Associate Director, Global Medical Information (Remote)

Role Summary

The Associate Director, Global Medical Information is responsible for the management of Hematology/Oncology medical information activities, ensuring medical accuracy for global promotional and medical materials, delivering high-quality written responses to inquiries, and guiding the Medical Information Call Center to comply with regulatory policies. It also includes surveying the literature to ensure up-to-date and clinically impactful information.

Responsibilities

• Supports global Promotional/Medical Review Committee meetings by reviewing and approving promotional/medical materials for medical accuracy.
• Provides timely medical information responses to questions about Jazz Pharmaceuticals marketed and investigational products and disease states from patients, health care professionals, and internal employees.
• Independently creates new Standard Responses (SRs) and updates existing SRs based on in-house data and literature.
• Trains the sales team on Medical Information processes.
• Assists in the management of Medical Information vendors.
• Helps develop standard processes related to Medical Information services.
• Performs critical analysis and synthesis of internal/external literature.
• Provides coverage for the Medical Information booth at US and international medical conferences.
• Up to 10-20% travel, domestic and international.

Qualifications

• Prior Hematology/Oncology experience preferred.
• Proven experience in a Medical Information Department in the pharmaceutical industry.
• Global medical information product lead experience preferred.
• Medical information product launch experience preferred.
• Ability to understand products and diseases to provide independent, accurate information meeting regulatory requirements.
• Excellent verbal and written communication skills.
• Ability to develop and maintain good working relationships with internal departments and external contacts.
• Demonstrated expertise in drug information communication.
• Knowledge of regulatory requirements and guidances for responding to unsolicited information requests.

Skills

• Medical information proficiency with regulatory awareness
• Strong written and verbal communication
• Literature review and data synthesis
• Cross-functional collaboration

Education

• Advanced degree preferred (PharmD, MD, PhD, or equivalent).

Additional Requirements

• Travel: Up to 10-20% travel, domestic and international.