Job details
Salary $60 - $65 an hour job type contract
Qualifications
Microsoft sql server: 3 years (preferred)
Full job description
Senior sas clinical trials programmer - remote role.
We are seeking an outstanding senior sas clinical trials programmer to join our teamYou will provide analytical services in support of customer’s clinical research studies and fdaOur team also puts a high value on work-life balanceStriking a healthy balance between your personal and professional life is crucial to your happiness and success here.
Description and responsibilities
Seeking a senior sas clinical trials programmer to work with our client, a
Clinical research organization clientConsultant will provide programming/analytical support utilizing sas as the primary programming language to create and manage the production of analysis reports, summary tables/listings and graphs for clinical trials submitted to various regulatory bodies worldwide.
The consultant must have excellent communication skills and must be able to communicate about the techniques developed and results of analysis both to executives and other analysts in the organization.
Qualifications – essential
Bachelor’s degree or equivalent, preferably in a scientific discipline such as statistics, computer science, mathematics, etcHealthcare or technology related field.
6+ years of sas programming experience working with clinical trials data in the pharmaceutical & biotech industry.
Sas certifications (base, advanced, etc.) are highly desiredBe proficient in base sas programming (data step), sql programming (i.e., use of sql pass-through or proc sql), as well as the sas macro language for use in making code more efficient.
Familiarity with programming to generate summary statistics (mean, median, etc.) and complex statistical methods (i.e., sas glm, logistic regression, and survival analysis).
Cdisc data models a necessity, especially sdtm then adam
Cdisc knowledge
Sdtm and adam dataset experience
Good written and spoken communications skills in english and thought-leadership skills.
Major responsibilties/activities:
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).
Develop sas programs and generate complete, accurate and validated statistical tlgs in
Well-defined formats.
Program sdtm and adam datasets according to the dataset specifications.
Create sdtm annotated patient case report forms.
Perform data conversion between datasets with two different formats according to
Conversion requirements/specifications, e.g., converting from excel data records to sas
Datasets, non-cdisc compliant datasets to cdisc compliant datasets.
Manage electronic data transfers from trial sponsors or other external clinical trial data
Vendors, such as central laboratories or other specialty laboratories.
Document data and programming information in accordance with corporate governing
Documents (policies, sops, or work instructions).
Archive clinical trial data (raw data, sdtm, and adam datasets) and programming
Documentation in accordance with corporate governing documents and/or clinical trial
Sponsor`s specific requirements.
Write sas programs to produce tables, listings, and graphs for ad hoc requests, annual progress reports, integrated summaries, publications and other clinical research reports.
Collaborate with biostatisticians, clinical research associates, medical writers, regulatory affairs and clinical data management teams to gather specifications for informative tables, listings and graphs.
Build sas data sets from various data sources which meet provided specifications.
Execute edit/logic checks to assist in data cleaning.
Maintain and execute programs for the evaluation and validation of incoming clinical data.
Perform validation of the analysis data sets, tables, listings and graphs.
Utilize macro libraries and complex data step techniques to standardize programming.
Maintain and enhance existing programs for clinical studies.
Gather and analyze programming requirements to develop clinical trial reporting systems.
Maintain detailed design specifications.
Ensure that programs and reports follow departmental/company standard operating procedures.
Assist in the development of departmental systems and generate/maintain systems documentation.
Participate in the preparation of clinical and statistical summary reports
Technex llc., is an equal opportunity employerTechnex, doesn`t not discriminate against any employee or applicant because of race, creed, color, religion, gender, sexual orientation, disability or any other basis protected by lawEmployment is based solely on a person`s merit and qualifications directly related to professional competence
Job type: contract
Pay: $60.00 - $65.00 per hour
Schedule:
8 hour shift
Experience:
Sas clinical: 6 years (required)
Sas macro: 6 years (required)
Microsoft sql server: 3 years (preferred)
Work location: remote
Hiring insights
Hiring 2 candidates for this role
Job activity
Employer reviewed job 1 day ago
Posted 14 days ago
