Director, Global Medical Information, Liver, Inflammation, Fibrosis & Established Products (LIFE)

Description

As the lead for LIFE therapeutic areas, the Director will oversee the development and delivery of medical information content for both marketed and investigational products to external (healthcare professionals, patients, and consumers) and internal (medical affairs staff in affiliates and distributors) customers in response to requests.

They will also be responsible for the medical input for promotional and medical review committees. Additionally, the Director will be responsible for business optimization, which may include oversight of QA processes, call center, and other operational areas.

The Director will be responsible for identifying and implementing strategies to enhance the efficiency and effectiveness of the Medical Information department.

The role involves analyzing current processes, identifying areas for improvement, and developing solution to optimize operational performance.

The director will oversee project management activities ensuring that projects are executed efficiently, on time and in alignment with the department’s strategic priorities.

The Director will provide clinical, strategic, and personnel oversight for a therapeutic area(s); lead strategic initiatives that improve the ability of the department to provide its services;

lead and manage staff; and foster the professional growth of individual team members through development, coaching and support.

Routine responsibilities may include performing and / or leading one or more staff members in :

• Utilizing Medical Information content to provide scientifically balanced responses to external parties (healthcare providers and patients) or internal parties (affiliates and distributors) requesting medical or product information
• Developing and maintaining up-to-date global response documents (GRDs) relevant to therapeutic area
• Ensuring medical and scientific accuracy of medical information content deliverables and input into the Promotional Review and Medical Review Committees
• Researching and proactively creating new scientific responses to unanticipated inquiries
• Reporting adverse events per Standard Operating Procedure
• Maintaining a record of all interactions via a relational database
• Recognizing, obtaining pertinent data on, and accurately transmitting adverse events or product complaints to the appropriate internal departments
• Evaluating drug compendia for accuracy, if applicable
• Drive business optimization and Medical Information vendor management to ensure high quality service delivery and operational efficiency
• Providing oversight and support for scientific conferences with medical information activities

including attending scientific conferences and answering questions at medical booths

• Partnering and providing support to colleagues in Medical Affairs for projects and deliverables specific to therapeutic area
• Identifying and analyzing medical information trends and data gaps for therapeutic area to contribute insights to medical affairs strategies and priorities
• Collaborating with publication teams for updates and review of medical information trends / data gaps to contribute to therapeutic area publication strategies
• Ensuring strategic alignment and cross functional communications with key internal stakeholders and partners across Gilead (Medical Affairs, Pharmacovigilance, Medical Scientists, Marketing, Business Conduct, Clinical Pharmacology, Analytic Operations, Supply Chain, etc.)
• Interacting with affiliates and ensuring the proper triage of queries and content development
• Developing and applying complex and often long-term strategies to promote global alignment across medical information geographies
• Updating and ensuring compliance to Medical Information standard work practices and operating procedures
• Developing departmental strategic initiatives to address major activities within assigned therapeutic area (product launches, labeling updates, etc)
• Developing and maintaining a deep knowledge of product, disease state and competitor landscape for assigned therapeutic area
• Building a strong global medical information community in collaboration with medical information regions / affiliates
• Cultivating a number of influential contacts within and outside of own work area and expertise
• Critically reviewing, editing, and / or writing scientific documents such reimbursement dossiers, draft manuscripts, and slide sets
• Developing policies and procedures
• Providing team leadership and coaching to the Global Medical Information Team staff; Training staff, fellows and interns

K n owledge / Skills

• Excellent leadership, interpersonal, and verbal and written communication skills
• Proven track record in working in a dynamic, cross-functional environment
• Highly self-motivated and able to perform multiple tasks in a timely fashion
• Excellent project management, analytical, strategic-thinking, and problem-solving skills
• Knowledge of applicable regulations regarding the dissemination of medical information, drug promotion and adverse event and product quality complaint reporting
• Strong people management skills and ability to effectively lead and motivate a high performing team of individuals

Sp ec ific Education and Experience Requirements

• Advanced scientific degree, MD, PhD, PharmD, or equivalent required
• Demonstrated ability to lead strategically, drive performance, build alignment and collaborate
• Minimum of 8 years of experience in the pharmaceutical industry, with a minimum of 5 years of experience in Medical Information or Medical Communications is required.
• Minimum of 4 years of line management experience
• Ability to travel up to 20% of the time
• Ability to flex working hours to meet the global business need

The salary range for this position is : $221,170.00 - $286,220.00. 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 :

As an equal opportunity employer, Gilead Sciences Inc. is committed to a diverse workforce. Employment decisions regarding recruitment and selection will be made without discrimination based on race, color, religion, national origin, gender, 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 for assistance.