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Internship Clinical Study Start Up Jobs (NOW HIRING)

In this vital role you will drive world-class study start-up planning and execution across a global portfolio, ensuring clinical trials launch with quality, efficiency, and speed. * Lead and manage a ...

Provide day-to-day study management support and oversight for assigned clinical study activities from start-up through close-out. * Coordinate with internal project team members, CROs, vendors ...

Provide day-to-day study management support and oversight for assigned clinical study activities from start-up through close-out. * Coordinate with internal project team members, CROs, vendors ...

Provide day-to-day study management support and oversight for assigned clinical study activities from start-up through close-out. * Coordinate with internal project team members, CROs, vendors ...

Provide day-to-day study management support and oversight for assigned clinical study activities from start-up through close-out. * Coordinate with internal project team members, CROs, vendors ...

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Internship Clinical Study Start Up information

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$13

$24

$40

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

As of Aug 11, 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 clinical study start up?

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 in clinical study start up?

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:

Director - Study Start-Up Project Management

Medpace, Inc.

CO • On-site, Remote

Full-time

Medical, Retirement, PTO

Re-posted 3 days ago


Medpace rating

8.6

Company rating: 8.6 out of 10

Based on 12 frontline employees who took The Breakroom Quiz

13th of 73 rated research


Job description

Job Summary

We are seeking an office-based Director of Study Start-Up to support our growing Study Start-Up/Regulatory Submissions team at Medpace! 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 clinical operations functions throughout Medpace. Study Start-Up/Regulatory Submissions experience within a CRO is required. 

Incentives can include: Competitive bonus program, sign-on/relocation bonus, and equity awards.

Location: Position can be office based in Cincinnati, Dallas or Denver.

Responsibilities
  • Contribute directly to the growth and strategic development of a large, global Study Start-Up team;
  • Develop and identify continuous improvement opportunities of internal processes;
  • Oversee Study Start-Up/Regulatory Submissions activities and timelines to ensure they are in accordance with Medpace standard operating procedures and study protocols;
  • Provide input on new business development opportunities; and
  • Develop and maintain relationships with clients.
Qualifications
  • Bachelor's degree in Life Sciences or related field, Advanced degree is preferred;
  • 8+ years as a study start-up senior leader within a CRO;
  • Excellent presentation, negotiation, documentation, leadership, team-orientation, and interpersonal skills;
  • Strong customer focus with ability to manage challenging priorities and remain flexible and adaptive in stressful situations;
  • Excellent written and oral communication; and
  • Experience managing and developing a team.
Medpace Overview

Medpace is a full-service clinical contract research organization (CRO) providing phase l-lV 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 the advancement of clinical research. We leverage in-country regulatory and therapeutic expertise across all major therapeutic areas including oncology, cardiology, metabolic, endocrinology, central nervous system, and anti-viral and anti-infective. Headquartered in Cincinnati, Ohio, we employ more than 6,500 people across 40+ countries.

Why Medpace?

When you join Medpace, you become part of an innovative team that brings cutting-edge therapies to market while building a meaningful and rewarding career focused on scientific excellence and improving patient outcomes around the world through continuous learning and cross-functional collaboration.

Purpose-Driven Work

    • Work alongside physicians, scientists, and industry-leading experts committed to advancing the global development of medical therapeutics through clinical research excellence

Collaborative Culture

    • Contribute to an interactive team environment that empowers decision making, creative thinking, and continuous learning through open communication and mutual trust.
    • Leadership throughout Medpace is both accessible and approachable

Continuous Growth & Development

    • Office based environment with on-site mentors
    • Defined career paths with clear advancement opportunities
    • Industry renowned onboarding and training programs designed to accelerate professional development
    • Ongoing training and continuous learning opportunities throughout your career
    • An environment that encourages employees to influence change, contribute ideas, and grow quickly

Other Employee Benefits

    • Competitive compensation programs that recognize and reward performance
    • Comprehensive health, wellness, retirement, and PTO benefits
    • Office based culture with occasional WFH that provides flexibility for eligible positions after training
    • Company-sponsored social events and intramural sports

Cincinnati Headquarters Experience

    • A modern corporate campus designed to support collaboration and productivity
    • Multiple on-site dining options in the heart of Madison Square
    • Free on-site parking
    • Convenient access to on-site 24-7 fitness and wellness facilities

What to Expect Next

A Medpace team member will review your application and if your profile matches our current needs, you will be contacted for an interview. While we review all applications carefully, we are unable to respond to every applicant, and only candidates selected for interviews will be contacted.

Employment Type: OTHER

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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