Senior Data Scientist for Clinical Trials

3 days ago

Gurgaon, Haryana, India Lifelancer Full time
Job Title: Senior Data Scientist for Clinical Trials

Salary: $120,000 - $180,000 per year

Location: Remote, India

About Syneos Health

Syneos Health is a leading biopharmaceutical solutions organization built to accelerate customer success. We translate unique clinical, medical affairs, and commercial insights into outcomes to address modern market realities.

Our Clinical Development model brings the customer and the patient to the center of everything that we do. We are continuously looking for ways to simplify and streamline our work to make Syneos Health easier to work with and easier to work for.

Job Responsibilities
  • Develop custom programming code using SAS or other software to generate summary tables, data listings, graphs, and derived datasets as specified in the statistical analysis plan and programming specifications.
  • Ensure outputs meet quality standards and project requirements.
  • Perform validation programming and collaborate with other Programmers, Biostatisticians, and project team members to resolve discrepancies or findings.
  • Maintain project team members informed of programming progress and issues requiring their attention.
  • Follow applicable SOPs, WIs, and relevant regulatory guidelines (e.g., ICH).
  • Keep project documentation, testing, and verification/quality control documents and programs up-to-date, ensuring inspection readiness.
  • Manage scheduling and time constraints across multiple projects, set goals based on priorities from management, and adapt to timeline or priority changes by reorganizing daily workload.
  • Develop specifications for datasets and outputs according to statistical and sponsor requirements, anticipating and addressing potential programming issues.
  • Prepare for internal meetings, contribute ideas, and demonstrate respect for others' opinions.
  • Conduct effective internal meetings, distribute relevant information, and maintain minutes.
  • Negotiate accurate time estimates for completion of study programming activities with internal team members and statistical programming management.
  • Review project documentation and provide feedback to project team members.
Qualifications
  • Undergraduate degree in a scientific or statistical discipline; equivalent combination of education and demonstrated programming experience accepted.
  • Extensive programming experience in SAS or other required software, preferably in a clinical trial environment.
  • Excellent written and verbal communication skills.
  • Ability to read, write, speak, and understand English.

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