
Assoc Director, Medical Information
米国 - カリフォルニア - フォスターシティメディカルアフェアーズ正社員仕事内容
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
- Performs 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 GMI strategy and represents GMI cross-functionally
- May lead department-wide and/or global projects, initiatives, and product launches
Responsibilities:
Routine responsibilities may include the following:
- 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
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 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
Basic Qualifications:
- 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 OR
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