Life Sciences Management Consultant

Infosys; Bengaluru; Presencial; INR 1.000.000 - 1.650.000; Jornada completa

Descripción de la vacante

Infosys in Bengaluru seeks an experienced Techno-Functional Business Analyst with 8–10 years in R&D Clinical Research. The role focuses on Clinical Data Management and operational systems integration (EDC, eTMF, CTMS, SSU) to optimize trial processes.

You will translate business needs into technical specs and drive cross-functional collaboration across lifecycle stages. Responsibilities include program planning, resource and risk management, stakeholder communication, and pursuit of

Formación

• 8–10 years of experience in R&D Clinical Research.
• Consultant/Senior Consultant level with delivery responsibility.
• Delivery of agile projects in Life Sciences.

Responsabilidades

• Analyze and translate business requirements into technical specs for cross-functional teams.
• Facilitate integration of EDC, eTMF, CTMS and SSU to streamline operations.
• Lead program planning, execution, reporting, risks, and budgets for successful delivery.
• Engage client stakeholders, provide updates, and ensure client satisfaction.

Conocimientos

Clinical Data Management

CTMS

EDC

eTMF

SSU

Stakeholder communication

Agile/Scrum

Client relationship management

Herramientas

VeeVa

Medidata RAVE

Oracle

Descripción del empleo

We are looking for 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. 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 analyst's 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. 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