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Intern Biotech Clinical Research Jobs (NOW HIRING)

Tranquil Clinical Research

Research Intern

Webster, TX · On-site

Description The Research Intern is an entry level clinical research position. The Intern will perform a variety of research, database and clerical duties of a routine and technical nature to support ...

Duke University

Clinical Research Intern

Durham, NC · On-site

$18 - $26.49/hr

As the Clinical Research Intern, you'll be a vital part of a collaborative, interdisciplinary research environment that exposes you to the full lifecycle of clinical research. Be Bold. The Clinical ...

Duke University

Clinical Research Intern

Durham, NC · On-site

$18 - $26.49/hr

As the Clinical Research Intern, you'll be a vital part of a collaborative, interdisciplinary research environment that exposes you to the full lifecycle of clinical research. Be Bold. The Clinical ...

Wake Research

Clinical Research Coordinator

Dallas, TX

$24 - $32/hr

Company Description M3 Wake Research, an M3USA Company, is an integrated network of premier investigational sites meeting the clinical research needs of global biopharmaceutical, biotechnology ...

New

Wake Research

Clinical Research Coordinator

Dallas, TX · On-site

$24 - $32/hr

Company Description M3 Wake Research, an M3USA Company, is an integrated network of premier investigational sites meeting the clinical research needs of global biopharmaceutical, biotechnology ...

Winaxis

Clinical Research Coordinator

Dallas, TX · On-site

$24 - $32/hr

Bachelor's or Master's degree in Life Sciences, Pharmacy, Nursing, Biotechnology, Microbiology, or a related field. * 0-3 years of experience in clinical research or clinical trial coordination.

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Intern Biotech Clinical Research information

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

As of Aug 29, 2026, the average monthly pay for intern 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 the difference between Intern Biotech Clinical Research vs Clinical Research Associate?

AspectIntern Biotech Clinical ResearchClinical Research Associate
CredentialsTypically pursuing or recent graduate in life sciences or related fieldBachelor's degree in life sciences; some roles prefer certifications
Work EnvironmentSupportive, entry-level, learning-focused in biotech or pharma settingsField and office-based, monitoring clinical trials
Employer & IndustryBiotech companies, research institutionsPharmaceutical companies, CROs

Intern Biotech Clinical Research roles are designed for students or recent graduates gaining initial industry experience, focusing on learning and support tasks. Clinical Research Associates are more experienced, responsible for monitoring and managing clinical trials, requiring some prior knowledge. Both roles are essential in the clinical research process but differ mainly in experience level and responsibilities.

What cities are hiring for Intern Biotech Clinical Research jobs?

Cities with the most Intern 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 Intern Biotech Clinical Research jobs?

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

Intern Biotech Clinical Research jobs near you

Research Intern

Webster, TX • On-site

Tranquil Clinical Research
Scientific Research and Development Services • 11 - 50 employees
Learn more about Tranquil Clinical Researchexternal

Other

Re-posted 7 hours ago

Job description

Please do not call our office - we will reach out to you.
Description
The Research Intern is an entry level clinical research position. The Intern will perform a variety of research, database and clerical duties of a routine and technical nature to support clinical trials and assist investigators to organize, gather and compile clinical research data. The Intern will primarily be responsible for the collection, aggregation, and analysis of data. The Research Intern will also form other duties such as data entry, and administrative duties such as filing, record keeping, photocopying, and creating flyers/posters. The Research Intern will be supervised by a senior research staff member or principal investigator.
Qualifications
Minimum Education
High School Diploma or GED (Required) Or
Bachelor's Degree May require a Bachelor's degree based on the specific internship program
Minimum Work Experience
0-2 years related experience. 2 years experience working in a medical or scientific research setting, preferred
Required Skills/Knowledge
Demonstrates adherence with the standards for the responsible conduct of research.
Work requires organizational skills, knowledge of basic mathematical, data collection and analysis, and research principles.
Knowledge of human subjects research.
Excellent computer skills in a Windows and/or Mac environment.
Excellent writing, editing, and proofing skills.
Required Licenses and Certifications
CITI Certification (Required)
Valid Driver's license
Functional Accountabilities
Research Projects

  • Maintain confidentiality of data, as required.
  • Plan, conduct and manage research projects.
  • Responsible for appropriate use of research funds and resources.
Project Administration
  • Ensure compliance with program guidelines and requirements of funding and regulatory agencies.
  • Stay informed of and adhere to human research protection guidelines, relevant best practices, and changes to any research protocol.
  • Accurately complete IRB submissions on time.
  • Anticipate study needs and work to accomplish them in a timely manner.
  • Seek assistance, when needed.
Data Collection
  • Collect data in order to facilitate operational and clinical research activities.
  • Enter clinical and research data and information into database, include electronic CRFs and sample tracking databases.
  • Follow established guidelines in the collection of clinical data and/or administration of clinical studies.
  • Support aggregation and analysis of study data, as directed by senior research staff.
Professional Development
  • Attend and contribute to team meetings, including working to set and achieve project timelines and deliverables.
  • Obtain training and certification as required by study protocol (e.g., CITI training).
  • Comply with all annual job-related training requirements.

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