Job details
Salary $110,000 - $130,000 a year job type full-time contract
Qualifications
Bachelor`s (required)
Cdisc standards: 4 years (required)
Sas: 4 years (required)
Benefits pulled from the full job description
401(k) 401(k) matching dental insurance employee assistance program flexible schedule health insurance show 5 more benefits
Full job 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 affairsYou 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.eDefine.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.
Job types: full-time, contract
Salary: $110,000.00 - $130,000.00 per year
Benefits:
401(k)
401(k) matching
Dental insurance
Employee assistance program
Flexible schedule
Health insurance
Life insurance
Paid time off
Professional development assistance
Referral program
Vision insurance
Schedule:
8 hour shift
Supplemental pay:
Bonus pay
Signing bonus
Education:
Bachelor`s (required)
Experience:
Cdisc standards: 4 years (required)
Sas: 4 years (required)
Work location: remote
Hiring insights
On-going need to fill this role
Job activity
Employer reviewed job 3 days ago
Posted 3 days ago
