Clinical Data Programmer Lead

2 weeks ago

Hyderabad, Telangana, India Lifelancer Full time
About the Role

We are seeking a highly skilled Clinical Data Programmer Lead to join our team at Lifelancer. As a key member of our data management team, you will be responsible for leading and mentoring a team of Clinical Data Programmers, creating and testing SAS code, and reviewing data specifications.

Key Responsibilities
  • Lead and mentor a team of Clinical Data Programmers to create and test SAS code for standard and non-standard data file creation.
  • Review Clario standard and non-standard data specifications and interact with the Data Manager to finalize specifications.
  • Develop programs to create Clario standard and non-standard data files.
  • Participate in the validation of encoding programs that generate Clario standard and non-standard data files.
  • Perform ad-hoc programming activities utilizing raw data based on internal and external requests.
  • Get exposed to all modalities and review user requirements to create, review, and approve functional and technical specifications.
  • Work with data management to provide programming support for DM activities, including data review.
  • Prepare and participate in internal and external audits.
  • Represent the service line through the NPI process.
  • Identify opportunities to improve 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 in Project Management, Data Management, or CDO meetings.
  • Organize team resources to meet client needs.
Requirements
  • BS/BA degree in Life Sciences or related field (preferred) or BS/BA degree in Computer Sciences or related field.
  • SAS Advanced certified.
  • Five or more years of experience in a pharmaceutical company or a CRO as a SAS Programmer, with 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, 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 REVS 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 language 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.
What We Offer
  • Competitive compensation and commission scheme.
  • Attractive benefits, including security, flexibility, support, and wellbeing.
  • Engaging employee programs.
  • Technology for hybrid working and great onsite facilities.
About Lifelancer

Lifelancer is a talent hiring platform in Life Sciences, Pharma, and IT. We connect talent with opportunities in pharmaceutical, biotech, health sciences, healthtech, data science, and IT domains.

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