IDAR Summer Intern (DM CM)

About Innovative Medicine

Our expertise in Innovative Medicine is informed and inspired by patients, whose insights fuel our science-based advancements. Visionaries like you work on teams that save lives by developing the medicines of tomorrow. Join us in developing treatments, finding cures, and pioneering the path from lab to life while championing patients every step of the way.

We are searching for the best talent for IDAR Summer Intern (DM CM) to be in Spring House, PA / Raritan, NJ or Titusville, NJ. The Intern term is from May to August, 2027. Full time requirement (40 hours per week). 2 vacancies are currently available.

Purpose

The Data Management and Central Monitoring (DM CM) Summer Internship provides undergraduate students with hands-on experience supporting clinical data management and data acquisition activities within Global Development. Based on business needs, interns may be assigned to a Clinical Data Manager or Data Acquisition Expert-EDC role. During this 12-week program, interns will gain practical exposure to clinical trials, data management processes, technology platforms, global regulations, and cross-functional drug development while contributing to projects that support the delivery of medicines to patients. The program also provides opportunities for professional development through coaching, mentoring, networking, and collaboration with cross-functional teams.

Responsibilities

• Executing assigned clinical trial activities within the scope of the internship.
• Performing activities in compliance with applicable J&J and Data Management and Central Monitoring SOPs, processes, policies, training requirements, Good Clinical Practice (GCP), and applicable regulatory requirements.
• Collaborating with colleagues within Data Management and Central Monitoring and other cross-functional partners.
• Supporting innovation and process improvement projects, as assigned.
• Contributing to projects aligned with strategic priorities and Our Credo values.

Clinical Data Manager Assignment

• Supporting scientific clinical study data review activities.
• Assisting with the management and resolution of Study Responsible Scientist (SRS) and Study Responsible Physician (SRP) queries within Electronic Data Capture (EDC) systems.
• Supporting additional clinical data review activities, including coding and Serious Adverse Event (SAE) reconciliation.

Data Acquisition Expert-EDC Assignment

• Supporting the setup and maintenance of Electronic Data Capture (EDC) systems for assigned clinical trials.
• Supporting EDC activities according to established best practices and guidelines.
• Gaining exposure to clinical technology platforms such as Medidata Rave.

Qualifications / Requirements

• Completion of Undergraduate Freshman year at an accredited University is required.
• Currently pursuing a bachelor’s degree in Science (Biology, Chemistry, Biochemistry, Neuroscience, Pharmacology, and others.), Data and/or Computer Science, Statistics, Analytics, Mathematics, IT and Systems, or related fields.
• Have a cumulative GPA of 3.5 or higher, which is reflective of all college coursework.
• Candidates must be enrolled in an undergraduate university program at the time of 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., must not require sponsorship of an employment visa (e.g., H-1B or green card) at the time of application or in the future.

Preferred Qualifications

• Experience or exposure to data review, data analysis, or data quality activities.
• Experience or familiarity with technology platforms and systems used for the collection, management, analysis, or reporting of data.
• Familiarity with Electronic Data Capture (EDC) systems or clinical data management technologies is 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.