×

Job Details

Click here to become a registered jobseeker.

Principal Statistical Programmer 1

Not Specified, United Kingdom, £ £ - Annual Annual, Permanent

Description:

At Cytel, we work hard to create successful careers with significant professional growth for our employees, as a result of which they work hard to make Cytel successful. Cytel is a place where talent, experience and integrity come together to advance the state of clinical development.

If you think you are the right match for the following opportunity, apply after reading the complete description.
As a Principal Statistical Programmer, you will lead studies and programmers, provide mentorshiop, you will leverage your advanced SAS programming skills and proficiency in CDISC standards (SDTM & ADaM) to support or lead one or more Phase I-IV clinical trials, with a focus on any of the following studies; Immunology, Oncology, Cardiovascular or Medical Affairs. You will report to the Director, Statistical Programming.
Additionally, you will contribute by:
performing data manipulation, analysis and reporting of clinical trial data, both safety and efficacy, utilizing SAS programming;
applying your CDISC know-how and proficiency in SDTM and ADaM, to create and validate datasets/analysis files, tables, listings, and figures ( TLF s);
generating complex ad-hoc reports
preparing and validating submission packages, i.e. define.xml, Reviewers Guide
applying your strong understanding/experience with Efficacy analysis;
preparing submission packages
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
What we're looking for:
Bachelor's degree or equivalent, preferably in a scientific discipline such as Statistics, Computer Science, Mathematics, etc.
Minimum 7 years of SAS programming experience in the Pharmaceutical & Biotech industry.
Familiarity with drug development life cycle and experience with the manipulation, analysis and reporting of clinical trials' data.
Study programming lead experience
Strong SAS data manipulation, analysis and reporting skills.
Ability to implement the latest CDISC SDTM / ADaM standards (production/validation).
Proficiency in SAS MACRO development
Strong ad-hoc reporting
Solid experience in Efficacy analysis
Experience with Pinnacle21
Submissions experience utilizing define.xml and other submission documents.
Experience supporting Medical Affairs, Immunology, Cardiovascular or Oncology strongly desirable.
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.

Cytel Inc. is an Equal Employment / Affirmative Action Employer. Applicants are considered for all positions without regard to race, color, religion, sex, national origin, age, veteran status, disability, sexual orientation, gender identity or expression, or any other characteristics protected by law.
Cytel does not accept referrals from employment businesses and/or employment agencies in respect of the vacancies posted on this site. All employment businesses/agencies are required to contact Cytel's human resources department to obtain prior written authorization before referring any candidates to Cytel. The obtaining of prior written authorization is a condition precedent to any agreement (verbal or written) between the employment business/ agency and Cytel. In the absence of such written authorization being obtained any actions undertaken by the employment business/agency shall be deemed to have been performed without the consent or contractual agreement of Cytel. Cytel shall therefore not be liable for any fees arising from such actions or any fees arising from any referrals by employment businesses/agencies.

Job Details

1592459737
Not Specified
Not Specified, United Kingdom
Permanent
£ £ - Annual Annual