Clinical Trial Manager (CTM)
- Istanbul
- Clinical Operations
- Internship
We usually respond within a week
Job Location :Istanbul
Department : Clinical Operations
Employment Type : Internship
Lead and manage the full lifecycle of clinical trials (planning, execution, monitoring, and close-out).
Develop study protocols, timelines, budgets, and risk-management plans.
Oversee site selection, site activation, and study training activities.
Monitor study performance and ensure adherence to GCP, SOPs, and regulatory requirements.
Coordinate with CROs, vendors, and internal teams to ensure smooth trial operations.
Review study documents including CRFs, monitoring reports, and regulatory submissions.
Ensure proper documentation, data quality, and timely reporting.
Resolve operational issues and track trial metrics to maintain study accuracy.
Manage study audits, inspections, and compliance activities.
Prepare and deliver study progress updates for leadership.
As a Clinical Trial Manager, you will be responsible for managing the day-to-day operations of clinical studies across multiple phases. You will collaborate with cross-functional teams, coordinate with vendors, monitor study progress, and ensure all clinical activities follow Good Clinical Practice (GCP) and regulatory guidelines. This role requires strong leadership, communication, and project management skills.
Bachelor’s or Master’s degree in Life Sciences, Pharmacy, Nursing, or a related field.
3–5+ years of experience in clinical research or clinical trial management.
Strong knowledge of GCP, ICH guidelines, and regulatory requirements.
Proven experience managing clinical trials across phases (Phase I–IV).
Excellent communication, leadership, and organizational skills.
Ability to manage multiple projects and meet strict timelines.
Experience working with CROs, vendors, and cross-functional teams.
Proficiency in clinical trial management systems (CTMS) and MS Office.
Detail-oriented with strong problem-solving abilities.
Excellent communication, leadership, and organizational skills.
Ability to manage multiple projects and meet strict timelines.
Experience working with CROs, vendors, and cross-functional teams.
Proficiency in clinical trial management systems (CTMS) and MS Office.
Detail-oriented with strong problem-solving abilities.