Experienced I Statistical Programmer (mumbai/hyderabad/bangalore)

Johnson & Johnson Johnson & Johnson · Pharma · Hyderabad, Andhra Pradesh, India +2

Experienced Statistical Programmer to support data analyses and reporting activities within clinical trial activities. Responsibilities include completing and leading programming trial activities, designing and developing programs for clinical research analysis and reporting, performing verification of programming and reporting, supporting submission activities with CDISC compliant data packages, and collaborating with team and cross-functional members. Requires a Bachelor's degree or higher in computer science, data science, mathematics, public health, or a related scientific field, with approximately 2+ years of relevant programming experience, preferably in the pharmaceutical industry. Knowledge of regulatory guidelines (ICH-GCP) and clinical R&D concepts is required. Proficiency in SAS is preferred, with knowledge of other languages like R and Python also relevant.

What you'd actually do

  1. Completes and may lead programming trial activities of low to medium complexity and/or criticality, with high quality and timeliness of deliverables.
  2. Accountable for the design and development of programs in support of clinical research analysis and reporting.
  3. Performs appropriate level of verification of programming and reporting activities. Reviews and provides input for project requirements and documentation.
  4. Supports submission activities including but not limited to creation, verification, and delivery of CDISC compliant and/or non-standard data packages and reviewer’s guides.
  5. Follows departmental processes and procedures, ensures use of latest standards and deployment of current technologies.

Skills

Required

  • Bachelor’s degree or higher and/or equivalent in computer science, data science/data engineering, mathematics, public health, or another relevant scientific field (or equivalent theoretical/technical depth).
  • Approx. 2+ years of relevant programming experience, preferably in Pharmaceutical, CRO or Biotech industry or related field or industry.
  • Basic knowledge of regulatory guidelines (e.g. ICH-GCP) and relevant clinical R&D concepts.
  • Knowledge of data structures and relevant programming languages for data manipulation/statistical analysis and reporting.
  • Basic knowledge of processes, methods, and concepts relevant to programming.

Nice to have

  • Experience working in a team environment preferred.
  • Excellent written and verbal communications skills.
  • SAS knowledge is preferred for Clinical Programming role.
  • Advanced Analytics
  • Analytical Reasoning
  • Biological Sciences
  • Biostatistics
  • Clinical Trials
  • Data Modeling
  • Data Privacy Standards
  • Data Quality
  • Data Savvy
  • Detail-Oriented
  • Good Clinical Practice (GCP)
  • Report Writing
  • Research Ethics
  • Researching
  • Statistical Analysis Systems (SAS) Programming
  • Statistics
  • Technologically Savvy

What the JD emphasized

  • SAS knowledge is preferred for Clinical Programming role