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Internship Clinical Research Startup information

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$2.1K

$6.4K

$7.8K

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

As of Aug 29, 2026, the average monthly pay for internship clinical research startup 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 Internship Clinical Research Startup vs Clinical Research Coordinator?

AspectInternship Clinical Research StartupClinical Research Coordinator
Required CredentialsTypically pursuing or recent graduate, some may have relevant courseworkUsually requires a bachelor's degree in health sciences or related field, certification preferred
Work EnvironmentInternship setting, often in startup or early-stage companies, learning-focusedClinical settings, hospitals, or research centers, more structured
Employer & Industry UsageStartups, biotech firms, research organizationsHospitals, research institutions, pharmaceutical companies
Common Search & ComparisonYesYes

The Internship Clinical Research Startup is an entry-level, learning-focused role often found in startup environments, while a Clinical Research Coordinator is a more experienced role with specific certifications, working in established clinical settings. Both roles support clinical research but differ in experience level and work environment.

What cities are hiring for Internship Clinical Research Startup jobs?

Cities with the most Internship Clinical Research Startup job openings:

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

The most popular types of Clinical Research Startup jobs are:

What states have the most Internship Clinical Research Startup jobs?

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

Internship Clinical Research Startup jobs near you

Clinical Research Manager (68740)

United Digestive

Atlanta, GA • On-site

Full-time

Posted 22 days ago

United Digestive rating

6.4

Company rating: 6.4 out of 10

Based on 20 frontline employees who took The Breakroom Quiz

Job description

GENERAL SUMMARY OF DUTIES: Leads day-to-day multi-site clinical research operations, staff, and study execution from feasibility through closeout in alignment with the Director's strategy.
 
Exceptional candidates with experience beyond the posted level are encouraged to apply. Based on qualifications, experience, and organizational needs, consideration may be given to placement at a higher level.
 
RESPONSIBILITIES: 
Duties include but are not limited to: 
  • Supervise and provide leadership to Clinical Research Coordinators and Research Assistants/Interns
  • Lead day-to-day multi-site clinical research operations and promote consistent, efficient study execution
  • Manage the study lifecycle from feasibility and startup through conduct, monitoring, and closeout
  • Track enrollment, timelines, milestones, compliance, and data quality; resolve issues and escalate significant risks
  • Serve as the operational liaison among investigators, sponsors, CROs, vendors, staff, and centralized support teams
  • Ensure regulatory documentation and study activities meet FDA, ICH-GCP, HIPAA, IRB, sponsor, and organizational requirements
  • Conduct quality reviews, implement SOPs and CAPAs, and maintain audit and inspection readiness
  • Recruit, onboard, train, mentor, evaluate, and allocate research staff based on study and site priorities
  • Support research systems, standardized workflows, and practical process improvements across sites
 
EDUCATION, SKILLS, & EXPERIENCE: 
  • Required: 
    • Bachelor's degree in nursing, life sciences, public health, healthcare administration, or a related field
    • At least five years of clinical research experience, including study coordination or site management and direct supervision of research personnel.
    • Demonstrated experience managing study startup, site activation, conduct, monitoring, closeout, and multi-site operational workflows
    • Knowledge of FDA regulations, ICH-GCP, HIPAA, and IRB requirements, with strong project management, people-leadership, communication, and organizational skills
  • Preferred: 
    • Master's degree in clinical research, healthcare administration, public health, nursing, or a related field
    • Clinical research certification and experience with research systems and process improvement
 
WORK ENVIRONMENT: 
Requires sitting and standing associated with a normal office environment. Travel required as business needs dictate.
 
DRUG FREE WORKPLACE: 
United Digestive is a drug-free workplace. All offers of employment are contingent upon passing a pre-employment drug screening.
 
EQUAL OPPORTUNITY EMPLOYER: 
United Digestive is an equal opportunity employer and will not tolerate discrimination in employment on the basis of race, color, age, sex, sexual orientation, gender identity or expression, religion, disability, ethnicity, national origin, marital status, veteran status, genetic information or any other legally protected classification or status.
 
 
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