As a Study Start Up Associate II at ICON, you will lead the initiation of clinical trials, ensuring compliance with regulatory requirements, and contribute to the advancement of innovative treatments ...
As a Study Start Up Associate II at ICON, you will lead the initiation of clinical trials, ensuring compliance with regulatory requirements, and contribute to the advancement of innovative treatments ...
As a Study Start Up Associate II at ICON, you will lead the initiation of clinical trials, ensuring compliance with regulatory requirements, and contribute to the advancement of innovative treatments ...
As a Study Start Up Associate II at ICON, you will lead the initiation of clinical trials, ensuring compliance with regulatory requirements, and contribute to the advancement of innovative treatments ...
As a Study Start Up Associate II at ICON, you will lead the initiation of clinical trials, ensuring compliance with regulatory requirements, and contribute to the advancement of innovative treatments ...
Quick apply
As a Study Start Up Associate II at ICON, you will lead the initiation of clinical trials, ensuring compliance with regulatory requirements, and contribute to the advancement of innovative treatments ...
Study Activation Manager
Raleigh, NC · On-site
Develop and lead the global study start-up and site activation strategy for assigned trials, including activation assumptions, country and site sequencing, critical path dependencies, milestone ...
Study Activation Manager
Raleigh, NC · On-site
Develop and lead the global study start-up and site activation strategy for assigned trials, including activation assumptions, country and site sequencing, critical path dependencies, milestone ...
Study Activation Manager
Raleigh, NC · On-site
Develop and lead the global study start-up and site activation strategy for assigned trials, including activation assumptions, country and site sequencing, critical path dependencies, milestone ...
Study Activation Manager
Raleigh, NC · On-site
Develop and lead the global study start-up and site activation strategy for assigned trials, including activation assumptions, country and site sequencing, critical path dependencies, milestone ...
Global Study Manager
Durham, NC · On-site
... Study Associate Director (GSAD). The role ensures compliance with AstraZeneca's Delivery Model ... Here, your start-up leadership shapes the path from promising data to approved medicines. You will ...
Global Study Manager
Durham, NC · On-site
... Study Associate Director (GSAD). The role ensures compliance with AstraZeneca's Delivery Model ... Here, your start-up leadership shapes the path from promising data to approved medicines. You will ...
Global Study Manager
Durham, NC · On-site
... Study Associate Director (GSAD). The role ensures compliance with AstraZeneca's Delivery Model ... Here, your start-up leadership shapes the path from promising data to approved medicines. You will ...
New
Global Study Manager
Durham, NC · On-site
... Study Associate Director (GSAD). The role ensures compliance with AstraZeneca's Delivery Model ... Here, your start-up leadership shapes the path from promising data to approved medicines. You will ...
New
Global Study Manager
Durham, NC · On-site
... Study Associate Director (GSAD). The role ensures compliance with AstraZeneca's Delivery Model ... Here, your start-up leadership shapes the path from promising data to approved medicines. You will ...
New
Global Study Manager
Durham, NC · On-site
... Study Associate Director (GSAD). The role ensures compliance with AstraZeneca's Delivery Model ... Here, your start-up leadership shapes the path from promising data to approved medicines. You will ...
New
Global Study Manager
Durham, NC · On-site
... Study Associate Director (GSAD). The role ensures compliance with AstraZeneca's Delivery Model ... Here, your start-up leadership shapes the path from promising data to approved medicines. You will ...
Global Study Manager
Durham, NC · On-site
... Study Associate Director (GSAD). The role ensures compliance with AstraZeneca's Delivery Model ... Here, your start-up leadership shapes the path from promising data to approved medicines. You will ...
Clinical Study Manager
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
Clinical Study Manager
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 ...
Clinical Study Manager
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
Clinical Study Manager
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 ...
Clinical Study Manager
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
Clinical Study Manager
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 ...
Clinical Study Manager
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
Clinical Study Manager
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 ...
Clinical Study Manager
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
Clinical Study Manager
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 ...
Clinical Study Manager
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
Clinical Study Manager
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 ...
Site Contracts Associate, IQVIA Biotech
Durham, NC · On-site
$49K - $123K/yr
IQVIA Biotech is hiring for Site Contracts Associate with 1-3 years' experience negotiating ... This role plays a critical part in ensuring timely and compliant study start-up and maintenance by ...
Site Contracts Associate, IQVIA Biotech
Durham, NC · On-site
$49K - $123K/yr
IQVIA Biotech is hiring for Site Contracts Associate with 1-3 years' experience negotiating ... This role plays a critical part in ensuring timely and compliant study start-up and maintenance by ...
Site Contracts Associate, IQVIA Biotech
Durham, NC · On-site
$49K - $123K/yr
IQVIA Biotech is hiring for Site Contracts Associate with 1-3 years' experience negotiating ... This role plays a critical part in ensuring timely and compliant study start-up and maintenance by ...
Site Contracts Associate, IQVIA Biotech
Durham, NC · On-site
$49K - $123K/yr
IQVIA Biotech is hiring for Site Contracts Associate with 1-3 years' experience negotiating ... This role plays a critical part in ensuring timely and compliant study start-up and maintenance by ...
Site Contracts Associate, IQVIA Biotech
Durham, NC · On-site
$49K - $123K/yr
IQVIA Biotech is hiring for Site Contracts Associate with 1-3 years' experience negotiating ... This role plays a critical part in ensuring timely and compliant study start-up and maintenance by ...
Site Contracts Associate, IQVIA Biotech
Durham, NC · On-site
$49K - $123K/yr
IQVIA Biotech is hiring for Site Contracts Associate with 1-3 years' experience negotiating ... This role plays a critical part in ensuring timely and compliant study start-up and maintenance by ...
Clinical Study Manager
Durham, NC · On-site
Primary Responsibilities " 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 ...
Quick apply
Clinical Study Manager
Durham, NC · On-site
Primary Responsibilities " 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 ...
Manager, Site Contracts
$86K - $115K/yr
Maintain study and site-specific CDA study start-up metrics * Global Site Contracts - Clinical ... Associate degree * At least 5 years of experience in a clinical site contract processing/management ...
Manager, Site Contracts
$86K - $115K/yr
Maintain study and site-specific CDA study start-up metrics * Global Site Contracts - Clinical ... Associate degree * At least 5 years of experience in a clinical site contract processing/management ...
Study Start Up Associate information
See Raleigh, NC salary details
$12.38 - $16.14
3% of jobs
$16.14 - $19.90
18% of jobs
$20.65 is the 25th percentile. Wages below this are outliers.
$19.90 - $23.66
20% of jobs
The median wage is $25.95 / hr.
$23.66 - $27.42
15% of jobs
$27.42 - $31.18
11% of jobs
$31.18 - $34.94
4% of jobs
$38.14 is the 75th percentile. Wages above this are outliers.
$34.94 - $38.70
5% of jobs
$38.70 - $42.46
8% of jobs
$42.46 - $46.22
6% of jobs
$46.22 - $49.98
6% of jobs
$49.98 - $53.74
3% of jobs
$12
$30
$53
How much do study start up associate jobs pay per hour?
As of Sep 14, 2026, the average hourly pay for study start up associate in Raleigh, NC is $30.66, according to ZipRecruiter salary data. Most workers in this role earn between $20.58 and $40.43 per hour, depending on experience, location, and employer.
What is the difference between Study Start Up Associate vs Clinical Trial Coordinator?
| Aspect | Study Start Up Associate | Clinical Trial Coordinator |
|---|---|---|
| Required Credentials | Bachelor's degree, knowledge of regulatory requirements | Bachelor's degree, familiarity with clinical procedures |
| Work Environment | Regulatory and site initiation activities | Participant management and site coordination |
| Employer & Industry Usage | Pharmaceuticals, biotech, CROs | Hospitals, research centers, CROs |
The Study Start Up Associate primarily focuses on regulatory submissions, site qualification, and initiation processes, ensuring trial readiness. In contrast, the Clinical Trial Coordinator manages participant recruitment, scheduling, and data collection. Both roles are essential in clinical research but differ in their core responsibilities and focus areas.
What are popular job titles related to Study Start Up Associate jobs in Raleigh, NC?
For Study Start Up Associate jobs in Raleigh, NC, the most frequently searched job titles are:
What job categories do people searching Study Start Up Associate jobs in Raleigh, NC look for?
The top searched job categories for Study Start Up Associate jobs in Raleigh, NC are:
What cities near Raleigh, NC are hiring for Study Start Up Associate jobs?
Cities near Raleigh, NC with the most Study Start Up Associate job openings:
Clinical Operations Specialist
Raleigh, NC • On-site
Full-time
Medical, Dental, Vision, Life, Retirement
Posted 28 days ago
Job description
Clinical Operations Specialist
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.
As a Study Start Up Associate II at ICON, you will lead the initiation of clinical trials, ensuring compliance with regulatory requirements, and contribute to the advancement of innovative treatments and therapies.
What You Will Do:
You will contribute to site start-up and activation activities, taking responsibility for your deliverables and working collaboratively.
Key responsibilities include:
Your Profile:
You will bring relevant site start-up and activation experience, along with the following qualifications and skills.
Required qualifications and experience:
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:
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 request here.
Are you a current ICON Employee? Please click here to apply
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.
As a Study Start Up Associate II at ICON, you will lead the initiation of clinical trials, ensuring compliance with regulatory requirements, and contribute to the advancement of innovative treatments and therapies.
What You Will Do:
You will contribute to site start-up and activation activities, taking responsibility for your deliverables and working collaboratively.
Key responsibilities include:
- Leading the preparation and submission of regulatory documents, including clinical trial applications, ethics committee submissions, and regulatory agency communications.
- Coordinating and liaising with internal and external stakeholders to obtain necessary approvals and authorizations for study initiation.
- Managing and maintaining comprehensive and accurate records of regulatory submissions, approvals, and correspondence
- Providing guidance and support to study teams on regulatory requirements and best practices for study start-up activities.
- Participating in process improvement initiatives to streamline study start-up processes and enhance efficiency.
Your Profile:
You will bring relevant site start-up and activation experience, along with the following qualifications and skills.
Required qualifications and experience:
- Bachelor's degree in life sciences or a related field.
- Minimum of 2 years of experience in clinical research or regulatory affairs, with specific experience in study start-up activities.
- Strong understanding of regulatory requirements and guidelines for clinical trials, including ICH-GCP and local regulatory requirements.
- Excellent organizational and project management skills, with the ability to prioritize and manage multiple tasks simultaneously.
- Excellent communication and interpersonal skills, with the ability to collaborate effectively with cross-functional teams.
- Willingness to travel as required (approximately 5%)
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 request here.
Are you a current ICON Employee? Please click here to apply