Senior Clinical Research Associate - Oncology - Northern Midwest (Remote)
About The Position
Worldwide Clinical Trials is a global, midsize CRO that is committed to changing the way the world experiences CROs by taking pioneering, creative approaches to cure the world’s most 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 for patients and their caregivers. We prioritize cultivating a diverse and inclusive environment that promotes collaboration and creativity, offering a supportive and team-oriented environment where professionals can thrive and do their best work. The Clinical Operations team at Worldwide Clinical Trials offers a rewarding journey where contributions have a profound impact on patients' lives. CRAs 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. 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 Line Managers, 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.
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 North Midwestern United States - Ohio, Michigan, Kentucky.
- 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, with most site management efforts performed remotely.
Benefits
- Competitive benefits package depending on location.
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What This Job Offers
Job Type
Full-time
Career Level
Senior
