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Location
In office (Hyderabad)
Seniority
Intern · 2+ years exp
Visa
Sponsors visas in United States; no register of this country names it
Employment
Internship

Confirmed on the employer's own hiring board on Nov 12, 2026. First seen by Alion on Nov 12, 2026. Johnson & Johnson scores A on the Alion truth index.

Overview
Company
Impact
Profile match
Johnson & Johnson is a global healthcare company headquartered in New Brunswick, New Jersey, working across Innovative Medicine, its pharmaceutical business, and MedTech, which covers orthopaedics, surgery, cardiovascular, vision and robotics. Founded in 1886 and listed on the NYSE, it operates research, manufacturing and commercial sites worldwide, including Raritan, West Chester, Cork, Leiden, Zug, Norderstedt, Madrid and Shanghai, and the Ottava soft-tissue surgical robotics program in Cincinnati. Its openings span production operators, supply chain and transport leads, quality, tax and HR managers, data transformation, digital product and scientific roles.

At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at jnj.com.

As guided by Our Credo, Johnson & Johnson is responsible to our employees who work with us throughout the world. We provide an inclusive work environment where each person is considered as an individual. At Johnson & Johnson, we respect the diversity and dignity of our employees and recognize their merit.

Job Function:

Career Programs

Job Sub Function:

Non-LDP Intern/Co-Op

Job Category:

Career Program

All Job Posting Locations:

Hyderabad, Andhra Pradesh, India

Job Description:

Position Summary:

The Experienced Programmer is an individual contributor with knowledge of data structures, industry standards, programming languages, and programming methods. This role supports data analyses and reporting activities within trial activities in accordance with departmental processes and procedures.

This position is a member of the programming team, capable of supporting programming activities of one or more trials of low to medium complexity/criticality and may contribute to departmental innovation and process improvement projects.

Principal Responsibilities:

  • Completes and may lead programming trial activities of low to medium complexity and/or criticality, with high quality and timeliness of deliverables.
  • Accountable for the design and development of programs in support of clinical research analysis and reporting.
  • Performs appropriate level of verification of programming and reporting activities. Reviews and provides input for project requirements and documentation.
  • Supports submission activities including but not limited to creation, verification, and delivery of CDISC compliant and/or non-standard data packages and reviewer’s guides.
  • Follows departmental processes and procedures, ensures use of latest standards and deployment of current technologies.
  • May contribute to departmental innovation and process improvement projects.
  • Collaborates effectively with team and cross-functional members.
  • Ensures continued compliance with required company and departmental training, time reporting and other business/operational processes as required for position.

Principal Relationships:

This role reports into a people manager position within the Delivery Unit and is accountable to the Portfolio and Study Leads for assigned activities and responsibilities

Functional contacts within IDAR include but are not limited to: Leaders and leads in Data Management and Central Monitoring, Programming Leads, Clinical Data Standards, Regulatory Medical Writing Leads, and system support organizations.

  • Functional Contacts within J&J Innovative Medicine (as collaborator or peer) include but are not limited to: Statistics, Clinical, Global Medical Safety, Project Management, Regulatory, Strategic Partnerships, Human Resources.
  • External contacts include but are not limited to external partners, CRO management and vendor liaisons, industry peers and working groups.

Education and Experience Requirements:

Bachelor’s degree or higher and/or equivalent in computer science, data science/data engineering,

mathematics, public health, or another relevant scientific field (or equivalent theoretical/technical

depth).

Experience and Skills Required:

  • Approx. 2+ years of relevant programming experience, preferably in Pharmaceutical, CRO or Biotech industry or related field or industry.
  • Basic knowledge of regulatory guidelines (e.g. ICH-GCP) and relevant clinical R&D concepts.
  • Experience working in a team environment preferred.
  • Excellent written and verbal communications skills.
  • Knowledge of data structures and relevant programming languages for data manipulation/statistical analysis and reporting. May include SAS, R, Python, etc. SAS knowledge is preferred for Clinical Programming role.
  • Basic knowledge of processes, methods, and concepts relevant to programming.

Required Skills:

Preferred Skills:

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