Coordinate clinical trial site activities and support site start-up and activation.
Serve as primary point of contact for investigative sites and cross-functional teams.
Ensure compliance with ICH/GCP guidelines and regulatory requirements.

Key Responsibilities:

Manage site identification, feasibility, regulatory submissions, and activation milestones.
Oversee essential documents, Trial Master File, and contract and budget negotiations.
Support pre-study visits, site initiation, and ongoing compliance monitoring.

Requirements:

University degree in life sciences or equivalent, or high school diploma with five years of clinical research experience.
At least one year of related experience in clinical research, healthcare, or data management.
Excellent communication, organization, and problem-solving skills with remote work readiness.

Benefits:

Remote-based working arrangement with limited travel.
Opportunity for professional development and career growth.
Cross-functional exposure to sponsors, CROs, and regulatory stakeholders.

Jobgether

This role is listed on behalf of a partner company in the clinical research sector, focused on coordinating site start-up and activation for clinical trials. The culture emphasizes operational excellence, collaboration, and patient safety, with a remote working environment.

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