A leading clinical research organization is seeking a Clinical Study Manager responsible for overseeing project management and site management for clinical studies. The role requires a Bachelor's degree in a relevant field and at least 1-3 years of experience in Oncology as a Clinical Research Associate. Key responsibilities include planning activities, managing budgets, leading meetings, and ensuring compliance with study protocols. Strong communication skills and an understanding of Good Clinical Practice are essential for success in this position.
Qualifications
Bachelor's degree or above required in relevant fields.
1-3 years of CRA experience in Oncology is preferred.
Strong understanding of GCP and clinical trial processes.
Responsibilities
Manage clinical study activities from selection to close-out.
Plan project activities and timelines based on goals.
Develop study management plans and budgets.
Organize and lead meetings and teleconferences.
Skills
Project management
Oncology CRA experience
Communication skills
Information-gathering skills
Good command of written and verbal English
Education
Bachelor degree in Medical, Pharmacology or Biology
Tools
Microsoft Word
Microsoft Excel
Microsoft PowerPoint
Microsoft Outlook
Job description
A leading clinical research organization is seeking a Clinical Study Manager responsible for overseeing project management and site management for clinical studies. The role requires a Bachelor's degree in a relevant field and at least 1-3 years of experience in Oncology as a Clinical Research Associate. Key responsibilities include planning activities, managing budgets, leading meetings, and ensuring compliance with study protocols. Strong communication skills and an understanding of Good Clinical Practice are essential for success in this position.