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Johnson & Johnson

Analyst II, Clinical Data Manager

Johnson & Johnson

Analyst II role providing oversight and performing data management activities for clinical trials. Contributing to healthcare innovations at Johnson & Johnson.

Posted 7/1/2026full-timeRaritan • New Jersey, Pennsylvania • 🇺🇸 United StatesJuniorMid-Level💰 $92,000 - $148,350 per yearWebsite

About the role

Key responsibilities & impact
  • Take on a leadership role with external suppliers, trial customers and other internal/external partners.
  • Gather and/or review content and integration requirements for Electronic Code of Federal Regulations (eCFR) and other data collection tools.
  • Establish conventions and quality expectations for clinical data.
  • Establish expectations for dataset content and structure.
  • Set timelines and follow-up regularly to monitor delivery of all data management milestones.
  • Review clinical data management documents for appropriate quality, scientific content, organization, clarity, accuracy, format, and consistency.
  • Ensure compliance with regulatory guidelines and the documentation matrix.
  • Ensure real-time inspection readiness of all DM deliverables for the trial.
  • Plan and track content, format, quality, and timing of applicable data management deliverables.
  • Create key functional plans ensuring appropriate quality, scientific content, organization, clarity, accuracy, format, and consistency.
  • Identify and communicate lessons learned, best practices, and frequently asked questions.
  • Identify and participate in process, system, and tool improvement initiatives.
  • Collaborate with the SRS/SRP to ensure that DM and Therapeutic Area trial needs and deliverables are achieved.

Requirements

What you’ll need
  • A minimum of a Bachelor's degree is required, preferably in Clinical Data Management, Life Sciences or Computer Sciences.
  • Advanced degree (Master’s, PharmD, PhD) preferred.
  • A minimum of 2 years of experience in the Pharmaceutical industry, Contract Research Organization (CRO), or related industry is required.
  • Clinical data management experience and/or knowledge of scientific concepts presented in clinical trial protocols is preferred.
  • Experience in clinical drug development within the Pharmaceutical industry or related industry is required.
  • Knowledge of current clinical drug development processes is preferred.
  • Knowledge of applicable international guidelines regarding data management of clinical trials is preferred.
  • Knowledge of technology platforms and systems to capture and process data (e.g., Medidata Rave, Inform) is preferred.
  • Understanding of data privacy rules in relation to clinical data exchange is preferred.
  • Experience in the Oncology Therapeutic Area is preferred.
  • Team leadership experience is preferred.
  • Project management experience is preferred.
  • Experience working with cross-functional stakeholders and teams is required.
  • 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 across a matrix environment is required.
  • This position will require up to 10% travel.

Benefits

Comp & perks
  • medical
  • dental
  • vision
  • life insurance
  • short- and long-term disability
  • business accident insurance
  • group legal insurance
  • consolidated retirement plan (pension)
  • savings plan (401(k))
  • long-term incentive program
  • vacation - 120 hours per calendar year
  • sick time - 40 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
  • Condolence Leave - 30 days for an immediate family member: 5 days for an extended family member
  • Caregiver Leave - 10 days
  • Volunteer Leave - 4 days
  • Military Spouse Time-Off - 80 hours

ATS Keywords

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Hard Skills & Tools
Clinical Drug DevelopmentData Management ProcessesScientific Content ReviewDataset Structure and ContentQuality Assurance
Soft Skills
Excellent Communication SkillsAdaptabilityProblem-Solving