Summer Intern - Clinical Development

Soleno Therapeutics, Inc.Redwood City, CA
51d$25 - $27Onsite

About The Position

Join Soleno Therapeutics, Inc. as a Summer Intern and gain hands-on experience in the pharmaceutical industry while contributing to meaningful projects. Interns will be aligned with a central function (i.e. Clinical Development, Technical Operations, Clinical Operations, Information Technology, Commercial, etc.) that matches their interests and will also collaborate with various departments. Throughout the internship, you will assist with administrative tasks and support cross functional projects. You’ll also have the opportunity to attend lunch and learn trainings and shadow senior staff. The ideal candidate is proactive, eager to learn, and able to multitask effectively in a team-oriented environment. This internship offers a unique chance to develop professional skills while playing a key role in advancing Soleno’s mission.

Requirements

  • Must be enrolled in a credited college or university at the time of the internship
  • Must be able to work onsite at our HQ office three days per week (Tuesday, Wednesday, and Thursday)
  • Possesses a can-do attitude with the ability to multi-task and take on various projects at a time
  • Team player with a willingness to take direction
  • Proficient in Microsoft Office Suite

Nice To Haves

  • A degree in a science-related field is preferred but not required

Responsibilities

  • Assist departments on various administrative projects such as organizing electronic and hard copy records and documents and assisting with literature reference searches
  • Assist with research and coordination for digital engagement initiatives
  • Support cross functional projects to improve patient and caregiver access to resources
  • Support research and analysis related to emerging health technologies
  • Support clinical trial design, setup and execution
  • Conducting background scientific and clinical research to support new indications
  • Assisting Clinical Development team with design and drafting of study protocols
  • Contributing to regulatory submission packages
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