Assoc Director, Medical Information - Oncology

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
 

Routine responsibilities may include the following:

• Develop and maintain a deep knowledge of product, disease state and competitor landscape for assigned therapeutic area

• Serve as the Medical Reviewer for promotional and medical materials by applying deep product, disease‑state, and therapeutic‑area expertise to ensure scientific accuracy, clinical relevance, and compliance, while providing solutions‑oriented guidance that supports strategic and timely content development

• Respond to unsolicited requests for medical and scientific information regarding Gilead products and documents in the request handling system  

• Research and collaborate with cross-functional colleagues to address complex requests.  

• Create, update, and participate in review, quality check and approval of MI response documents  

• Collaborate with affiliate MI and relevant internal partners who may include medical affairs, development, regulatory, global patient safety and operations, commercial, to manage global response topics and content 

• Prepare and approve data on file to support response documents and complex requests 

• Maintain document repository with routine review of approved documents for new data from regulatory updates, scientific conferences, up-to-date literature searches, proactive literature surveillance, or newly published materials 

• Understand the needs and preferences of internal and external partners and customers 

• Review and provide analysis of MI databases for trends, customer insights and data gaps to guide content development and prepare customer interaction reports to share with internal stakeholders 

• Participate and support MI booths at scientific congresses  

• Serve as liaison for department specific training for new staff members, cross-functional colleagues and vendors, as required 

• Contribute to departmental strategic initiatives by supporting key activities within the TA, including product launches, labeling updates, patient engagement etc. 

• Execute and drive global MI initiatives and actions in a timely way to advance the provision of MI to improve patient care 

• Identify, report and record adverse events and product complaints in a timely manner in accordance with SOP 

• Serve as department SME for one or more product(s) or TA 

• Build and cultivate relationships with appropriate functions                        

Basic Qualifications:

• 10+ Years with BS/BA
  OR

• 8+ Years with MS/MA or MBA

Preferred Qualifications:

• Excellent written, verbal and interpersonal communication skills, and the ability to work well in multidisciplinary teams, across geographies 

• Ability to create and clearly communicate scientific data for different audiences,  

• Knowledge of applicable regulatory and legal requirements for the provision of MI in the pharmaceutical environment 

• Ability to analyze and evaluate clinical, biomedical and scientific data 

• Demonstrates Gilead’s core values and Leadership Commitments 

• Has a strong attention to detail, excellent project management and problem-solving skills 

• Previous experience with problem-solving and project management preferred 

• PharmD, PhD or MD preferred

• Experience in MI preferred or comparable experience within a healthcare/clinical environment preferred

• Experience in the pharmaceutical industry or a MI vendor preferred 

• Experience in conducting medical/promotional reviews preferred

This role is Foster City CA based.

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: $195,670.00 - $253,220.00. 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 Applican