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Analyst Ii Global Data Manager - Hyderabad/Bangalore/Mumbai

Johnson & Johnson
Johnson & Johnson
2 years
preferred by company
10 Jan. 29, 2026
Job Description
Job Type: Hybrid Education: B.Sc./ M.Sc./ M.Pharm/ B.Pharm/ Life Sciences 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

Analyst II – Global Data Manager

Locations: Hyderabad / Bangalore / Mumbai, India
Function: Data Analytics & Computational Sciences
Sub-Function: Clinical Data Management
Job Category: Experienced Analyst (Clinical Data Management, P5)
Work Model: Hybrid
Requisition Number: R-054319
Date Posted: January 22, 2026


About Johnson & Johnson

At Johnson & Johnson, we are committed to transforming healthcare through innovation. Our expertise spans pharmaceuticals, medical devices, and consumer health, enabling smarter, less invasive treatments and personalized solutions. With a global presence and a focus on advanced data-driven healthcare, we empower teams to deliver breakthroughs that improve patient outcomes worldwide. Learn more at jnj.com.


Position Overview

We are seeking a highly motivated Analyst II – Global Data Manager to join our Clinical Data Management team. This hybrid role offers flexibility to work remotely and on-site across Hyderabad, Bangalore, or Mumbai. You will oversee clinical data management activities, ensure data integrity, and support trials of varying complexity. The role requires active collaboration with internal teams, external vendors, and clinical stakeholders to maintain regulatory compliance and optimize trial data quality.


Key Responsibilities

  • Lead coordination with internal teams, external vendors, and trial sponsors to define clinical data management expectations and deliverables

  • Gather and review content requirements for electronic Case Report Forms (eCRFs) and other data collection tools

  • Establish and monitor quality standards, dataset structure, and timelines for clinical trial data deliverables

  • Review clinical data management documents for accuracy, consistency, clarity, and compliance with regulatory guidelines

  • Ensure inspection readiness for all data management deliverables and support internal and external audits

  • Track and report on the status, quality, and timing of deliverables, identifying risks and escalation points

  • Collaborate with cross-functional trial teams to ensure seamless execution and alignment with Therapeutic Area needs

  • Develop and maintain trial-level functional plans such as Integrated Review Plans

  • Identify lessons learned, best practices, and contribute to process improvement initiatives

  • Execute data management activities under direction from Data Management Leaders (DML) and ensure adherence to Standard Operating Procedures (SOPs)

  • Support knowledge sharing and mentorship within the Clinical Data Management team


Principal Relationships

  • Reports to the Data Management Leader (DML)

  • Works closely with Data Management, Clinical & Statistical Programming, Clinical Data Standards, Regulatory, Medical Writing, and Therapeutic Area Leads

  • Interfaces with Global Program Leaders, Biostatisticians, Clinical Teams, Procurement, Finance, Legal, Privacy, and Project Coordinators

  • Engages with external partners, vendors, and CROs to manage clinical data deliverables


Education & Experience Requirements

Required:

  • Bachelor’s degree (BS/BA) or equivalent professional experience in Clinical Data Management, Health Sciences, or Computer Sciences

  • Minimum 2 years’ experience in pharmaceutical, biotech, or CRO environments in clinical data management or related roles

  • Strong experience in clinical drug development, cross-functional collaboration, and stakeholder communication

Preferred:

  • Master’s or PhD in Life Sciences, Clinical Data Management, or related field

  • Experience in leading teams or mentoring junior analysts

  • In-depth knowledge of clinical trial protocols, GCP, data management processes, and international regulatory standards

  • Proficiency in data management technology platforms, electronic data capture (EDC) systems, and understanding of clinical data privacy regulations

  • Familiarity with SOPs, reporting standards, and integrated trial data review

Other Requirements:

  • Willingness to travel domestically or internationally (<10%) as required

  • Strong analytical, problem-solving, and report-writing skills


Key Skills

  • Clinical Data Management (CDM) and trial oversight

  • Advanced analytics and database applications

  • Biostatistics fundamentals

  • GCP compliance and regulatory knowledge

  • Cross-functional collaboration and effective communication

  • Data privacy and security standards

  • SOP and process adherence


Why Johnson & Johnson

  • Work at a global leader in healthcare innovation with opportunities to impact patient care worldwide

  • Hybrid work model promoting flexibility and work-life balance

  • Exposure to complex clinical trials across therapeutic areas

  • Opportunity to develop leadership and domain expertise in clinical data management

  • Collaborative and inclusive culture fostering professional growth


Apply now on ThePharmaDaily.com to join Johnson & Johnson as an Analyst II – Global Data Manager and contribute to innovative clinical solutions shaping the future of healthcare.