Senior Clinical Research Associate — Remote (Southeast)

Worldwide Clinical Trials; North Carolina; Remote; USD 97,000 - 193,000; Full time

Job summary

Worldwide Clinical Trials is seeking a Remote Clinical Research Associate to support sites across the Southeast. You will manage activities from start-up through close-out, train sites on data collection and safety reporting, and collaborate with sponsors and study teams to ensure quality trial delivery.

The role requires 5+ years as a CRA, experience in Psychiatry, and proficiency with CTMS, EDC, and Microsoft Office. Strong communication and remote oversight are essential.

Qualifications

• Minimum 5+ years as a Clinical Research Associate.
• Experience in Psychiatry required.
• Proficient with CTMS, EDC and MS Office.

Responsibilities

• Manage research activities at investigative sites participating in Worldwide’s clinical research projects.
• Conduct Study Initiation Visits (SIVs) and train sites on data collection and safety-event reporting.
• Coordinate site start-up activities, regulatory documentation, and contract/budget support.
• Oversee ongoing site activities remotely with strong communication and oversight.
• Ensure compliance with informed consent requirements, safety reporting, and regulatory needs.

Skills

Communication skills

Site management

Team collaboration

Attention to detail

English proficiency

Education

Four-year degree or Nursing degree

Tools

CTMS

EDC systems

Microsoft Office

Job description

Worldwide Clinical Trials is seeking a Remote Clinical Research Associate to support sites across the Southeast. You will manage activities from start-up through close-out, train sites on data collection and safety reporting, and collaborate with sponsors and study teams to ensure quality trial delivery.

The role requires 5+ years as a CRA, experience in Psychiatry, and proficiency with CTMS, EDC, and Microsoft Office. Strong communication and remote oversight are essential.