Description
Role:The Clinical Trial Manager will ensure that clinical study deliverables are planned, executed and well documented in accordance with standard operating procedures (SOPs), regulatory and legal requirements. It is important that you are an experienced and independent Clinical Trial Manager who is professionally and personally capable of spanning across more projects and comfortable in making own decisions in a fast-paced environment across many stakeholders.Essential Functions and Duties:
- Laboratory test site selection and contracting
- Vendor/CRO selection and management
- Ensure monitoring of clinical studies either by way of outsourcing or by own execution
- Create, maintain and oversee trial files
- Prepare, revise and maintain SOPs for the conduct of clinical studies
- May be involved in preparation of study protocols and reports
Requirements:
- Advanced degree preferred, e.g. university degree in pharmaceutical, medical or other relevant biological science
- A minimum of 5 years of Clinical Trial Management experience for diagnostic, medical device or pharmaceutical products
- Experience working in projects as part of project teams as well as a solid understanding of working in a project organization
- Knowledge of pathology and/or oncology is preferred
- Experience in CRO/vendor management and contracting
****This is a small start up company currently waiting to begin Phase 2 trials on the drug.
To find out more about Real please visit www.realstaffing.com