Associate Director, Medical Information
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Associate Director, Medical Information United States - California - Foster City Medical Affairs Regular Job Description 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
Job Overview
Responds to unsolicited medical requests regarding Gilead products from HCPs, members of the public, and internal Gilead colleagues. Responses are provided in a timely manner using approved scientific response documents, up-to-date literature support , and other resources
Uses scientific and MI expertise to drive strategic initiatives and empower Gilead partners, HCPs, and patients to enable timely , informed decisions and improved patient outcomes
P erform s appropriate medical review for promotional and/or medical materials
Prepares global scientific resources in collaboration with local affiliate teams
Identifies , reports and records adverse events and product complaints in a timely manner in accordance with SOP.
Contributes to development of G MI strategy and represents G MI cross - functionally
Responsibilities
Routine responsibilities may include the following :
D evelop and maintain a deep knowledge of product, disease state and competitor landscape for assigned therapeutic area
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 approv al of MI response documents
C ollaborate 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
P repare 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
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 congress es
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, inclu ding 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
Build and cultivate relationships with appropriate functions
Knowledge and Skills
Excellent written, verbal and interpersonal communication skills, and the ability to work well in multidisciplinary teams, across geographies
Knowledge of applicable regulatory and legal requirements for the provision of MI in the pharmaceutical environment
Ability to analy ze and evaluate clinical, biomedical and scientific data
Demonstrates Gileads 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
Education and Experience
Pharmacy, Nursing or Medical/ Life Sciences degree/advanced degree or equivalent
Experience in MI preferred or comparable experience within a healthcare/clinical environment required
Experience in the pharmaceutical industry or a MI vendor required
Experience in conducting medical/promo tional reviews required
Previous experience minimum 5 years preferred (may include advanced degree course)
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*. Job Description 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
Job Overview
Responds to unsolicited medical requests regarding Gilead products from HCPs, members of the public, and internal Gilead colleagues. Responses are provided in a timely manner using approved scientific response documents, up-to-date literature support , and other resources
Uses scientific and MI expertise to drive strategic initiatives and empower Gilead partners, HCPs, and patients to enable timely , informed decisions and improved patient outcomes
P erform s appropriate medical review for promotional and/or medical materials
Prepares global scientific resources in collaboration with local affiliate teams
Identifies , reports and records adverse events and product complaints in a timely manner in accordance with SOP.
Contributes to development of G MI strategy and represents G MI cross - functionally
May lead department-wide and/or global projects, initiatives, and product launches
Responsibilities
Routine responsibilities may include the following :
D evelop and maintain a deep knowledge of product, disease state and competitor landscape for assigned therapeutic area
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 approv al of MI response documents
C ollaborate 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
P repare 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 congress es
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, inclu ding 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
Knowledge and Skills
Excellent written, verbal and interpersonal communication skills, and the ability to work well in multidisciplinary teams, across geographies
Ability to create and clear ly communicat e scientific data for different audiences
Knowledge of applicable regulatory and legal requirements for the provision of MI in the pharmaceutical environment
Ability to analy ze and evaluate clinical, biomedical and scientific data
Demonstrates Gileads 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
Education and Experience
Pharmacy, Nursing or Medical/ Life Sciences degree/advanced degree or equivalent
Experience in MI preferred or comparable experience within a healthcare/clinical environment required
Experience in the pharmaceutical industry or a MI vendor required
Experience in conducting medical/promo tional reviews required
Levelling Guide
Previous experience minimum 5 years preferred (may include advanced degree course)
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:
* 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@ for assistance.
For more information about equal employment opportunity protections, please view the 'Know Your Rights' poster.
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Job Requisition ID R0045781
Full Time/Part Time Full-Time
Job Level Associate Director
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- Location:
- San Mateo, CA, United States
- Job Type:
- PartTime
- Category:
- Management Occupations