Assoc Director, Medical Information

Descripción del trabajo

At Gilead our pursuit of a healthier world for all people has yielded a cure for hepatitis C, revolutionary improvements in HIV treatment and prevention as well as advancements in therapies for viral and inflammatory diseases and certain cancers.

We set and achieve bold ambitions in our fight against the world’s most devastating diseases, united in our commitment to confronting the largest public health challenges of our day and improving the lives of patients for generations to come.

As a Assoc Director, Medical Information, at Gilead you will ...

Responsibilities

• 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
  

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

Basic Qualifications:

• 10+ Years with BS/BA
  OR

• 8+ Years with MS/MA or MBA

Preferred Qualifications:

• PharmD, MD, PhD 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/promotional reviews required

• 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

This role is Foster City CA or Parsippany NJ based.
​There are two openings available.

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.