Gilead Sciences, Inc. Posted September 14, 2026

Assoc Director, Operations Oversight Lead Medical Affairs Research Global Operations (MARGO)

Foster City, United States Full time
Clinical Development Associate Director
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Gilead Sciences, Inc. is the source of truth for this posting and owns the application process. We surface normalized context and market comparison you won't find on the original listing.

About this opportunity

At Gilead, we’re creating a healthier world for all people. For more than 35 years, we’ve tackled diseases such as HIV, viral hepatitis, COVID-19 and cancer – working relentlessly to develop therapies that help improve lives and to ensure access to these therapies across the globe. We continue to fight against the world’s biggest health challenges, and our mission requires collaboration, determination and a relentless drive to make a difference.

Every member of Gilead’s team plays a critical role in the discovery and development of life-changing scientific innovations. Our employees are our greatest asset as we work to achieve our bold ambitions, and we’re looking for the next wave of passionate and ambitious people ready to make a direct impact.

We believe every employee deserves a great leader. People Leaders are the cornerstone to the employee experience at Gilead and Kite. As a people leader now or in the future, you are the key driver in evolving our culture and creating an environment where every employee feels included, developed and empowered to fulfil their aspirations. Join Gilead and help create possible, together.

Job Description

MARGO Background:

The MARGO function is part of the wider Medical Affairs Research (MAR) department within the Development organization and operationalises Non Interventional Studies scientifically led from MAR. MAR conducts observational research and generates analysis results to inform decisions throughout the product lifecycle across research, development, post-approval, and commercialization. Observational research is conducted on data collected from individuals assessed for biomedical, health and other outcomes, and includes observational studies and observational analyses. Source data for observational studies may be based on primary data

collection, secondary data use, or both. The study results, generated using a rigorous process, provide insights and evidence for internal (e.g., program, safety) and external (e.g., regulators, healthcare providers) stakeholders.

Position Summary:

This role provides end-to-end operational oversight of observational studies within the MAR portfolio across all therapeutic areas (TA). This position supports the MAR team in high-quality, compliant and timely study execution of the study portfolio through effective vendor oversight, risk management and issue resolution. This role reports to the Director, MAARGO and is the primary point of contact for study operations for vendors and service providers. While not responsible for day-to-day execution, the role is responsible for collaborating with MAR scientific leads, Quality, Clinical Operations, Regulatory Affairs, Medical Affairs and other stakeholders to ensure vendors and service providers meet agreed-upon timelines and are compliant with process requirements and relevant regulatory guidelines.

Key Responsibilities:

• Responsible for working with the MARGO Leadership Team to track, prioritize and manage the execution of observational studies across all TA portfolios

• Collaborate with MARGO Leadership Team on strategic sourcing options to optimize the execution of the TA portfolio

• Responsible for vendor performance management, issue management and escalation of risks impacting the portfolio

• Responsible for the vendor oversight plans, and performance and quality checks of study deliverables per the vendor oversight process

• Partner with vendor outsourcing to support initiation and execution of study vendor and service provider agreements

• Collaborate with MAR scientific leads to ensure alignment of study objectives and timelines across all stakeholders and vendors

• Own end-to-end oversight of study deliverables, ensuring timely, high-quality completion aligned to TA priorities, with proactive risk identification and mitigation

• Track study milestones, timelines, deliverables and financials; proactively identify and mitigate risks

• Collaborate with MAR scientific leads to monitor utilization and assignment of resources to deliver on priorities established by the MARGO Leadership Team

• Ensure onboarding of study vendors and service provider resources to support the study portfolio priorities established with the MARGO Leadership Team

• Monitor end-to-end processes to ensure compliance with process requirements, regulatory guidelines and study objectives

• Serve as an escalation point to resolve quality, scope and timeliness issues with operational stakeholders, including vendors and service providers

• Maintain regular communication with operational stakeholders, study vendors and service providers to ensure delivery against priorities and commitments

• Identify opportunities for process improvement, increased standardization and operational efficiency

• Collaborate with other oversight roles within MAR to drive consistency across study execution processes and implement best practices

• Liaison with Quality on periodic quality reviews and other quality related activities

• Escalate study specific issues to Quality for guidance and consultation

Basic Qualifications:

Bachelor's Degree and Ten Years' Experience

OR

Masters' Degree and Eight Years' Experience

OR

PhD and Two Years' Experience

Preferred Qualifications:

• 5+ years of experience in study operations or project management providing operational and financial oversight of observational studies

• Degree in Biology, Business, Operations Research or equivalent

• Hands-on training and experience in managing study lifecycles in GxP compliant environment

• Demonstrated experience in managing cross-functional study teams and vendor resources to balance priorities and timelines in a matrixed environment

• Proven ability to communicate the scope, requirements, expectations and standards for executing observational studies

• Proven track record of assessing vendor proposals e.g., timelines, deliverables and budget to meet study objectives

• Demonstrated vendor management experience to conduct primary data collection and secondary data use studies

• Demonstrated ability to collaborate cross-functionally with program, study and functional teams, and vendor resources

• Knowledge of global NIS regulatory landscape

• Experience in working with international entities to conduct observational studies

• Ability to work collaboratively with global cross-functional stakeholders

• Ability to communicate study requirements and results

• Strong problem-solving skills using data driven approaches

• Excellent written and verbal communication skills

People Leader Accountabilities :

Create Inclusion - knowing the business value of diverse teams, modeling inclusion, and embedding the value of diversity in the way they manage their teams.

Develop Talent - understand the skills, experience, aspirations and potential of their employees and coach them on current performance and future potential. They ensure employees are receiving the feedback and insight needed to grow, develop and realize their purpose.

Empower Teams - connect the team to the organization by aligning goals, purpose, and organizational objectives , and holding them to account. They provide the support needed to remove barriers and connect their team to the broader ecosystem.

The salary range for this position is:

Bay Area: $195,670.00 - $253,220.00.

Other US Locations: $177,905.00 - $230,230.00.

Gilead considers a variety of factors when determining base compensation, including experience, qualifications, and geographic location. These considerations mean actual compensation will vary. This position may also be eligible for a discretionary annual bonus, discretionary stock-based long-term incentives (eligibility may vary based on role), paid time off, and a benefits package. Benefits include company-sponsored medical, dental, vision, and life insurance plans*.

For additional benefits information, visit:

https://www.gilead.com/careers/compensation-benefits-and-wellbeing

* Eligible employees may participate in benefit plans, subject to the terms and conditions of the applicable plans.

For jobs in the United States:

Gilead Sciences Inc. is committed to providing equal employment opportunities to all employees and applicants for employment, and is dedicated to fostering an inclusive work environment comprised of diverse perspectives, backgrounds, and experiences. Employment decisions regarding recruitment and selection will be made without discrimination based on race, color, religion, national origin, sex , age, sexual orientation, physical or mental disability, genetic information or characteristic, gender identity and expression, veteran status, or other non-job related characteristics or other prohibited grounds specified in applicable federal, state and local laws. In order to ensure reasonable accommodation for individuals protected by Section 503 of the Rehabilitation Act of 1973, the Vietnam Era Veterans' Readjustment Act of 1974, and Title I of the Americans with Disabilities Act of 1990, applicants who require accommodation in the job application process may contact ApplicantAccommodations@gilead.com  for assistance.

For more information about equal employment opportunity protections, please view the  'Know Your Rights' poster.

NOTICE: EMPLOYEE POLYGRAPH PROTECTION ACT

YOUR RIGHTS UNDER THE FAMILY AND MEDICAL LEAVE ACT

Gilead Sciences will not discharge or in any other manner discriminate against employees or applicants because they have inquired about, discussed, or disclosed their own pay or the pay of another employee or applicant. However, employees who have access to the compensation information of other employees or applicants as a part of their essential job functions cannot disclose the pay of other employees or applicants to individuals who do not otherwise have access to compensation information, unless the disclosure is (a) in response to a formal complaint or charge, (b) in furtherance of an investigation, proceeding, hearing, or action, including an investigation conducted by the employer, (c) consistent with the  legal duty to furnish information; or (d) otherwise protected by law.

Our environment respects individual differences and recognizes each employee as an integral member of our company. Our workforce reflects these values and celebrates the individuals who make up our growing team.

Gilead provides a work environment free of harassment and prohibited conduct. We promote and support individual differences and diversity of thoughts and opinion.

For Current Gilead Employees and Contractors:

Please apply via the Internal Career Opportunities portal in Workday.

Job details

Seniority
Associate Director
Function
Clinical Development
Therapeutic area
Not listed
Location
Foster City, United States
Employment type
Full time

How this role compares

Computed from every other active Clinical Development role in our database, not just this employer's listings.

We currently track 384 comparable Associate Director Clinical Development roles across 80 biopharma companies.

384Comparable roles tracked
369Currently active
80Companies hiring similar roles
27Countries represented

Salary context

103 of 384 peers report a salary range (USD, annualized)

Peers share this role's job function and a matching or adjacent seniority level -- not necessarily the same therapeutic area or country.

This roleSubject $195,670/yr – $253,220/yr
Lowest disclosed · Sr. Research Associate, Clinical Biomarker Laboratory · ModernaTX, Inc. $74,000/yr – $118,400/yr
Highest disclosed · Sr Statistical Advisor · Gilead Sciences, Inc. $261,375/yr – $338,250/yr
Peer group range $96,200 – $299,813 (median $175,600)

Where these roles are based

Top locations among the 384 comparable roles

United States163
India81
United Kingdom20
Poland20
Japan12
China12

+ 21 more countries

Seniority mix

384 of 384 peers have a known seniority level

Manager171
Associate Director113
Senior100

Therapeutic area mix

43 of 384 peers have a known therapeutic area; the rest are genuinely unlabeled, not hidden

Oncology19
Immunology11
Neuroscience8
Rare Disease1
Cardiovascular / CVRM1
Respiratory1
Ophthalmology1
Dermatology & Aesthetics1

Similar opportunities

The closest matches from our peer group, ranked by how similar they are, not how well you'd qualify for them -- treat this as market context, not a guaranteed shortlist; a weak match is labeled as one below.

60%similar
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Regeneron Pharmaceuticals, Inc (USA) Tarrytown, United States Associate Director
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Gilead Sciences, Inc. Foster City, United States Associate Director
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Notify me about similar jobs

Get an email when we spot other openings like this one – same job function, comparable seniority, roles you'd actually want to see.

How we calculate "similar"

No black box, no LLM guesswork: a deterministic score built from four normalized attributes. Here's this role's own peer group at different match levels, so you can see the mechanism, not just the result.

Every comparison starts from the same 100-point budget: 25 for working in the same function, 40 for the same therapeutic area, 20 for the same or adjacent seniority, 15 for the same country. A dimension we can't confirm on both sides contributes nothing, never a guess, never a free pass.

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Unmatched or unknown dimensions score exactly the same: 0 points, never a partial guess. A role we know almost nothing about beyond its function bottoms out at 25%; it never inflates to 100% just because there's little to compare against. Seniority uses a defined ladder (Associate → Manager → Associate Director → Senior → Principal → Director → Senior Director → Executive/VP) so "Director" and "Senior Director" count as adjacent, but "Director" and "Executive/VP" do not.