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Costello Medical

Analyzes clinical and cost data for drug and device makers

Analyst/Medical Writer

Technical WritingConfirmed live in the last 24 hours
Full-timeBoston, MA, USA$71k - $76.5k /yr

About the Job

Requirements

  • A bachelor's degree in a scientific discipline and a minimum GPA of 3.3 are required; coursework in the life sciences is particularly welcomed.
  • Excellent written and spoken fluency in English is required.
  • Ability to communicate scientific materials clearly in written and oral form is required.
  • Understanding of scientific concepts and ability to apply them are required.
  • Close attention to detail is required.
  • Aptitude for and experience with scientific writing are required; relevant examples may include dissertations, research summaries, lab reports, poster or oral presentations, peer-reviewed scientific publications, book chapters, literature reviews, grant applications, regulatory documents, and articles for websites or student magazines.
  • Competency in Microsoft Word, Excel, and PowerPoint is required.
  • Strong organizational skills and the ability to manage time effectively and meet deadlines are required.
  • No previous experience in the sector is necessary, but applicants should demonstrate genuine interest in healthcare and eagerness to learn about new areas of clinical science.
  • Applicants with higher-level qualifications in a scientific discipline are welcome, but these qualifications are not required.
  • Applicants must have the right to work in the United States independently of the company; temporary visa holders such as those on OPT may be considered.
  • Applicants must submit a resume and cover letter explaining why they are suited to the role and want to join Costello Medical, with supporting examples; the resume should state qualification dates and grades where applicable.

Responsibilities

  • Analyze clinical-trial data and assimilate and creatively present the analysis in formats including posters, slide sets, value dossiers, reports, and peer-reviewed publications.
  • Work on three or four projects at a time across disease areas and products, collaborating with project teams and clients.
  • Participate increasingly in teleconferences and face-to-face client meetings following the induction period.
  • For publications projects, develop abstracts, manuscripts, posters, oral presentations, regulatory documents, lay summaries, and policy-related publications as assigned.
  • For medical affairs projects, present scientific information through medical education events, advisory boards, and medical information materials; support expert advisors and event speakers; and provide on-site support at certain events.
  • For market access projects, contribute to evidence generation through literature reviews, advisory boards with clinicians and payers, and economic modelling, and develop evidence-based materials presenting product value.
  • For literature review and synthesis projects, identify clinical, economic, and real-world evidence; conduct evidence reviews from searching through interpretation of results; ensure reviews conform to industry guidelines where applicable; and transform methods and results into reports and slide sets.
  • For real-world evidence projects, design, execute, and report prospective, retrospective, or cross-sectional studies; develop protocols and statistical analysis plans with statisticians, epidemiologists, clients, and external experts; acquire and analyze data; and communicate methods and results in written and oral formats.
  • For rare-disease projects, contribute across service offerings, including literature reviews, global economic models, publications, and medical education events.

About the Company

Costello Medical

Analyzes clinical and cost data for drug and device makers

Costello Medical analyzes, interprets and communicates clinical and health economic data for pharmaceutical and medical technology companies. Its evidence teams run statistical analyses, literature reviews and real-world evidence studies, while health economists build the cost and value cases that health systems weigh before paying for a treatment. Medical writers and designers turn trial results into journal articles, conference posters and slide sets, and other groups cover health policy, patient engagement, rare diseases and medical devices. Clients commission projects from these teams under one roof, and the firm also does pro bono work for charities. It was founded in 2008 and is headquartered in Cambridge, England.

Company size
501-1,000
Company stage
Not listed
Total funding
Not listed
Headquarters
Not listed
Founded
2008

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