• PRA Health Sciences
  • $116,035.00 -96,800.00/year*
  • Flemington , NJ
  • Scientific Research
  • Full-Time
  • 18 Brentwood Ct

Responsibilities

  • In collaboration with the medical team develop and implement the US publication plan according to the medical strategy for assigned products
  • Attend publication working group (PWG) meeting for assigned products to discuss status of projects, get guidance from medical team on any issues/conflicts arising for any project
  • Ensure that publication of manuscripts, abstracts, oral presentations, and posters, developed in collaboration with medical directors, biostatistics team, and external authors are in line with Novartis publication policy and industry guidelines (GPP2, ICJME).
  • Manage projects, including tracking and updating of timelines on behalf of assigned product team
  • Identify opportunities for new posters, publications or presentations.
  • Review/fact check draft publication/abstract/poster content to ensure alignment with clinical trial data and for consistency
  • Provide appropriate recommendations to team on journal selection and meetings for manuscripts and abstract submission
  • Manage external publication agency deliverables and quality of work
  • Responsible for the maintenance of publication records in the publication management system.
  • Responsible for the budget of his/her activities and deliverables (budget planning, monthly/quarterly budget accruals and tracking appropriate spend) for his/her assigned successful completion of objectives
  • Escalate concerns or issues related to departmental processes
  • Recommend process improvements that can help reduce cycle times, improve quality or increase productivity
  • Qualifications

    Education and Work Experience:

  • BS in science or related field required
  • 3-5 years pharmaceutical publication development experience required
  • Knowledge, Skills, and Abilities:

  • Good working knowledge of publication appropriate guidelines/regulations; ICMJE, GPP2, CONSORT etc.
  • Effective communication and computer (MS Office Suite) skills
  • Familiarity with the use of DataVision Publication software
  • Project management skills to track and update timelines
  • Medical writing experience preferred
  • Ability to interpret a clinical study report required

  • Associated topics: biopharmaceutical, dietetic, drug development, immuno oncology, injury, microbiology, pharmaceutical, physiologist, protein, trauma

    * The salary listed in the header is an estimate based on salary data for similar jobs in the same area. Salary or compensation data found in the job description is accurate.

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