Lead Clinical Data Programmer

3 days ago

puducherry, India Lifelancer Full time

About the job

Are you a seasoned Clinical Data Programming professional looking for an opportunity to join an industry leading data technology organisation in the clinical research space? Clario are looking for a Lead, Clinical Data Programmer to join our well established team in India, working alongside a global team of data specialists to provides our customers with best in class data to support the development of life changing therapies from clinical trials.

What We Offer

  • Competitive compensation + commission scheme
  • Attractive benefits (security, flexibility, support and well-being)
  • Engaging employee programs
  • Technology for hybrid working and great onsite facilities

What You Will Be Doing

  • Lead and Mentor a team of Clinical Data Programmers, Create and test SAS code used for standard and non-standard data file creation; Review Clario standard and non-standard data specifications.
  • Attend client meetings as appropriate to understand data collection requirements.
  • Review standard CLARIO and non-standard data specifications and interact with the Data Manager (DM) to finalize specifications.
  • Develop programs to create Clario standard and non-standard data files.
  • Participate in the validation of encoding programs which generates CLARIO standard and non-standard data files.
  • Performing ad-hoc programming activities utilizing raw data based on internal and external requests for:
  • Esoteric quality control checks requested by QC.
  • Data resolution/Mining.
  • Other client requirements.
  • Get exposed to all modalities.
  • Review User Requirements and create, review and approve Functional and Technical Specifications.
  • Work with data management in providing programming support for DM activities including data review.
  • Prepare and participate in internal and external audits.
  • Represent the service line through the NPI (New Product Initiative) process.
  • Identify opportunities to improve the methodology and provide practical solutions for problems.
  • Contribute to the development of best practices to improve quality, efficiency and effectiveness.
  • Drive client deliverables by performing the role of CDP SME when attending Project Management, Data Management or CDO meetings.
  • Organize team resources to meet client needs.
  • Lead and Mentor a team of Clinical Data Programmers:
  • Develop the orientation and training plan for assigned Clinical Data Programing personnel.
  • Oversee training of new Clinical Data Programmers.
  • Assist with orientation and training of personnel as determined by management.
  • Contribute to process development. Review and development of SOPs and associated documents related to Clinical Data Programming activities.
  • Complete administrative tasks as needed within Clinical Data Programming.
  • Mentoring other Clinical Data Programming resources.
  • Participate in new hire interviews and provide feedback to management

What We Look For

  • BS/BA Degree in Life Sciences or related field preferred or BS/BA Degree in computer sciences or related field
  • SAS ADVANCED certified
  • Ideally five or more years of experience in a pharmaceutical company or a CRO as a SAS Programmer experience in SAS/BASE, SAS/MACRO and SAS/SQL products and procedures and one or more years of experience in database design and data structures
  • Understanding of the pharmaceutical drug development process, as gained through a minimum of five years of experience in the pharmaceutical or healthcare industry.
  • Strong organization, analytical and communication skills.
  • Detail-oriented
  • Extensive experience in implementing CDISC SDTM and Define standards including EG, CO, DM, RE, VS, SUPP CDISC SDTM domains.
  • Experience with Windows and Microsoft Office products preferred.
  • Strong written and verbal communication skills.
  • Fluency in English (spoken and written).
  • Experience with another programming languages is a plus.
  • Proven experience working with large, complex real-world data sets (more specifically, patient data)
  • Knowledge of technical and regulatory requirements related to the role.
  • Excellent time management skills, contributing to multiple projects with competing timelines.
  • Leadership/Mentoring skills: Proven ability to motivate people, instill accountability and achieve results.
  • Prior leadership experience a plus.

Please use the below link for job application and quicker response.

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