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 ...
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 ...
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 ...
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 ...
Maintain timelines for study start-up through both internal and external collaboration; * Provide ... associates, as well as those that are new to the industry. The SAM Training Program embraces ...
Maintain timelines for study start-up through both internal and external collaboration; * Provide ... associates, as well as those that are new to the industry. The SAM Training Program embraces ...
Study Start-Up Coordinator - Clinical Research Coordinator Experience
Irving, TX · On-site
$22.50 - $30/hr
Maintain timelines for study start-up through both internal and external collaboration; * Provide ... associates, as well as those that are new to the industry. The SAM Training Program embraces ...
Study Start-Up Coordinator - Clinical Research Coordinator Experience
Irving, TX · On-site
$22.50 - $30/hr
Maintain timelines for study start-up through both internal and external collaboration; * Provide ... associates, as well as those that are new to the industry. The SAM Training Program embraces ...
Regulatory Start-Up Specialist The Regulatory Start-Up Specialist serves as the main point of contact for project-specific study start-up activities within the regulatory department and provides ...
Regulatory Start-Up Specialist The Regulatory Start-Up Specialist serves as the main point of contact for project-specific study start-up activities within the regulatory department and provides ...
Clinical Project Manager II - Early Phase Virology /Healthy Volunteer Studies (Sponsor Dedicated -
Plano, TX · On-site
You will oversee timelines, budgets, operational risks, study start-up activities, vendor performance, and cross-functional collaboration while ensuring studies are conducted in accordance with ...
Clinical Project Manager II - Early Phase Virology /Healthy Volunteer Studies (Sponsor Dedicated -
Plano, TX · On-site
You will oversee timelines, budgets, operational risks, study start-up activities, vendor performance, and cross-functional collaboration while ensuring studies are conducted in accordance with ...
... start up to monitoring through to study close out, across commercial and government contracts ... Under the general direction of the Clin Ops Supervisor, the Study Team Associate is responsible for ...
... start up to monitoring through to study close out, across commercial and government contracts ... Under the general direction of the Clin Ops Supervisor, the Study Team Associate is responsible for ...
... start up to monitoring through to study close out, across commercial and government contracts ... Under the general direction of the Clin Ops Supervisor, the Study Team Associate is responsible for ...
... start up to monitoring through to study close out, across commercial and government contracts ... Under the general direction of the Clin Ops Supervisor, the Study Team Associate is responsible for ...
... start up to monitoring through to study close out, across commercial and government contracts ... Under the general direction of the Clin Ops Supervisor, the Study Team Associate is responsible for ...
... start up to monitoring through to study close out, across commercial and government contracts ... Under the general direction of the Clin Ops Supervisor, the Study Team Associate is responsible for ...
Job Purpose ARTIDIS is a medical device start-up company that conducts clinical studies to validate and develop new cases for its medical products. Given that ARTIDIS's medical devices are unique ...
Job Purpose ARTIDIS is a medical device start-up company that conducts clinical studies to validate and develop new cases for its medical products. Given that ARTIDIS's medical devices are unique ...
... start up to monitoring through to study close out, across commercial and government contracts ... Under the general direction of the Clin Ops Supervisor, the Study Team Associate is responsible for ...
... start up to monitoring through to study close out, across commercial and government contracts ... Under the general direction of the Clin Ops Supervisor, the Study Team Associate is responsible for ...
Clinical Study Manager
Houston, TX · On-site
Job Purpose ARTIDIS is a medical device start-up company that conducts clinical studies to validate and develop new cases for its medical products. Given that ARTIDIS's medical devices are unique ...
Clinical Study Manager
Houston, TX · On-site
Job Purpose ARTIDIS is a medical device start-up company that conducts clinical studies to validate and develop new cases for its medical products. Given that ARTIDIS's medical devices are unique ...
Study Manager I (4011)
Sugar Land, TX · On-site
Completing all the relevant training prior to study-start and on a continued basis in a timely ... Working closely with the Associate Site Director/Site Director to achieve strategic goals for the ...
Study Manager I (4011)
Sugar Land, TX · On-site
Completing all the relevant training prior to study-start and on a continued basis in a timely ... Working closely with the Associate Site Director/Site Director to achieve strategic goals for the ...
Study Manager I (4011)
Sugar Land, TX · On-site
Completing all the relevant training prior to study-start and on a continued basis in a timely ... Working closely with the Associate Site Director/Site Director to achieve strategic goals for the ...
Study Manager I (4011)
Sugar Land, TX · On-site
Completing all the relevant training prior to study-start and on a continued basis in a timely ... Working closely with the Associate Site Director/Site Director to achieve strategic goals for the ...
Senior Research Coordinator
Houston, TX · On-site
Position requires leading rapid study start-up, high participant volumes, and intricate protocol requirements. Participates in study qualification and feasibility assessments and provides operational ...
Senior Research Coordinator
Houston, TX · On-site
Position requires leading rapid study start-up, high participant volumes, and intricate protocol requirements. Participates in study qualification and feasibility assessments and provides operational ...
To provide general administrative support to the Clinical Operation team and assistance to Project Manager(s) and Study Start-up Specialist in start-up from site selection to site activation. * To ...
To provide general administrative support to the Clinical Operation team and assistance to Project Manager(s) and Study Start-up Specialist in start-up from site selection to site activation. * To ...
Study Manager I (4012)
Houston, TX · On-site
Completing all the relevant training prior to study-start and on a continued basis in a timely ... Working closely with the Associate Site Director/Site Director to achieve strategic goals for the ...
Study Manager I (4012)
Houston, TX · On-site
Completing all the relevant training prior to study-start and on a continued basis in a timely ... Working closely with the Associate Site Director/Site Director to achieve strategic goals for the ...
Completing all the relevant training prior to study-start and on a continued basis in a timely ... Working closely with the Associate Site Director/Site Director to achieve strategic goals for the ...
Completing all the relevant training prior to study-start and on a continued basis in a timely ... Working closely with the Associate Site Director/Site Director to achieve strategic goals for the ...
Study Manager I (4012)
Houston, TX · On-site
Completing all the relevant training prior to study-start and on a continued basis in a timely ... Working closely with the Associate Site Director/Site Director to achieve strategic goals for the ...
Study Manager I (4012)
Houston, TX · On-site
Completing all the relevant training prior to study-start and on a continued basis in a timely ... Working closely with the Associate Site Director/Site Director to achieve strategic goals for the ...
Study Start Up Associate information
See Texas salary details
$11.87 - $15.47
3% of jobs
$15.47 - $19.08
18% of jobs
$19.79 is the 25th percentile. Wages below this are outliers.
$19.08 - $22.68
20% of jobs
The median wage is $24.87 / hr.
$22.68 - $26.28
15% of jobs
$26.28 - $29.89
11% of jobs
$29.89 - $33.49
4% of jobs
$36.55 is the 75th percentile. Wages above this are outliers.
$33.49 - $37.10
5% of jobs
$37.10 - $40.70
8% of jobs
$40.70 - $44.30
6% of jobs
$44.30 - $47.91
6% of jobs
$47.91 - $51.51
3% of jobs
$11
$29
$51
How much do study start up associate jobs pay per hour?
What is the difference between Study Start Up Associate vs Clinical Trial Coordinator?
| Aspect | Study Start Up Associate | Clinical Trial Coordinator |
|---|---|---|
| Required Credentials | Bachelor's degree, knowledge of regulatory requirements | Bachelor's degree, familiarity with clinical procedures |
| Work Environment | Regulatory and site initiation activities | Participant management and site coordination |
| Employer & Industry Usage | Pharmaceuticals, biotech, CROs | Hospitals, research centers, CROs |
The Study Start Up Associate primarily focuses on regulatory submissions, site qualification, and initiation processes, ensuring trial readiness. In contrast, the Clinical Trial Coordinator manages participant recruitment, scheduling, and data collection. Both roles are essential in clinical research but differ in their core responsibilities and focus areas.

Other
Medical, Retirement, PTO
Re-posted 27 days ago
Medpace rating
8.6
Based on 12 frontline employees who took The Breakroom Quiz
14th of 72 rated research
Job description
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.
- 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 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
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- Work alongside physicians, scientists, and industry-leading experts committed to advancing the global development of medical therapeutics through clinical research excellence
Collaborative Culture
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- 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
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- 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
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- 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
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- 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: OTHERAbout 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