Senior to Manager Biostatistics (depending on experience)
Job Location: N/A
Pharmaceutical / Biotechnology - South Jersey
Provide statistical input into the design of clinical trials applying statistical designs and methodology needed to meet the overall objective and regulatory requirements. Prepare input to protocols and statistical analysis plans. Ascertain that the clinical data are appropriately analyzed and reported. Provide statistical support for integrated reports and submissions preparation. Contribute to Clinical Development Plans. Support preparation of manuscripts. Work closely with different departments within the company. Interact and co-ordinate activities with CROs and consultants. Represent the company on statistical matters in meetings with regulatory authorities, key opinion leaders and similar experts. Quality control of statistical deliverables.
PhD in a statistical discipline with 3-4 years pharmaceutical experience or MS and 5-7 years. Thorough understanding of statistical issues. At least 5 years of industry experience in statistical analysis in a clinically related subject. Experience in the areas of Oncology a must. Strong knowledge in SAS programming. Good oral and written English communication skills are mandatory.
Please contact Darren Gutowski at firstname.lastname@example.org
125-160K+15% target bonus and stock
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