Study Start-Up Manager
Wilmington, DE · On-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 ...
Wilmington, DE · On-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 ...
Wilmington, DE · On-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 ...
Wilmington, DE · On-site
Working across clinical operations, sites, and strategy, you will remove obstacles, compress ... Study Start Up Lead work (must be full time, not a partial mix of maintenance or close-out ...
Wilmington, DE · On-site
Working across clinical operations, sites, and strategy, you will remove obstacles, compress ... Study Start Up Lead work (must be full time, not a partial mix of maintenance or close-out ...
Wilmington, DE · On-site
Working across clinical operations, sites, and strategy, you will remove obstacles, compress ... Study Start Up Lead work (must be full time, not a partial mix of maintenance or close-out ...
Wilmington, DE · On-site
Working across clinical operations, sites, and strategy, you will remove obstacles, compress ... Study Start Up Lead work (must be full time, not a partial mix of maintenance or close-out ...
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 ...
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 ...
The Study Start-Up Manager serves as the primary operational lead for startup execution, coordinating closely with Regulatory, Clinical Operations, Clinical Data, sponsors, CROs, investigators, and ...
The Study Start-Up Manager serves as the primary operational lead for startup execution, coordinating closely with Regulatory, Clinical Operations, Clinical Data, sponsors, CROs, investigators, and ...
The Study Start-Up (SSU) Manager is responsible for overseeing and driving operational study startup activities across the clinical research network from study award through activation. This role ...
The Study Start-Up (SSU) Manager is responsible for overseeing and driving operational study startup activities across the clinical research network from study award through activation. This role ...
Princeton, NJ · On-site
... study start-up, site contact and budget negotiation, and managing relationships with clinical ... You will support clinical benchmarking and site budget development, escalation, and payment ...
Princeton, NJ · On-site
... study start-up, site contact and budget negotiation, and managing relationships with clinical ... You will support clinical benchmarking and site budget development, escalation, and payment ...
The Study Start-Up (SSU) Manager is responsible for overseeing and driving operational study startup activities across the clinical research network from study award through activation. This role ...
The Study Start-Up (SSU) Manager is responsible for overseeing and driving operational study startup activities across the clinical research network from study award through activation. This role ...
Watertown, MA · On-site
$195K - $275K/yr
Provide strategic and operational leadership for end-to-end study start-up activities across ... Strong understanding of clinical trial management, ICH-GCP, and regulatory compliance * Proven ...
Watertown, MA · On-site
$195K - $275K/yr
Provide strategic and operational leadership for end-to-end study start-up activities across ... Strong understanding of clinical trial management, ICH-GCP, and regulatory compliance * Proven ...
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 ...
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 ...
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 ...
Boston, MA · On-site
... study start up and enrollment ... This role will support the overall planning and management of clinical trials, including CRO and ...
Boston, MA · On-site
... study start up and enrollment ... This role will support the overall planning and management of clinical trials, including CRO and ...
This role is crucial in managing site agreements to support our programs. The ideal candidate will ... Partner with Clinical Finance team to provide study-wide site payment estimates and forecasts
This role is crucial in managing site agreements to support our programs. The ideal candidate will ... Partner with Clinical Finance team to provide study-wide site payment estimates and forecasts
This position will be an integral part of the Clinical Operations leadership team and requires a ... Study Start-Up/Regulatory Submissions experience within a CRO is required. Incentives can include:
This position will be an integral part of the Clinical Operations leadership team and requires a ... Study Start-Up/Regulatory Submissions experience within a CRO is required. Incentives can include:
Pacific, MO · On-site
$150 - $200/hr
Who We Are Emerald Clinical Trials is a global leader in clinical research, partnering with over ... Develop and manage study start-up plans, forecasts, and deliverables * Oversee IRB/EC and hospital ...
Pacific, MO · On-site
$150 - $200/hr
Who We Are Emerald Clinical Trials is a global leader in clinical research, partnering with over ... Develop and manage study start-up plans, forecasts, and deliverables * Oversee IRB/EC and hospital ...
Durham, NC · On-site
Provide day-to-day study management support and oversight for assigned clinical study activities from start-up through close-out. * Coordinate with internal project team members, CROs, vendors ...
Quick apply
Durham, NC · On-site
Provide day-to-day study management support and oversight for assigned clinical study activities from start-up through close-out. * Coordinate with internal project team members, CROs, vendors ...
Durham, NC · On-site
Provide day-to-day study management support and oversight for assigned clinical study activities from start-up through close-out. * Coordinate with internal project team members, CROs, vendors ...
Quick apply
Durham, NC · On-site
Provide day-to-day study management support and oversight for assigned clinical study activities from start-up through close-out. * Coordinate with internal project team members, CROs, vendors ...
Durham, NC · On-site
Provide day-to-day study management support and oversight for assigned clinical study activities from start-up through close-out. * Coordinate with internal project team members, CROs, vendors ...
Quick apply
Durham, NC · On-site
Provide day-to-day study management support and oversight for assigned clinical study activities from start-up through close-out. * Coordinate with internal project team members, CROs, vendors ...
$57/hr
Clinical Study Manager duties are ... Develop project cross-functional, integrated study plan to study start up (in-house) and validate ...
$57/hr
Clinical Study Manager duties are ... Develop project cross-functional, integrated study plan to study start up (in-house) and validate ...
$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
The most popular types of Clinical Study Start Up jobs are:
For Clinical Study Start Up Manager jobs, the most frequently searched job titles are:
Wilmington, DE • On-site
Full-time
Re-posted 15 days ago
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.
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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.
It services
11 - 50 Employees
Plano, TX, US
2008