Senior Team Lead– Cytel (6 – 8 years of experience)

deepak Last Updated : 11 Nov, 2014
2 min read

Is statistics your first love? Can you co-ordinate with internal and external stakeholders while making sure that the required work is top notch. Are you a team leader with hands on experience in SAS Programming? Here is an excellent opportunity for you to look at.

Designation – Senior Team Lead – Statistical Programming

About employer Cytel

Responsibilities:

  • Lead multiple study teams in terms of providing technical and domain related guidance
  • Lead and manage a team of 8 – 10 team members
  • Be responsible for the timeliness and quality of work of the team members and manage their leaves, appraisals and aspirations etc.
  • Ability to work on data migration from legacy datasets to standards such as CDISC or any other client specific standard
  • May need to work with internal and client biostatisticians
  • Read and understand the program specifications document
  • Prepare SAS analysis datasets, tables, listings, and figures as per specifications. Create programs to create graphs and tables that are required in CSRs, safety reports, efficacy reports, etc. ensuring on-time quality delivery
  • Validate and transform datasets as per client assignment specifications
  • Validate tables, listings, and figures as per client assignment specifications. Co-ordinate with the client and US-team for clarity of specifications, data issues, outliers, reviews, schedules, etc.
  • Contribute in the organization’s recruitment process by identifying need and required skill set of resources and conducting interviews to hire appropriate resources
  • Collect data for different metrics and share it project managers
  • Ensure adherence to compliance of standard operating procedures (SOPs) as defined in Quality Management System or the respective client(s) standards as applicable

Qualification and Skills Required:

  • BS or MS degree in Computer Science, Statistics, or related health science field
  • A minimum of 6 – 8 years of SAS programming experience with clinical trial data
  • Profound understanding of regulatory requirements and drug development process
  • Excellent understanding of Clinical trial domain and good SAS programming skills
  • Excellent Communication skills

Interested candidates can send their CV’S to [email protected] with subject as Senior Team Lead ,Statistical Programming – Cytel.

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