Collect, review, organize, and assemble regulatory start-up submissions (including submissions to ... associates, as well as those that are new to the industry. The SAM Training Program embraces ...
Collect, review, organize, and assemble regulatory start-up submissions (including submissions to ... associates, as well as those that are new to the industry. The SAM Training Program embraces ...
Study Start-Up Coordinator- PhD
Cincinnati, OH · On-site +1
Collect, review, organize, and assemble regulatory start-up submissions (including submissions to ... associates, as well as those that are new to the industry. The SAM Training Program embraces ...
Study Start-Up Coordinator- PhD
Cincinnati, OH · On-site +1
Collect, review, organize, and assemble regulatory start-up submissions (including submissions to ... associates, as well as those that are new to the industry. The SAM Training Program embraces ...
Regulatory Associate
Maitland, FL · On-site
K2 is seeking an organized, detail-oriented Regulatory Associate to manage site-level regulatory ... Study Start-Up & Timeline Management: Drive study start-up workflows from initial packet receipt ...
Regulatory Associate
Maitland, FL · On-site
K2 is seeking an organized, detail-oriented Regulatory Associate to manage site-level regulatory ... Study Start-Up & Timeline Management: Drive study start-up workflows from initial packet receipt ...
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 ...
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 ...
Regulatory Associate
Ocala, FL · On-site
K2 is seeking an organized, detail-oriented Regulatory Associate to manage site-level regulatory ... Study Start-Up & Timeline Management: Drive study start-up workflows from initial packet receipt ...
Regulatory Associate
Ocala, FL · On-site
K2 is seeking an organized, detail-oriented Regulatory Associate to manage site-level regulatory ... Study Start-Up & Timeline Management: Drive study start-up workflows from initial packet receipt ...
Regulatory Associate
Lady Lake, FL · On-site
K2 is seeking an organized, detail-oriented Regulatory Associate to manage site-level regulatory ... Study Start-Up & Timeline Management: Drive study start-up workflows from initial packet receipt ...
Regulatory Associate
Lady Lake, FL · On-site
K2 is seeking an organized, detail-oriented Regulatory Associate to manage site-level regulatory ... Study Start-Up & Timeline Management: Drive study start-up workflows from initial packet receipt ...
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 ...
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 ...
Job Summary We are currently seeking a full-time Regulatoy (Study Start Up) Submissions Manager to ... Review pertinent regulations to develop proactive solutions to start-up issues and challenges; and
Job Summary We are currently seeking a full-time Regulatoy (Study Start Up) Submissions Manager to ... Review pertinent regulations to develop proactive solutions to start-up issues and challenges; and
Director - Study Start-Up Project Management
CO · On-site +1
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 ...
Director - Study Start-Up Project Management
CO · On-site +1
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 ...
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 ...
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 ...
Job Summary We are currently seeking a full-time, office based Regulatory (Study Start up) Submissions Coordinator to join our Clinical Operations team in the Seoul office. This role is a vital part ...
Job Summary We are currently seeking a full-time, office based Regulatory (Study Start up) Submissions Coordinator to join our Clinical Operations team in the Seoul office. This role is a vital part ...
Manager Study Start-up
San Clemente, CA · On-site
What You'll Do: • Lead the operational execution of clinical studies from start-up through close ... Strong working knowledge of FDA regulations, GCP, and global clinical research requirements, with ...
Manager Study Start-up
San Clemente, CA · On-site
What You'll Do: • Lead the operational execution of clinical studies from start-up through close ... Strong working knowledge of FDA regulations, GCP, and global clinical research requirements, with ...
Study Start-Up Intern
Cincinnati, OH · On-site
The Regulatory Submissions Intern will provide support to the Regulatory Submissions Coordinators ... Medpace training programs are curated to educate and support experienced associates, as well as ...
Study Start-Up Intern
Cincinnati, OH · On-site
The Regulatory Submissions Intern will provide support to the Regulatory Submissions Coordinators ... Medpace training programs are curated to educate and support experienced associates, as well as ...
Study Start-Up Lead
South San Francisco, CA · On-site
$70 - $75/hr
Demonstrated experience in clinical trial start-up, regulatory submissions, and cross-functional ... Drive and facilitate efficient study start-up processes to contribute to the delivery of clinical ...
Quick apply
Study Start-Up Lead
South San Francisco, CA · On-site
$70 - $75/hr
Demonstrated experience in clinical trial start-up, regulatory submissions, and cross-functional ... Drive and facilitate efficient study start-up processes to contribute to the delivery of clinical ...
Collect, review, organize, and assemble regulatory start-up submissions (including submissions to ... associates, as well as those that are new to the industry. The SAM Training Program embraces ...
Collect, review, organize, and assemble regulatory start-up submissions (including submissions to ... associates, as well as those that are new to the industry. The SAM Training Program embraces ...
Oversee consistent application of appropriate study start-up standards and processes to deliver high quality, cost effective clinical studies in line with local operational, legal and regulatory ...
Oversee consistent application of appropriate study start-up standards and processes to deliver high quality, cost effective clinical studies in line with local operational, legal and regulatory ...
Collect, review, organize, and assemble regulatory start-up submissions (including submissions to ... associates, as well as those that are new to the industry. The SAM Training Program embraces ...
Collect, review, organize, and assemble regulatory start-up submissions (including submissions to ... associates, as well as those that are new to the industry. The SAM Training Program embraces ...
Manager Study Start Up
Princeton, NJ · On-site
Manage and may lead the day-to-day operations within Study Start Up to ensure completion of established goals and objectives in compliance with applicable GCP/ICH guidelines and other regulatory ...
Manager Study Start Up
Princeton, NJ · On-site
Manage and may lead the day-to-day operations within Study Start Up to ensure completion of established goals and objectives in compliance with applicable GCP/ICH guidelines and other regulatory ...
Experienced Study Start-Up Coordinator
Cincinnati, OH · On-site +1
Collect, review, organize, and assemble regulatory start-up submissions (including submissions to ... associates, as well as those that are new to the industry. The SAM Training Program embraces ...
Experienced Study Start-Up Coordinator
Cincinnati, OH · On-site +1
Collect, review, organize, and assemble regulatory start-up submissions (including submissions to ... associates, as well as those that are new to the industry. The SAM Training Program embraces ...
Job Summary We are currently seeking a full-time, office based Regulatory (Study Start up) Submissions Coordinator to join our Clinical Operations team in the Seoul office. This role is a vital part ...
Job Summary We are currently seeking a full-time, office based Regulatory (Study Start up) Submissions Coordinator to join our Clinical Operations team in the Seoul office. This role is a vital part ...
Regulatory Study Start Associate information
See salary details
$17.07 - $19.95
12% of jobs
$19.95 - $22.84
6% of jobs
$24.48 is the 25th percentile. Wages below this are outliers.
$22.84 - $25.72
12% of jobs
$25.72 - $28.61
12% of jobs
The median wage is $30.77 / hr.
$28.61 - $31.49
11% of jobs
$31.49 - $34.38
14% of jobs
$37.17 is the 75th percentile. Wages above this are outliers.
$34.38 - $37.26
9% of jobs
$37.26 - $40.14
11% of jobs
$40.14 - $43.03
3% of jobs
$43.03 - $45.91
5% of jobs
$45.91 - $48.80
5% of jobs
$17
$32
$48
How much do regulatory study start associate jobs pay per hour?
As of Sep 14, 2026, the average hourly pay for regulatory study start associate in the United States is $32.21, according to ZipRecruiter salary data. Most workers in this role earn between $24.52 and $38.22 per hour, depending on experience, location, and employer.
What are popular job titles related to Regulatory Study Start Associate jobs?
For Regulatory Study Start Associate jobs, the most frequently searched job titles are:
Study Start-Up Coordinator- PhD
Cincinnati, OH • On-site
Medpace, Inc.
• Medical Equipment and Supplies Manufacturing • 1 - 5K employees1,001 - 5,000 employees
Other
Medical, Retirement, PTO
Re-posted 29 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 Regulatory Submissions Coordinators to join our Study Start-up team. This position works both independently and collaboratively with a team to meet common goals and plays a key role in the clinical trial management and study start-up process at Medpace. We are seeking entry level employees. If you want an exciting career where you can build a foundation in industry knowledge through our robust training program and develop and grow your career even further, 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...
• 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
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 Regulatory Submissions Coordinators to join our Study Start-up team. This position works both independently and collaboratively with a team to meet common goals and plays a key role in the clinical trial management and study start-up process at Medpace. We are seeking entry level employees. If you want an exciting career where you can build a foundation in industry knowledge through our robust training program and develop and grow your career even further, 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 (including submissions to Institutional Review Boards (IRB);
- Maintain timelines for study start-up through both internal and external collaboration; and
- Review pertinent regulations and guidance to develop proactive solutions to regulatory issues and challenges.
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
- PhD 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