What this posting tells you

Natera seeks a Director/Associate Director to build and manage the operational backbone of its Pharma Discovery Lab, overseeing cross-functional portfolio execution, budgets, resourcing, governance, and pharma-partner engagements. The role is remote in the United States and lists a base pay range of $184,600–$230,700. Requires 10+ years of relevant experience and an advanced life-sciences degree.

Role lane

Data, DevOps, Finance and investments, Healthcare admin, HR and recruiting, Legal, Operations, Product, QA and testing, Software, Customer support

Where you can work

United States

Working hours

Timezone overlap is not stated.

Arrangement

Director / Associate Director · Contract

Required signals
Portfolio and program managementCross-functional program leadershipGovernance and portfolio trackingStakeholder managementBiomarker sample operations or biorepository workflowsBudget forecasting and resource planningDeal or contract structuring supportExecutive communication and meeting facilitation
Preferred signals
Biopharma translational medicine or biomarker portfolio experienceLiquid biopsy/MRD, CGP, spatial transcriptomics, single-cell, or digital pathology familiarityBiomarker strategy for regulatory submissions or clinical trialsMBA or equivalent business training
Confirm before applying
  • Required timezone overlap is not stated
Market context

Data hiring on WFH.team

8,216active related roles
3,372new in the latest period
320.3jobs per 100 candidates
$179kmedian of comparable listed ranges

This role's listed pay is above the median among 200 comparable roles shown here. Category counts come from WFH.team's latest published remote job market snapshot.

Explore the remote job market
Skills and signals
Portfolio and program managementCross-functional program leadershipGovernance and portfolio trackingStakeholder managementBiomarker sample operations or biorepository workflowsBudget forecasting and resource planningDeal or contract structuring supportExecutive communication and meeting facilitationBiopharma translational medicine or biomarker portfolio experienceLiquid biopsy/MRD, CGP, spatial transcriptomics, single-cell, or digital pathology familiarityBiomarker strategy for regulatory submissions or clinical trialsMBA or equivalent business trainingRemote (US)
Job description

Director/Associate Director, BioPharma Portfolio & Program Management at Natera

Summary

Natera’s Pharma Discovery Lab (PDL) bridges R&D execution, analytics, and target and biomarker discovery and development. We are seeking an Director/Associate Director of Portfolio & Program Management to build and run the operational backbone of PDL. The successful candidate will manage a broad portfolio of internal and external projects from inception to execution — managing portfolio metrics, tracking budgets, stage-gating project milestones, coordinating wet lab / dry lab / bioinformatics, RWD analytics resourcing, and managing pharma-partner engagements (biomarker consultation, translational research contracts, and target discovery/co-development projects) from intake through delivery. The role sits at the intersection of science, business, and operations, and reports into PDL leadership.

Key Responsibilities

Internal Project Management - Cross-Functional & Operational Coordination

-Work closely with lab and IT operations to build out PDL on time and on budget

-Serve as the operational lead for internal cross-functional projects across PDL and the BioPharma BU

-Track deliverables, timelines, and resourcing for PDL pharma contracts and flag risks to scope, budget, or timeline early

-Work with R&D and Commercial project management operations to ensure line of sight for PDL projects and ensure transparency between the organizations

-Coordinate shared infrastructure and CapEx planning between the pharma-facing PDL and the internal R& Lab to maximize ROI on shared equipment and space.

-Coordinate across wet lab (DNA/RNA/digital pathology, biorepository, spatial transcriptomics, single-cell RNA,advanced microscopy), dry lab/bioinformatics, and BD/pharma partnerships teams to keep PDL commitments on track.

-Support resourcing and hiring plans to close identified capability gaps in partnership with lab and discovery leadership.

-Facilitate recurring working groups, client status meetings, and internal review forums; author agendas, minutes, and action-item tracking.

Business & Financial Operations

-Support go-to-market and monetization structuring for PDL offerings in partnership with BD and finance.

-Maintain program-level budget visibility, resource forecasts, and spend tracking against the approved investment case.

Communications & Stakeholder Management

-Act as a trusted cross-functional partner to scientific, laboratory, BD, and commercial stakeholders, translating

scientific priorities into operational plans.

-Prepare client-facing materials, KOL engagement support, and scientific narratives supporting regulatory and

commercial adoption of PDL-enabled diagnostics.

-Manage change and communication strategies as PDL scales, including team structure, roles, and process updates as the portfolio grows.

Qualifications

-10+ years of experience in oncology drug development, translational research, or biomarker/CDx program

management, ideally spanning both pharma and diagnostics/lab-services environments.

-Demonstrated track record leading complex, cross-functional programs — governance operations, portfolio/program

tracking, and stakeholder management at the senior leadership level.

-Experience managing biomarker sample operations, biorepository/biobank workflows, or CDx-adjacent laboratory

operations.

  • Financial acumen, including budget forecasting, resource planning, and experience supporting deal or contract

structuring (fee-for-service, milestone, royalty, or licensing models).

  • Strong meeting facilitation, executive communication, and document-authoring skills; comfortable presenting to

senior leadership and external pharma partners.

  • Ability to navigate ambiguity in a newly-formed business line and build process/governance from the ground up.
  • Advanced degree (PhD, PharmD, or MS) in a life sciences required; MBA or equivalent business training a plus.

Preferred Experience

-Prior experience in a biopharma translational medicine, biomarker portfolio, or clinical operations role at a large

pharma or biotech (e.g., governance, franchise-level portfolio management, or business/program management

supporting a $M+ budget).

-Familiarity with liquid biopsy/MRD (e.g., Signatera-type assays), CGP (WES/WTS/WGS), spatial transcriptomics,

single-cell, or digital pathology platforms.

-Experience supporting biomarker strategy for regulatory submissions (IND/IDE, companion diagnostics) or Phase 1–3 clinical trial biomarker operations.

The pay range is listed and actual compensation packages are based on a wide array of factors unique to each candidate, including but not limited to skill set, years & depth of experience, certifications and specific office location. This may differ in other locations due to cost of labor considerations.

Remote USA

$184,600 — $230,700 USD

Compensation & Total Rewards

This range reflects a good-faith estimate of the base pay we reasonably expect to offer at the time of hire. Final compensation will vary based on experience, qualifications, and internal equity considerations.

This position is also eligible for additional compensation and benefits through Natera’s robust Total Rewards program, including:

  • Annual performance incentive bonus
  • Long-term equity awards
  • Comprehensive health benefits (medical, dental, vision)
  • 401(k) with company match
  • Generous paid time off and company holidays
  • Additional wellness and work-life benefits

Compensation Range

$184,600 — $230,700 USD

OUR OPPORTUNITY

Natera™ is a global leader in cell-free DNA (cfDNA) testing, dedicated to oncology, women’s health, and organ health. Our aim is to make personalized genetic testing and diagnostics part of the standard of care to protect health and enable earlier and more targeted interventions that lead to longer, healthier lives.

The Natera team consists of highly dedicated statisticians, geneticists, doctors, laboratory scientists, business professionals, software engineers and many other professionals from world-class institutions, who care deeply for our work and each other. When you join Natera, you’ll work hard and grow quickly. Working alongside the elite of the industry, you’ll be stretched and challenged, and take pride in being part of a company that is changing the landscape of genetic disease management.

WHAT WE OFFER

Competitive Benefits - Employee benefits include comprehensive medical, dental, vision, life and disability plans for eligible employees and their dependents. Additionally, Natera employees and their immediate families receive free testing in addition to fertility care benefits. Other benefits include pregnancy and baby bonding leave, 401k benefits, commuter benefits and much more. We also offer a generous employee referral program!

For more information, visit www.natera.com .

Natera is proud to be an Equal Opportunity Employer. We are committed to ensuring a diverse and inclusive workplace environment, and welcome people of different backgrounds, experiences, abilities and perspectives. Inclusive collaboration benefits our employees, our community and our patients, and is critical to our mission of changing the management of disease worldwide.

All qualified applicants are encouraged to apply, and will be considered without regard to race, color, religion, gender, gender identity or expression, sexual orientation, national origin, genetics, age, veteran status, disability or any other legally protected status. We also consider qualified applicants regardless of criminal histories, consistent with applicable laws.

If you are based in California, we encourage you to read this important information for California residents.

Link: https://www.natera.com/notice-of-data-collection-california-residents/

Please be advised that Natera will reach out to candidates with a @ natera.com email domain ONLY. Email communications from all other domain names are not from Natera or its employees and are fraudulent. Natera does not request interviews via text messages and does not ask for personal information until a candidate has engaged with the company and has spoken to a recruiter and the hiring team. Natera takes cyber crimes seriously, and will collaborate with law enforcement authorities to prosecute any related cyber crimes.

For more information

  • BBB announcement on job scams
  • FBI Cyber Crime resource page
Company context

Working remotely at Natera

Natera is a global leader in cell-free DNA (cfDNA) testing, specializing in reproductive health, oncology, and organ transplantation.

Headquarters
France, United Kingdom, Italy, United States, and Germany
Team size
1001-5000
Founded
2004
Remote policy

Remote hiring signal is inferred from active confirmed-remote job listings.

Application process

Review current openings on Natera's official careers page before applying.

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