Summary We are looking for a Study Start-Up Manager with extensive experience to lead clinical study start-up activities. This role requires a strong background in regulatory processes, site ...
Summary We are looking for a Study Start-Up Manager with extensive experience to lead clinical study start-up activities. This role requires a strong background in regulatory processes, site ...
Clinical Study Start-Up Associate
Boston, MA · On-site
$36.25 - $49.50/hr
Join our Clinical Operations team and play a key role in getting clinical studies off the ground. As a Study Start-Up Associate, you'll help drive study activation by coordinating essential start-up ...
Clinical Study Start-Up Associate
Boston, MA · On-site
$36.25 - $49.50/hr
Join our Clinical Operations team and play a key role in getting clinical studies off the ground. As a Study Start-Up Associate, you'll help drive study activation by coordinating essential start-up ...
Summary We are looking for a Study Start-Up Manager with extensive experience to lead clinical study start-up activities. This role requires a strong background in regulatory processes, site ...
Summary We are looking for a Study Start-Up Manager with extensive experience to lead clinical study start-up activities. This role requires a strong background in regulatory processes, site ...
Summary We are looking for a Study Start-Up Manager with extensive experience to lead clinical study start-up activities. This role requires a strong background in regulatory processes, site ...
Summary We are looking for a Study Start-Up Manager with extensive experience to lead clinical study start-up activities. This role requires a strong background in regulatory processes, site ...
The Director of Clinical Operations Study Start-Up will oversee the Study Start-Up portfolio managing Study Start-Up activities. This role takes direction from the Clinical Operations Leadership ...
The Director of Clinical Operations Study Start-Up will oversee the Study Start-Up portfolio managing Study Start-Up activities. This role takes direction from the Clinical Operations Leadership ...
The Associate Director, Clinical Operations Program Lead, Study Start-up and Feasibility will report to the Director, Patient Recruitment and Start-Up Strategy and will lead a team to drive the ...
The Associate Director, Clinical Operations Program Lead, Study Start-up and Feasibility will report to the Director, Patient Recruitment and Start-Up Strategy and will lead a team to drive the ...
The Associate Director, Clinical Operations Program Lead, Study Start-up and Feasibility will report to the Director, Patient Recruitment and Start-Up Strategy and will lead a team to drive the ...
The Associate Director, Clinical Operations Program Lead, Study Start-up and Feasibility will report to the Director, Patient Recruitment and Start-Up Strategy and will lead a team to drive the ...
Support the execution of Phase I-IV studies including study start-up, site management and clinical operations activities in compliance with principles of ICH-GCP guidelines, SOPs, local laws and ...
Quick apply
Support the execution of Phase I-IV studies including study start-up, site management and clinical operations activities in compliance with principles of ICH-GCP guidelines, SOPs, local laws and ...
Director, Study Start-Up
Watertown, MA · On-site
$195K - $275K/yr
Kymera is a clinical-stage biotechnology company pioneering the field of targeted protein ... Provide strategic and operational leadership for end-to-end study start-up activities across ...
Director, Study Start-Up
Watertown, MA · On-site
$195K - $275K/yr
Kymera is a clinical-stage biotechnology company pioneering the field of targeted protein ... Provide strategic and operational leadership for end-to-end study start-up activities across ...
Study Start-Up Manager
$80K - $100K/yr
Tempus created the TIME clinical trials network to increase patient access to clinical trials by ... We are looking for an experienced Study Start-Up Manager who will work with our cross- functional ...
Study Start-Up Manager
$80K - $100K/yr
Tempus created the TIME clinical trials network to increase patient access to clinical trials by ... We are looking for an experienced Study Start-Up Manager who will work with our cross- functional ...
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Clinical Study Manager
Durham, NC · On-site
$57 - $71/hr
We are seeking an experienced Clinical Study Manager to lead the operational execution of clinical studies from start-up through close-out. This position is responsible for coordinating study ...
New
Quick apply
Be Seen First
Clinical Study Manager
Durham, NC · On-site
$57 - $71/hr
We are seeking an experienced Clinical Study Manager to lead the operational execution of clinical studies from start-up through close-out. This position is responsible for coordinating study ...
New
Study Start-Up Manager
Chicago, IL · On-site
$80K - $100K/yr
Tempus created the TIME clinical trials network to increase patient access to clinical trials by ... We are looking for an experienced Study Start-Up Manager who will work with our cross- functional ...
Study Start-Up Manager
Chicago, IL · On-site
$80K - $100K/yr
Tempus created the TIME clinical trials network to increase patient access to clinical trials by ... We are looking for an experienced Study Start-Up Manager who will work with our cross- functional ...
The Director of Clinical Operations Study Start-Up will oversee the Study Start-Up portfolio managing Study Start-Up activities. This role takes direction from the Clinical Operations Leadership ...
New
The Director of Clinical Operations Study Start-Up will oversee the Study Start-Up portfolio managing Study Start-Up activities. This role takes direction from the Clinical Operations Leadership ...
New
Job Summary Our clinical operations activities are growing rapidly, and we are currently seeking a 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 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 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 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 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 ...
Clinical Study Manager The Clinical Study Manager is responsible for the end-to-end management and ... Lead the operational execution of clinical studies from start-up through close-out, including site ...
Clinical Study Manager The Clinical Study Manager is responsible for the end-to-end management and ... Lead the operational execution of clinical studies from start-up through close-out, including site ...
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 ...
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 ...
Manager Study Start-up
San Clemente, CA · On-site
Clinical Study Manager The Clinical Study Manager is responsible for the end-to-end management and ... Lead the operational execution of clinical studies from start-up through close-out, including site ...
Manager Study Start-up
San Clemente, CA · On-site
Clinical Study Manager The Clinical Study Manager is responsible for the end-to-end management and ... Lead the operational execution of clinical studies from start-up through close-out, including site ...
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 Jul 15, 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 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?
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 Clinical Study Start Up, and why are they important?
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 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 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:
Job description
Summary
Qualifications
We are looking for a Study Start-Up Manager with extensive experience to lead clinical study start-up activities. This role requires a strong background in regulatory processes, site management, and expertise in ensuring compliance with local and international guidelines, particularly ICH-GCP.
- Lead and manage start-up activities for clinical studies, ensuring compliance with local and international guidelines (ICH-GCP).
- Prepare, review, and track site regulatory documentation throughout the study start-up phase.
- Collaborate with Clinical Research Associates (CRAs) and the local study team to meet start-up milestones.
- Participate in Local Study Team meetings and report on site performance metrics.
- Ensure the timely submission of documents to regulatory authorities and maintain the trial master file (eTMF).
Qualifications
- Minimum 3 years of experience in Clinical Study Start-Up (full-time).
- At least 1 year of hands-on experience with Veeva Vault.
- Strong background in informed consent review and negotiation.
- Bachelor’s degree (higher degree preferred) with knowledge of clinical trial processes (Phases II-IV) and ICH-GCP.
- Excellent communication, organizational, and project management skills.
- Strong problem-solving and negotiation abilities.
About Cedent
Sourced by ZipRecruiter
CEDENT strives to attract and retain the best people and provide an environment where they can all develop professionally and build a rewarding career. As a result, we create an inclusive environment that is rich in diversity, acknowledges each individual's uniqueness and promotes respect, personal achievement and stewardship. Our clients are global and so is CEDENT. We build and maintain a global workforce that includes people from different backgrounds, with a vast range of skills and experience all united by a common culture and commitment to help our clients achieve high performance. Cultivating a diverse workforce and inclusive work environment makes business sense. Our peoples varied skills are the talent engine that powers CEDENT, enabling it in turn to deliver the innovative solutions that help our clients outperform competitors.
Industry
It services
Company size
11 - 50 Employees
Headquarters location
Plano, TX, US
Year founded
2008