Remote Clinical Site Activation Specialist

Worldwide; Durham (NC); Remote; USD 60,000 - 119,000; Full time

Benefits offered by this job

Remote work opportunity

Job summary

Worldwide Clinical Trials is seeking a Site Activation Specialist for a remote US-based role, with Durham, NC as a reference location. You will coordinate site regulatory activities, support activation milestones, and partner with cross-functional teams to ensure timely study start-up and regulatory readiness.

Ideal candidates hold a bachelor’s degree in a related scientific field and have 1+ year of clinical research experience, with strong knowledge of ICH GCP and regulatory requirements.

Qualifications

• 1+ year of clinical research experience, preferably in site activation or regulatory roles.
• Knowledge of ICH GCP and regulatory guidance.
• Strong organizational and communication skills.

Responsibilities

• Coordinate collection and maintenance of site regulatory documents for activation.
• Ensure timely completion of start-up activities and activation milestones.
• Review regulatory documentation to identify gaps and drive corrective actions.
• Support informed consent development and site-specific documentation.
• Coordinate site feasibility, confidentiality agreements, and site qualification.
• Monitor submission activities and communicate status to teams.
• Contribute to country/site intelligence for study planning and activation.
• Maintain SOPs, ICH GCP compliance, and study processes.

Skills

Clinical research

Site activation

Regulatory documentation

Communication

Organization

Education

Bachelor's degree

Tools

Microsoft Word

Excel

PowerPoint

Job description

Worldwide Clinical Trials is seeking a Site Activation Specialist for a remote US-based role, with Durham, NC as a reference location. You will coordinate site regulatory activities, support activation milestones, and partner with cross-functional teams to ensure timely study start-up and regulatory readiness.

Ideal candidates hold a bachelor’s degree in a related scientific field and have 1+ year of clinical research experience, with strong knowledge of ICH GCP and regulatory requirements.