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Internship Biotech Clinical Research Jobs (NOW HIRING)

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Clinical Research Coordinator

Fort Worth, TX · On-site

$45K - $55K/yr

Clinical Research Coordinator Prime Clinical Research Location: On-Site Employment Type: Full-Time ... companies, biotechnology organizations, and contract research organizations. Our mission is to ...

IQVIA

Clinical Research Associate, IQVIA Biotech

Austin, TX · On-site

$71K - $169K/yr

IQVIA Biotech is now hiring for CRA 2 with a minimum of 1 year of on-site monitoring and will also ... Job Overview We are seeking a dedicated Clinical Research Associate (CRA) to join our team and play ...

IQVIA

Clinical Research Associate, IQVIA Biotech

Ithaca, NY · On-site

$71K - $169K/yr

IQVIA Biotech is now hiring for CRA 2 with a minimum of 1 year of on-site monitoring and will also ... Job Overview We are seeking a dedicated Clinical Research Associate (CRA) to join our team and play ...

IQVIA

Clinical Research Associate, IQVIA Biotech

Austin, TX · On-site

$71K - $169K/yr

IQVIA Biotech is now hiring for CRA 2 with a minimum of 1 year of on-site monitoring and will also ... Job Overview We are seeking a dedicated Clinical Research Associate (CRA) to join our team and play ...

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Internship Biotech Clinical Research information

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How much do internship biotech clinical research jobs pay per month?

As of Sep 5, 2026, the average monthly pay for internship biotech clinical research in the United States is $6,439.50, according to ZipRecruiter salary data. Most workers in this role earn between $4,416.67 and $7,666.67 per month, depending on experience, location, and employer.

What is an internship in biotech clinical research?

An Internship in Biotech Clinical Research is a temporary position, typically for students or recent graduates, that provides hands-on experience in the field of biotechnology and clinical research. Interns assist with research studies, data collection, regulatory documentation, and lab work, gaining practical skills under the guidance of experienced professionals. This opportunity allows interns to understand the clinical trial process, learn about regulatory requirements, and build a foundation for a career in the biotech or pharmaceutical industry.

What are the typical responsibilities of an intern in biotech clinical research?

As an intern in biotech clinical research, you can expect to assist with data collection, maintain accurate study documentation, and support the coordination of clinical trials. Interns often help prepare study materials, monitor lab results under supervision, and attend team meetings to discuss project progress. These responsibilities provide hands-on experience with the clinical research process, while also allowing you to contribute meaningfully to the success of ongoing studies. Collaboration with clinical coordinators, scientists, and regulatory staff is common, offering valuable networking and learning opportunities.

What are the key skills and qualifications needed for an internship in biotech clinical research?

To thrive in a Biotech Clinical Research Internship, you need a solid understanding of biological sciences, data analysis, and research methodologies, often supported by current enrollment in a life sciences degree program. Familiarity with laboratory tools, statistical software (such as SPSS or R), and clinical trial management systems is highly valued. Strong attention to detail, effective communication, and teamwork are crucial soft skills for collaborating with research teams and handling complex data. These skills and qualities are important to ensure accurate research processes, data integrity, and successful clinical trial outcomes.

What is the difference between Internship Biotech Clinical Research vs Clinical Research Associate?

AspectInternship Biotech Clinical ResearchClinical Research Associate
Required CredentialsTypically students or recent graduates, some may have relevant coursework or certificationsBachelor's degree in life sciences, often with certifications like CCRP or RAC
Work EnvironmentEducational setting, laboratory, or clinical trial sites under supervisionMonitoring clinical trials at sites, data review, and regulatory compliance
Employer & Industry UsagePharmaceutical companies, biotech firms, research institutions, often as a learning rolePharmaceutical companies, CROs, biotech firms, as a professional role

Internship Biotech Clinical Research positions are primarily educational opportunities for students or recent graduates to gain industry experience. In contrast, Clinical Research Associates are trained professionals responsible for monitoring and managing clinical trials. The internship serves as a stepping stone toward a career as a CRA, which requires more experience and certifications.

What cities are hiring for Internship Biotech Clinical Research jobs?

Cities with the most Internship Biotech Clinical Research job openings:

What are the most commonly searched types of Biotech Clinical Research jobs?

The most popular types of Biotech Clinical Research jobs are:

What states have the most Internship Biotech Clinical Research jobs?

States with the most job openings for Internship Biotech Clinical Research jobs include:

Internship Biotech Clinical Research jobs near you
Infographic showing various Internship Biotech Clinical Research job openings in the United States as of August 2026, with employment types broken down into 3% As Needed, 71% Full Time, 18% Part Time, and 8% Contract. Highlights an 95% Physical, 1% Hybrid, and 4% Remote job distribution, with an average salary of $77,274 per year, or $37.2 per hour.

Senior Clinical Research Coordinator

Headlands Research

Riverside, CA • On-site

$25.25 - $33.75/hr

Full-time

Re-posted 5 days ago

Job description

 Riverside, CA
Artemis Institute for Clinical Research (a Headlands Research site)
 Full-time | Onsite (no opportunities for hybrid or remote)

For experienced CRCs looking for stability, collaboration, and meaningful work

If you're an experienced Clinical Research Coordinator who values strong operations, multidisciplinary collaboration, and a schedule that actually supports work-life balance, Artemis Institute for Clinical Research may be the right next step in your career.

Our Riverside site is known for its depth of experience, thoughtful study execution, and team-based approach to clinical research-particularly in vaccines, CNS, general medicine, and psychiatry.

About Artemis Institute for Clinical Research

Artemis Institute for Clinical Research in Riverside is a patient-centered clinical research site and part of the Headlands Research family. Founded with a core mission to prioritize patients, advance medicine, and improve the world, Artemis combines rigorous, process-driven trial management with a compassionate approach to care. The site conducts high-quality clinical trials across multiple therapeutic areas-including psychiatric, metabolic, vaccine, and healthy volunteer studies-and has helped thousands of participants contribute to meaningful medical advancements. Artemis is known for its collaborative team culture, strong operational standards, and commitment to excellence in delivering reliable, protocol-compliant research on behalf of pharmaceutical and biotech sponsors.

Why Experienced CRCs Choose Artemis
  • Multi-disciplinary collaboration with seasoned investigators and clinical staff
  • Strong operational support and clear SOPs
  • Exposure to complex, meaningful studies-not just high-volume turnover
  • Backing of a growing research network with resources and stability

This role is ideal for CRCs who enjoy owning their studies, working with competent teams, and being trusted to execute with precision.

Responsibilities:

  • Provide the highest level of care for study patients
  • Deliver excellent customer service to pharmaceutical clients
  • Coordinate all aspects of assigned clinical trials from site initiation through close-out
  • Conduct subject visits and ensure accurate, timely documentation in compliance with protocol and standards
  • Maintain compliance with protocols, GCP/ICH guidelines, FDA regulations, IRB requirements, and SOPs
  • Manage subject recruitment, informed consent, and retention activities
  • Ensure timely EDC data entry and resolution of queries
  • Report and follow up on AEs, SAEs, and protocol deviations
  • Collaborate with investigators, sponsors/CROs, labs, and internal teams
  • Prepare for and participate in monitoring visits, audits, and inspections
  • Maintain regulatory documentation and ensure training compliance for amendments and systems
  • Perform study procedures such as phlebotomy, ECGs, and sample processing (as trained)
  • Attend investigator meetings and provide cross-functional support as needed
  • Maintain working knowledge of protocols, lab manuals, equipment calibration, and inventory

Requirements:

  • At least two years of experience managing multiple phase 2-4 industry-sponsored clinical trial studies as the primary coordinator required
  • High school diploma or GED required
  • Strong understanding of FDA regulations, ICH-GCP, and clinical trial operations
  • Experience with EDC, IVRS, and clinical research platforms
  • Proficiency in medical terminology and clinical documentation
  • Strong organizational skills with the ability to manage multiple studies
  • Clear, professional verbal and written communication skills
  • Comfortable working onsite in a collaborative, clinical environment
Who Thrives in This Role
  • CRCs who want structure, support, and accountability
  • Those interested in taking the next step in managing people
  • Professionals who value teamwork over silos
  • Coordinators who care about data quality, patient experience, and compliance
  • Those ready to grow within a stable, well-established research site

 Apply today if you're looking for a CRC role where your experience is respected, your schedule is predictable, and your work directly contributes to advancing meaningful medical research.

Apply