Senior Clinical Research Associate - Oncology - Northeast/Midwest (Remote)

Worldwide Clinical Trials•Virtual United States Ohio, MI

5d•$97,000 - $193,000•Remote

About The Position

We are Worldwide Clinical Trials, a global, midsize CRO that pushes boundaries and innovates to find cures for persistent diseases. Our mission is to work with passion and purpose every day to improve lives. We are looking for individuals who value this pursuit and want to make a difference. In Clinical Operations, your contributions will profoundly impact patients' lives. You will work alongside brilliant minds across diverse therapeutic areas, including Cardiovascular, Metabolic, Neuroscience, Oncology, and Rare Diseases. Collaboration is ingrained in our culture, and we foster a supportive, team-oriented environment. We offer extensive support through regulatory submissions, TMF management, and in-house CRAs for projects with heavy site management needs. Professional development is a top priority, with regular touchpoints and coaching conversations with your Line Manager. We offer a clear career path and development opportunities that can lead to Clinical Trial Manager roles. Our accessible Executive Leadership team is committed to advancing science and overcoming obstacles to improve patients' lives. Experience a world of difference with us!

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 Oncology is required.
Candidates must reside in the Northeast or Midwest United States (Michigan, Ohio, New York, Pennsylvania ideal).
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.