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 ...
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 ...
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 ...
Ensures all clinical trials are executed in compliance with ICH/GCP guidelines/regulations and ... Demonstrated experience operating at a Senior Clinical Trial Lead or Associate Director level.
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Ensures all clinical trials are executed in compliance with ICH/GCP guidelines/regulations and ... Demonstrated experience operating at a Senior Clinical Trial Lead or Associate Director level.
Associate Clinical Lead Directors are an integral part of clinical trial delivery, leading and ... Work as the primary Clinical Lead alongside other Clinical Leads to deliver large, global trials.
Associate Clinical Lead Directors are an integral part of clinical trial delivery, leading and ... Work as the primary Clinical Lead alongside other Clinical Leads to deliver large, global trials.
Ensures all clinical trials are executed in compliance with ICH/GCP guidelines/regulations and ... Demonstrated experience operating at a Senior Clinical Trial Lead or Associate Director level.
Ensures all clinical trials are executed in compliance with ICH/GCP guidelines/regulations and ... Demonstrated experience operating at a Senior Clinical Trial Lead or Associate Director level.
Senior Clinical Project Manager
Raleigh, NC · On-site
$140 - $200/hr
Ensures all clinical trials are executed in compliance with ICH/GCP guidelines/regulations and ... Demonstrated experience operating at a Senior Clinical Trial Lead or Associate Director level.
Senior Clinical Project Manager
Raleigh, NC · On-site
$140 - $200/hr
Ensures all clinical trials are executed in compliance with ICH/GCP guidelines/regulations and ... Demonstrated experience operating at a Senior Clinical Trial Lead or Associate Director level.
Associate Clinical Lead Directors are an integral part of clinical trial delivery, leading and ... Work as the primary Clinical Lead alongside other Clinical Leads to deliver large, global trials.
Associate Clinical Lead Directors are an integral part of clinical trial delivery, leading and ... Work as the primary Clinical Lead alongside other Clinical Leads to deliver large, global trials.
Associate Clinical Lead Directors are an integral part of clinical trial delivery, leading and ... Work as the primary Clinical Lead alongside other Clinical Leads to deliver large, global trials.
Associate Clinical Lead Directors are an integral part of clinical trial delivery, leading and ... Work as the primary Clinical Lead alongside other Clinical Leads to deliver large, global trials.
Lead CRA
Raleigh, NC · On-site
Extensive experience as a Clinical Research Associate within the pharmaceutical, biotech, or CRO industry, with a proven track record of managing complex clinical trials. * In-depth knowledge of ICH ...
Quick apply
Lead CRA
Raleigh, NC · On-site
Extensive experience as a Clinical Research Associate within the pharmaceutical, biotech, or CRO industry, with a proven track record of managing complex clinical trials. * In-depth knowledge of ICH ...
Associate Clinical Project Manager, Immuno-Oncology, Cell and Gene Therapy, IQVIA Biotech
Durham, NC · On-site
$68K - $171K/yr
As an Associate Project Manager (APM), you'll play a critical role in delivering clinical trials ... Support delivery of clinical trials across Immuno-Oncology and Cell & Gene Therapy programs
New
Associate Clinical Project Manager, Immuno-Oncology, Cell and Gene Therapy, IQVIA Biotech
Durham, NC · On-site
$68K - $171K/yr
As an Associate Project Manager (APM), you'll play a critical role in delivering clinical trials ... Support delivery of clinical trials across Immuno-Oncology and Cell & Gene Therapy programs
New
Associate Clinical Project Manager, Immuno-Oncology, Cell and Gene Therapy, IQVIA Biotech
Durham, NC · On-site
$68K - $171K/yr
As an Associate Project Manager (APM), you'll play a critical role in delivering clinical trials ... Support delivery of clinical trials across Immuno-Oncology and Cell & Gene Therapy programs
New
Associate Clinical Project Manager, Immuno-Oncology, Cell and Gene Therapy, IQVIA Biotech
Durham, NC · On-site
$68K - $171K/yr
As an Associate Project Manager (APM), you'll play a critical role in delivering clinical trials ... Support delivery of clinical trials across Immuno-Oncology and Cell & Gene Therapy programs
New
... clinical trials, including studies involving Investigational Products (IP). You will play a ... Graduation from an accredited BSN, Associate Degree in Nursing, or Nursing Diploma program
... clinical trials, including studies involving Investigational Products (IP). You will play a ... Graduation from an accredited BSN, Associate Degree in Nursing, or Nursing Diploma program
Clinical Research Nurse Coordinator - Duke Cancer Institute
Durham, NC · On-site
$66K - $83K/yr
... clinical trials, including studies involving Investigational Products (IP). You will play a ... Graduation from an accredited BSN, Associate Degree in Nursing, or Nursing Diploma program
Clinical Research Nurse Coordinator - Duke Cancer Institute
Durham, NC · On-site
$66K - $83K/yr
... clinical trials, including studies involving Investigational Products (IP). You will play a ... Graduation from an accredited BSN, Associate Degree in Nursing, or Nursing Diploma program
Manager, Site Contracts with Clinical Trials experience Hybrid or Remote in USA-NC
Morrisville, NC · On-site
$80 - $140/hr
Manager, Site Contracts with Clinical Trials experience Hybrid or Remote in USA-NC Updated ... May conduct oversight visits as required for Clinical Research Associates. Responsible for all ...
Manager, Site Contracts with Clinical Trials experience Hybrid or Remote in USA-NC
Morrisville, NC · On-site
$80 - $140/hr
Manager, Site Contracts with Clinical Trials experience Hybrid or Remote in USA-NC Updated ... May conduct oversight visits as required for Clinical Research Associates. Responsible for all ...
Clinical Studies Registered Nurse II, Cardiology
Wake Forest, NC · On-site
$38.20 - $57.30/hr
Primary area is cardiovascular device and pharmaceutical clinical trials. EDUCATION/EXPERIENCE Associate's degree in Nursing from an accredited School of Nursing with one year of nursing experience ...
Clinical Studies Registered Nurse II, Cardiology
Wake Forest, NC · On-site
$38.20 - $57.30/hr
Primary area is cardiovascular device and pharmaceutical clinical trials. EDUCATION/EXPERIENCE Associate's degree in Nursing from an accredited School of Nursing with one year of nursing experience ...
Clinical Trial Assistant
Raleigh, NC · On-site
Provide administrative support to Clinical Research Associates (CRAs), including preparing site ... Experience supporting multiple clinical studies, including multicenter or global trials.
Clinical Trial Assistant
Raleigh, NC · On-site
Provide administrative support to Clinical Research Associates (CRAs), including preparing site ... Experience supporting multiple clinical studies, including multicenter or global trials.
Associate Merck Clinical Trials information
See Raleigh, NC salary details
$16.82 - $21.50
4% of jobs
$21.50 - $26.17
8% of jobs
$26.17 - $30.84
12% of jobs
$30.99 is the 25th percentile. Wages below this are outliers.
$30.84 - $35.52
26% of jobs
$35.52 - $40.19
18% of jobs
$41.81 is the 75th percentile. Wages above this are outliers.
$40.19 - $44.87
19% of jobs
$44.87 - $49.54
6% of jobs
$49.54 - $54.21
2% of jobs
$54.21 - $58.89
1% of jobs
$58.89 - $63.56
1% of jobs
$63.56 - $68.23
2% of jobs
$16
$38
$68
How much do associate merck clinical trials jobs pay per hour?
As of Aug 23, 2026, the average hourly pay for associate merck clinical trials in Raleigh, NC is $38.87, according to ZipRecruiter salary data. Most workers in this role earn between $31.30 and $42.74 per hour, depending on experience, location, and employer.
What is the difference between Associate Merck Clinical Trials vs Clinical Research Coordinator?
| Aspect | Associate Merck Clinical Trials | Clinical Research Coordinator |
|---|---|---|
| Required Credentials | Bachelor's degree, relevant certifications (e.g., CCRP) | Bachelor's degree, often similar certifications |
| Work Environment | Pharmaceutical company, clinical trial sites, research labs | Hospital, research sites, clinics |
| Employer & Industry | Pharmaceutical industry, biotech firms | Healthcare facilities, research organizations |
| Common Search & Comparison | Yes | Yes |
The Associate Merck Clinical Trials role typically involves supporting clinical trial activities within a pharmaceutical company, focusing on drug development and regulatory compliance. In contrast, a Clinical Research Coordinator manages patient recruitment, data collection, and trial logistics at research sites. Both roles require similar educational backgrounds and certifications, but their work environments and specific responsibilities differ, with the Associate Merck Clinical Trials position being more industry-focused and the Clinical Research Coordinator more patient-facing.
What are the most commonly searched types of Merck Clinical Trials jobs in Raleigh, NC?
The most popular types of Merck Clinical Trials jobs in Raleigh, NC are:
What are popular job titles related to Associate Merck Clinical Trials jobs in Raleigh, NC?
For Associate Merck Clinical Trials jobs in Raleigh, NC, the most frequently searched job titles are:
What job categories do people searching Associate Merck Clinical Trials jobs in Raleigh, NC look for?
The top searched job categories for Associate Merck Clinical Trials jobs in Raleigh, NC are:
- Clinical Research Assistant
- Clinical Trial Management Associate
- Entry Level Biotech Clinical Research
- Clinical Trial Data Entry
- Full Time Clinical Research Rater
- Entry Level Clinical Study Startup
- Full Time Clinical Trials Test Subject
- Cra Training
- Clinical Research Coordinator Hybrid
- Clinical Research Associate Manager
What cities near Raleigh, NC are hiring for Associate Merck Clinical Trials jobs?
Cities near Raleigh, NC with the most Associate Merck Clinical Trials job openings:
Full-time
Medical, Dental, Vision, Life, Retirement
Posted 8 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:
- 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 requesthere.
Are you a current ICON Employee? Please click here to apply