Assoc Director – Medical Information

Assoc Director – Medical Information

Requirements

• 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
• Doctorate and 5+ years of relevant experience OR
• Master’s and 8+ years of relevant experience OR
• Bachelor’s and 10+ years of relevant experience

Responsibilities

• Develop 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 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

Preferred Qualifications

• Pharmacy, Nursing or Medical/ Life Sciences degree/advanced degree or equivalent
• Experience in MI preferred or comparable experience within a healthcare/clinical environment
• Experience in the pharmaceutical industry or a MI vendor
• Experience in conducting medical/promotional reviews