Clinical Research Associate II - Psychiatry - United States (Remote)

Worldwide Clinical Trials•Durham, NC

2d•$79,500 - $158,500•Remote

About The Position

Worldwide Clinical Trials is a global, midsize CRO that focuses on innovative and pioneering approaches to find cures for persistent diseases. We are a team of over 3,500 experts dedicated to improving lives. Our Clinical Operations team offers a rewarding journey where contributions profoundly impact patient lives. As a Clinical Research Associate (CRA) at Worldwide, you will collaborate with brilliant minds across diverse therapeutic areas, including Cardiovascular, Metabolic, Neuroscience, Oncology, and Rare Diseases. Our culture fosters collaboration and creativity within a supportive, team-oriented environment. We provide extensive support for regulatory submissions, TMF management, and in-house CRAs for projects with heavy site management needs. Regular touchpoints and coaching conversations with your Line Manager ensure professional development is a top priority, with a clear career path that can lead to Clinical Trial Manager roles. Our accessible Executive Leadership team is committed to advancing science and overcoming obstacles to improve patient lives. We offer an unparalleled experience where you can drive scientific breakthroughs and be at the core of every successful clinical trial.

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.
2 - 5 years of experience as a regional, traveling Clinical Research Associate.
4-year university degree OR Nursing Degree.
Experience in Psychiatric monitoring is required.
Willingness to travel regionally required.

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.
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, while most site management efforts will be performed remotely.