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Scientific Director
2 months ago
Responsibilities
Independently provide client-ready deliverables
Oversee content development on a wide range of complex projects across multiple teams/therapeutic areas and guide the decision-making process in data analysis
Review scientific content developed by scientific team members and guide others to develop this skill
Contribute to scope creation and provide feedback on scientific aspects of budget development
Collaborate with the Client Services partner for forecasting, staffing, and resource planning
Serve as scientific lead on assigned accounts, providing strategic direction and leadership
Develop understanding of the big picture in therapeutic categories through fundamental review of literature
Demonstrate strong knowledge of pharmaceutical industry standards and compliance
Moderate and facilitate effective, productive client sessions
Build and manage strong relationships with clients and medical experts communication channels with physicians and guides others in developing this skill
Partner with Client Services on account / issues management
Communicate effectively and propose rational and appropriate solutions when conflicts arise
Guide career development and performance management for direct reports
Work with functional teams and Client Services to cross sell services showing an understanding of business environment and client business strategy/implications
Participate in business development initiatives with existing clients and contribute to RFPs and pitches for business with new clients
Qualifications
- An advanced scientific degree (PhD, MD, PharmD) with 3 to 5 years of experience in a Medical Communications agency setting
- Strong therapeutic category knowledge and experience.
- Experience working directly with pharmaceutical clients
- Demonstrated ability to interpret data and provide strategic/scientific direction to clients
- Proficiency organizing teams and managing projects
- Strong self-motivation and enthusiasm with demonstrated ability to thrive in a fast-paced, dynamic, highly detail-oriented environment
- Strong knowledge of pharmaceutical standards, compliance, and regulations