Works with medical colleagues to facilitate the dissemination of clinical research data. Collaborates in the preparation of study reports and manuscripts.

Works with outside advisory groups to develop new approaches to studying and developing the assigned products.

Provides scientific analysis of candidate products for licensing and/or further clinical development.

Responsible for providing scientific 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.

Provide scientific training to the Sales and Marketing Department as needed.

Provides medical input and support for local regulatory processes pertaining to his/her designated products. Also collaborates with the Senior Regulatory Affairs Manager and Medical Director in the revision of LPDs.

Promotes proactively the relationships with new professionals and support the existing liaison with Key Opinion leaders in the areas of interest to Pfizer.

Strengthen and create professional bonds with Medical Associations and Health Organizations within their areas of expertise.

Provides scientific counsel and expertise to the members of the Marketing Team.

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 and the local WIs 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.

Forwards any safety or product quality information to the appropriate group within the timelines specified in accordance with local and global procedures.

Responsible for operational excellence and timely production of high-quality deliverables, including those related to:

Promotional materials review and approval.

• Educational symposia.
• Advisory board meetings.
• Clinical plans, protocols, study reports.
• Clinical abstracts / manuscripts.
• Regulatory submissions.
• Pharmacoeconomic submissions.
• Health outcome study manuscripts.
• Medical information enquiries.
• Product safety complaints & responses

REQUIRED SKILL SET

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 Colombia regulatory environment.

Managerial

• Analytical and Strategic Thinking
• Problem solving
• Quality
• Customer focus
• Flexibility
• Drive for Results
• Networking
• Communication
• Integrity
• Teamwork
• Pfizer Community and environment
• Negotiation and Influence
• Leadership
• Planning and organizing

Education

• Medical Degree.
• Medical Specialty - MSc (Desired)

Experience

• Previous related experience in the pharmaceutical or health related industry is an asset.
• Previous experience in clinical research is an asset.
• Fluency in English.
• At least 3 years of prior experience in medical advising positions

Work Location Assignment: On Premise

EEO (Equal Employment Opportunity) & Employment Eligibility

Pfizer is committed to equal opportunity in the terms and conditions of employment for all employees and job applicants without regard to race, color, religion, sex, sexual orientation, age, gender identity or gender expression, national origin, or disability.
Medical

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