Study Start Up Associate II

Job Summary

A company is looking for a Site & Study Start Up Specialist.

Key Responsibilities

• Lead the preparation and submission of regulatory documents for clinical trials
• Coordinate with internal and external stakeholders to obtain necessary approvals
• Manage and maintain records of regulatory submissions and approvals

Required Qualifications

• Bachelor's degree in life sciences or a related field
• Minimum of 2 years of experience in clinical research or regulatory affairs
• Strong understanding of regulatory requirements for clinical trials
• Excellent organizational and project management skills
• Ability to collaborate effectively with cross-functional teams