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ApotheCom

Associate Medical Director

Biology & BiotechConfirmed live in the last 24 hours
Full-timeYardley, PA, USA$1In-person

About the Job

Requirements

  • An advanced degree in life sciences, pharmacology, or medicine is required.
  • Previous experience within a medical communications agency is required.
  • Excellent written and verbal communication and interpersonal skills are required.
  • Ability to work in a fast-paced environment, meet deadlines, and manage multiple projects is required.
  • Strong financial, administrative, and organizational skills, including the ability to multitask, are required.
  • Strong client communication skills and the ability to work with clients and faculty members are required.
  • Attention to detail, ability to prioritize responsibilities, and ability to work both in a team-oriented environment and independently are required.

Responsibilities

  • Provide scientific support for assigned client projects and be responsible for scientific content across medical affairs and publications deliverables.
  • Develop scientifically accurate and strategically sound content under the supervision of senior medical staff, meet with clients, and work with faculty.
  • Ensure assigned medical communications are accurate, clinically relevant, and reflect recent advances in the medical field.
  • Consult with key opinion leaders in the appropriate therapeutic area and provide expert resources and information.
  • Maintain knowledge of pharmaceutical industry developments and trends regarding appropriate drugs.
  • Partner with pharmaceutical industry clients, when appropriate, on communications program goals and objectives and ensure delivery of high-quality products.
  • Stay current with medical developments and conduct literature searches to provide accurate medical information for assigned projects.
  • Analyze, interpret, and use complex medical documents under the supervision of senior scientific staff.
  • Synthesize clinical trial data and translate its relevance for physician and consumer audiences according to client requirements for assigned projects.
  • Attend and help 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.
  • Edit medical documents, verify scientific accuracy, and provide quality control for writers and freelancers.

About the Company

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