Ref #: 25464
Employment type: Permanent - Full-Time
Location: Bangalore/Chennai
Posted: 13-Jan-2021
Description
We have an exciting opportunity and looking for talents to join our team. Below are the insights about the role.
Job Title : Senior Report Programmer
Job location : Chennai /Bangalore Office based
No of years of experience: 4+ years of relevant exp in Clinical Review and Report Programming
Education Qualification: Bachelor Degree
Salary : As per Industry standards with attractive benefits
Skill set : SAS Programming, SAS Listing ,SAS Report, Base SAS, Advance SAS,Macros
Job responsibilities/ Role Expectations:
• We are looking for an experienced person in clinical review and reporting programming, business analytics clinical trial setup, gained in the Pharmaceutical /CRO industry
• Strong knowledge of Data Review and/or Business Intelligence tools (such as Spotfire, JReview)
• Hands on experience in Creating SAS Macros, SAS Report
• Knowledge of clinical data management systems and/or relational databases (e.g. OC/RDC, INFORM, RAVE) as applied to clinical trials
• Understanding of Drug Development Process, ICH-GCP, CDISC standards and Health Authority guidelines and regulations
• Ability to train and supervise new or less experienced associates
• Ability to translate technical concepts for non-technical users in the areas of clinical database design and data review reporting development
• Great learning opportunity embedded with a single sponsor.
Job Title : Senior Report Programmer
Job location : Chennai /Bangalore Office based
No of years of experience: 4+ years of relevant exp in Clinical Review and Report Programming
Education Qualification: Bachelor Degree
Salary : As per Industry standards with attractive benefits
Skill set : SAS Programming, SAS Listing ,SAS Report, Base SAS, Advance SAS,Macros
Job responsibilities/ Role Expectations:
• We are looking for an experienced person in clinical review and reporting programming, business analytics clinical trial setup, gained in the Pharmaceutical /CRO industry
• Strong knowledge of Data Review and/or Business Intelligence tools (such as Spotfire, JReview)
• Hands on experience in Creating SAS Macros, SAS Report
• Knowledge of clinical data management systems and/or relational databases (e.g. OC/RDC, INFORM, RAVE) as applied to clinical trials
• Understanding of Drug Development Process, ICH-GCP, CDISC standards and Health Authority guidelines and regulations
• Ability to train and supervise new or less experienced associates
• Ability to translate technical concepts for non-technical users in the areas of clinical database design and data review reporting development
• Great learning opportunity embedded with a single sponsor.