Clinical Data Specialist

Experience Range : 8 – 14 years

About the Role

Primarily responsible for quality and timely delivery of CP reports (Data Validation Listings, Reconciliation Reports, Coding Review, CRF Metrics, Patient Profiles and Narratives). Thorough understanding of End-to-End Drug Development Process. Good data understanding and Analytical skills. Keen knowledge on Data Management and Data cleaning process and willingness to work for adhoc requests. Having a skill set of Database Knowledge and flow, Study Protocol, CRF Design, Coding Dictionaries, Central vs Local lab concepts. Experience in debugging system level macros and modifying them for study level. Develop utility macros for reusability and efficiency. Coordinate work on multiple projects according to priorities. Communicate with project team / stakeholders / other departments and / or groups effectively.

Responsibilities

• Ability to program with and without specifications
• Reviewing and providing feedback on specifications when client provides them
• Ability to develop Macro from scratch or update existing macros
• Client Level Interaction not restricted to cascading work but setting up a project
• Ability to work independently and as part of a team
• Being open to new learnings and sharing with team members
• Excellent communication skills [Written, Verbal, Interpersonal and organizational skills]
• Proficient in using SAS EG / Studio for programming
• Familiar with Unix environment and programming
• Experience with additional programming languages (R / Python, Spotfire) will be an added advantage.

Qualifications

Post-graduate degree in statistics, computing, life science related field B.E / B tech

Required Skills

Good data understanding and Analytical skills.

Preferred Skills

Experience with additional programming languages (R / Python, Spotfire) will be an added advantage

Equal Opportunity Statement

We are committed to diversity and inclusivity.