Senior Clinical Research Associate – Psychiatry

This is a fully remote position, open to applicants in Michigan, +1 more state.

📋 Description

• Oversee research operations at sites involved in Worldwide’s clinical research initiatives.

• Identify and evaluate potential sites for participation in research activities.

• Execute study startup processes, which include gathering regulatory documentation and assisting in contract and budget discussions.

• Provide training to sites on accurate data collection and reporting of any safety-related incidents.

• Supervise site operations throughout the study's duration.

• Conclude research activities at sites following the completion of the study.

• Carry out study initiation visits (SIVs).

• Ensure adherence to informed consent protocols, safety event reporting, and relevant regulatory standards.

⛳️ Requirements

• Exceptional interpersonal, verbal, and written communication abilities in English.

• Outstanding organizational skills with a keen eye for detail.

• Capability to operate independently with minimal supervision.

• Proficient in Microsoft Office, CTMS, and EDC Systems.

• A minimum of 5 years of experience as a Clinical Research Associate.

• Bachelor’s degree or Nursing degree required.

• Experience in Psychiatry is mandatory.

• Familiarity with General Anxiety Disorder (GAD) is an advantage.

• Candidates must be residents of the Midwestern United States.

• Willingness to travel regionally is essential.

🏝️ Benefits

• Comprehensive support for regulatory submissions, TMF management, and in-house CRAs for projects with significant site management demands.

• Regular check-ins and coaching sessions with the Line Manager.

• Defined career trajectory and development opportunities leading to Clinical Trial Manager positions.

• Access to the Executive Leadership team.

• Competitive benefits package tailored to location.