Senior Statistical Programmer Information

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Covance Inc.

Covance, with headquarters in Princeton, New Jersey, is one of the world’s largest and most comprehensive drug development services companies, with annual revenues greater than $2 billion, employees in more than 60 countries, and more than 11,000 employees worldwide. NONCLINICAL DEVELOPMENT(Toxicology, Research Products, Analytical Services) * Managed 443 compound development programs (>250 IND/CTA enabling), with over 100 different sponsors, which led to 41 IND/CTA applications in 2... Read More

Address	210 Carnegie Ctr Princeton, NJ 08540 (609) 452-8550
Website	www.covance.com/
Holding	No Holding Details

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Senior Statistical Programmer

At Covance, your imagination, your dedication, and your drive to find solutions to challenging projects begin on your very first day. Covance is one of the world’s largest and most respected contract research organizations. Our clients are a Who’s Who of the pharmaceutical and biotechnology industry. If you’re looking for a diverse and stimulating work environment, you'll find it at Covance.

We are currently seeking a Senior Statistical Programmer for our Princeton, NJ office!

The role of the Senior Statistical Programmer is to assist in provisional of Statistical Programming service. This individual will develop and review SAS programs and output for the management and reporting of clinical trial data. They will act as Lead Programmer for increasingly complex or multi-protocol projects and to act as a Statistical Programming consultant to clients and internal customers.
Education/Qualifications   •BSc in a computing, life science, mathematical or statistical subject.
•A high computing content is considered to be beneficial; however proven computing skills are most important.
•Alternative academic qualifications or experience are assessed to ensure equivalent background.
Experience   •Approximately 3.5 years experience in provision of programming support for clinical trial management and reporting, or equivalent experience.
•Extensive experience and proven skills in the use of SAS within a clinical trials environment.
•A good understanding of the fundamental principles of programming, program development and review.
•Experience in the preparation and review of Programming Plans, study set-p and review of study specific documents, e.g. CRF and data validation guidelines.
•Extensive experience in the development and review of SAS programs for management and reporting of clinical trail data.

Covance believes that their best-in-class employees deserve first-class benefits. Covance offers an outstanding benefits package including medical & dental insurance, tuition reimbursement, a 401(k) plan with a generous company match, short and long-term disability, and life insurance, all of which are effective on your first day of employment!

At Covance, we help make the miracles of medicine a reality. We offer opportunities to work on diverse, challenging projects with bright, interesting colleagues while building a flexible and rewarding career.
EEO Employer   Covance is committed to diversity in the workplace and is an equal opportunity employer. (M/F/D/V). Your confidentiality and privacy are important to us.

Other Job Information

Vacancy type:	Full Time	Contact Mode:	not provided
Fax:	+1-302-6555049	Contact Name:	not provided
Job Duration:	not provided	Phone:	+1-609-4524440
Email:	not provided