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Senior Biostatistician

Covance 10/22/2018 4:45:47 PM
JOB ID: 24713 Category: Biostatistics Programming
Chicago, Illinois



Job Overview

Senior Biostatistician

*These remote opportunities can be done from anywhere in the U.S. or Canada

Are you ready to discover your extraordinary potential at Covance? A career here provides the unique chance to create a lasting impact and difference in patients' lives. Joining our team will offer you a rewarding career, an opportunity to work in a high-energy, innovative & collaborative work place, along with access to comprehensive benefits. Your work is meaningful, and the results are lasting. With the support of exceptional people from across the globe and an energized purpose, you'll be empowered to own your career journey with mentoring, training and personalized development planning. Our mission is to help our clients bring the miracles of medicine to market sooner -- join us for your next career move.

We are seeking Senior Biostatisticians to lead large global or other major projects, analyze all parts of any clinical study, and provide planning on multiple clinical studies from multiple clients including tracking project activities and project time management. The selected candidate will provide statistical input into other disciplines' activities and participate in interdepartmental processes; provide technical solutions and advice to staff and clients on statistical processes; supervise and train less Experience d biostatisticians within project activities; and be responsible for the development of Statistical Analysis Plans including statistical methodology, statistical programming procedures, definition of derived variables, and data handling rules and mockups.

Additional responsibilities include:

* Ensure mechanisms in place to maintain flow of appropriate information between disciplines on project team.
* Responsible for development of Statistical Analysis Plans, to include statistical methodology, statistical programming procedures, definition of derived variables, data-handling rules and mockups.
* Responsible for Biostatistics deliverables within assigned projects.
* Develop and coordinate QC procedures for Biostatistics deliverables, ensuring activities are appropriate for effectively and efficiently delivering quality output within specific project.
* Statistical analysis of clinical trial data and related decision-making.
* Responsible for statistical input to statistical reports and Clinical Study Reports. Authorizes final reports as one of Covance signatories.
* Provide statistical guidance in development of clinical research program and in design of individual studies as part of multi-disciplinary team; responsible for statistical input to protocol; approves protocol as signatory.
* Provide statistical input into design/review of format of CRFs.
* Prepare randomization specifications; generate schedules; verify randomization components (specification and schedule). Provide input into planning activities related to the preparation of, distribution of and access to randomization and unblinding information.
* Determine documentation requirements for Biostatistics aspects of projects. Give guidance to support business and regulatory requirements including definition of appropriate documentation, storage/communication media, and retention/return of documents at study close-out.
* Independent peer review of statistical deliverables, e.g., protocols, Statistical Analysis Plans, Tables, Figures and Patient Data Listings, statistical reports, Clinical Study Reports.
* SAS programming and related activities for the presentation and analysis of clinical trial data.
* Contribute to review and amendment of departmental processes and supporting documentation.
* Project management activities for identified projects including financial, resource planning and utilization, timelines and milestone management.
* Contact with client across multiple disciplines.
* Contribute to proposal activities and client presentations.
* Represent the department during audits.
* Carry out all activities according to appropriate Covance SOPs, working within the framework of the Quality Management System and to GCP.
* Perform other duties as requested by management.


* MA or MS in statistics subject, preferably with a strong medical statistics component.
* 3 to 5 years of postgraduate Experience in the application of statistics to clinical trials for
employees with a PhD in statistics subject; 5 to 8 years of postgraduate Experience in the application of statistics to clinical trials for employees with an MA/MS in statistics subject


* Interpersonal and effective communication skills; cooperative, team-oriented and proactive
* Self-motivation and able to motivate others.
* The ability to work to tight deadlines while maintaining high standards.
* SAS proficiency including use of a variety of statistical procedures, e.g., nonparametric analysis, linear and non-linear models, categorical data and survival analysis, SAS Macro language.
* Ability to adhere to strict guidelines and codes of practice.
* A good knowledge of the overall Clinical Trial process and of its application within Covance Clinical Development.
* Competence in the preparation of Statistical Analysis Plans, analysis, reporting, etc., across a variety of trials.
* Ability to explain statistical concepts to non-statisticians.
* Supervisory, project management and organizational skills.
* A proactive approach to management of day-to-day activities and actions that may affect Covance as a business.
* A professional approach at all times.

Position Type: Full-Time

Location: Chicago, IL - Illinois


Covance Recruiting Process

Below is a general Overview of Our Recruiting Process

If you’d like to work for us, please submit your resume/CV online. If your ability to use or access our electronic application is limited due to a disability, please visit or call 1-800-978-4473 for help.

We consider applications from everyone who is interested in a position with us and who meets the required criteria and qualifications.

If your application is selected, someone from our recruiting team will contact you to arrange an initial screen. We may carry this out over the phone or at a face-to-face meeting. You must complete the screen to be considered for the position.

Based on the results of the initial screen, we may invite you to an interview. One of our recruiting team members will contact you to arrange this. The process may involve several interviews, initially over the phone, and then face-to-face with different members of the hiring team.

Our interviews follow a behavioral-based format. This means we’ll ask you to give us information that’s specific to your professional and educational experiences.

Hiring team members will share and discuss their input and then make their decision.

If you’re the person who best meets the requirements of the position, a member of the hiring team will get in touch to make you an offer of employment. Covance is an eVerify employer (United States only).