The Medical Director at MedEvoke acts as the scientific lead across multiple accounts. The Medical Director is proficient in writing and editing technical scientific documents and managing content at all stages of development. This person is delegated the responsibility and authority for reviewing all deliverables prior to client submission and is integrally involved with new business development and strategic recommendations.
At MedEvoke, you will:
· Produce documents that are technically accurate and meet intended objectives
·... Participate in teleconferences and attend client and scientific meetings such as advisory boards and workshops
· Manage multiple work streams and projects simultaneously from a scientific perspective
· Types of projects include:
o Workshop material for client working sessions
o Scientific narratives based on extensive literature analysis
o Executive summaries and meeting reports
o Digitally medical strategy and communications solutions including value proposition, strategic differentiation, analytic insights and data translation
o Clinical trial alignment initiation, acceleration, and optimization strategies
· Lead scientific discussions as subject matter expert with cross-functional client groups during meetings, workshops or advisory board meetings
· Participate in discussions with Business Development to support new business requests and needs
· Work closely with Account Directors on existing business to ensure scientific accuracy, integrity, and client vision
· Perform other duties and assignments as directed
Required knowledge, skills, and abilities:
· Advanced degree in life sciences (MD, PharmD or PhD) with at least two years of relevant healthcare agency, medical education, or pharmaceutical industry experience in multiple therapeutic areas including rare diseases
· Knowledge of clinical development, FDA and global regulations and guidelines, and assessment of the evolving competitive landscape
· Ability to conduct literature analysis, write and edit the content, for a wide range of projects
· Ability to interact with all levels of internal and external stakeholders
· High level of proficiency with Microsoft Office Suite
· Be well versed in pharma regulations, have a strong attention to detail, and demonstrate strong verbal and written communication skills
You bring:
In addition to a competitive package that includes health, dental, vision, matching 401(K), unlimited vacation, holiday, and sick time, we have a flexible, friendly, informal working environment, and offer a sign on bonus
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