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Johnson & Johnson

IDAR Summer Intern – DM CM

Johnson & Johnson

. Support clinical data management and data acquisition activities within Global Development .

Posted 11/9/2026full-timeUnited StatesEntry Level💰 $24 - $53 per hourWebsite

Core Competencies

Role fit
Core Competencies

Use this summary to align your resume positioning with the role.

Demonstrates strong analytical skills and attention to detail in clinical data management and data acquisition activities. Familiar with Electronic Data Capture (EDC) systems and Good Clinical Practice (GCP) guidelines, with the ability to collaborate effectively in a hybrid work environment.

Highest-signal resume keywords
Clinical Data ManagementElectronic Data Capture (EDC)Good Clinical Practice (GCP)Data AnalysisAnalytical Skills

ATS Keywords

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Applicant Tracking System Keywords

Tip: use these terms in your resume and cover letter to boost ATS matches.

Hard Skills
Data ReviewData Quality ActivitiesData AcquisitionStatistical AnalysisClinical Trial Support
Soft Skills
Problem-Solving SkillsCommunication SkillsTeam CollaborationSelf-StarterTime Management
Tools & Technologies
Medidata RaveClinical Technology Platforms
Industry Keywords
Clinical TrialsPharmaceutical Drug DevelopmentRegulatory RequirementsSOPsProcess Improvement

About the role

Key responsibilities & impact
  • Support clinical data management and data acquisition activities within Global Development
  • Execute assigned clinical trial activities within the scope of the internship
  • Perform activities in compliance with J&J and Data Management and Central Monitoring SOPs, processes, policies, training requirements, Good Clinical Practice (GCP), and applicable regulatory requirements
  • Collaborate with Data Management and Central Monitoring colleagues and cross-functional partners
  • Support innovation and process improvement projects
  • Contribute to projects aligned with strategic priorities and Our Credo values
  • Clinical Data Manager assignment: support scientific clinical study data review activities
  • Clinical Data Manager assignment: assist with management and resolution of Study Responsible Scientist and Study Responsible Physician queries in EDC systems
  • Clinical Data Manager assignment: support clinical data review activities, including coding and Serious Adverse Event reconciliation
  • Data Acquisition Expert-EDC assignment: support setup and maintenance of EDC systems for assigned clinical trials
  • Data Acquisition Expert-EDC assignment: support EDC activities according to established best practices and guidelines
  • Gain exposure to clinical technology platforms such as Medidata Rave

Requirements

What you’ll need
  • Completion of Undergraduate Freshman year at an accredited University is required
  • Currently pursuing a bachelor’s degree in Science, Data and/or Computer Science, Statistics, Analytics, Mathematics, IT and Systems, or related fields
  • Cumulative GPA of 3.5 or higher
  • Must be enrolled in an undergraduate university program during the internship and must not graduate during the internship period
  • Ability to work within the designated hybrid model, including three days at a local New Jersey or Pennsylvania site and two days remotely
  • Candidates are responsible for transportation to the applicable local site
  • Ability to work effectively within established processes, procedures, policies, and regulatory requirements
  • Permanently authorized to work in the U.S. without current or future employment visa sponsorship
  • Students currently on CPT, OPT, or STEM OPT generally do not meet the program requirements unless eligible for an alternative long-term status without company sponsorship
  • Under-18 candidates may need required working papers or documentation and parental consent for background checks
  • Preferred: experience or exposure to data review, data analysis, or data quality activities
  • Preferred: familiarity with technology platforms and systems for data collection, management, analysis, or reporting
  • Familiarity with Electronic Data Capture (EDC) systems or clinical data management technologies preferred
  • Exposure to Medidata Rave or similar clinical data platforms is a plus
  • Interest in clinical trials, clinical data management, data acquisition, or pharmaceutical drug development
  • Strong analytical and problem-solving skills with attention to detail
  • Excellent written and verbal communication and presentation skills
  • Ability to manage multiple assignments and priorities while delivering results
  • Ability to work independently as a self-starter while contributing effectively to team objectives
  • Demonstrated leadership or participation in academic programs, campus organizations, or community service activities

Benefits

Comp & perks
  • Company sponsored employee medical benefits in accordance with the terms of the plan
  • Sick time benefits: up to 40 hours per calendar year; employees residing in Washington State may receive up to 56 hours per calendar year
  • Participation in the Company’s consolidated retirement plan (pension)
  • Professional development through coaching, mentoring, networking, and collaboration with cross-functional teams