***URGENT OPENINGS FOR A PHARMA MAJOR IN PA. Kindly reply ASAP***

Clinical Research Scientist (10 positions)

Our client, a major pharmaceutical company in PA has multiple requirements for Clinical
Research Scientist.

Duration: 3+ months

Drafts protocols, reviews data in CDRS, process and reviews AE�s and SAE's, participates in
writing study reports
 
Complete Description: 
- AE/SAE reconciliation
- compile the Integrated Data Review Plan
- identify and communicate database errors with CDM
- manage central labs
- Manage telephone contact documentation
- Handle inbound communications -- clinical / scientific
- prepare and revise study manuals (eg. SRM)
- preparing Confidentiality Disclosure Agreements
- Respond to scientific questions on clinical execution
- Review and Analyze Laboratory Data
- Review scientific data for content and perform exploratory data analyses
- review site specific ICFs and HIPAAs
- Telephone communications with labs
- Telephone communications with sites
- write narratives rite 
- write protocols and amendments

Medical data review (not data management or data entry) and patient narrative writing