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Clinical Trial Internship Jobs (NOW HIRING)

Clinical Research Coordinator

Dallas, TX ยท On-site

$24 - $32/hr

Fresh graduates with relevant internships or clinical research training are encouraged to apply ... Maintain Trial Master File (TMF), Investigator Site File (ISF), and essential study documents.

Clinical Research Coordinator

Dallas, TX ยท On-site

$24 - $32/hr

Fresh graduates with relevant internships or clinical research training are encouraged to apply ... Maintain Trial Master File (TMF), Investigator Site File (ISF), and essential study documents.

... Clinical Trial Research. We are looking for bright and motivated individuals to join our Data Management team in Horsham, PA for a paid Internship. You will have the opportunity to learn and ...

... Clinical Trial Research. We are looking for bright and motivated individuals to join our Data Management team in Horsham, PA for a paid Internship. You will have the opportunity to learn and ...

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Clinical Trial Internship information

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How much do clinical trial internship jobs pay per hour?

As of Sep 2, 2026, the average hourly pay for clinical trial internship in the United States is $37.67, according to ZipRecruiter salary data. Most workers in this role earn between $25.72 and $48.08 per hour, depending on experience, location, and employer.

What is a clinical trial internship?

A Clinical Trial Internship is a temporary position designed for students or recent graduates to gain hands-on experience in the field of clinical research. Interns typically assist with tasks such as data collection, patient recruitment, regulatory documentation, and coordinating study logistics under the supervision of experienced professionals. This role provides valuable exposure to how clinical trials are conducted, including ethical considerations and regulatory requirements. Clinical Trial Internships are ideal for those interested in careers in medicine, pharmaceuticals, or healthcare research.

What types of projects or tasks can I expect to work on during a clinical trial internship?

During a Clinical Trial Internship, you can expect to assist with a variety of tasks such as data entry, reviewing case report forms, supporting regulatory documentation, and helping coordinate study logistics. Interns often work closely with clinical research coordinators and project managers, gaining exposure to the entire trial process from start-up to closeout. This hands-on experience provides a valuable understanding of Good Clinical Practice (GCP) guidelines and the opportunity to develop skills in teamwork, communication, and compliance within a fast-paced environment.

What are the key skills and qualifications needed to thrive as a clinical trial intern, and why are they important?

To thrive as a Clinical Trial Intern, you typically need a background in life sciences or a related field, along with knowledge of clinical research principles and regulatory guidelines. Familiarity with electronic data capture (EDC) systems, Microsoft Office, and Good Clinical Practice (GCP) certification are often expected. Strong organizational skills, attention to detail, and effective communication set outstanding interns apart. These skills are crucial for ensuring data integrity, regulatory compliance, and smooth collaboration within clinical research teams.

What is the difference between Clinical Trial Internship vs Clinical Research Coordinator?

AspectClinical Trial InternshipClinical Research Coordinator
Required CredentialsTypically students or recent graduates, some healthcare backgroundUsually requires a bachelor's degree in health sciences or related field
Work EnvironmentTemporary, educational setting, often part-time or summerFull-time, clinical setting, ongoing responsibilities
Employer & Industry UsagePharmaceutical companies, research institutions, universitiesHospitals, research centers, pharmaceutical companies

While a Clinical Trial Internship provides hands-on experience for students or entry-level individuals, a Clinical Research Coordinator manages ongoing clinical trials, overseeing patient recruitment, data collection, and compliance. Internships are ideal for gaining initial exposure, whereas coordinators handle the day-to-day operations of clinical studies.

What cities are hiring for Clinical Trial Internship jobs?

Cities with the most Clinical Trial Internship job openings:

What are the most commonly searched types of Clinical Trial jobs?

The most popular types of Clinical Trial jobs are:

What states have the most Clinical Trial Internship jobs?

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

Clinical Trial Operations Specialist II

Boston Scientific Gruppe

Maple Grove, MN โ€ข On-site

$68 - $129/hr

Other

Posted yesterday

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Job description

Additional Location(s): US-MA-Marlborough; US-MN-Maple Grove

Diversity - Innovation - Caring - Global Collaboration - Winning Spirit- High Performance

At Boston Scientific, weโ€™ll give you the opportunity to harness all thatโ€™s within you by working in teams of diverse and high-performing employees, tackling some of the most important health industry challenges. With access to the latest tools, information and training, weโ€™ll help you in advancing your skills and career. Here, youโ€™ll be supported in progressing โ€“ whatever your ambitions.

About the role:

Boston Scientific was recognized as a Glassdoor Best Place to Work in 2026, ranking No. 15 on the Top 100 list, reflecting the culture our employees experience every day.

At Boston Scientific Urology, we are committed to developing innovative technologies that improve the lives of patients with urologic and pelvic health conditions. As a Clinical Trial Operations Specialist II, you will support clinical research programs that generate the evidence needed to advance therapies across areas such as neuromodulation, pelvic floor disorders, stone management, benign prostatic hyperplasia, and prosthetic urology.

In this role, you will work closely with cross-functional teams to support the planning, execution, and oversight of global clinical studies that evaluate the safety, effectiveness, and real-world impact of innovative medical technologies. This position offers an excellent opportunity to build foundational clinical researchexpertisewhile contributing toevidencegeneration that informs regulatory submissions, scientific publications, healthcare provider education, and patient access to life-changing therapies

At Boston Scientific, we value collaboration andsynergy. This role follows a hybrid work model requiring employees to be in our localofficeMaple Grove,MNor Marlborough, MAat least three days per week. Boston Scientific will not offer sponsorship or take over sponsorship of an employment visa for thispositionat this time.Relocation assistance is not available for this position at this time.

Your responsibilities will include:

Support the project team in planning,executing,and managing operational aspects of global clinical trials.

Participatewith supervision, in the execution of clinical studiesin accordance withproject plans, budgets and resource allocations while following applicable regulatory requirements and standard operating procedures.

Track the development of project materials and collaborate with cross-functional team members on internal and external study materials, processes, manuals, plans,committees,and study systems.

Support-required sponsor regulatory submissions, as applicable.

Maintain documentation and processes that support a continuous state of audit readiness.

Collaborate with the project teamtoidentify,assess,and manage clinical study risks.

Partner effectively with departmental and cross-functional stakeholders to support clinical study and programobjectives.

Required qualifications:

Minimum bachelor's degree in biology, life sciences, nursing, biomedical engineering, public health, clinical research, or related field and 2 years of clinical research experience, for example, Clinical Research Coordinator, Clinical Trial Assistant, Clinical Operations Associate, Research Assistant, Regulatory Coordinator, or internship/co-op in clinical research.

Basic understanding of clinical research or healthcare environment.

Experience working with multiple stakeholders to complete projects, coordinate activities, and meet established timelines.

Demonstrated ability to organize andmaintainproject documentation, track deadlines, follow up on action items, and manage multiple assigned tasks simultaneously.

Abilityto work within established procedures, projectplans,and quality requirements.

Strong written and verbal communication skills.

Strong project management skills and experienced with Microsoft Office Suite

Demonstrated knowledge of Trial Master Files and essential clinical and regulatory documents

Preferredqualifications:

Proven experience supporting clinical studies, clinicalresearchor clinical trial operations, especially in medical devices

Working knowledge of Good Clinical Practice (GCP) principles; familiarity with ICH-GCP, ISO 14155, and applicable FDA clinical research regulations preferred.

Exposure to EDC, CTMS, eTMF or electronic medical records

Familiarity with clinical study documentation, studysystems,and regulatory processes.

Understanding clinical research quality requirements and audit-readiness practices.

Experience supporting global or cross-functional projectspreferred.

PreferredAssociation of Clinical Research Professionals (ACRP) accreditation.

Requisition ID:633925

Minimum Salary:$68100

Maximum Salary: $129400

The anticipated compensation listed above and the value of core and optional employee benefits offered by Boston Scientific (BSC) โ€“ see www.bscbenefitsconnect.comโ€” will vary based on actual location of the position and other pertinent factors considered in determining actual compensation for the role. Compensation will be commensurate with demonstrable level of experience and training, pertinent education including licensure and certifications, among other relevant business or organizational needs. At BSC, it is not typical for an individual to be hired near the bottom or top of the anticipated salary range listed above.

Compensation for non-exempt (hourly), non-sales roles may also include variable compensation from time to time (e.g., any overtime and shift differential) and annual bonus target (subject to plan eligibility and other requirements).

Compensation for exempt, non-sales roles may also include variable compensation, i.e., annual bonus target and long-term incentives (subject to plan eligibility and other requirements).

For MA positions: It is unlawful to require or administer a lie detector test for employment. Violators are subject to criminal penalties and civil liability.

Boston Scientific transforms lives through innovative medical technologies that improve the health of patients around the world. As a global medical technology leader for more than 45 years, we advance science for life byprovidinga broad range of high-performance solutions that address unmet patient needs and reduce the cost of healthcare. Our portfolio of devices and therapies helps physicians diagnose and treat complex cardiovascular, respiratory, digestive, oncological,neurologicaland urological diseases and conditions. Learn more at www.bostonscientific.com and follow us on LinkedIn .

Boston Scientific Corporation has been and will continue to be an equal opportunity employer. To ensure full implementation of its equal employment policy, the Company will continue to take steps to assure that recruitment, hiring, assignment, promotion, compensation, and all other personnel decisions are made and administered without regard to race, religion, color, national origin, citizenship, sex, sexual orientation, gender identity, gender expression, veteran status, age, mental or physical disability, genetic information or any other protected class.

Please be advised that certain US based positions, including without limitation field sales and service positions that call on hospitals and/or health care centers, require acceptable proof of COVID-19 vaccination status. Candidates will be notified during the interview and selection process if the role(s) for which they have applied require proof of vaccination as a condition of employment. Boston Scientific continues to evaluate its policies and protocols regarding the COVID-19 vaccine and will comply with all applicable state and federal law and healthcare credentialing requirements. As employees of the Company, you will be expected to meet the ongoing requirements for your roles, including any new requirements, should the Companyโ€™s policies or protocols change with regard to COVID-19 vaccination.

Among other requirements, Boston Scientific maintains specificprohibited substancetest requirements for safety-sensitive positions. This role is deemed safety-sensitive and, as such, candidates will be subject to a prohibited substance test as a requirement. The goal of the prohibited substance testing is to increase workplace safety in compliance with the applicable law.


Nearest Major Market: Minneapolis
Job Segment: Clinical Research, Medical Research, EMR, Compliance, Urology, Healthcare, Legal

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