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Internship Clinical Study Start Up Jobs (NOW HIRING)

Medpace, Inc.

CO · Hybrid

This position will be an integral part of the Clinical Operations leadership team and requires a strong understanding of how study start-up and regulatory submissions are integrated with other ...

Amgen, Inc.

Associate Director Study Start-up

$182K - $212K/yr

Career Category Clinical Join Amgen's Mission of Serving Patients At Amgen, if you feel like you're ... Study Start Up Hub - Associate Director Study Start-up What you will do Let's do this. Let's change ...

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BeiGene, Inc.

Regional Clinical Study Manager

Generates, manages, and maintains high quality study start up and recruitment timelines for region and tracks progress towards these * Ensures that the clinical study is operationally feasible in the ...

TechData Service Company LLC

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Clinical Research Specialist (LC18246-1)

Irvine, CA · On-site

$54 - $56/hr

The main function of a clinical research specialist is to perform study start-up and conduct activities including ICF review that meets regulatory requirements, creating study specific essential ...

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Internship Clinical Study Start Up information

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How much do internship clinical study start up jobs pay per hour?

As of Jul 20, 2026, the average hourly pay for internship clinical study start up in the United States is $24.09, according to ZipRecruiter salary data. Most workers in this role earn between $20.19 and $24.76 per hour, depending on experience, location, and employer.

What is the difference between Internship Clinical Study Start Up vs Clinical Research Coordinator?

AspectInternship Clinical Study Start UpClinical Research Coordinator
CredentialsTypically pursuing or holding a relevant degree (e.g., life sciences, healthcare)Often requires a degree in health sciences or related field, with certifications preferred
Work EnvironmentAssists in preparing sites for clinical trials, often in a training or entry-level capacityManages daily trial activities at clinical sites, coordinating with investigators and staff
Employer & Industry UsageUsed in pharmaceutical companies, CROs, and research institutions during early trial phasesCommonly employed in hospitals, research centers, and clinical trial sites

While both roles support clinical trials, an Internship Clinical Study Start Up focuses on assisting with trial preparations and site readiness, often as an entry-level position or trainee. In contrast, a Clinical Research Coordinator manages ongoing trial activities, ensuring compliance and data integrity at clinical sites.

What types of projects and tasks can an intern expect to handle in a Clinical Study Start Up role?

As an intern in Clinical Study Start Up, you will typically support activities such as preparing regulatory submission documents, tracking site activation milestones, and assisting with communication between study sites and sponsors. You'll gain hands-on experience with study documentation, database entry, and compliance checks, often working closely with clinical operations teams and regulatory specialists. This role offers valuable insight into the clinical trial initiation process and provides a strong foundation for future roles in clinical research.

What are the key skills and qualifications needed to thrive as an Internship Clinical Study Start Up, and why are they important?

To thrive as an Internship Clinical Study Start Up, you need foundational knowledge of clinical research processes, regulatory requirements, and attention to detail, often gained through coursework in life sciences or related fields. Familiarity with clinical trial management systems (CTMS), Microsoft Office Suite, and understanding of ICH-GCP guidelines are typically important. Strong organizational, communication, and teamwork skills help you coordinate study start-up activities and collaborate with diverse stakeholders. These competencies ensure efficient study initiation, regulatory compliance, and effective cross-functional collaboration in clinical research environments.

What is an Internship in Clinical Study Start Up?

An Internship in Clinical Study Start Up is a temporary position where students or recent graduates assist with the initial phases of clinical trials. This role typically involves helping with regulatory document preparation, site selection, ethics committee submissions, and coordination between study teams. Interns gain hands-on experience in clinical research processes, compliance requirements, and project management. It’s a valuable opportunity for those interested in pharmaceutical, biotechnology, or healthcare research careers.
What cities are hiring for Internship Clinical Study Start Up jobs? Cities with the most Internship Clinical Study Start Up job openings:
What are the most commonly searched types of Clinical Study Start Up jobs? The most popular types of Clinical Study Start Up jobs are:
What states have the most Internship Clinical Study Start Up jobs? States with the most job openings for Internship Clinical Study Start Up jobs include:
Internship Clinical Study Start Up jobs near you
Entry-Level Study Start-Up Coordinator

Entry-Level Study Start-Up Coordinator

Medpace, Inc.

Cincinnati, OH

Other

Medical, PTO

Re-posted 22 days ago

Medpace rating

8.5

Company rating: 8.5 out of 10

Based on 9 frontline employees who took The Breakroom Quiz

14th of 59 rated research

Job description

Job Summary

Our clinical operations activities are growing rapidly, and we are currently seeking full-time, office-based Study Start-Up Coordinators to join our Regulatory Submissions team. In this position you will work independently and collaboratively to manage timelines, meet goals, and play a key role in the clinical trial management and study start-up process at Medpace. If you are seeking an exciting, entry-level position where you can build a foundation in the clinical research industry and develop/grow your career through our robust training program, then this is the opportunity for you.

Responsibilities
  • Communicate with research sites (doctor's offices, universities, hospitals, etc.) to collect all essential documents required before the site begins to screen patients to participate in the clinical trial;
  • Maintain and perform ongoing quality review of trial documents within the Trial Master File (TMF);
  • Collect, review, organize, and assemble regulatory start-up submissions (includes submissions to Institutional Review Boards); and
  • Maintain timelines for study start-up through internal team collaboration.

SITE ACTIVATION & MAINTENANCE (SAM) TRAINING PROGRAM

Medpace training programs are curated to educate and support experienced associates, as well as those that are new to the industry. The SAM Training Program embraces evidence based learning & development models to advance professional learning and employee performance. In the program, you will...

  • Complete independent learning modules, interactive exercises, and team workshops through the core curriculum;
  • Gain exposure to real-world tasks through a robust mentoring program; and
  • Join other professionals revolutionizing efficient and seamless study start-up to advance clinical trials.
Qualifications
  • Bachelor's degree is required (Life Sciences field preferred);
  • Some experience in an office setting is preferred;
  • Excellent organizational and prioritization skills;
  • Knowledge of Microsoft Office; and
  • Great attention to detail and excellent oral and written communication skills.

Travel: None

Medpace Overview

Medpace is a full-service clinical contract research organization (CRO). We provide Phase I-IV clinical development services to the biotechnology, pharmaceutical and medical device industries. Our mission is to accelerate the global development of safe and effective medical therapeutics through its scientific and disciplined approach. We leverage local regulatory and therapeutic expertise across all major areas including oncology, cardiology, metabolic disease, endocrinology, central nervous system, anti-viral and anti-infective. Headquartered in Cincinnati, Ohio, employing more than 6,000 people across 40+ countries.

Why Medpace?

People. Purpose. Passion. Make a Difference Tomorrow. Join Us Today.

The work we've done over the past 30+ years has positively impacted the lives of countless patients and families who face hundreds of diseases across all key therapeutic areas. The work we do today will improve the lives of people living with illness and disease in the future.

Cincinnati Perks

  • Flexible work environment
  • Competitive PTO packages, starting at 20+ days
  • Competitive compensation and benefits package
  • Company-sponsored employee appreciation events
  • Employee health and wellness initiatives
  • Community involvement with local nonprofit organizations
  • Discounts on local sports games, fitness gyms and attractions
  • Modern, ecofriendly campus with an on-site fitness center
  • Structured career paths with opportunities for professional growth
  • Discounted tuition for UC online programs

Awards

  • Named a Top Workplace in 2024 by The Cincinnati Enquirer

  • Recognized by Forbes as one of America's Most Successful Midsize Companies in 2021, 2022, 2023 and 2024
  • Continually recognized with CRO Leadership Awards from Life Science Leader magazine based on expertise, quality, capabilities, reliability, and compatibility

What to Expect Next

A Medpace team member will review your qualifications and, if interested, you will be contacted with details for next steps.

Employment Type: OTHER

What Medpace employees say

Pay

Benefits

Hours and flexibility

Workplace

Get the full story on Breakroom

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About Medpace

Sourced by ZipRecruiter

Medpace is a globally recognized clinicial contract research organization (CRO) based in Cincinnati, OH, in the United States. Established in 1992, it operates in the healthcare sector, providing scientifically-driven outsourcing solutions for the development of drugs and medical devices. It offers comprehensive services like full-service clinical development services, regulatory affairs management, clinical pharmacology, data management, statistical analysis, and medical writing. By applying a scientifically-driven, therapeutically-focused, and patient-centric approach, Medpace's mission is to accelerate the global development of safe and effective medical therapies.

Industry

Medical equipment and supplies manufacturing

Company size

1,001 - 5,000 Employees

Headquarters location

Cincinnati, OH, US

Year founded

1992

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