Senior Clinical Research Associate - Psychiatry - East Coast (Remote)

Worldwide Clinical Trials•Carolina, NC

2d•Remote

About The Position

Worldwide Clinical Trials is a global, midsize CRO that is dedicated to pushing boundaries and innovating to find cures for persistent diseases. We are a global team of over 3,500+ experts committed to changing the way the world experiences CROs. Our mission is to work with passion and purpose every day to improve lives. Within Clinical Operations, your contributions will leave a profound impact on the lives of patients. As a Clinical Research Associate (CRA) at Worldwide, you will work alongside brilliant minds across diverse therapeutic areas, including Cardiovascular, Metabolic, Neuroscience, Oncology, and Rare Diseases. Collaboration with top-tier colleagues is ingrained in our culture. Our commitment to advancing clinical research is nurtured within a supportive and team-oriented environment. In a CRA role, you'll receive extensive support through regulatory submissions, TMF management, and in-house CRAs for projects with heavy site management needs. Through regular touchpoints and coaching conversations with your Line Manager, we ensure that your professional development remains a top priority. We offer a clear career path and development that can lead to Clinical Trial Manager roles. Our accessible Executive Leadership team is committed to advancing science and surmounting obstacles to make a difference in the lives of patients. We offer an unparalleled experience where you can drive remarkable scientific breakthroughs and be at the very 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
5+ years of experience as a Clinical Research Associate
4-year university degree OR Nursing Degree
Experience in Psychiatry required
Candidates must reside on the East Coast
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, 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.