Associate Director, Statistical Programming - Oncology
Eisai (digital)
Woodcliff Lake, New Jersey 07675

Job Description


The Associate Director, Statistical Programming serves the critical role for providing lead and oversight to programming team/activities. Assist in managing liaisons across the company, with external alliances, vendors, and with regulatory agencies. The position will also be responsible for providing input into submission strategies and will support process and infrastructural improvement, resource and cost management for multiple oncology clinical studies/programs.

Assist in managing collaborations with external alliances for all programming related activities.

Ensure successful and effective coordination and communications

Manages, reviews and / or executes statistical programming deliverables for planned statistical analysis, related to study monitoring, clinical study reports, data integrations and regulatory query responses, covering multiple compounds and studies

Leads global submission activities including cross company projects.

Acts as a programming functional and technical expert to support submission strategy planning, regulatory communication

Sets and leads key business objectives or projects within the department; Leads development and updating company policies/SOPs; Recommends enhancements for improvement

Manages and leads development and enhancement towards standardization and process for consistency, efficiency and accuracy

Supports computer infrastructure improvement with data integrity by working with internal resources and external

Participates in recruitment activities; Supports planning
and directing work between internal resources and external vendors

Manages CROs and contractors with regarding the
compliance, deliverable qualities, timelines and budgets


Job Qualifications

Minimum of a Master degree in Biostatistics (preferred), Statistics, computer science, or related discipline. Bachelor degree with extensive experience might also be considered.

At least 10 years relevant experience in the pharmaceutical industry/CRO environment with people and project management experience.

Highly experienced in clinical development statistical programming methods and processes in industry setting required.

Regulatory submission experiences in the area of Oncology indications. Have lead programming activities involving CDISC SDTM, ADaM, eSub.

Experience with CRO oversight.

Strong organizational skills with ability to effectively manage multiple studies/projects.

Excellent technical writing and verbal communication skills JOB REQUIREMENTS: <img height=1 width=1 border=0 src= /> To apply for this position, please copy and paste the following link into your browser address bar:

Date Posted : 01/16/2020