Clinical Research Associate II - Cardio - East Coast/Central (Remote)

Worldwide Clinical Trials•Carolina, NC

1d•Remote

About The Position

Worldwide Clinical Trials is a global, midsize CRO that focuses on innovative and creative approaches to developing cures for diseases. We are looking for individuals who are passionate about improving lives and contributing to scientific breakthroughs. Our Clinical Operations team works on diverse therapeutic areas, including Cardiovascular, Metabolic, Neuroscience, Oncology, and Rare Diseases. We foster a supportive, collaborative, and inclusive environment where professionals can thrive and develop their careers. As a Clinical Research Associate (CRA), you will play a crucial role in managing research activities at participating sites, contributing to all stages of clinical studies, from site identification and start-up to data collection, safety monitoring, and study close-out. We provide extensive support through regulatory submissions, TMF management, and in-house CRAs, along 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 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.
2+ years of experience as a Clinical Research Associate.
4-year university degree OR Nursing Degree.
Experience in Cardiology or Hypertension 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).
Ensuring compliance with obtaining informed consent, reporting potential safety-related events, and adhering to all applicable regulatory requirements, primarily through remote efforts.