Senior Psychiatry Clinical Research Associate: Site Leader

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

Job summary

Worldwide Clinical Trials in the United States seeks a Clinical Research Associate with 5+ years of CRA experience. You will monitor sites, ensure regulatory compliance, and support TMF management across therapeutic areas.

Candidates must reside in the Central United States, hold a 4-year degree or nursing degree, and be willing to travel regionally; strong English communication and MS Office/CTMS/EDC proficiency are essential.

Qualifications

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

Responsibilities

• Responsible for managing the research activities at sites participating in Worldwide’s clinical research projects.
• Typically involved in all stages of the clinical study, including identifying potential sites to participate in the research effort, performing various study start‑up activities such as working with sites to collect appropriate regulatory documents and supporting the negotiation of contracts and budgets, training the sites to collect data properly and report any potential safety‑related events, managing the site's activities during study maintenance, and closing down research activities at the sites once the study has concluded.
• Conduct study initiation visits (SIVs)
• While most of the site management efforts will be performed remotely, you will be required to ensure compliance with obtaining informed consent, reporting potential safety‑related events, and adhering to all applicable regulatory requirements

Skills

Communication skills

English proficiency

Organizational skills

Independence

Education

Bachelor's or Nursing degree

Tools

MS Office

CTMS

EDC Systems

Job description

Worldwide Clinical Trials in the United States seeks a Clinical Research Associate with 5+ years of CRA experience. You will monitor sites, ensure regulatory compliance, and support TMF management across therapeutic areas.

Candidates must reside in the Central United States, hold a 4-year degree or nursing degree, and be willing to travel regionally; strong English communication and MS Office/CTMS/EDC proficiency are essential.