Teva Intern - Clinical Operations 

United States, Pennsylvania, East Bradford Township 

753714932

Embark on a future with an international pharmaceuticals company, contributing your creative energy to high-impact projects from the moment you arrive through the course of this 12-week experience. You will take part in meaningful work and real-life projects that will help you grow both professionally and personally throughout the program.

During the 12-week rotational program, you will learn the basics of clinical trial management, including:
• Gaining insights into the management of clinical trials for innovative medicines and biosimilars, including vendor oversight and clinical trial site management.
• Participating in activities related to clinical supply chain design, execution, and monitoring.
• Learning about the operational support for generic and clinical pharmacology studies.
• Acquiring hands-on experience in clinical trial data management.
• Understanding the importance of trial master file quality, operations, and maintenance.

The program will maximize your exposure to different study phases and aspects of managing clinical trials within Teva Global Clinical Operations. Specifically, you will gain experience in the following groups:
• Innovative Medicines and Biosimilars (6 weeks)
• Clinical Supply Chain, Secondary Packaging, and Logistics (2 weeks)
• Generics and Clinical Pharmacology Operations (1 week)
• Data Management (2 weeks)
• Strategy, Systems, and Business Operations (2 weeks)

Supported by a mentor and experienced colleagues, you will be directly involved in our daily business and be assigned tasks within diverse projects. You will also present a lunch and learn session of your choice within the clinical operations department.
Interns are required to develop a solid understanding of good clinical and manufacturing practices during the internship.

Qualifications
• Experience and/or interest in the biotechnology, pharmaceutical or health-care industry
• Must be currently enrolled in an undergraduate, ideally in health science discipline, with a good academic standing within your program with an accumulated GPA of at least 3.0
• Effective time management as this internship requires balancing simultaneous project completion, team and study meetings, introductory sessions on relevant topics, and following up on previous rotation tasks
• Adaptability: The ability to pivot every two weeks—transitioning to a new department, embracing different teams, methodologies, knowledge domains, and projects—is essential.
• Knowledge bridging: Quickly acquiring the necessary knowledge to comprehend meetings and ongoing projects is crucial. In the initial days, understanding team dynamics, information sources, and identifying helpful colleagues is essential.
• Eligible to work in the United States.
• Candidates are required to live within a commutable distance of West Chester, Pennsylvania
• Interns are required to be able to work from May 19th to August 8th
• Excellent communication, collaboration, and interpersonal skills.
• Demonstrate enthusiasm and curiosity about drug development in biotech industry
• Desire to learn

The internal career site is available from your home network as well. If you have trouble accessing your EC account, please contact your local HR/IT partner.