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Analyst II, Clinical Data Manager
Johnson & JohnsonAnalyst 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
✓ Tailor your resumeApplicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard Skills & Tools
Clinical Drug DevelopmentData Management ProcessesScientific Content ReviewDataset Structure and ContentQuality Assurance
Soft Skills
Excellent Communication SkillsAdaptabilityProblem-Solving