Medical Affairs Intern

StrykerPortage, MI
21dOnsite

About The Position

Stryker, a global leader in medical technology takes great pride in their people, and that’s why we’re looking to expand our talent. As a result, we are looking for the best and brightest students to strengthen our team and drive our business going forward. As an intern at Stryker, you will: Apply classroom knowledge and gain experience in a fast-paced and growing industry setting Implement new ideas, be constantly challenged, and develop your skills Network with key/high-level stakeholders and leaders of the business Be a part of an innovative team and culture Opportunities Available As a Clinical intern at Stryker, you will: Work cross functionally with different departments including R&D Engineering, Project Management, Health Care Solutions, Marketing, and Regulatory Affairs to assist in clinical research programs and develop a broad understanding of the regulated clinical research landscape Perform clinical intelligence activities to ensure a thorough understanding of available treatment options and clinical studies Accompany Clinical Research Associate to monitor clinical data at clinical investigative sites Prepare literature review summaries for comprehensive evaluation of current clinical outcomes in recent published trials Shadow Clinical Research Associates at cross functional team meetings to gain exposure to the collaborative development process associated with executing a clinical trial.

Requirements

  • Currently working on completion of a Bachelor’s or Master’s degree in related field or equivalent; we will only consider students who plan to be enrolled in a degree- seeking program after the summer.
  • Cumulative 3.0 GPA or above; must be the case at the date of hire and will be verified during background check in the spring
  • Must be legally authorized to work in the U.S. and not require employment-based sponsorship now or in the future.
  • Excellent written and verbal communication skills.
  • Strong interpersonal skills.
  • Ability to exercise independent judgment and proven leadership and business acumen skills.
  • Proven ability to handle multiple projects and meet deadlines.
  • Versatility, flexibility, and a willingness to work within constantly changing priorities with enthusiasm.
  • Strong organizational, problem-solving, and analytical skills; able to manage priorities and workflow.
  • Proficient on basic computer programs: Microsoft Excel, Word, PowerPoint

Responsibilities

  • Assist in clinical research programs
  • Develop a broad understanding of the regulated clinical research landscape
  • Perform clinical intelligence activities
  • Monitor clinical data at clinical investigative sites
  • Prepare literature review summaries
  • Shadow Clinical Research Associates at cross functional team meetings
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