Consultant - Business Consulting (Life Sciences)
Infosys · Pune · onsite · Posted 51d ago
Undisclosed8–10 yrsfulltimeSourced from
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About this role
Job Summary
Techno-Functional Business Analyst with 8-10 years of experience in RnD Clinical Research, focusing on Clinical Data Management and trial operations including Electronic Data Capture (EDC), Electronic Trial Master File (eTMF), Clinical Trial Management System (CTMS), and Study Start-Up (SSU).
Responsibilities - Manage program planning, execution and reporting, responsible for program resources, Deliverables, Quality, Stakeholder communication, Client Buy-in, program risks, mitigations and budgets leading to successful program delivery and client delight.
- Understand areas of concerns for a Pharma Organization and being able to suggest Innovative ideas to improve their existing processes
- Lead and support initiatives for the improvement initiatives, organizational SOPs, working practice guidance documents.
- Engage and maintain contacts with key client stakeholders, proactively identifies opportunities for business development.
- Lead sales pursuits in collaboration with Larger Infosys teams, Lead proposal development process, solution formulation, Proposal pricing, client presentations, contract negotiations and deal closure
- Develop solutions that enable adoption of digital capabilities for life sciences organizations. Participate in analysts meetings, industry speaking engagements, publish white papers in leading industry journals
- Participate in practice development activities, coach consultants, participate in consultant training and staffing process.
- 8-10 years experienced RnD Clinical Research professionals as Consultant/ Senior Consultant to join our team as a Techno-Functional Business Analyst.
- The ideal candidate should possess practical experience and in-depth knowledge of Clinical Data Management and Clinical Trial Operations, including Electronic Data Capture (EDC), Electronic Trial Master File (eTMF), Clinical Trial Management System (CTMS), and Study Start-Up (SSU).
- Analyze and translate business requirements into technical specifications. Collaborate with cross-functional teams to implement and optimize Modules.
- Facilitate the integration of EDC, eTMF, CTMS, and SSU systems to streamline clinical trial operations.
- Additional Responsibility Demonstrate excellent core competence and experience in delivery of agile projects using scrum or various other methodologies across value chain in Life Sciences
- Industry experiences working directly at Consulting organization for pharmaceutical, medical devices or Bio- pharmaceutical clients is a plus.
- Proficiency with IT tools supporting delivery CDM - VeeVa, Medidata RAVE, Oracle etc
- Bachelor of Engineering
- Domain->Healthcare->Regulatory Compliance Standards
- Domain->LifeSciences->Pharma Regulations->Computer Systems Validation (CSV)
- Foundational->Project Management->Project Management
- Technology->Life Sciences->Regulatory Systems
- Technology->Risk Management->Risk Management System
Sourced from naukri
Skills
Business ConsultingAgileclinical data managementclinical researchdeal closureBusiness AnalystBusiness Requirementsclient presentationsCSVdigital servicesClinical Trial ManagementBusiness Developmentcompliance
About Infosys
Infosys
IT Services & Consulting
323.6k+
employees
1981
45 years old
Bengaluru/Bangalore, Karnataka
India
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