Clinical Data Programmer (SAS)
Princeton, NJ  / Audubon, PA  / Durham, NC  / New York, NY  / Franklin, TN  / Baltimore, MD ...View All
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Posted 21 days ago
Job Description

At Clario, we put people first, always. We are united and driven by patients, committed to making a difference, and we are always looking for the best talent to help us transform lives. We value the contribution each of our people brings. It's only through our people that we can continue to innovate technology that will shape the future of clinical trials. We are investing resources to create an environment our people are proud to be a part of. We want people who know their efforts are valued. This in turn leads to fantastic customer service and allows us to transform patients' lives.

Primary Responsibilities

Provides data to clients (internal and external) in functional format by:

  • Creating and executing SAS edit check programs
  • Validating edit check programs using standard validation practices and processes
  • Creating, validating and executing SAS programs and macros
  • Utilizing SAS programming skills to provide ad-hoc reports (external and internal)
  • Assist in developing programming specifications
  • Assist in creating program specific validation plans
  • Identifying and implementing solutions for complex reporting needs

Ensures client data accuracy and integrity by:

  • Creating and/or reviewing data editing and export specifications
  • Working directly with clinical data manager, and where needed with clinical project manager and other team members to ensure specifications are clear and accurate.
  • Has a clear understanding of the contextual requirements for reporting outputs; and provides feedback
  • Programming data cleaning/consistency checking programs to support internal applications for all therapeutic areas
  • Programming and testing data export programs in accordance with specific client needs
  • Documenting all programming and validation efforts in accordance with Good Clinical Practices
  • Monitoring data integrity throughout a given study
  • Utilizing SDTM guidelines to create transfer datasets
  • Participating in project meetings (internal and external)

Develops and maintains clinical programming standard operating procedures by:

  • Participating in the development of data editing conventions, specification documents and Clinical Data Management (CDM) processes
  • Contributing to, designing and maintaining a library of reusable code
  • Leading and managing enhancements to current CDM systems and providing inputs in the implementation of new systems.

Ensures project timelines are maintained by:

  • Working independently and efficiently with minimal input required from the manager. Reviewing timelines; and projecting estimates and target dates in conjunction with direct supervisor and project team
  • Adhering to target dates for project timelines
  • Communicating any changes in target date to appropriate personnel including Project Manager
  • Keeping department head informed of progress as well as potential impediments

Maintains Quality Service and Departmental Standards by:

  • Adhering to established processes and standards
  • Reading, understanding and adhering to organizational Standard Operating Procedures (SOP)
  • Assisting in establishing and enforcing departmental standards
  • Maintain and review clinical programming SOPs
  • Participating in the modification of company SOPs

Secondary Responsibilities

Contributes to team effort by:

  • Working with internal staff to resolve issues
  • Exploring new opportunities to add value to organization and departmental processes
  • Helping others to achieve results
  • Performing other duties as assigned

Maintains Technical and Industry Knowledge by:

  • Attending and participating in applicable company-sponsored training



  • Bachelor's or Master's degree in computer science, life sciences or related field required
  • SAS Certified Professional considered a plus


  • 3 years SAS programming experience in pharmaceutical related industry required (1 year with Master's degree)
  • Experience working with CDISC, SQL, and Relational Databases preferred
  • Demonstrated programming skills required
  • Working knowledge and solid understanding of database organization and how to extract data in order to generate listings and reports
  • Proven ability in analyzing data
  • Understanding of medical and/or clinical trial terminology is desirable
  • Proven ability in problem solving

Additional skill set:

  • Ability to work in group setting and independently; ability to adjust to changing priorities
  • Excellent attention to detail and orientation toward meticulous work
  • Strong interpersonal and communication skills, both verbal and written
  • Strong documentation and organizational skills
  • Ability to project and maintain a professional and positive attitude

Working conditions:

Travel: 0-5%

Lifting: 0-10lbs

Other: Computer work for long periods of time

EEO Statement

Clario is an equal opportunity employer. Clario evaluates qualified applicants without regard to race, color, religion, gender, national origin, age, sexual orientation, gender identity or expression, protected veteran status, disability/handicap status or any other legally protected characteristic

Delivery, Intangibles / Other, Issue/Risk Management, Learning Agility, Sponsor/Internal Feedback, Team Player/ Contributor
Bioclinica is an equal opportunity employer. Bioclinica evaluates qualified applicants without regard to race, color, religion, gender, national origin, age, sexual orientation, gender identity or expression, protected veteran status, disability/handicap status or any other legally protected characteristic.


Job Summary
Start Date
As soon as possible
Employment Term and Type
Regular, Full Time
Required Education
Bachelor's Degree
Required Experience
3+ years
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