Clinical Research Associate – Neurology, Oncology
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Job Description
Clinical Research Associate managing neurology and oncology trial sites for Worldwide Clinical Trials, a global CRO. Conducting monitoring, compliance, safety, and data-quality activities remotely in Bulgaria.
Responsibilities:
- Conduct site qualification, initiation, interim monitoring, site management, and study close-out visits
- Provide mentoring and guidance to less experienced CRAs and site staff when needed
- Document site visit findings via written reports
- Assess, monitor, and train study site staff on protocol adherence as required
- Review study subject safety information and informed consent
- Conduct source document verification for compliance, patient safety, and veracity of data
- Review CRFs using paper or electronic data capture systems and assist sites with data query resolution
- Provide applicable updates for site-related documentation for filing in the Trial Master File (TMF)
- Ensure site compliance with IP receipt, accountability, and return or destruction
- Conduct accompanied site visits for assessment or training of other CRAs as requested and appropriate
- Collaborate with colleagues across diverse therapeutic areas and specialties to advance clinical research
Requirements:
- Excellent interpersonal, oral, and written communication skills in English
- Superior organizational skills with attention to details
- 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 RN/BSN in Nursing
- Experience in Neurology and Oncology is required
- Willingness to travel required
Benefits:
- Supportive and team-oriented work environment
- Extensive support through regulatory submissions, TMF management, and in-house CRAs for projects with heavy site management needs
- Diverse and inclusive workplace
- Equal employment opportunities
- Exceptional employee experiences
- Access to equal opportunity
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