
Research Professional
5 days ago
As a highly skilled Research Assistant, you will play a pivotal role in the coordination and delivery of clinical trials. Your expertise will be invaluable in ensuring the success of these projects.
You will maintain accurate and compliant clinical trial documentation, including Investigator Site Files and essential records in accordance with Good Clinical Practice (GCP). This will involve supporting trial investigators with documentation reviews and sign-offs, ensuring timely and accurate data collection.
About this OpportunityThis is a full-time, 12-month contract role that provides a unique opportunity to gain diverse, real-world research experience in oncology. You will be part of a forward-thinking research team, with access to the resources and career pathways that only a large, integrated organisation can offer.
Your Responsibilities- Support the coordination and administration of oncology and haematology clinical trials across multiple phases.
- Maintain accurate and compliant clinical trial documentation.
- Assist trial investigators with documentation reviews and sign-offs.
- Support remote and on-site monitoring visits by study sponsors and CROs.
We are looking for someone passionate about Clinical Research with a keen interest in the field of Oncology & Clinical Research. Relevant undergraduate degree and excellent written, verbal and interpersonal skills are required.
Key Requirements- Relevant undergraduate degree.
- Excellent written, verbal and interpersonal skills.
- Proficient in MS Office suite and database management.
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