Job Description:

Who are we
Infosys is a global leader in next generation digital services and consulting with annual revenues of 16
31B FY 22
Infosys Consulting partners with clients from strategy through execution to transform their businesses in areas such as business IT strategy processes organization systems and risk
Infosys Consulting has 2 500 people across the US Europe APAC and India
We are Value Integrators we deliver realized business value by managing transformations from strategy setting direction through execution including operating and optimizing delivered solutions

Key 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

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

Proven efficiency in conflict management influencing and negotiating skills with the ability to lead or manage stakeholders effectively
Deep Domain knowledge and work experience in areas of virtual trials clinical trial process real world data research studies site payment management clinical trial audits monitoring clinical trial management technology and data
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

Foundational->Project Management->Project Management,Technology->Consulting - Data Management->Data Management,Technology->Life Sciences->LIMS