MDWerks Inc. logo
MDWerks Inc.

MDWerks is a forward-thinking company that is leading the charge in the world of sustainable technology.

Director, Medical Publications – Medical Affairs

DirectorDirectorFull TimeRemoteLeadTeam 1-10H1B No SponsorCompany SiteLinkedIn

Location

United States

Posted

91 days ago

Salary

$225K - $240K / year

Seniority

Lead

Postgraduate Degree8 yrs expEnglish

Job Description

• Own and lead the Scientific Publications Team meeting and workshops to drive the development of the strategic global publication plan • Provide writing and editorial support for clinical and disease state abstracts, posters, manuscripts, and other publications • Ensure and communicate regular updates to relevant key stakeholders • Ensure that all publication-related activities are conducted according to standards, SOPs, applicable working instructions and, industry standards • Ensure high scientific quality, alignment with medical strategy and adherence to compliance/legal requirements • Manage 3rd-party vendors to ensure delivery of quality publications on time and on budget • Utilize and champion the use of AI and digital technologies to optimize publication workflows and processes • Create, review and oversee the publication budget and serve as a financial steward • Ensure that vendors are properly trained to and comply with company standards, on SOPs, company systems and tools while managing all vendor partners to execute the tactical plan effectively • Lead special projects with team and Med Affairs departments

Job Requirements

  • A higher education degree (M.D., Pharm.D., Ph.D.), or master’s degree in biomedical discipline or equivalent with demonstrated experience in publication management
  • 8-10+ years of pharmaceutical industry experience, at least half of which is in Medical Affairs
  • 5-8+ years’ experience in medical publications/communications, or other related areas within the biopharmaceutical industry, preferably within a matrix structure, in Medical Affairs or Clinical Development
  • CMPP certification preferred
  • Prior experience in hypertension, chronic kidney disease, and/or sleep apnea
  • Demonstrated experience in leveraging AI tools and/or digital technologies in scientific communications and publication planning
  • Understanding of the pharmaceutical drug development process, clinical trial design and execution, statistical methods, and clinical trial data reporting requirements
  • Deep knowledge of scientific publication planning processes and industry standards for reporting scientific studies
  • Experience and knowledge of publication management software/systems
  • Ability to foster diversity of opinion and an environment of open communication and trust
  • Demonstrated ability in coordinating and implementing simultaneous projects within a complex matrix
  • Demonstrated ability to formalize governance structures and develop operational processes and SOPs
  • Experience in vendor and budget management

Benefits

  • standard Company benefits including medical, dental, vision, time off and 401K
  • participating in Mineralys incentive plans are contingent on achievement of personal and company performance

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