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 ...
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 ...
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 ...
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 ...
CO · Hybrid
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 ...
CO · Hybrid
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 ...
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 ...
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 ...
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 ...
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 Associate (Medical Device) - Arden Hills, MN ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to ...
New
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Study Start Up Associate (Medical Device) - Arden Hills, MN ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to ...
New
Study Start Up Associate (Medical Device) - Arden Hills, MN ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to ...
New
Quick apply
Study Start Up Associate (Medical Device) - Arden Hills, MN ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to ...
New
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 ...
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 ...
Associate Director Study Start-up
$182K - $212K/yr
Career Category Clinical Join Amgen's Mission of Serving Patients At Amgen, if you feel like you're ... Study Start Up Hub - Associate Director Study Start-up What you will do Let's do this. Let's change ...
Associate Director Study Start-up
$182K - $212K/yr
Career Category Clinical Join Amgen's Mission of Serving Patients At Amgen, if you feel like you're ... Study Start Up Hub - Associate Director Study Start-up What you will do Let's do this. Let's change ...
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 ...
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 ...
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 ...
Be Seen First
Clinical Research Specialist (LC18246-1)
Irvine, CA · On-site
$54 - $56/hr
The main function of a clinical research specialist is to perform study start-up and conduct activities including ICF review that meets regulatory requirements, creating study specific essential ...
Quick apply
Be Seen First
Clinical Research Specialist (LC18246-1)
Irvine, CA · On-site
$54 - $56/hr
The main function of a clinical research specialist is to perform study start-up and conduct activities including ICF review that meets regulatory requirements, creating study specific essential ...
Clinical Study Manager
Durham, NC · On-site
Onsite Hours: 40.0 Overview The Clinical Study Manager provides onsite operational oversight for assigned clinical studies from start-up through close-out, ensuring delivery aligns with ICH/GCP ...
Clinical Study Manager
Durham, NC · On-site
Onsite Hours: 40.0 Overview The Clinical Study Manager provides onsite operational oversight for assigned clinical studies from start-up through close-out, ensuring delivery aligns with ICH/GCP ...
Senior Clinical Study Manager
Sunnyvale, CA · On-site +1
Primary Function of the Position This position requires a candidate with extensive experience with planning, study start-up, and execution of clinical studies. This Lead Clinical Study Manager-4 (CSM ...
Senior Clinical Study Manager
Sunnyvale, CA · On-site +1
Primary Function of the Position This position requires a candidate with extensive experience with planning, study start-up, and execution of clinical studies. This Lead Clinical Study Manager-4 (CSM ...
Clinical Study Manager
Durham, NC · On-site
Onsite Hours: 40.0 Overview The Clinical Study Manager provides onsite operational oversight for assigned clinical studies from start-up through close-out, ensuring delivery aligns with ICH/GCP ...
Quick apply
Clinical Study Manager
Durham, NC · On-site
Onsite Hours: 40.0 Overview The Clinical Study Manager provides onsite operational oversight for assigned clinical studies from start-up through close-out, ensuring delivery aligns with ICH/GCP ...
Clinical Study Manager
Durham, NC · On-site
Onsite Hours: 40.0 Overview The Clinical Study Manager provides onsite operational oversight for assigned clinical studies from start-up through close-out, ensuring delivery aligns with ICH/GCP ...
Quick apply
Clinical Study Manager
Durham, NC · On-site
Onsite Hours: 40.0 Overview The Clinical Study Manager provides onsite operational oversight for assigned clinical studies from start-up through close-out, ensuring delivery aligns with ICH/GCP ...
Clinical Study Manager
Durham, NC · On-site
Onsite Hours: 40.0 Overview The Clinical Study Manager provides onsite operational oversight for assigned clinical studies from start-up through close-out, ensuring delivery aligns with ICH/GCP ...
Quick apply
Clinical Study Manager
Durham, NC · On-site
Onsite Hours: 40.0 Overview The Clinical Study Manager provides onsite operational oversight for assigned clinical studies from start-up through close-out, ensuring delivery aligns with ICH/GCP ...
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?
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 types of projects and tasks can an intern expect to handle in a Clinical Study Start Up role?
What are the key skills and qualifications needed to thrive as an Internship Clinical Study Start Up, and why are they important?
What is an Internship in Clinical Study Start Up?
Other
Medical, PTO
Posted 11 days ago
Medpace rating
8.5
Based on 9 frontline employees who took The Breakroom Quiz
14th of 59 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). 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: 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