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Senior Clinical Research Associate (Oncology Experience Required) - UK - FSP - R
UKPosted today
Parexel is a clinical research organization dedicated to improving global health through clinical trials, regulatory, consulting, and market access services. They are seeking a Senior Clinical Research Associate for UK-based sponsor roles, with experience in oncology trials and RECIST criteria.
Location: UK
Responsibilities
- Ensuring regulatory, ICH-GCP and protocol compliance.
- Verifying informed consent process.
- Protecting subject confidentiality and assessing safety and data integrity.
- Conducting monitoring activities both on site and remotely.
- Reviewing source documents and verifying clinical data.
- Managing protocol deviations and follow-up.
- Applying query resolution techniques.
- Performing Investigational Product inventory and reconciliation.
- Verifying IP dispensing and administration.
- Ensuring proper labeling, import, and release of IP.
- Reporting issues and managing follow-up.
- Documenting activities and maintaining records.
- Managing site personnel training and delegation.
- Tracking data and project timelines.
- Reviewing data entry and site logs.
- Follow-up on adverse event reports.
- Checking site facilities and supplies.
- Collaborating with site staff and attending meetings.
Requirements
- Networking and relationship building skills.
- Ability to adapt to new technologies and processes.
- Excellent communication and interpersonal skills.
- Proficiency in local language.
- Fluency in English.
- Bachelor’s degree or RN in a related field or equivalent experience.