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Clinical Sas Programmer

5-12 years years
Preffered by Company
Not Disclosed May 28, 2024
Job Description
Job Type: Full Time Education: B.Pharm/M.Pharm/PharmD Skills: Clinical SAS Programming, Communication Skills, ICD-10 CM, CPT, HCPCS Coding, Interpersonal Skill, Narrative Writing, Technical Skill

Job Title: Clinical SAS Programmer

Location: PAN India (primary location Mumbai)

Experience Required: 5 - 12 years

Application Deadline: 22-Jul-2024

Job ID: 309071

Job Function: BUSINESS PROCESS SERVICES

Role Category: Executive

Job Description: The Clinical SAS Programmer is responsible for leading and executing clinical programming tasks across studies or regulatory submissions. This role requires comprehensive clinical data knowledge, strong expertise in SAS/Spotfire programming, and the ability to drive projects independently. Familiarity with RBQM or Medical/Safety analytics is advantageous.

Key Responsibilities:

  • Develop and manage SAS macros, templates, and utilities for data cleaning and reporting.
  • Lead or co-lead the clinical programming aspects of a study or regulatory submission.
  • Participate in project team meetings and contribute to project management with minimal supervision.
  • Review and provide feedback on documents such as Issue logs, Change Control forms, and extraction plans to ensure clarity and appropriateness of requested changes.
  • Perform quality control checks on final reports to ensure accuracy.
  • Establish and monitor data transfers for ongoing trials to identify any potential study conduct or data quality issues.

Required Skills:

  • Strong SAS/Spotfire programming background.
  • Excellent communication and sound project management skills.
  • Experience with RBQM or Medical/Safety analytics is preferred.

Qualifications:

  • Bachelor of Pharmacy (B.Pharm)

Desired Skills:

  • Proficiency in statistics.

Additional Information: This role is ideal for a highly skilled Clinical SAS Programmer looking to take on significant responsibilities within a dynamic environment. The position offers the opportunity to impact critical aspects of clinical trials and regulatory processes.

Apply Now: Interested candidates with the requisite experience and skills are encouraged to apply by the specified deadline. Please ensure your application includes an updated resume highlighting relevant programming expertise and project management capabilities.