job title: Study start up associate - 1 (icon)

Roles and Responsibilities

• Assisting in the preparation and submission of regulatory documents, such as clinical trial applications and ethics committee submissions.

• Coordinating with internal and external stakeholders to obtain necessary approvals and authorizations for study initiation.

• Maintaining accurate and up-to-date records of regulatory submissions and approvals.

• Supporting study teams in the development of study documents, including protocols, informed consent forms, and investigator brochures.

• Participating in study start-up meetings and providing input on regulatory requirements and timelines.
  

Your profile

• Bachelor's degree in life sciences or a related field.

• Previous experience in clinical research or regulatory affairs preferred, but Nt required.

• Strong attention to detail and organizational skills.

• Excellent communication and interpersonal skills, with the ability to collaborate effectively with cross-functional teams.

• Ability to work independently and manage multiple tasks simultaneously in a fast-paced environment.