Senior Clinical Research Associate – Oncology Experience Preferred
Parexel
full-time
Posted on:
Location Type: Remote
Location: United Kingdom
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Job Level
Tech Stack
About the role
- Responsible for data integrity, data quality and ensuring compliance with ICH GCP and local requirements at the site level.
- Monitoring will be conducted in line with the Study Monitoring Plan (SMP) and will be performed virtually for the majority of activities to supplement on site visit requirements.
- Collaborate with the Site Manager to assure that the site complies with the protocol and is inspection ready.
- Conduct monitoring activities using different methods, e.g., both on site and remote, where allowed by country regulations.
- Maintains a working knowledge of ICH/GCP Guidelines or other applicable guidance, relevant regulations, and company Standard Operating Procedures (SOPs)/processes.
Requirements
- Oncology experience preferred
- Bachelor’s degree or Registered Nurse (RN) in a related field or equivalent combination of education, training, and experience.
- Advanced level or fluency in English is required.
Benefits
- Flexible working arrangements
Applicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard Skills & Tools
data integritydata qualitymonitoring activitiesICH GCPStudy Monitoring PlancomplianceStandard Operating Procedures
Soft Skills
collaborationcommunication
Certifications
Bachelor’s degreeRegistered Nurse (RN)