Senior Clinical Research Associate – Oncology Experience Essential
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Job Description
Senior Clinical Research Associate ensuring site compliance and data integrity in oncology studies. Collaborating with site managers and conducting remote monitoring as required in the UK.
Responsibilities:
- Responsible for data integrity, data quality and ensuring compliance with ICH GCP and local requirements
- Monitoring will be conducted in line with the Study Monitoring Plan (SMP)
- Collaborate with the Site Manager to assure that the site complies with the protocol and is inspection ready
- Conduct monitoring activities using different methods, both on site and remote
- Conducts source document review and verification of appropriate site source documents and medical records
Requirements:
- Recent oncology experience is essential
- Networking and relationship building skills
- Ability to communicate effectively and appropriately with internal and external stakeholders
- Ability to adapt to changing technologies and processes
- Excellent communication (verbal and written), presentation, and interpersonal skills
- Advanced level or fluency in English is required
- Bachelor's degree or Registered Nurse (RN) in a related field or equivalent combination of education, training, and experience
Benefits:
- Competitive salary
- Flexible working hours
- Professional development budget
- Home office setup allowance
- Global team events
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