Life Sciences Management Consultant

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 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.

Additional Responsibilities:

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

Technical and Professional Requirements:

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.