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 ...
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 ...
The Study Start-Up (SSU) Manager is responsible for overseeing and driving operational study startup activities across the clinical research network from study award through activation. This role ...
The Study Start-Up (SSU) Manager is responsible for overseeing and driving operational study startup activities across the clinical research network from study award through activation. This role ...
Job Summary Our clinical operations activities are growing rapidly, and we are currently seeking full-time, office-based Regulatory Submissions Coordinators to join our Study Start-up team. This ...
Job Summary Our clinical operations activities are growing rapidly, and we are currently seeking full-time, office-based Regulatory Submissions Coordinators to join our Study Start-up team. This ...
Clinical Research Regulatory & Study Start-Up Coordinator
Nashville, TN · On-site
$23.50 - $31.25/hr
C. is seeking a detail-oriented and regulatory-minded Clinical Research Regulatory & Study Start-Up Coordinator to join our growing Clinical Research Department. This role serves as the department ...
Clinical Research Regulatory & Study Start-Up Coordinator
Nashville, TN · On-site
$23.50 - $31.25/hr
C. is seeking a detail-oriented and regulatory-minded Clinical Research Regulatory & Study Start-Up Coordinator to join our growing Clinical Research Department. This role serves as the department ...
Study Start-Up Coordinator- PharmD
Cincinnati, OH · On-site +1
Job Summary Our clinical operations activities are growing rapidly, and we are currently seeking full-time, office-based Regulatory Submissions Coordinators to join our Study Start-up team. This ...
Study Start-Up Coordinator- PharmD
Cincinnati, OH · On-site +1
Job Summary Our clinical operations activities are growing rapidly, and we are currently seeking full-time, office-based Regulatory Submissions Coordinators to join our Study Start-up team. This ...
Job Summary Our clinical operations activities are growing rapidly, and we are currently seeking a full-time, office-based Regulatory Submissions Coordinator to join our Study Start-up team. This ...
Job Summary Our clinical operations activities are growing rapidly, and we are currently seeking a full-time, office-based Regulatory Submissions Coordinator to join our Study Start-up team. This ...
Study Start-Up Associate II
Rockville, MD · On-site +1
$34.25 - $46.75/hr
Overview Study Start-Up Associate II US Remote Emmes Group: Building a better future for us all ... Emmes Group is transforming the future of clinical research, bringing the promise of new medical ...
Study Start-Up Associate II
Rockville, MD · On-site +1
$34.25 - $46.75/hr
Overview Study Start-Up Associate II US Remote Emmes Group: Building a better future for us all ... Emmes Group is transforming the future of clinical research, bringing the promise of new medical ...
Job Summary Our clinical operations activities are growing rapidly, and we are currently seeking a full-time, office-based Regulatory Submissions Coordinator to join our Study Start-up team. This ...
Job Summary Our clinical operations activities are growing rapidly, and we are currently seeking a full-time, office-based Regulatory Submissions Coordinator to join our Study Start-up team. This ...
Study Start-Up Associate II
Rockville, MD · On-site
$34.25 - $46.75/hr
Overview Study Start-Up Associate II US Remote Emmes Group: Building a better future for us all ... Emmes Group is transforming the future of clinical research, bringing the promise of new medical ...
Study Start-Up Associate II
Rockville, MD · On-site
$34.25 - $46.75/hr
Overview Study Start-Up Associate II US Remote Emmes Group: Building a better future for us all ... Emmes Group is transforming the future of clinical research, bringing the promise of new medical ...
Study Start-Up Associate II
Rockville, MD · On-site
$34.25 - $46.75/hr
Overview Study Start-Up Associate II US Remote Emmes Group: Building a better future for us all ... Emmes Group is transforming the future of clinical research, bringing the promise of new medical ...
Study Start-Up Associate II
Rockville, MD · On-site
$34.25 - $46.75/hr
Overview Study Start-Up Associate II US Remote Emmes Group: Building a better future for us all ... Emmes Group is transforming the future of clinical research, bringing the promise of new medical ...
Study Start-Up Project Manager
Irving, TX · On-site
Our clinical operations activities are growing rapidly, and we are currently seeking a full-time Study Start-Up Project Manager to join our Site Activation and Maintenance team. This position plays a ...
Study Start-Up Project Manager
Irving, TX · On-site
Our clinical operations activities are growing rapidly, and we are currently seeking a full-time Study Start-Up Project Manager to join our Site Activation and Maintenance team. This position plays a ...
Clinical Study Manager
Durham, NC · On-site
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 ...
Quick apply
Clinical Study Manager
Durham, NC · On-site
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 ...
Clinical Study Manager
Durham, NC · On-site
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 ...
Quick apply
Clinical Study Manager
Durham, NC · On-site
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 ...
Clinical Study Manager
Durham, NC · On-site
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 ...
Quick apply
Clinical Study Manager
Durham, NC · On-site
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 ...
Clinical Study Manager
Durham, NC · On-site
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 ...
Quick apply
Clinical Study Manager
Durham, NC · On-site
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 ...
Clinical Study Manager
Durham, NC · On-site
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 ...
Quick apply
Clinical Study Manager
Durham, NC · On-site
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 ...
Clinical Study Manager
Durham, NC · On-site
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 ...
Quick apply
Clinical Study Manager
Durham, NC · On-site
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 ...
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 ...
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 ...
Study Start-Up Project Manager
Irving, TX · On-site +1
Our clinical operations activities are growing rapidly, and we are currently seeking a full-time Study Start-Up Project Manager to join our Site Activation and Maintenance team. This position plays a ...
Study Start-Up Project Manager
Irving, TX · On-site +1
Our clinical operations activities are growing rapidly, and we are currently seeking a full-time Study Start-Up Project Manager to join our Site Activation and Maintenance team. This position plays a ...
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 ...
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 ...
Internship Clinical Study Start Up information
See salary details
$13.22 - $15.73
11% of jobs
$15.73 - $18.25
10% of jobs
$19.41 is the 25th percentile. Wages below this are outliers.
$18.25 - $20.76
7% of jobs
$20.76 - $23.27
19% of jobs
The median wage is $23.45 / hr.
$23.27 - $25.79
37% of jobs
$25.79 - $28.30
0% of jobs
$28.30 - $30.81
3% of jobs
$30.81 - $33.33
3% of jobs
$33.33 - $35.84
3% of jobs
$35.84 - $38.35
3% of jobs
$38.35 - $40.87
3% of jobs
$13
$24
$40
How much do internship clinical study start up jobs pay per hour?
As of Sep 12, 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 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 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 the difference between Internship Clinical Study Start Up vs Clinical Research Coordinator?
| Aspect | Internship Clinical Study Start Up | Clinical Research Coordinator |
|---|---|---|
| Credentials | Typically 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 Environment | Assists in preparing sites for clinical trials, often in a training or entry-level capacity | Manages daily trial activities at clinical sites, coordinating with investigators and staff |
| Employer & Industry Usage | Used in pharmaceutical companies, CROs, and research institutions during early trial phases | Commonly 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 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:
Entry-Level Study Start-Up Coordinator
Cincinnati, OH • On-site
Medpace, Inc.
• Medical Equipment and Supplies Manufacturing • 1 - 5K employees1,001 - 5,000 employees
Other
Medical, Retirement, PTO
Re-posted 15 days ago
Medpace rating
8.6
Based on 12 frontline employees who took The Breakroom Quiz
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
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...
Qualifications
Travel: None
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
Collaborative Culture
Continuous Growth & Development
Other Employee Benefits
Cincinnati Headquarters Experience
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.
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) 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.
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