Job DescriptionIn the assigned Job Role of Domain Consultant 1, your Area Of Responsibility will be as below:• Assist in data analysis and business modelling to support informed decision-making based on domain-specific standards
• Contribute to benchmarking studies by analysing performance data against domain-specific industry standards and identifying improvement opportunities
• Support translating technical details into clear, user-friendly documentation for communication and reporting
• Assist in researching third-party products within the domain, focusing on features, scalability, and conducting preliminary assessments
• Provide support during the implementation of domain-specific systems, assist with configuration, and identify opportunities for enhancements
Your contribution to the team:• An agile mindset with effective communication and problem-solving skills.
• Familiarity with domain-specific standards, methodologies, and best practices
• Ability to assist in system configurations and troubleshooting within domain-specific workflows
• Passion for innovating solutions that drive progress and meet future challenges
• Commitment to continuous learning, knowledge sharing, and fostering team development
Required Skill and Experienceo End-end Clinical trial management process and related applications.
o Experience in Clinical data management applications such as oc/rdc/tms.
o Experience on clinical reporting (internal, FDA) during study start to closeout phases.
o Knowledge of Clinical Data Management processes with knowledge of Clinical Data Warehouse
o Experience in Computer systems Validation activities
o Familiarity with Good Clinical Practices, Good Documentation practices, Clinical Trial Quality & Compliance.
o 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.
o Must be able to translate business requirements into well-formed technical and system requirements
Preferred Skill and Experienceo Experience in Computer systems Validation activities
o Familiarity with Good Clinical Practices, Good Documentation practices, Clinical Trial Quality & Compliance.
Additional Required Qualifications• Bachelor's degree or foreign equivalent required from an accredited institution. Will also consider three years of progressive experience in the specialty in lieu of every year of education.
• This position may require relocation and/or travel to work/project location.
• Candidates authorized to work for any employer in the United States without employer-based visa sponsorship are welcome to apply. Infosys is unable to provide immigration sponsorship for this role now or in the future.
BenefitsAlong with competitive pay, as a full-time Infosys employee you are also eligible for the following benefits:
- Medical/Dental/Vision/Life Insurance
- Long-term/Short-term Disability
- Health and Dependent Care Reimbursement Accounts
- Insurance (Accident, Critical Illness , Hospital Indemnity, Legal)
- 401(k) plan and contributions dependent on salary level
- Paid holidays plus Paid Time Off
