Description
Responsibilities will include, but are not limited to, the following:-Work under the direction of Medical Affairs Statistics Disease Lead atively provide statistical support to the Medical Affairs Department.
-Provide statistical support for publications, presentations, posters at medical meetings and any other requests not covered in the clinical study report. Interact with authors, referees and in-house reviewers in the preparation of publications, presentation
-Provide statistical reviews of proposed design and analysis of protocols for investigator initiated trials.
-Provide statistical input for design, sample size and protocol for Medical Affairs studies.
-Provide review of statistical analysis plan including table shells, analysis dataset specifications and all deliverables for Medical Affairs studies provided by CRO
Manage outside CROs and consultants as needed.
Skills/Knowledge Required:
*Masters in Statistics with a focus on statistical methods appropriate for clinical trials is essential.
*3-5 years of experience and demonstrated skill in the planning, analysis and reporting of clinical trials.
*Oncology experience is a plus.
*Good planning and project management skills.
*Detailed knowledge of currently acceptable statistical methodologies.
*Excellent SAS skills including report generation. Willingness to be hands-on when needed.
*Knowledge of MS Office products (Word, Excel, PowerPoint)
To find out more about Real please visit www.realstaffing.com