Study Start Up Associate II(m/w/x)

Description

In this role, you will be at the forefront of initiating clinical trials, ensuring compliance with regulations, and collaborating with various stakeholders to facilitate the approval process for innovative treatments.

Requirements

• •Bachelor's degree in life sciences or related field
• •Minimum of 2 years of experience in clinical research or regulatory affairs
• •Strong understanding of regulatory requirements and guidelines for clinical trials
• •Excellent organizational and project management skills
• •Excellent communication and interpersonal skills

Tasks

• •Lead preparation and submission of regulatory documents
• •Coordinate with internal and external stakeholders for approvals
• •Manage records of regulatory submissions and correspondence
• •Provide guidance on regulatory requirements to study teams
• •Participate in process improvement initiatives for study start-up

Benefits