Required Skills
- Familiarity with Good Clinical Practices, Good Documentation practices, Clinical Trial Quality & Compliance.
- Good Knowledge of Study life cycle activities (Study Protocols /study design for IRT and EDC Studies), various study milestones, clinical trial regulatory reports and other metrics reports at study level /site level.
- Basic- Must be able to translate business requirements into well-formed technical and system requirements
- Basic Experience with modeling business processes, data flows, and workflow processes depicting relationships between Clinical data entities.
- Agile – Scrum …
- Strong business consulting skills associated with complex IT system implementation spanning over 12-18 months.
- Strong oral & written communication skills, Business stakeholder management
- Must have performed business requirement analysis, use case modeling from a business analysis/consulting standpoint.
- Experience and desire to work in a management consulting environment that requires regular travel
- A basic knowledge writing custom queries in SQL or PL/SQL is needed for data extraction and validation.
- Experience in the full System Development Life Cycle (SDLC) on a variety of technologies and platforms preferably in pharma IT space
- U.S. citizens and those authorized to work in the U.S. are encouraged to apply. We are unable to sponsor at this time.
Preferred Skills
- Experience with project management
- Planning and Co-ordination skills.
- Experience and desire to work in a management consulting environment that requires regular travel.
- Experience and desire to work in a Global delivery environment.
- Ability to write design documents and walk the audience through the design.
- Able to estimate for the end to end delivery of Integration projects.
- Able to work on technical aspects and help tackle complex items including Integration.
Excellent communication skills to efficiently manage client stakeholders and Infosys internal teams.
