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.
Minimum Bachelors/ Master in statistics
For more information, Please contact
Akriti Gupta
(973) 967-3409
Morristown, NJ 07960
Job details are sourced from the employer's original posting.
Open job postingAbout the company
Artech is an employer-of-choice for the last 25 years to over 7,500 consultants across the globe. We recruit top-notch talent for over 70 Fortune and Government clients coast-to-coast across the U.S., India, and China. We are #1 Largest Women-Owned IT Staffing Firm in the US and this may be your opportunity to join us! For more check: www.artechinfo.com