Biostatistician III : 4601430

Job Description: Support the Trial Statistician; Write and review statistical sections and other relevant parts of study synopses and protocols. Support study start up activities (including review of Data Handling plan, CRF review, study specific documentation)Develop SAP, program TLFs, preparation for database lock, dry run and CSR activities; support analyses as required for decision making at project level; support analyses and activities during submission and response to HA questions. Ensure timeliness and adequate quality of statistical deliverables. Provide input as required at all meetings and activities related to set up of trials he/she will be assigned to Maintain efficient interfaces with internal and external customers and communicate effectively across line functions.

Skills: At least 5 years experience in pharmaceutical development and clinical research Sound statistical skills and knowledge of clinical trials methodology: experience with analysis planning and reporting of clinical trials Experience using SAS in the analysis and the reporting of pharmaceutical data Working knowledge of database design/structures Expertise with SAS (including SAS macro language)Experience in Oncology therapeutic area would be appreciated Fluent in English, good oral and written communication skills Knowledge and experience in reporting activities for Clinical Pharmacology trials preferred

Education: Minimum Master in statistics No C2C.

Qualifications: Minimum Bachelors/ Master in statistics

Additional Information: For more information, Please contact Akriti Gupta(973) 967-3409 Morristown, NJ 07960

Type: Contract

Function: Research

Experience level: Mid-Senior Level

Industry: Pharmaceuticals