Senior CNS CRA – Mid-Atlantic (Remote)

Worldwide Clinical Trials; Oregon; Hybrid; USD 97,000 - 193,000; Full time

Job summary

Worldwide Clinical Trials is seeking a Clinical Research Associate to manage investigative sites across the study lifecycle, ensuring compliant trial delivery and training site staff on data collection and safety reporting.

This home-based role supports sites across the US Mid-Atlantic with travel about 8–10 days per month; some travel to other regions may be required. Psychiatry experience and full-service monitoring is preferred.

Qualifications

• Excellent interpersonal, organizational, and communication skills, with strong attention to detail.
• Ability to work effectively with little or no supervision.
• Proficiency in Microsoft Office, CTMS, and EDC systems.
• Proficiency in English, including strong oral and written communication skills.

Responsibilities

• Manage research activities at investigative sites participating in Worldwide's clinical research projects.
• Support sites throughout the full study lifecycle, from site identification and start-up through study maintenance and close-out.
• Coordinate study start-up activities, including collecting required regulatory documentation and supporting contract and budget negotiations.
• Conduct Study Initiation Visits (SIVs) and train sites on accurate data collection and safety-event reporting.
• Manage ongoing site activities, primarily remotely, while maintaining effective communication and oversight.
• Ensure sites comply with informed consent requirements, safety reporting expectations, and applicable regulatory requirements.

Skills

Interpersonal skills

Organizational skills

Communication skills

Ability to work with little supervisor

Attention to detail

Education

4-year university degree or Nursing Degree

Tools

Microsoft Office

CTMS

EDC systems

Job description

Worldwide Clinical Trials is seeking a Clinical Research Associate to manage investigative sites across the study lifecycle, ensuring compliant trial delivery and training site staff on data collection and safety reporting.

This home-based role supports sites across the US Mid-Atlantic with travel about 8–10 days per month; some travel to other regions may be required. Psychiatry experience and full-service monitoring is preferred.