Job Description

Company DescriptionAbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas - immunology, oncology, neuroscience, and eye care - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at . Follow @abbvie on , , , and .Primary Function:Represent the affiliate's medical/scientific voice of expertise for assigned product(s) and relevant therapeutic areas. Provide medical / scientific expert advice / guidance to key customers for assigned products and relevant therapeutic areas, including scientific exchange and professional relationship development with key thought leaders / external experts. Provide medical / scientific input into Medical Affairs strategies for the affiliate medical department and commercial plans, as required, and medical / scientific support for medical department activities under the overall direction of the Affiliate Medical Director. Provide medical affairs support to cross- functional affiliate teams. Ensure that the medical affairs role is fully integrated to support the strategy and execution of affiliate business, while being functionally independent.Responsibilities:1- Develop and maintain in depth knowledge for assigned product(s) / relevant therapeutic area(s) through attendance / participation at key internal meetings/training sessions, relevant congresses, and seminars and by regular self-study of the national/international literature.2- Provide expert medical/scientific advice for assigned products and related therapeutic areas, including responding to requests for scientific/technical information; contribute to the development and medical and scientific accuracy of core dossiers generated by the medical department (i.e. pricing and reimbursement dossiers, HEOR dossiers, medical information packs, clinical expert reviews etc.).3- Establish and maintain professional and credible relationships with key thought leaders /external experts and academic centers; this will involve participating in scientific congresses, coordinating advisory boards, round-table meetings, discussion fora etc.4- Deliver scientific presentations and medical education programs to healthcare professionals individually or in groups (meetings, clinical sessions, etc.), where appropriate.5- Screen relevant literature and other information from relevant scientific societies meetings and conferences and develop summaries of key messages for use within the Company (e.g. key areas of scientific/company interest, new trends in diagnosis, monitoring and treatments in the therapeutic area, etc.)6- Deliver training to sales forces and other departments; develop and update relevant training materials.7- Clinical Research Activities:

• Design and implement clinical research projects within defined standards and budgets (e.g. Phase IV, post marketing clinical activities such as registry/database projects, epidemiological surveys, and PMOS studies).
• Provide the required oversight to manage review, approval and conduct of IIS studies.
• Support the affiliate Clinical Research Department in the management of clinical studies, as appropriate (e.g. review new clinical study protocols, identifying potential investigators/sites, conducting feasibility surveys).

8- Review and preparation of promotional and non promotional material. Ensure the medical/scientific content is correct and fully compliant with Abbvie's internal policies, guidelines and the marketing code.9- Provide medical/scientific input into marketing strategy and key commercial initiatives, as required. Monitor the environment for competitive intelligence (e.g. product strategies, studies, commercial messages, positioning, etc.) and communicate, where appropriate, within the Company.10- Ensure compliance with all applicable national laws and regulations, guidelines, codes of conduct, AbbVie's policies and procedures and accepted standards of best practice.ACCOUNTABILITY & SCOPE:

• Provide input, as required, into the development of product or TA specific strategic medical affairs plans for the affiliate medical department and local commercial plans; collaborate and partner with local business partners to ensure that medical activities for assigned products / therapeutic areas are aligned with local business-related strategic plans.
• Ensure that local medical affairs implementation plans for assigned products / therapeutic areas are executed efficiently.
• Ensure adherence to all applicable national laws and regulations, guidelines, codes of conduct, AbbVie standards, policies and procedures.
• Operate as a scientific interface and resource to HCPs/Customer(s), Health Care Institutions, External Experts, professional associations and payers regarding assigned AbbVie Products or Products in Development.
• Provide specialist medical/scientific strategic input and operational support of core activities such as local clinical research, HCP/Customer interactions, generation and communication of clinical and scientific data, educational initiatives and patient safety for assigned products / therapeutic areas.

Qualifications

• Medical Degree or Bachelor's degree in a scientific discipline or higher.
• Minimum of 3-4 years' medical affairs experience within the pharmaceutical industry
• Experience and general knowledge on drug development and clinical research an advantage.
• Keen interest in developing and maintaining expert knowledge for assigned therapeutic area/product and in medical research in general.
• Excellent written/spoken communication and presentation skills.
• Fluency in written and oral English is highly desirable in order to facilitate communications between the affiliate medical department, Regional and International Medical Affairs and other AbbVie functional staff.
• High customer orientation
• Strong commitment to compliance with the relevant rules and procedures, and to scientific quality and integrity
• Collaborative, team-oriented approach, able to develop and support relationships across an organization as well as with key external stakeholders and the healthcare community at large. Experience being an active contributor to cross-functional teams and/or working in matrix organizations will be an advantage. Works independently: limited guidance/oversight. Works broadly across functions to facilitate and support the affiliate's medical and clinical activities as necessary.
• Sound judgment, strong planning and organizational skills, and the ability to get things done.
• Demonstrated strong sense of urgency.

Additional Information

• Affiliate medical personnel: Clinical Research Manager, Clinical Operations Manager, Medical
• Advisors/Managers; Medical Information team / specialists; affiliate pharmacovigilance / drug safety personnel; Medical Science Liaisons.
• Marketing and Sales personnel for assigned product and therapeutic area; Market access teams;
• Affiliate Brand teams Leads and members.
• Affiliate Government Affairs; Affiliate Public Affairs; Regulatory Affairs.
• Global Medical Information; Global HEOR.
• Library Information Resources.
• Regionally and HQ based Therapeutic Area medical affairs teams.
• Area/Regional commercial Staff / Brand Team members
• International Medical Affairs teams.
• Project/Medical Directors and Clinical Teams within Clinical Development and Global Medical Affairs.
• Healthcare personnel, Investigators, External Experts.
• Academic Institutions and Scientific or Medical Societies.
• Hospitals and Local Regulatory Authorities.
• Payers

AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives, serving our community and embracing diversity and inclusion. It is AbbVie's policy to employ qualified persons of the greatest ability without discrimination against any employee or applicant for employment because of race, color, religion, national origin, age, sex (including pregnancy), physical or mental disability, medical condition, genetic information, gender identity or expression, sexual orientation, marital status, status as a protected veteran, or any other legally protected group status.US & Puerto Rico only - to learn more, visitUS & Puerto Rico applicants seeking a reasonable accommodation, click here to learn more:

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