Analyst/Medical Writer Summer Internship

Costello MedicalBoston, MA
9h$24 - $30Hybrid

About The Position

Our Analyst/Medical Writer Internship is ideal for current students and recent graduates in scientific disciplines, eager to gain valuable insights into life at a leading healthcare consultancy. You will gain practical experience by contributing to two or three projects during the internship, each of which involve the interpretation, assimilation, and creative presentation of clinical or health economic data. Depending on your team and project allocations, you may work on anything from medical communications to market access and evidence synthesis. Specific tasks may include: The preparation of medical education slides Performing systematic searches of medical literature Developing clinical trial manuscripts Assimilating clinical and cost-effectiveness evidence to support HTA submissions to NICE These meaningful and exciting projects contribute to improving healthcare outcomes globally. Interns will receive one-to-one training on the technical aspects of the role and learn about project management and effective communication with clients. Your designation as either an Analyst Intern or Medical Writer Intern will depend on your team allocation; however, the core responsibilities of both roles remain the same. Our teams are generally organised under the service areas of Medical Communications , Value and Access , and Evidence Development , and also encompass specialist areas such as Rare Diseases . If you have a particular interest in any of these service areas, include this in your cover letter. Please note that your team allocation will be confirmed closer to your start date. Whilst we will do our best to accommodate your preferences, final team allocations will be determined by business needs.

Requirements

  • A degree or enrolled in a degree program in a scientific discipline (minimum or expected GPA 3.3). We welcome applications from candidates with a diverse range of educational backgrounds, but particularly those with coursework in the life sciences
  • Exceptional attention to detail
  • Strong analytical skills
  • Excellent written English and spoken English, and the ability to communicate scientific material clearly in both written and oral form for a variety of audiences
  • Strong organizational skills and the ability to plan your own work effectively, with a proactive approach to task prioritization and time management
  • The ability to communicate effectively and work collaboratively as part of a team
  • Strong self-motivation, self-awareness and willingness to learn, with a desire to contribute to the company above and beyond project work
  • Fluency in Microsoft Word, Excel and PowerPoint
  • A genuine interest in healthcare and an eagerness to learn about new areas of science
  • You must have the right to work in the US independently from the company.

Responsibilities

  • You will be given hands-on experience working across Medical Communications, Evidence Development and/or Value and Access projects, all of which involve the assimilation, interpretation and creative presentation of scientific data related to pharmaceuticals or medical devices
  • The preparation of medical education slides
  • Performing systematic searches of medical literature
  • Developing clinical trial manuscripts
  • Assimilating clinical and cost-effectiveness evidence to support HTA submissions to NICE

Benefits

  • Generous vacation leave allowance
  • Flexible working hours and the chance to work from home 1 day per week
  • Access to medical, dental and vision insurance, as well as funded social activities
  • We provide exceptional internal training, opportunities to work on pro bono and charitable projects, and regular company-funded social activities.
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