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Biopharmaceutical Intern Jobs (NOW HIRING)

PhRMA

Fall Internship, Public Affairs

Washington, DC · On-site

$25 - $35/hr

The intern will broadly assist members of the Public Affairs Department and work with multiple ... PhRMA represents the country's leading innovative biopharmaceutical research companies, which are ...

Forus Inc

Senior Talent Partner

New York, NY · On-site

$200K - $325K/yr

The resulting network enables biopharma companies to design better research, launch new drugs more effectively, and invest in harder-to-treat conditions. Forus has exceptional product-market fit and ...

Labcorp

Associate Inside Sales Manager

$50/hr

... biopharma, biotech, and related sectors. * Clearly articulate Labcorp's RWD, genetic, and ... Employees regularly scheduled to work less than 20 hours, Casual, Intern, and Temporary employees ...

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Biopharmaceutical Intern information

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How much do biopharmaceutical intern jobs pay per hour?

As of Aug 7, 2026, the average hourly pay for biopharmaceutical intern in the United States is $17.04, according to ZipRecruiter salary data. Most workers in this role earn between $14.42 and $19.23 per hour, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive as a biopharmaceutical intern?

To thrive as a Biopharmaceutical Intern, you generally need a background in biology, chemistry, or a related field, often supported by progress toward a relevant degree. Familiarity with laboratory techniques, data analysis software, and compliance systems such as Good Laboratory Practices (GLP) is typically required. Strong attention to detail, teamwork, and effective communication are standout soft skills in this role. These competencies ensure that interns can support research, adhere to safety standards, and contribute meaningfully to scientific projects in a regulated environment.

What does a biopharmaceutical intern do?

A Biopharmaceutical Intern typically assists with research, development, and quality control of pharmaceutical products derived from biological sources. Responsibilities may include conducting laboratory experiments, analyzing data, maintaining lab equipment, and supporting the development of new drugs or therapies. Interns often work closely with scientists and engineers to gain hands-on experience in various aspects of the biopharmaceutical industry. This role provides valuable exposure to regulatory standards, lab techniques, and the drug development process. It's an excellent opportunity for students or recent graduates interested in careers in biotechnology or pharmaceutical sciences.
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Biopharmaceutical Intern jobs near you
Infographic showing various Biopharmaceutical Intern job openings in the United States as of August 2026, with employment types broken down into 17% Internship, 1% As Needed, 51% Full Time, 28% Part Time, 1% Temporary, and 2% Contract. Highlights an 93% Physical, 2% Hybrid, and 5% Remote job distribution, with an average salary of $35,436 per year, or $17 per hour.

Clinical Development Medical Director, MD Required

Jobtailor

California, MO • On-site

$180 - $280/hr

Other

Posted 2 days ago

New

Job description

Responsibilities
  • Responsible for medical and scientific oversight of clinical trials in Internal Medicine
  • Provides timely, study-related medical information and guidance
  • Conducts and documents periodic safety data review and ongoing clinical/medical data review
  • Represents the study team in internal protocol review governance submissions and interactions
  • Develops site selection criteria and ensures protocol training is delivered to site-facing colleagues
  • Ensures TMF compliance for clinical documents
  • Develops clinical guidance and reviews safety data
Requirements
  • Primary medical degree (e.g., MD, DO, MBBS, MBChB)
  • 4+ years of experience in biopharmaceutical industry in clinical research and development
  • Licensed by a licensing body to prescribe medicines for at least 2 years post intern/house officer/foundation period
  • Cardiometabolic disease experience preferred
  • Clinical research experience in study design, start-up, conduct, and close-out, including regulatory submissions and inspections
  • Scientific productivity via publications, posters, abstracts, and/or presentations
  • Extensive knowledge of clinical development, global and regional regulation, and ICH/GCP
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