Support the day-to-day operational activities of the different clinical trials within the Global Clinical Operations team
Collaborate with the Clinical Project Lead (CPL) and gain experience in tasks typically performed by Global Trial Managers (GTMs) and Clinical Trial Administrators (CTAs)
Assist in coordinating trial-related documentation and tracking activities to ensure compliance with study timelines and quality standards
Support the maintenance of trial management systems, preparing meeting materials, and contributing to the organization of investigator and vendor communications
Help monitor study progress by reviewing operational metrics and assisting with follow-up actions as directed by the CPL
Additional tasks may involve supporting regulatory and ethics submissions, managing essential documents, and contributing to the preparation of status reports for internal stakeholders

Must be a current student enrolled at an accredited college or university pursuing at least a bachelor’s degree
An in progress undergraduate degree in Biology, Biochemistry, Chemistry, Research, or a related discipline preferred
Strong academic record with a preferred cumulative GPA of 3.0 or higher
Conscientious self-starter with good organizational skills, project management skills and attention to detail
Ability to balance multiple projects and priorities, must be able to multi-task
Strong interpersonal communication and ability to collaborate with teams; must effectively operate independently, across functional lines, and with internal customers
Demonstrated personal initiative, self-motivation, flexibility, adaptability and willingness to learn
Proficient in Microsoft Office Tools including Word, Excel, PowerPoint, etc.

Intern, R&D Clinical Operations

Key skills