Analyst, Global Data Manager

Johnson & Johnson

Analyst, Global Data Manager contributing to clinical trials and data management. Supporting the development of innovative medicines at Johnson & Johnson.

Posted 7/16/2026full-timeSpring House • New Jersey, Pennsylvania • 🇺🇸 United StatesMid-LevelSenior💰 $76,000 - $121,900 per yearWebsite

Core Competencies

Role fit

Core Competencies

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Demonstrates expertise in Clinical Data Management, ensuring compliance with regulatory guidelines and industry standards while effectively collaborating with cross-functional teams. Proficient in managing data deliverables and maintaining high-quality standards throughout the clinical trial process.

Highest-signal resume keywords

Clinical Data ManagementRegulatory ComplianceData Quality AssuranceClinical Trial Protocol KnowledgeProject Management

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Clinical Data ManagementData Quality AssuranceClinical Trial Protocol KnowledgeKnowledge of CDISC StandardsKnowledge of SDTMKnowledge of CDASHData Integration RequirementsTrial Level Oversight ControlsData Management ActivitiesContent and Format Review

Soft Skills

Excellent Verbal CommunicationExcellent Written CommunicationAdaptabilityCollaborationCross-Functional Teamwork

Tools & Technologies

Electronic Code of Federal Regulations (eCFR)Data Exchange PlatformsProject Management Tools

Industry Keywords

Clinical Drug DevelopmentPharmaceutical IndustryContract Research Organization (CRO)International GuidelinesProcess Improvement Initiatives

About the role

Key responsibilities & impact

Work with external suppliers, trial customers and other internal/external partners to establish, align and confirm data management and/or clinical data management expectations to the business for assigned trial(s) to include but not limited to: Gather and/or review content and integration requirements for Electronic Code of Federal Regulations (eCFR) and other data collection tools.
Participate in establishing conventions and quality expectations for clinical data.
Participate in establishing expectations for dataset content and structure.
Work with others to set timelines and follow-up regularly to monitor delivery of all data management milestones.
Review clinical data management documents (including submission package) for appropriate quality, scientific content, organization, clarity, accuracy, format, and consistency.
Work with DML to facilitate compliance with regulatory guidelines and the documentation matrix.
Work with DML to facilitate real-time inspection readiness of all assigned deliverables for the trial.
Participate in regulatory agency inspections and Johnson & Johnson internal audits as necessary.
Work with DML to plan and track content, format, quality, and timing of applicable data management deliverables.
Work with DML to ensure deliverables are on time.
Support the assigned clinical working group(s) to ensure that DM and TA trial needs and deliverables are met.
Identify and communicate lessons learned with support from DML and frequently asked questions at trial level.
Contribute to the creation of key functional plans (e.g., study Integrated Review Plan) ensuring appropriate quality, scientific content, organization, clarity, accuracy, format, and consistency.
Participate in process, system, and tool improvement initiatives.
Perform trial level oversight controls and/or execute data management activities per applicable procedures, with DML direction.

Requirements

What you’ll need

A minimum of a Bachelor's degree is required, preferably in Clinical Data Management, Life Sciences or Computer Sciences.
Clinical data management experience is preferred.
Knowledge of scientific concepts presented in clinical trial protocols is preferred.
Experience in clinical drug development within the pharmaceutical industry, Contract Research Organization (CRO) or related industry is preferred.
Knowledge of applicable international guidelines regarding data management of clinical trials is preferred.
Knowledge of current industry standards (e.g., Clinical Data Interchange Standards Consortium (CDISC), Study Data Tabulation Model (SDTM), Clinical Data Acquisition Standards Harmonization (CDASH), etc.) is preferred.
Knowledge of technology platforms for data exchange and project management is preferred.
Must have excellent verbal and written communication skills.
Must have the ability to adapt to a rapidly changing organization and business environment.
The ability to collaborate with all levels of management in a cross-functional team environment is preferred.
This position will require up to 10% travel.

Benefits

Comp & perks

Subject to the terms of their respective plans, employees are eligible to participate in the Company’s consolidated retirement plan (pension) and savings plan (401(k)).
This position is eligible to participate in the Company’s long-term incentive program.
Subject to the terms of their respective policies and date of hire, employees are eligible for the following time off benefits:
Vacation –120 hours per calendar year
Sick time - 40 hours per calendar year; for employees who reside in the State of Colorado –48 hours per calendar year; for employees who reside in the State of Washington –56 hours per calendar year
Holiday pay, including Floating Holidays –13 days per calendar year
Work, Personal and Family Time - up to 40 hours per calendar year
Parental Leave – 480 hours within one year of the birth/adoption/foster care of a child
Bereavement Leave – 240 hours for an immediate family member: 40 hours for an extended family member per calendar year
Caregiver Leave – 80 hours in a 52-week rolling period
Volunteer Leave – 32 hours per calendar year
Military Spouse Time-Off – 80 hours per calendar year