Catalyst Clinical Research · 3 days ago
Senior Statistical Programmer
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Pharmaceutical
H1B Sponsor Likely
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Responsibilities
Creation of safety and efficacy SAS datasets.
Creation of SDTM specifications.
Creation of project specific macros and formats.
Performing data checks as needed, to ensure integrity and correctness of data displays and to understand structure and content of data.
Perform QC/validation of datasets, tables, listings, figures to verify the output.
Establish, maintain, and strengthen professional working relationships with clients, potential clients, regulatory agencies, collaborating staff, vendor, and subcontract personnel.
Represent department and company in a multi-disciplinary setting, including project team meetings, client meetings/presentations.
Ensure the quality and integrity of data analysis and reporting.
Maintain awareness of project budgets and tasks, and effectively communicate the status of such tasks to management.
Contribute to the development of functional-level standards, tools, and templates.
Interact across operational areas as required.
Interact with sponsor representatives as required.
Qualification
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Required
Bachelor’s Degree in Computer Science/Mathematics or equivalent
A minimum of 5 years SAS programming experience
Hands on Experience with CDISC/SDTM/ADaM Programming including but not limited to SAS: Data Step Manipulation, Merge, Sort, Transpose, Reporting (Proc Report), Comparison (Proc Compare), Error Checking (Log resolution), modeling, missing data handling approaches/procedures, figure development
Experience developing custom SAS programs
Experience with P21 reporting and DEFINE, SDRG, ADRG development
Creation of annotated CRFs
Previous experience in pharmaceutical research or CRO setting
Proficient with Microsoft Office Suite
Excellent written and oral communication skills
Excellent presentation skills
Strong organizational, problem-solving, and analytical skills
Ability to manage priorities and workflow for self and study teams
Ability to track, report, and escalate as needed on study level financials and resourcing needs
Ability to work on a SAS server environment using windows based PC SAS
Versatility, flexibility, and a willingness to work within constantly changing priorities
Proven ability to handle multiple projects and meet deadlines
Strong interpersonal skills
Ability to deal effectively with a diversity of individuals at all organizational levels
Commitment to excellence and high standards
Creative, flexible, and innovative team player
Ability to work independently and as a member of various teams and committees
Good judgement with the ability to make timely and sound decisions
Ability to be discreet with sensitive company information
Ability to travel for meetings or training activities may be required
Preferred
Master’s Degree preferred
Base or Advance SAS certification preferred
Company
Catalyst Clinical Research
Catalyst Clinical Research is a provider of clinical operation solutions to the biotechnology, pharmaceutical and medical device companies.
H1B Sponsorship
Catalyst Clinical Research has a track record of offering H1B sponsorships. Please note that this does not
guarantee sponsorship for this specific role. Below presents additional info for your
reference. (Data Powered by US Department of Labor)
Distribution of Different Job Fields Receiving Sponsorship
Represents job field similar to this job
Trends of Total Sponsorships
2022 (1)
2021 (1)
2020 (3)
Funding
Current Stage
Late StageTotal Funding
unknown2018-11-01Acquired
Recent News
The Hindu BusinessLine
2024-04-08
2024-02-14
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