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Technical Subject Matter Expert

Cognizant
Cognizant
15+ years
$155,000–$170,000 Annually
10 June 27, 2025
Job Description
Job Type: Hybrid Education: B.Sc./M.Sc/B.Pharm/M.Pharm/Life Science Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

 

Job Title

Technical Subject Matter Expert – Life Sciences Regulatory | $155K–$170K | Hybrid – Bridgewater, NJ


Job Summary

Cognizant is hiring a Technical Subject Matter Expert – Life Sciences Regulatory to drive account growth, regulatory transformation, and stakeholder engagement across key life sciences clients. This hybrid position is based in Bridgewater, NJ and involves up to 30–40% travel. As a senior leader with deep R&D regulatory compliance knowledge and strong experience in Regulatory Information Management Systems (RIMS), you’ll manage the go-to-market strategy, build long-term client relationships, and lead impactful regulatory transformation initiatives. This is a high-visibility role with a competitive salary range of $155,000–$170,000 annually, plus performance bonuses.


Key Responsibilities

  • Lead account strategy for R&D transformation across regulatory, pharmacovigilance, clinical, and research

  • Build strong relationships with regulatory stakeholders in top life sciences companies

  • Develop and execute account growth plans, including cross-sell and up-sell strategies

  • Drive commercial success by meeting revenue and margin goals

  • Identify opportunities for digital transformation in Regulatory Affairs using tools like RIMS

  • Collaborate with global sales and delivery teams to align client engagement strategies

  • Manage technical and commercial proposal development for high-value opportunities

  • Oversee contract negotiation and manage ongoing client communications

  • Maintain accurate records in CRM and support marketing events

  • Monitor customer satisfaction and ensure consistent value delivery


Required Skills & Qualifications

  • Minimum 15 years of experience in client-facing roles in pharma consulting, software, IT services, or product companies

  • Deep domain expertise in Regulatory Compliance and R&D

  • Strong experience with Regulatory Information Management Systems (RIMS)

  • Proven ability to sell and implement regulatory solutions across large accounts

  • Track record of engaging with C-level executives and aligning business-IT strategy

  • Strong commercial acumen and contract negotiation capabilities

  • Excellent storytelling, communication, and interpersonal skills

  • Ability to travel up to 40% and work hybrid from Bridgewater, NJ office


Perks & Benefits

  • Annual Salary: $155,000–$170,000

  • Performance Bonus: Annual discretionary incentive program

  • Medical, Dental, Vision & Life Insurance

  • Paid Holidays & Paid Time Off

  • 401(k) plan with company contributions

  • Paid Parental Leave

  • Long-term/Short-term Disability

  • Employee Stock Purchase Plan


Company Description

Cognizant is a global leader in transforming healthcare and life sciences through digital innovation. With over 300,000 employees worldwide, Cognizant empowers pharmaceutical and biotech clients with cutting-edge solutions in Regulatory Affairs, R&D, Clinical Development, and Compliance. Recognized as one of Forbes’ World’s Best Employers 2024, Cognizant delivers high-impact results through a unique industry-first consultative model.


Work Mode

Hybrid – Based in Bridgewater, NJ with 30–40% travel


Call-to-Action

Are you a regulatory R&D expert ready to shape the future of pharma transformation? Apply today and join Cognizant’s elite Life Sciences team as a trusted technical leader.