Senior Clinical Research Associate - Psychiatry - Midwest

Worldwide Clinical Trials•Virtual United States Ohio, MI

10d•$97,000 - $193,000•Remote

About The Position

Worldwide Clinical Trials is a global, midsize CRO that focuses on innovation and quality to find cures for persistent diseases. We are a team of over 3,500+ experts dedicated to changing the way the world experiences CROs. Our mission is to improve lives through passionate and purposeful work. We are committed to fostering a diverse and inclusive environment where professionals from all backgrounds can succeed and thrive. In Clinical Operations, CRAs contribute to advancing clinical research and impacting patients' lives. We offer support through regulatory submissions, TMF management, and in-house CRAs. Professional development is a priority, with regular coaching and a clear career path towards Clinical Trial Manager roles. Our accessible Executive Leadership team is dedicated to advancing science and overcoming obstacles.

Requirements

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.
5+ years of experience as a Clinical Research Associate.
4-year university degree OR Nursing Degree.
Experience in Psychiatry required.
Candidates must reside in the Midwestern United States.
Willingness to travel regionally required.

Nice To Haves

General Anxiety Disorder (GAD) experience a plus.

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).
Ensure compliance with obtaining informed consent, reporting potential safety-related events, and adhering to all applicable regulatory requirements, with most site management efforts performed remotely.