The internship program provides a learning experience, mentoring and valuable work experience in the field of clinical trials. We provide our interns the opportunity to work on meaningful assignments and make sure that they gain real world experiences (in the areas of Regulatory & Finance and Supply & CRA support).
This program provides comprehensive trial and site administration experience. Under the oversight of the Clinical Operation Manager Leads/Clinical Operation Managers and Clinical Trial Coordinators, the person prepares, collates, distributes and archives clinical documents. The Interns supports clinical supply & non-clinical supply management and ensures timely maintenance of tracking and reporting tools, as applicable.
Requirements: CORE Competency Expectations:
Fluent in Local Languages and business proficient in English (verbal and written) and excellent communication skills.
Behavioral Competency Expectations:
Effective time management, organizational and interpersonal skills, conflict management.
Educational Requirements:
B.A./B.S. (Life Science preferred) or equivalent healthcare experience.
GCP course/ CRA course.
Required Skills:
Biological Sciences, Clinical Research, Clinical Trials, Data Analysis, Database Management, Data Science, Detail-Oriented, Document Management, Key Performance Indicators (KPI), Life Science, Project Management, Software Proficiency
This position is open to all candidates.