Clinical Development Intern
About The Position
Overview Xeris is a growth-oriented biopharmaceutical company committed to improving patient lives by developing and commercializing innovative products across a range of therapies. Xeris is headquartered in Chicago, Illinois and has a strong foundation built on proprietary formulation technologies and deep expertise in clinical development and commercialization. We are seeking a motivated and enthusiastic intern to join our Clinical Development Department. This internship offers hands-on experience in clinical research, exposure to real-world projects, and an opportunity to develop professional skills in a collaborative environment. The intern will gain an understanding of the clinical research operational activities across all phases of clinical research, become familiar with the essential documents required and gain a cross functional appreciation of drug development through interfacing with key internal and external collaborators and participating in wider study team discussions.
Requirements
- Currently pursuing a Bachelor’s/Masters/PhD and/or has completed a minimum of 2 years of undergraduate studies
- Minimum GPA 3.0
- Returning to academic program at a credentialed institution for at least one semester post-internship
- Strong interest in Clinical Development (eg. Clinical Research Operations, Data Management, Biostatistics, Clinical Supply Chain)
- Excellent verbal and written communication skills
- Ability to work independently and as part of a team
- Proficiency in Microsoft suite of products (eg. Word, Power Point, Excel)
- Thrive in a fast-paced, diverse work environment
- Competencies : Written and Verbal Communication, Teamwork & Collaboration, Attention to Detail, Self-Starter, Analytical skills, Problem Solving, Organizational skills, Adaptability, Professionalism.
Responsibilities
- Assist with review of key study documentation including protocols, informed consent forms, investigator brochures, case report forms, and clinical study reports and other activities including conducting research, preparing reports or presentations, etc.
- Assist in the implementation of new systems and tools to streamline clinical trial operations
- Perform tasks related to supporting operational execution of clinical studies, including trial master file documentation filing and reviews, preparation of materials, and study inspection readiness activities
- Work on assigned projects and participate in study team activities and meetings
- Support the team in day-to-day operations as needed
- Participate in team meetings and contribute ideas
- Collaborate with cross-functional teams as needed
- At the conclusion of the internship, prepare a comprehensive review of the internship experience and present to the organization
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What This Job Offers
Career Level
Intern
