{bc}
Apply
oracle

Senior Statistical Programmer FSP

Cytel
IND
Full-time
Senior · 8+ years experience
Onsite
Discovered 1 weeks ago
sas

Full Job Posting

Qualifications

  • Here at Cytel we want our employees to succeed and we enable this success through consistent training, development and support. To be successful in this position you will have:
  • Bachelor’s degree in one of the following fields Statistics, Computer Science, Mathematics, etc.
  • At least 8 years of SAS programming working with clinical trial data in the Pharmaceutical & Biotech industry with a bachelor’s degree or equivalent. At least 6 years of related experience with a master’s degree or above.
  • Study lead experience, preferably juggling multiple projects simultaneously preferred.
  • Strong SAS data manipulation, analysis and reporting skills.
  • Solid experience implementing the latest CDISC SDTM / ADaM standards.
  • Strong QC / validation skills.
  • Good ad-hoc reporting skills.
  • Proficiency in Efficacy analysis.
  • Familiarity with drug development life cycle and experience with the manipulation, analysis and reporting of clinical trials’ data.
  • Submissions experience utilizing define.xml and other submission documents.
  • Experience supporting immunology, respiratory or oncology studies would be a plus.
  • Excellent analytical & troubleshooting skills.
  • Ability to provide quality output and deliverables, in adherence with challenging timelines.
  • Ability to work effectively and successfully in a globally dispersed team environment with cross-cultural partners.

Responsibilities

  • How you will contribute:
  • Performing data manipulation, analysis and reporting of clinical trial data, both safety and efficacy (ISS/ISE), utilizing SAS programming
  • Generating and validating SDTM and ADaM datasets/analysis files, and tables, listings, and figures (TLFs)
  • Production and QC / validation programming
  • Generating complex ad-hoc reports utilizing raw data
  • Applying strong understanding/experience of Efficacy analysis
  • Creating and reviewing submission documents and eCRTs
  • Communicating with and/or responding to internal cross-functional teams and client for project specifications, status, issues or inquiries
  • Performing lead duties when called upon
  • Serving as team player, with a willingness to go the extra distance to get results, meet deadlines, etc.
  • Being adaptable and flexible when priorities change

Preferred Qualifications

  • Study lead experience, preferably juggling multiple projects simultaneously preferred.
  • Experience supporting immunology, respiratory or oncology studies would be a plus.

Apply for this job in 1 click

Skip the repetitive application forms

Install the Base Career Chrome Extension and autofill job applications across major job boards with your profile.

Sarah M.James T.Maya R.

Trusted by over 500,000 job seekers on Base Career

Start Free Today

More from this employer

More jobs at Cytel

Director, Biostatistics FSP

, USA

Discovered 2 days agoFull-time

Clinical Data Manager II- QC Specialist

, IND

Discovered 2 days agoFull-time

Senior Statistical Programmer FSP-Hybrid 3 days a week in PA a must

, USA

Discovered 3 days agoFull-time

Senior Statistical Programmer FSP

, GBR

Discovered 3 days agoFull-time

Principal Statistical Programmer FSP

, IND

Discovered 1 weeks agoFull-time

Principal Biostatistician FSP

, USA

Discovered 1 weeks agoFull-time

Manager - Global Accounts Payable and Employee Expenses

Pune, IND

Discovered 1 weeks agoFull-time

Senior Director, HR Business Partner

, USA

Discovered 2 weeks agoFull-time