Description
The successful candidate will be accountable for the overall management of all clinical studies. They must be comfortable for collaborating with other functional teams to coordinate the development and finalisation of key study documents including protocols, case report forms, informed consent documents, study management plans and final clinical study reports.They will be responsible for monitoring studies against defined milestones and timelines to assure that all deliverables are met. Expected to facilitate the development and implementation of remedial activities when necessary. Must be willing to assume monitoring, co-monitoring responsibilities as needed.
Experience with eCRFs and InForm database required.
Key requirements:
- Minimum of 5 years of Study Management required.
- Oncology experience preferred, advanced degree desired (MS/ Nursing Preferred)
- Big Pharma experience and Longevity in work history also preferred.
Location: New Jersey
Duration: 12 Months
Rate: $70-$75 per hour
If you are interested in this opportunity please forward me your most up to date CV ASAP.
To find out more about Real please visit www.realstaffing.com