Senior Consultant- Research and Development, Life Sciences

Senior Consultant- Research and Development, Life Sciences
We're seeking a Senior Consultant who blends R&D domain depth (Clinical, Safety, Regulatory) with consulting excellence (problem framing, stakeholder influence, structured delivery, and thought leadership) for Life Sciences Practice. You will translate complex R&D business needs into scalable processes, data, and platform solutions, enabling efficiencies across Clinical Operations, Pharmacovigilance, and Regulatory while advancing data governance and automation/AI use cases.
This role spans end-to-end R&D operations, supporting clients through Regulatory/Clinical/Safety functions while driving impactful system implementations, data-centric initiatives, and automation programs.

Key Responsibilities

1. R&D Systems & Process Consulting (Regulatory, Clinical & Safety)

• Engage with cross-functional R&D teams-Regulatory, Clinical Operations, Medical Writing, Safety/Pharmacovigilance-to understand process pain points and define harmonized, scalable solutions.

• Conduct workshops, requirement gathering, business analysis, and process mapping across R&D functions.

• Provide consulting support for Clinical and Safety workflows such as protocol amendments, safety reporting, signal management, CTA/IND submissions, and compliance tracking.

2. Regulatory Information Management (RIMS) & Data Governance

• Lead/support RIMS implementations, upgrades, and enhancements by connecting Regulatory needs with Clinical and Safety data flows.

• Develop RIMS-eDMS-Safety-Clinical interoperability frameworks to ensure consistent product, submission, and registration data.

• Establish data governance operating models across full R&D, defining stewardship roles, data ownership, business rules, and data quality KPIs.

3. Clinical & Safety Data Enablement

• Support configuration and process alignment for Clinical Trial Applications, tracking systems, clinical documentation lifecycles, and inspection readiness.

• Partner with safety teams to enable accurate Safety Case Management data, Label updates, safety variation submissions, and compliance reporting.
• Assist in aligning R&D master data (Product, Study, Molecule, Substance) across Clinical, Safety, and Regulatory systems.

4. IDMP, xEVMPD & Structured Data Across R&D

• Guide IDMP/SPOR/xEVMPD readiness and implement structured data models that align Regulatory, Clinical, and Safety data sources.

• Support automation of IDMP data extraction and mapping from clinical documents, CMC files, safety datasets, and eCTD modules.

5. Regulatory CMC, Publishing & Documentation

• Provide consulting support for CMC variation management, product lifecycle maintenance, change controls, and regulatory strategies.

• Oversee publishing workflows: eCTD compilation, QC, hyperlinking automation, and submission compliance.

6. Digital Transformation, Automation & AI in R&D

• Identify, define, and lead automation initiatives across Regulatory, Clinical, and Safety-such as RegIntel crawlers, content generation, publishing automation, safety data ingestion, and clinical document processing.

• Collaborate with engineering, AI, and platform teams to build proof-of-concept, evaluate tools, and demonstrate solutions to clients.

7. Consulting Excellence & Client Engagement

• Serve as a trusted advisor to global R&D leaders, bringing structured consulting practices and domain intelligence together.

• Drive PMO activities-JIRA management, sprint planning, stakeholder communication, RAID logs, reporting, and release preparation.

• Simplify complex technical topics into clear business recommendations and influence decision-making across R&D functions.

Required Qualifications

• Bachelor's/Master's in Life Sciences/Pharmacy/ or related

• 5 years in R&D Clinical Research and/or cross-functional Life Sciences consulting with hands-on exposure to EDC, eTMF, CTMS, SSU and clinical data/operations.

• Demonstrated ability to analyze/translate business requirements into technical specs, collaborate with cross-functional/technical teams, and drive agile delivery (Scrum/Kanban).

• Practical knowledge across Regulatory (RIMS, Publishing/eCTD, IDMP), Safety/PV (case processing, signal management), and CMC processes.
• 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 at this time

Preferred Skills & Tools

• Hands-on with Veeva (Vault Clinical/RIM), Medidata Rave, Oracle clinical solutions (or equivalents).

• Experience with virtual/decentralized trials, RWD/RWE, site payments, and clinical audits/monitoring.

• Awareness of AI/ML implementation across the clinical research lifecycle and regulatory operations; comfort shaping POCs and scaling.

• Proficiency in JIRA/Confluence, Agile delivery tooling; familiarity with structured content/authoring and documentation standards.

• Strong consulting soft skills: structured communication, facilitation, conflict resolution, influencing without authority, and crisp storytelling.

Client-provided location(s): Bridgewater, NJ

Job ID: Infosys-145548BR

Employment Type: OTHER

Posted: 2026-04-28T19:09:30