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.
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.
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.
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.
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 ...
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 ...
The Senior Manager, Study Start-up partners closely with the Clinical Operations study team leading ... Pay Range $140,300.00 - $189,900.00 The pay range reflects the full-time base salary range we ...
The Senior Manager, Study Start-up partners closely with the Clinical Operations study team leading ... Pay Range $140,300.00 - $189,900.00 The pay range reflects the full-time base salary range we ...
Manager Study Start Up
Princeton, NJ · On-site
HARMONi: Phase 3 clinical study which was intended to evaluate ivonescimab combined with ... Manage and may lead the day-to-day operations within Study Start Up to ensure completion of ...
Manager Study Start Up
Princeton, NJ · On-site
HARMONi: Phase 3 clinical study which was intended to evaluate ivonescimab combined with ... Manage and may lead the day-to-day operations within Study Start Up to ensure completion of ...
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
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 ...
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 ...
Kymera Therapeutics is seeking a senior leader to drive end-to-end study start-up activities across clinical programs, ensuring timely activation and high-quality documentation. You will shape start ...
Kymera Therapeutics is seeking a senior leader to drive end-to-end study start-up activities across clinical programs, ensuring timely activation and high-quality documentation. You will shape start ...
Manager Study Start Up
Princeton, NJ · On-site
You will support clinical benchmarking and site budget development, escalation, and payment ... Manage and may lead the day-to-day operations within Study Start Up to ensure completion of ...
Manager Study Start Up
Princeton, NJ · On-site
You will support clinical benchmarking and site budget development, escalation, and payment ... Manage and may lead the day-to-day operations within Study Start Up to ensure completion of ...
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 ...
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 ...
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 ... What You'll Do: • Lead the operational execution of clinical studies from start-up through close ...
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 ... What You'll Do: • Lead the operational execution of clinical studies from start-up through close ...
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 ...
Experienced Study Start-Up Coordinator
Cincinnati, OH · On-site +1
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 ...
Experienced Study Start-Up Coordinator
Cincinnati, OH · On-site +1
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 ...
Director - Study Start-Up Project Management
CO · On-site +1
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 ...
Director - Study Start-Up Project Management
CO · On-site +1
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 ...
Study Start-Up Coordinator- PhD
Cincinnati, OH · On-site +1
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 ...
Study Start-Up Coordinator- PhD
Cincinnati, OH · On-site +1
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 ...
Study Start-Up Specialist
$55K - $70K/yr
... study start-up related questions ... Coordinate with TIME sites and sponsor teams to activate clinical trials through the JIT and ...
Study Start-Up Specialist
$55K - $70K/yr
... study start-up related questions ... Coordinate with TIME sites and sponsor teams to activate clinical trials through the JIT and ...
Study Start-Up Specialist
$55K - $70K/yr
... study start-up related questions ... Coordinate with TIME sites and sponsor teams to activate clinical trials through the JIT and ...
Study Start-Up Specialist
$55K - $70K/yr
... study start-up related questions ... Coordinate with TIME sites and sponsor teams to activate clinical trials through the JIT and ...
Full Time Clinical Study Start Up information
See salary details
$22K - $38.7K
1% of jobs
$38.7K - $55.5K
3% of jobs
$55.5K - $72.2K
7% of jobs
$87.1K is the 25th percentile. Wages below this are outliers.
$72.2K - $88.9K
15% of jobs
$88.9K - $105.6K
9% of jobs
$105.6K - $122.4K
14% of jobs
The median wage is $123.4K / yr.
$122.4K - $139.1K
17% of jobs
$150.9K is the 75th percentile. Wages above this are outliers.
$139.1K - $155.8K
13% of jobs
$155.8K - $172.5K
11% of jobs
$172.5K - $189.3K
7% of jobs
$189.3K - $206K
3% of jobs
$22K
$125.3K
$206K
How much do full time clinical study start up jobs pay per year?
As of Aug 26, 2026, the average yearly pay for full time clinical study start up in the United States is $125,290.00, according to ZipRecruiter salary data. Most workers in this role earn between $85,000.00 and $157,000.00 per year, depending on experience, location, and employer.
What is the difference between Full Time Clinical Study Start Up vs Clinical Research Coordinator?
| Aspect | Full Time Clinical Study Start Up | Clinical Research Coordinator |
|---|---|---|
| Responsibilities | Planning, site selection, regulatory submissions, startup documentation | Participant recruitment, data collection, site coordination |
| Credentials | Typically requires a degree in health sciences or related field, experience in study startup | Often requires a degree or certification in health or research, with focus on coordination |
| Work Environment | Office-based, regulatory and planning focus | Site-based, patient interaction and data management |
Full Time Clinical Study Start Up professionals focus on preparing and initiating clinical trials, handling regulatory and site setup tasks. Clinical Research Coordinators primarily manage participant interactions and data collection at study sites. Both roles require related credentials but differ in daily responsibilities and work environment.
More about Full Time Clinical Study Start Up jobs
What cities are hiring for Full Time Clinical Study Start Up jobs?
Cities with the most Full Time 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 Full Time Clinical Study Start Up jobs?
States with the most job openings for Full Time Clinical Study Start Up jobs include:
What job categories do people searching Full Time Clinical Study Start Up jobs look for?
The top searched job categories for Full Time Clinical Study Start Up jobs are:
Study Start-Up Manager
Wilmington, DE
CEDENT •
IT Services • 11 - 50 employees11 - 50 employees
Full-time
Re-posted 29 days ago
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