Remote CRA for Psychiatry Trials — Impactful Research

Worldwide Clinical Trials; Minnesota; On-site; USD 97,000 - 193,000; Full time

Benefits offered by this job

Competitive benefits package

Pay equity and transparency

Job summary

Worldwide Clinical Trials in the United States is seeking a seasoned Clinical Research Associate to support site activities across multiple therapeutic areas, with emphasis on site management, regulatory submissions, and TMF processes.

The ideal candidate has 5+ years of CRA experience, a 4-year degree or nursing degree, and will reside in the Midwest. Willingness to travel regionally and collaborate with cross-functional teams is required.

Qualifications

• 5+ years of experience as a Clinical Research Associate.
• 4-year university degree OR Nursing Degree.
• Experience in Psychiatry required, General Anxiety Disorder (GAD) a plus.
• Candidates must reside in the Midwestern United States.
• Willingness to travel regionally required.

Responsibilities

• Manage the research activities at sites participating in Worldwide’s clinical research projects.
• Typically involved in all stages of the clinical study, including site identification, regulatory document collection, and contract/budget support.
• Conduct study initiation visits (SIVs).
• Ensure regulatory compliance, informed consent, and safety reporting with remote site management.

Skills

Clinical Research

Site management

Regulatory knowledge

Communication

MS Office

CTMS

EDC Systems

Education

Bachelor's degree or Nursing degree

Tools

CTMS

EDC

MS Office

Job description

Worldwide Clinical Trials in the United States is seeking a seasoned Clinical Research Associate to support site activities across multiple therapeutic areas, with emphasis on site management, regulatory submissions, and TMF processes.

The ideal candidate has 5+ years of CRA experience, a 4-year degree or nursing degree, and will reside in the Midwest. Willingness to travel regionally and collaborate with cross-functional teams is required.