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AM
Ashfield MedComms
Associate Medical Director
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Based on Pennsylvania data
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What they do
A Medical Director directs and manages a medical practice, clinic, lab or public health program. Organizes and manages of staff physicians, policy implementation, and ensures that standards for medical care are communicated and maintained.
$257,197 / year median in Pennsylvania
+7% projected growth
Job Description
Associate Medical Direct - Publications About ApotheCom ApotheCom is an exciting leader in the field of medical communications. Drawn together from several backgrounds including the pharmaceutical industry, research, marketing, medical and regulatory writing, sales, publishing, digital media and design, we have the experience and all-round ability to conceive and deliver the best quality medical communications programs. About the role The Associate Medical Director ("AMD") will assist senior scientific staff in providing scientific support for assigned client projects. The AMD will be responsible for scientific content on specific projects across both medical affairs and publications deliverables. With supervision of senior medical staff, the AMD will develop content that is scientifically accurate and strategically sound, meet with the client and work with faculty. You will report to the Senior Vice President. Here's what you'll be doing: Responsible for ensuring that assigned medical communications are accurate, clinically relevant and reflect the most recent advances in the medical field. Consults with key opinion leaders in the appropriate therapeutic area and provides expert resources and information. Maintains knowledge of developments and trends in the pharmaceutical industry regarding appropriate drugs When appropriate will partner with pharmaceutical industry clients on goals and objectives of communications programs, ensuring delivery of the highest quality product. Remains current with medical developments and conducts literature searches to ensure delivery of accurate medical information for assigned projects. Analyzes, interprets and uses complex medical documents under the supervision of senior scientific staff. Synthesizes clinical trial data and translates relevance for the appropriate physician and consumer audiences according to client requirements for assigned projects. Attends and helps design clinical trial investigator meetings and advisory boards. Help write medical manuscripts, white papers, monographs, slide kits, abstracts, and posters under the supervision of senior scientific staff. Edits medical documents, verify scientific accuracy and provide quality control for writers and freelancers.