Senior Clinical Research Associate - Rare Disease - East Coast/Central (Remote)

Worldwide Clinical Trials•Virtual United States North Carolina, TX

5d•$97,000 - $193,000•Remote

About The Position

Worldwide Clinical Trials is a global, midsize CRO that focuses on innovative and creative approaches to find cures for persistent diseases. We are a team of over 3,500 experts dedicated to improving lives. Our Clinical Operations team works on diverse therapeutic areas including Cardiovascular, Metabolic, Neuroscience, Oncology, and Rare Diseases. We foster a supportive and collaborative environment, offering extensive support for 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 committed to advancing science and overcoming obstacles to improve patient lives.

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 Rare Disease required.
Candidates must reside in the East Coast or Central United States.
Willingness to travel regionally required.

Responsibilities

Managing the research activities at sites participating in Worldwide’s clinical research projects.
Involved in all stages of the clinical study, including identifying potential sites, performing study start-up activities (collecting regulatory documents, supporting contract and budget negotiation), training sites on data collection and safety reporting, managing site activities during study maintenance, and closing down research activities at sites.
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.