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 ...
Efficiently manage successful execution of global start-up, maintenance, and close-out studies; * Effectively lead others in a matrix environment; * Perform quality checks on submission documents and ...
Efficiently manage successful execution of global start-up, maintenance, and close-out studies; * Effectively lead others in a matrix environment; * Perform quality checks on submission documents and ...
Study Start-Up Project Manager
Irving, TX · On-site
Efficiently manage successful execution of global start-up, maintenance, and close-out studies; * Effectively lead others in a matrix environment; * Perform quality checks on submission documents and ...
Study Start-Up Project Manager
Irving, TX · On-site
Efficiently manage successful execution of global start-up, maintenance, and close-out studies; * Effectively lead others in a matrix environment; * Perform quality checks on submission documents and ...
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 ...
... 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 ...
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 ...
Clinical Research Site Manager
Sugar Land, TX · On-site
$65K - $72K/yr
Study start-up task completion timeliness and reduction of activation delays * Data quality metrics: query aging, EDC timeliness, monitoring findings closure rate Required Qualifications * 3+ years ...
Quick apply
Clinical Research Site Manager
Sugar Land, TX · On-site
$65K - $72K/yr
Study start-up task completion timeliness and reduction of activation delays * Data quality metrics: query aging, EDC timeliness, monitoring findings closure rate Required Qualifications * 3+ years ...
Pharmacy Graduate Intern
Houston, TX · On-site
$16 - $19.75/hr
Study Start-Up & Documentation: • Assist in the development, preparation, and maintenance of protocol-specific documents, including: • Compounding worksheets • Drug accountability logs • ...
Pharmacy Graduate Intern
Houston, TX · On-site
$16 - $19.75/hr
Study Start-Up & Documentation: • Assist in the development, preparation, and maintenance of protocol-specific documents, including: • Compounding worksheets • Drug accountability logs • ...
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 ...
Clinical Trials Activation Coordinator
Houston, TX · On-site +1
Responsibilities Feasibility, Start-Up & Activation Support (70%) Serve as primary liaison for feasibility review processes for Phase I-V clinical trials Analyze study feasibility documentation and ...
Clinical Trials Activation Coordinator
Houston, TX · On-site +1
Responsibilities Feasibility, Start-Up & Activation Support (70%) Serve as primary liaison for feasibility review processes for Phase I-V clinical trials Analyze study feasibility documentation and ...
Pharmacy Graduate Intern
$33K - $82K/yr
Study Start-Up & Documentation: Assist in the development, preparation, and maintenance of protocol-specific documents, including: Compounding worksheets Drug accountability logs Patient medication ...
Pharmacy Graduate Intern
$33K - $82K/yr
Study Start-Up & Documentation: Assist in the development, preparation, and maintenance of protocol-specific documents, including: Compounding worksheets Drug accountability logs Patient medication ...
Pharmacy Graduate Intern
$33K - $82K/yr
Study Start-Up & Documentation: Assist in the development, preparation, and maintenance of protocol-specific documents, including: Compounding worksheets Drug accountability logs Patient medication ...
Pharmacy Graduate Intern
$33K - $82K/yr
Study Start-Up & Documentation: Assist in the development, preparation, and maintenance of protocol-specific documents, including: Compounding worksheets Drug accountability logs Patient medication ...
Pharmacy Graduate Intern
$33K - $82K/yr
Study Start-Up & Documentation: Assist in the development, preparation, and maintenance of protocol-specific documents, including: Compounding worksheets Drug accountability logs Patient medication ...
Pharmacy Graduate Intern
$33K - $82K/yr
Study Start-Up & Documentation: Assist in the development, preparation, and maintenance of protocol-specific documents, including: Compounding worksheets Drug accountability logs Patient medication ...
Pharmacy Graduate Intern
$33K - $82K/yr
Study Start-Up & Documentation: Assist in the development, preparation, and maintenance of protocol-specific documents, including: Compounding worksheets Drug accountability logs Patient medication ...
Pharmacy Graduate Intern
$33K - $82K/yr
Study Start-Up & Documentation: Assist in the development, preparation, and maintenance of protocol-specific documents, including: Compounding worksheets Drug accountability logs Patient medication ...
Pharmacy Graduate Intern
$33K - $82K/yr
Study Start-Up & Documentation: Assist in the development, preparation, and maintenance of protocol-specific documents, including: Compounding worksheets Drug accountability logs Patient medication ...
Pharmacy Graduate Intern
$33K - $82K/yr
Study Start-Up & Documentation: Assist in the development, preparation, and maintenance of protocol-specific documents, including: Compounding worksheets Drug accountability logs Patient medication ...
Pharmacy Graduate Intern
$33K - $82K/yr
Study Start-Up & Documentation: Assist in the development, preparation, and maintenance of protocol-specific documents, including: Compounding worksheets Drug accountability logs Patient medication ...
Pharmacy Graduate Intern
$33K - $82K/yr
Study Start-Up & Documentation: Assist in the development, preparation, and maintenance of protocol-specific documents, including: Compounding worksheets Drug accountability logs Patient medication ...
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?
As of Jul 14, 2026, the average hourly pay for study start up associate in Texas is $29.38, according to ZipRecruiter salary data. Most workers in this role earn between $19.71 and $38.75 per hour, depending on experience, location, and employer.
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.
What are popular job titles related to Study Start Up Associate jobs in Texas? For Study Start Up Associate jobs in Texas, the most frequently searched job titles are:
What job categories do people searching Study Start Up Associate jobs in Texas look for? The top searched job categories for Study Start Up Associate jobs in Texas are:
What cities in Texas are hiring for Study Start Up Associate jobs? Cities in Texas with the most Study Start Up Associate job openings:
Other
Medical, PTO
Posted 5 days ago
Medpace rating
8.5
Based on 9 frontline employees who took The Breakroom Quiz
14th of 59 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.
- 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). 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
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