Senior Clinical Research Associate - Oncology - Southeast/Mid-Atlantic (Remote)
About The Position
Worldwide Clinical Trials is a global, midsize CRO that is dedicated to changing the way the world experiences CROs by taking pioneering, creative approaches to developing cures for 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. At Worldwide, we believe everyone plays an important role in making a world of difference for patients and their caregivers. We are committed to enabling professionals from all backgrounds and experiences to succeed in a diverse and inclusive environment that promotes collaboration and creativity. 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 Oncology is required.
- Candidates must reside in the Southeastern or Mid-Atlantic United States.
- Willingness to travel regionally required.
Responsibilities
- Managing the research activities at sites participating in Worldwide’s clinical research projects.
- Identifying potential sites to participate in the research effort.
- Performing study start-up activities such as working with sites to collect appropriate regulatory documents and supporting the negotiation of contracts and budgets.
- Training sites to collect data properly and report any potential safety-related events.
- Managing the site's activities during study maintenance.
- Closing down research activities at the sites once the study has concluded.
- Conducting 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 site management efforts.
Benefits
- Competitive benefits package depending on location.
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What This Job Offers
Job Type
Full-time
Career Level
Senior
