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 ...
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 ...
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 ...
Manager of Study Start Up
Blue Bell, PA · On-site
Manager of Study Start Up ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster. As a values-driven ...
Manager of Study Start Up
Blue Bell, PA · On-site
Manager of Study Start Up ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster. As a values-driven ...
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 ...
Senior Manager, Study Start Up
San Diego, CA · On-site
$130K - $160K/yr
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 ...
Senior Manager, Study Start Up
San Diego, CA · On-site
$130K - $160K/yr
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 ...
Job Requirements Position Summary The Clinical Research Study Start-Up Specialist is responsible for leading and coordinating all activities associated with the initiation of clinical research ...
Job Requirements Position Summary The Clinical Research Study Start-Up Specialist is responsible for leading and coordinating all activities associated with the initiation of clinical research ...
Senior Manager, Study Start Up
San Diego, CA · Remote
$130K - $160K/yr
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
Senior Manager, Study Start Up
San Diego, CA · Remote
$130K - $160K/yr
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 ...
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
$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 ...
Job Requirements Position Summary The Clinical Research Study Start-Up Specialist is responsible for leading and coordinating all activities associated with the initiation of clinical research ...
Job Requirements Position Summary The Clinical Research Study Start-Up Specialist is responsible for leading and coordinating all activities associated with the initiation of clinical research ...
Study Start-Up Lead
South San Francisco, CA · On-site
$70 - $75/hr
Enable innovative clinical trial delivery and address study start-up needs across various ... therapeutic areas. * Collaborate with local internal and external country teams, global study teams ...
Quick apply
Study Start-Up Lead
South San Francisco, CA · On-site
$70 - $75/hr
Enable innovative clinical trial delivery and address study start-up needs across various ... therapeutic areas. * Collaborate with local internal and external country teams, global study teams ...
Study Start Up Associate II ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster. As a values ...
Study Start Up Associate II ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster. As a values ...
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 ...
Study Start Up Associate II ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster. As a values ...
Study Start Up Associate II ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster. As a values ...
Study Start Up Associate II
Blue Bell, PA · On-site
Study Start Up Associate II ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster. As a values ...
Study Start Up Associate II
Blue Bell, PA · On-site
Study Start Up Associate II ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster. As a values ...
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 ...
Executive Clinical Study Start Up information
See salary details
$11.54 - $16.74
4% of jobs
$16.74 - $21.94
15% of jobs
$24.54 is the 25th percentile. Wages below this are outliers.
$21.94 - $27.14
13% of jobs
$27.14 - $32.34
8% of jobs
The median wage is $35.23 / hr.
$32.34 - $37.54
19% of jobs
$37.54 - $42.74
13% of jobs
$44.83 is the 75th percentile. Wages above this are outliers.
$42.74 - $47.95
10% of jobs
$47.95 - $53.15
5% of jobs
$53.15 - $58.35
11% of jobs
$58.35 - $63.55
1% of jobs
$63.55 - $68.75
1% of jobs
$11
$37
$68
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Job description
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
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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