About The Position

The Scientist in Medical Affairs will be responsible for organizing and delegating work to meet project deadlines while mentoring team members and ensuring high-quality deliverables. The role requires independent task execution with minimal supervision, functional review of team outputs, and proactive planning to mitigate risks. The Scientist will also provide therapeutic area knowledge support, conduct literature searches, create product information manuals, and collaborate with physicians on cross-functional teams. Additional responsibilities include training employees, generating safety reports, and supporting investigator-initiated studies.

Requirements

  • Bachelor’s degree in science or above
  • PhD in Nutritional is preferred
  • Minimum of 5 to 8 years of relevant experience in identified functional domain/business workstream

Responsibilities

  • Effectively organize and delegate work to complete assigned tasks to meet deadlines
  • Mentor and bestow domain knowledge to the team
  • Ensure tasks are delivered 100% on time or before deadlines
  • Demonstrate quality of work and commitment through excellence in deliverables
  • Independently perform tasks with minimal guidance
  • Functionally review the team’s work for accuracy and compliance
  • Plan deliverables and foresee potential risks
  • Ensure error-free and high-quality deliverables
  • Meet assigned goals for utilization and efficiency
  • Ensure training and timesheet compliance
  • Conduct functional training for team members
  • Support functional capability development of junior members
  • Provide therapeutic area knowledge support and contribute to research activities
  • Conduct and evaluate literature searches and analyze scientific literature
  • Create standard language for product information reference manuals
  • Provide medical support in reviewing printed packaging components and labeling
  • Collaborate with physicians on cross-functional teams for medical/scientific accuracy
  • Participate in creation of medical training materials and programs
  • Train employees in scientific/medical knowledge of relevant products
  • Create strategically targeted information in response to scientific literature
  • Assist in generating safety reports and regulatory submissions
  • Support investigator-initiated studies and facilitate review of proposals
  • Perform quality review of Epidemiology authored sections of the RMP
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