Manager, Regulatory Submission Management

At Gilead were creating a healthier world for all people. For more than 35 years weve 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 worlds biggest health challenges and our mission requires collaboration determination and a relentless drive to make a difference.

Every member of Gileads 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 were 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

Regulatory Submission Management acts as a partner for strategic planning and execution of the portfolio to ensure global Regulatory submissions are scalable seamless and optimized. We are a trusted companion across Regulatory Affairs bridging strategy and execution while building knowledge across the portfolio to bring therapies to patients faster together.

You will execute a wide range of regulatory submissions independently including submissions of high complexity contribute to global submission content plans and lead review and planning processes for multiple products or projects. You will represent Regulatory Submission Management (RSM) on relevant product project and/or regulatory submissions teams providing specialist guidance on regulatory submissions requirements and timing. You may also represent RSM on other cross-functional initiatives. You will plan and have oversight for assigned deliverables and may serve as the RSM lead for small to medium regulatory submissions. You will participate in identifying/developing process improvements new standards and updating systems in support of submissions. You may coach train and provide guidance to less experienced RSM colleagues.

Essential Duties and Job Functions:

• Manages a wide variety of global submissions such as clinical study reports (CSRs) investigators brochures DSURs regulatory responses original INDs and amendments.
• May represent RSM in cross-functional teams such as product project and/or regulatory submissions teams; providing guidance for optimal strategies to achieve speed-to-filing or meet technical health authority requirements; may act as a technical and operational lead for submission execution.
• Plans and oversees assigned submissions with responsibilities including development and management of global and regional content plans and resource planning for assigned submissions.
• Acts as a Subject Matter Expert for various expertise related to RSM Core Capabilities
• Supports regulatory maintenance activities for early development and late-stage products.
• Supports the planning and preparation activities of regulatory deliverables with direction from an RA Liaison and/or GRAD Affiliate
• May serve as the RSM lead for small to medium regulatory submissions.
• May serve as lead submission manager and department representative across development programs.
• Organizes preparation of high-quality documents for internal stakeholders. Author documents and/or procedures for submissions such as cover letters forms and other documents as assigned.
• Participates in development/improvement of submission standards submission templates and validation decision trees.
• May also participate in other special projects and/or represent RSM in other cross-functional initiatives.
• Where applicable oversees the work of external contractors supporting deliverables and other activities.
• Act as the primary interface with the publishing team to plan and negotiate publishing timelines and deliverables.
• May coach train and provide guidance to less experienced Submission Management colleagues.
• Ensures own work complies with established practices policies and processes and any regulatory or other requirements.
  

Basic Qualifications:

6 Years with BS/BA
OR
4 Years with MS/MA

Preferred Qualifications:

• BA/ BS with 6 relevant submission management regulatory project management or regulatory operations experience in the biopharma industry or 4 years relevant experience with MA/MS/MBA or 0 years relevant experience with PharmD/PhD.
• Significant experience in the biopharma industry is strongly preferred.
• Experience managing a broad range of submission types across multiple stages of drug development.
• Experience working with one or more Gilead TAs and varying stages of drug development is strongly preferred.
• Demonstrated ability to be a fast learner.
• Demonstrated ability to be flexible and adaptable to change to move between projects easily and provide support/expertise where needed.
• Recognized as a SME in a broad range of regulatory submission types and a resource for technical advice and guidance.
• Able to advise cross-functional partners on technical health authority requirements and RSM processes to meet business goals and objectives.
• In-depth knowledge of relevant health authorities including system processes and regulatory requirements.
• In-depth knowledge of regulatory document requirements and guidelines relevant to assigned products projects and markets as evidenced by effectiveness and successes with technically compliant and rapid filings.
• Able to advise cross-functional partners on technical health authority requirements and processes to meet business goals and objectives.
• Demonstrates strong analytical thinking skills attention-to-detail strong communication and writing skills project management skills and proficiencies with Microsoft Office suite Smartsheet and Sharepoint as evidenced through accomplishments in past roles.
• Ability to lead and influence submissions projects and/or initiatives.
• Strong interpersonal skills and understanding of team dynamics.
• Proven ability to work successfully in a team-oriented highly matrixed environment.
• When needed ability to travel.

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:

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:

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

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 disabilitygenetic 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 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 for assistance.

For more information about equal employment opportunity protections please view theKnow Your Rights poster.

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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.

Please apply via the Internal Career Opportunities portal in Workday.