Medical Manager
hace 4 semanas
3866 Upjohn Export B.V. sucursal Costa Rica
At VIATRIS, we see healthcare not as it is but as it should be.
We act courageously and are uniquely positioned to be a source of stability in a world of evolving healthcare needs.
Viatris empowers people worldwide to live healthier at every stage of life.
We do so via:
Access - Providing high quality trusted medicines regardless of geography or circumstance;
Leadership - Advancing sustainable operations and innovative solutions to improve patient health; and
Partnership - Leveraging our collective expertise to connect people to products and services.
Every day, we rise to the challenge to make a difference and here's how the Medical Manager role will make an impact:
Key responsibilities for this role include:
- Provides support, information, and advice on medical and scientific issues to internal (marketing, sales, etc.
), and external customers (medical population, investigators, regulatory authorities, etc.
)- Collaborates in the implementation of regional clinical development program to support medical strategies of assigned products.
Identify new research areas/studies, publications and/or guidelines that could capitalize on the strengths of the assigned products and further differentiate them from other agents.- Collaborates with in country and above country Medical Affairs colleagues to ensure coordination of scientific/medical efforts at the country level.- Is actively involved in the development and review of pre-launch and launch marketing programs of assigned products, as required.
Ensures the promotional material is prepared according to the PhRMA Code, Viatris guidelines/SOPs/Policies on Good Promotional Practices and Local Regulations.- Is actively involved and the responsible person for the interaction with the investigator, review and tracking of Investigator Initiated Research (IIR) programs of assigned products, with interaction with appropriate internal colleagues, according to the current IIR Global SOP.- Works with marketing and medical colleagues to facilitate the dissemination of clinical research data.- Collaborates in the preparation of study reports and manuscripts, as required.- Works with outside advisory groups to develop new approaches to studying and developing the assigned products.-
- As required by the Marketing and Sales Departments, the Medical Manager will be responsible of providing input in the creation process of promotional and training materials, ensuring their clinical pertinence as well as compliance with applicable regulatory, medical and ethical standards, as well as corporate Standard Operating Procedures.
The Medical Manager should identify potentially problematic medical/clinical issues in the promotional materials, and, if appropriate, liaise with the Medical Director to address them.- Collaborates with the Sales, Marketing Department and Training & Cap.
Dev.
in the Field Force Training Program and Process.- Provides medical input and support for local regulatory processes pertaining to his/her designated products.
Also collaborates with Regulatory Affairs in the revision of LPDs/LLDs.- Promotes proactively the relationships with new professionals and support the existing liaison with Key Opinion leaders in the areas of interest to Viatris.- Strengthen and create professional bonds with Medical Associations and Health Organizations within their areas of expertise.- Provides counsel and expertise to the members of the Marketing Team for the elaboration of programs, strategies and tactical approaches of the drugs under his/her responsibility.- Provides and documents an accurate, consistent, timely, and balanced response to written and oral Medical Information inquiries from internal (e.g.
Medical, Marketing) and external customers (Healthcare Professionals, consumers etc.)
according to the Global SOP when acting as a back-up of the Medical Information Officer or any other Medical Managers outside his/her product lines, or whenever applicable.- Conducts literature review activities of his/her products for potential adverse events and/or product complaints and documents this review, according to applicable SOPs/WI.- Provides counsel and expertise to WRD colleagues upon request.- Forwards any safety or product quality information to the appropriate group within the timelines specified in accordance with global policies.
The minimum qualifications for this role are:
Technical- Knowledge of PhRMA Code of Pharmaceutical Marketing practices- Knowledge of pharmaceutical business- Training skills- Presentation skills- Excellent command of informatics tools- Knowledge of medical Information and regulatory procedures and local regulatory environment- Knowledge of copyright guidelines- Knowledge about how to handle national and international databases and other bibliographical sources- Understanding of local business needs and/or business coursework is desirable- Knowledge of the Central America and Caribbean regulatory en
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