Prepare and QC clinical study specific materials. * Ensure that proper guidelines for communication are set at study start-up and maintained throughout a study by creating and updating the study ...
Prepare and QC clinical study specific materials. * Ensure that proper guidelines for communication are set at study start-up and maintained throughout a study by creating and updating the study ...
Clinical Trial Manager
Morrisville, NC · On-site
The Clinical Trial Manager (CTM) is responsible for managing various aspects of clinical trials including study start-up, site management and monitoring activities. This includes vendor management ...
Clinical Trial Manager
Morrisville, NC · On-site
The Clinical Trial Manager (CTM) is responsible for managing various aspects of clinical trials including study start-up, site management and monitoring activities. This includes vendor management ...
Prepare and QC clinical study specific materials. * Ensure that proper guidelines for communication are set at study start-up and maintained throughout a study by creating and updating the study ...
Quick apply
Prepare and QC clinical study specific materials. * Ensure that proper guidelines for communication are set at study start-up and maintained throughout a study by creating and updating the study ...
... study start-up and maintained throughout a study by creating and updating the study specific Communication and Escalation Plan. Maintain clinical study specific study files and ensure that all ...
Quick apply
... study start-up and maintained throughout a study by creating and updating the study specific Communication and Escalation Plan. Maintain clinical study specific study files and ensure that all ...
... study start-up and maintained throughout a study by creating and updating the study specific Communication and Escalation Plan. Maintain clinical study specific study files and ensure that all ...
... study start-up and maintained throughout a study by creating and updating the study specific Communication and Escalation Plan. Maintain clinical study specific study files and ensure that all ...
Clinical Trials Manager- Remote
Chapel Hill, NC · Remote
$62 - $64.73/hr
Remote Schedule: Full-Time | Eastern Time Zone Hours Pay: $62.00-$64.73 per hour Position Overview ... Coordinate study start-up activities and support timely ethics committee and regulatory submissions.
Quick apply
Clinical Trials Manager- Remote
Chapel Hill, NC · Remote
$62 - $64.73/hr
Remote Schedule: Full-Time | Eastern Time Zone Hours Pay: $62.00-$64.73 per hour Position Overview ... Coordinate study start-up activities and support timely ethics committee and regulatory submissions.
Clinical Research Nurse Coordinator - Duke Cancer Institute
Durham, NC · On-site
$66K - $83K/yr
From study start-up through closeout, you will be a central driver of clinical trial execution, ensuring excellence in patient care, regulatory compliance, and data integrity. In your day-to-day work ...
Clinical Research Nurse Coordinator - Duke Cancer Institute
Durham, NC · On-site
$66K - $83K/yr
From study start-up through closeout, you will be a central driver of clinical trial execution, ensuring excellence in patient care, regulatory compliance, and data integrity. In your day-to-day work ...
Clinical Research Nurse Coordinator - Duke Cancer Institute
Durham, NC · On-site
$66K - $83K/yr
From study start-up through closeout, you will be a central driver of clinical trial execution, ensuring excellence in patient care, regulatory compliance, and data integrity. In your day-to-day work ...
Clinical Research Nurse Coordinator - Duke Cancer Institute
Durham, NC · On-site
$66K - $83K/yr
From study start-up through closeout, you will be a central driver of clinical trial execution, ensuring excellence in patient care, regulatory compliance, and data integrity. In your day-to-day work ...
... activities for assigned clinical studies. What You Will Do: You will oversee site start-up and activation workstreams, ensuring deliverables meet quality and timeline expectations. Key ...
... activities for assigned clinical studies. What You Will Do: You will oversee site start-up and activation workstreams, ensuring deliverables meet quality and timeline expectations. Key ...
... activities for assigned clinical studies. What You Will Do: You will oversee site start-up and activation workstreams, ensuring deliverables meet quality and timeline expectations. Key ...
... activities for assigned clinical studies. What You Will Do: You will oversee site start-up and activation workstreams, ensuring deliverables meet quality and timeline expectations. Key ...
This role requires demonstrated success in leading complex global clinical studies through all phases of execution, from study start-up to close-out. As a Global Clinical Operations Leader/ Clinical ...
This role requires demonstrated success in leading complex global clinical studies through all phases of execution, from study start-up to close-out. As a Global Clinical Operations Leader/ Clinical ...
Clinical Program Manager
Durham, NC · On-site
Provide oversight and direction to study team members for study deliverables, study start up and ... Minimum 8 years of clinical trial experience with at least the two most recent years in a people ...
Clinical Program Manager
Durham, NC · On-site
Provide oversight and direction to study team members for study deliverables, study start up and ... Minimum 8 years of clinical trial experience with at least the two most recent years in a people ...
Provide oversight and direction to study team members for study deliverables, study start up and ... Minimum 8 years of clinical trial experience with at least the two most recent years in a people ...
Provide oversight and direction to study team members for study deliverables, study start up and ... Minimum 8 years of clinical trial experience with at least the two most recent years in a people ...
Clinical Program Manager
Durham, NC · On-site
Main Purpose of the Role The CPM Clinical Program Manager (CPM) will plan, initiate, and execute ... Provide oversight and direction to study team members for study deliverables, study start up and ...
Clinical Program Manager
Durham, NC · On-site
Main Purpose of the Role The CPM Clinical Program Manager (CPM) will plan, initiate, and execute ... Provide oversight and direction to study team members for study deliverables, study start up and ...
Clinical Research Coordinator
Durham, NC · On-site
$23.50 - $31.25/hr
... as study start up and close out, IRB tasks, etc.). You will have an essential role in the ... Duke clinical trial experience and a desire to expand their knowledge and to share knowledge in an ...
Clinical Research Coordinator
Durham, NC · On-site
$23.50 - $31.25/hr
... as study start up and close out, IRB tasks, etc.). You will have an essential role in the ... Duke clinical trial experience and a desire to expand their knowledge and to share knowledge in an ...
Clinical Research Coordinator
Durham, NC · On-site
$23.50 - $31.25/hr
... as study start up and close out, IRB tasks, etc.). You will have an essential role in the ... Duke clinical trial experience and a desire to expand their knowledge and to share knowledge in an ...
Clinical Research Coordinator
Durham, NC · On-site
$23.50 - $31.25/hr
... as study start up and close out, IRB tasks, etc.). You will have an essential role in the ... Duke clinical trial experience and a desire to expand their knowledge and to share knowledge in an ...
This role requires demonstrated success in leading complex global clinical studies through all phases of execution, from study start-up to close-out. As a Global Clinical Operations Leader/ Clinical ...
This role requires demonstrated success in leading complex global clinical studies through all phases of execution, from study start-up to close-out. As a Global Clinical Operations Leader/ Clinical ...
This role requires demonstrated success in leading complex global clinical studies through all phases of execution, from study start-up to close-out. As a Global Clinical Operations Leader/ Clinical ...
This role requires demonstrated success in leading complex global clinical studies through all phases of execution, from study start-up to close-out. As a Global Clinical Operations Leader/ Clinical ...
Site Contracts Associate, IQVIA Biotech
$49K - $123K/yr
... for clinical trials. This role plays a critical part in ensuring timely and compliant study start-up and maintenance by managing financial and operational aspects of site contracts. Essential ...
Site Contracts Associate, IQVIA Biotech
$49K - $123K/yr
... for clinical trials. This role plays a critical part in ensuring timely and compliant study start-up and maintenance by managing financial and operational aspects of site contracts. Essential ...
Clinical Research Associate
$71K - $189K/yr
Clinical Research Associate II & Senior Clinical Research Associate (CRA II/Sr. CRA) Multiple ... May participate in study start-up activities, site budget tracking, financial management, and site ...
Clinical Research Associate
$71K - $189K/yr
Clinical Research Associate II & Senior Clinical Research Associate (CRA II/Sr. CRA) Multiple ... May participate in study start-up activities, site budget tracking, financial management, and site ...
Full Time Clinical Study Start Up information
See Raleigh, NC salary details
$21.4K - $37.6K
1% of jobs
$37.6K - $53.9K
3% of jobs
$53.9K - $70.2K
7% of jobs
$84.7K is the 25th percentile. Wages below this are outliers.
$70.2K - $86.4K
15% of jobs
$86.4K - $102.7K
9% of jobs
$102.7K - $118.9K
14% of jobs
The median wage is $120K / yr.
$118.9K - $135.2K
17% of jobs
$146.7K is the 75th percentile. Wages above this are outliers.
$135.2K - $151.5K
13% of jobs
$151.5K - $167.7K
11% of jobs
$167.7K - $184K
7% of jobs
$184K - $200.2K
3% of jobs
$21.4K
$121.8K
$200.2K
How much do full time clinical study start up jobs pay per year?
As of Sep 4, 2026, the average yearly pay for full time clinical study start up in Raleigh, NC is $121,792.00, according to ZipRecruiter salary data. Most workers in this role earn between $82,600.00 and $152,600.00 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.
What are the most commonly searched types of Clinical Study Start Up jobs in Raleigh, NC?
The most popular types of Clinical Study Start Up jobs in Raleigh, NC are:
What are popular job titles related to Full Time Clinical Study Start Up jobs in Raleigh, NC?
For Full Time Clinical Study Start Up jobs in Raleigh, NC, the most frequently searched job titles are:
What job categories do people searching Full Time Clinical Study Start Up jobs in Raleigh, NC look for?
The top searched job categories for Full Time Clinical Study Start Up jobs in Raleigh, NC are:
What cities near Raleigh, NC are hiring for Full Time Clinical Study Start Up jobs?
Cities near Raleigh, NC with the most Full Time Clinical Study Start Up job openings:
Full-time
Medical, Dental, Vision, Life, Retirement
Re-posted 6 days ago
Job description
Project Manager, II Labs- hybrid
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 organisation, integrity, collaboration, agility, and inclusion are at the heart of how we work and interact with each other, customers, patients and suppliers.
Project Manager II, Laboratory- Farmingdale NY- Blue Bell PA- hybrid
The Project Manager, Labs will ensure client satisfaction by acting as the Client's main contact in all matters regarding ICON Laboratory Services (ILS), including the setup and day-to-day management of studies, attend and represent ILS at Client meetings, manage studies in accordance with Good Clinical Practice, provide Clients with regular study updates and communicate study progress to Clients and PM Leadership in a responsible and professional manner.
The role
- Act as the sponsor's main contact person in all matters regarding our central laboratory services, following up and responding to clinical study specific inquiries from Sponsors, Physicians, CRA and CRO representatives and the ICON Site Services Department.
- Review newly assigned protocols and Amendments. Coordinate and manage the completion of the Clinical Laboratory Worksheet (CLW) and communicate information as required to other departments within ICON Laboratories (and ICON Clinical CRO if appropriate).
- Enter protocol parameter information into PACS//ICOLIMS and other systems for new and/or amended protocols. Prepare and QC clinical study specific materials.
- Ensure that proper guidelines for communication are set at study start-up and maintained throughout a study by creating and updating the study specific Communication and Escalation Plan. Ensure adherence to the protocol specific monitoring plan. Maintain clinical study specific study files and ensure that all appropriate documents are properly maintained. Ensure that all necessary documents are archived at study closure.
- Provide Sponsors with study management reports. Provide client with support on ICOLabs system. Inform team leader about study progress.
- Proactively monitor study budget.
- Set the timelines for and monitor the progress of shipment requests for storage samples and verify data.
- Attend and represent ICON at Sponsor Investigator Meetings, Kick-Off Meeting, Bid Defenses or Initiations.
- Develop new tools, train new employees.
- Performs additional relevant responsibilities as requested by management.
What you need
- Bachelor's degree or local equivalent in Science, Business or related Field
- Minimum of 2 years of experience working in a clinical laboratory, clinical trials, or customer management/account management role in a life science related organization
- Minimum of 2 years of Project Management experience in a service area serving clinical trials, such as IVRS, Clinical Supplies Packaging and Distribution, Medical Imaging, Data Management, or Electronic Data Capture.
- Working familiarity with Word, Excel, PowerPoint
#LI-FL1
Employment with ICON is contingent upon having the legal right to work in the country where the role is based.
Rewards & Benefits
ICON offers a competitive and comprehensive total rewards package designed to support your health, wellbeing, and career development.
Benefits may include:
- Competitive base salary and performance related incentives
- Health and wellbeing programmes including medical, dental, and vision coverage where applicable
- Retirement and pension plans
- Life assurance and disability coverage
- Employee assistance programmes and wellbeing resources
- Learning and development opportunities through structured training and career pathways
Benefits may vary depending on role and location.
Visit our careers site to read more about the benefits ICON offers.
Inclusion and Accessibility
ICON is an equal opportunity employer. We are committed to building an inclusive and accessible workplace where everyone feels valued and supported.
If you require reasonable accommodations during the recruitment process, please let us know or submit a requesthere.
Are you a current ICON Employee? Please click here to apply