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Scientific Director

2 months ago


New York, United States SourceLab Search Full time

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