Req 1): SAS Analyst / Clinical Trials Specialist
Skills: 1. Provides/lead primary statistical input for clinical study design. 2. Provides/lead analysis planning for clinical studies. 3. Provides/lead statistical input to clinical study reports. 4. Provides statistical support to other disciplines related to clinical statistics. OTHER RESPONSIBILITIES / DETAILED DUTIES: 1. Works with team on protocol design and writes statistics section of protocols. 2. Writes analytical plan and leads detailed analysis planning; participates in other trial setup activities. 3. Analyzes and interprets data; writes statistical methods section for clinical study reports. 4. Assists in clinical development planning for new drug indications. 5. Provides statistical consulting and support to other disciplines related to clinical statistics. 6. Ensures compliance with department SOPs and regulatory guidance. Location: NJ Duration: 12+ months ---------------------------------------------------- Please provide me resume, rate and contact # asap. -- Kind Regards, Haresh Patel cyberThink, Inc. -- You received this message because you are subscribed to the Google Groups "it req" group. To post to this group, send email to [email protected]. For more options, visit this group at http://groups.google.com/group/it-req?hl=.
