Are you a motivated Clinical Research Associate with 2-3 years of monitoring experience who is looking for more than just your next job? Are you seeking a company that will invest in your development ...
Are you a motivated Clinical Research Associate with 2-3 years of monitoring experience who is looking for more than just your next job? Are you seeking a company that will invest in your development ...
Clinical Research Associate 2, IQVIA
Durham, NC · On-site
$71K - $189K/yr
IQVIA is hiring a Clinical Research Associate 2 with on-site monitoring experience in CNS, GLP-1/Obesity/Diabetes (Type II) and/or Cardiovascular clinical trials. Phase 1 experience is a plus! Job ...
Clinical Research Associate 2, IQVIA
Durham, NC · On-site
$71K - $189K/yr
IQVIA is hiring a Clinical Research Associate 2 with on-site monitoring experience in CNS, GLP-1/Obesity/Diabetes (Type II) and/or Cardiovascular clinical trials. Phase 1 experience is a plus! Job ...
Clinical Research Associate 2, IQVIA
Durham, NC · On-site
$71K - $189K/yr
IQVIA is hiring a Clinical Research Associate 2 with on-site monitoring experience in CNS, GLP-1/Obesity/Diabetes (Type II) and/or Cardiovascular clinical trials. Phase 1 experience is a plus! Job ...
Clinical Research Associate 2, IQVIA
Durham, NC · On-site
$71K - $189K/yr
IQVIA is hiring a Clinical Research Associate 2 with on-site monitoring experience in CNS, GLP-1/Obesity/Diabetes (Type II) and/or Cardiovascular clinical trials. Phase 1 experience is a plus! Job ...
Clinical Research Associate, Sponsor Dedicated, Oncology
Durham, NC · On-site
$90K - $197K/yr
As a Clinical Research Associate, you'll be at the forefront of ensuring our study sites operate smoothly and efficiently. Your work will be pivotal in advancing groundbreaking research. Key ...
Clinical Research Associate, Sponsor Dedicated, Oncology
Durham, NC · On-site
$90K - $197K/yr
As a Clinical Research Associate, you'll be at the forefront of ensuring our study sites operate smoothly and efficiently. Your work will be pivotal in advancing groundbreaking research. Key ...
Clinical Research Associate, Sponsor Dedicated, Oncology
Durham, NC · On-site
$90K - $197K/yr
As a Clinical Research Associate, you'll be at the forefront of ensuring our study sites operate smoothly and efficiently. Your work will be pivotal in advancing groundbreaking research. Key ...
Clinical Research Associate, Sponsor Dedicated, Oncology
Durham, NC · On-site
$90K - $197K/yr
As a Clinical Research Associate, you'll be at the forefront of ensuring our study sites operate smoothly and efficiently. Your work will be pivotal in advancing groundbreaking research. Key ...
Research Associate
Durham, NC · On-site
Research Associate 1 Year Durham (RTP), NC $32 Qualifications: Requirements Experience with antibody conjugation and general surface modification chemistry. Hands on experience in a lab working with ...
Research Associate
Durham, NC · On-site
Research Associate 1 Year Durham (RTP), NC $32 Qualifications: Requirements Experience with antibody conjugation and general surface modification chemistry. Hands on experience in a lab working with ...
Senior Clinical Trial Manager - Oncology
Durham, NC · On-site +1
What Clinical Operations Site Management does at Worldwide Clinical Trial Managers (CTMs) and Clinical Research Associates (CRAs) play a vital role in ensuring our clinical research programs are ...
Senior Clinical Trial Manager - Oncology
Durham, NC · On-site +1
What Clinical Operations Site Management does at Worldwide Clinical Trial Managers (CTMs) and Clinical Research Associates (CRAs) play a vital role in ensuring our clinical research programs are ...
Clinical Research Associate II
Durham, NC · On-site
$48/hr
Job Overview: Requirement/Must Have: * Minimum 2+ years monitoring experience. * One year or more obesity monitoring experience. * Strong endocrinology monitoring experience (2+ years monitoring) is ...
Quick apply
Clinical Research Associate II
Durham, NC · On-site
$48/hr
Job Overview: Requirement/Must Have: * Minimum 2+ years monitoring experience. * One year or more obesity monitoring experience. * Strong endocrinology monitoring experience (2+ years monitoring) is ...
Clinical Research Associate III
Durham, NC · On-site
$70/hr
Job Overview: Requirement/Must Have: * Minimum 3+ years monitoring experience with one year or more obesity monitoring experience. * Prior contracting experience preferred. * Strong endocrinology ...
Quick apply
Clinical Research Associate III
Durham, NC · On-site
$70/hr
Job Overview: Requirement/Must Have: * Minimum 3+ years monitoring experience with one year or more obesity monitoring experience. * Prior contracting experience preferred. * Strong endocrinology ...
Senior Clinical Trial Manager - Oncology
Durham, NC · On-site +1
Join us! n What Clinical Operations Site Management does at Worldwide Clinical Trial Managers (CTMs) and Clinical Research Associates (CRAs) play a vital role in ensuring our clinical research ...
Senior Clinical Trial Manager - Oncology
Durham, NC · On-site +1
Join us! n What Clinical Operations Site Management does at Worldwide Clinical Trial Managers (CTMs) and Clinical Research Associates (CRAs) play a vital role in ensuring our clinical research ...
Clinical Research Associate, Sponsor Dedicated
Durham, NC · On-site
$71K - $189K/yr
Good knowledge of, and skill in applying, applicable clinical research regulatory requirements. i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines. Good ...
Clinical Research Associate, Sponsor Dedicated
Durham, NC · On-site
$71K - $189K/yr
Good knowledge of, and skill in applying, applicable clinical research regulatory requirements. i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines. Good ...
Clinical Research Associate, Full Service
Durham, NC · On-site
$49K - $175K/yr
Basic knowledge of, and skill in applying, applicable clinical research regulatory requirements (i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines)
Clinical Research Associate, Full Service
Durham, NC · On-site
$49K - $175K/yr
Basic knowledge of, and skill in applying, applicable clinical research regulatory requirements (i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines)
Clinical Research Associate, Sponsor Dedicated
Durham, NC · On-site
$71K - $189K/yr
Good knowledge of, and skill in applying, applicable clinical research regulatory requirements. i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines. Good ...
Clinical Research Associate, Sponsor Dedicated
Durham, NC · On-site
$71K - $189K/yr
Good knowledge of, and skill in applying, applicable clinical research regulatory requirements. i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines. Good ...
Clinical Research Associate - Sponsor Dedicated
Durham, NC · On-site
$87K - $182K/yr
Req Good knowledge of, and skill in applying, applicable clinical research regulatory requirements. i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines.
Clinical Research Associate - Sponsor Dedicated
Durham, NC · On-site
$87K - $182K/yr
Req Good knowledge of, and skill in applying, applicable clinical research regulatory requirements. i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines.
Clinical Research Associate, Sponsor Dedicated
Durham, NC · On-site
$71K - $189K/yr
IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to ...
Clinical Research Associate, Sponsor Dedicated
Durham, NC · On-site
$71K - $189K/yr
IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to ...
Clinical Research Associate (CRA 2), Sponsor Dedicated
Durham, NC · On-site
$71K - $182K/yr
IQVIA is hiring Clinical Research Associates (CRA) at the CRA 2 level. Ideal candidates will have 1-2 years of onsite monitoring experience with expertise in Cardiovascular/Renal/Metabolic, Oncology ...
Clinical Research Associate (CRA 2), Sponsor Dedicated
Durham, NC · On-site
$71K - $182K/yr
IQVIA is hiring Clinical Research Associates (CRA) at the CRA 2 level. Ideal candidates will have 1-2 years of onsite monitoring experience with expertise in Cardiovascular/Renal/Metabolic, Oncology ...
Clinical Research Assistant
Wake Forest, NC · On-site
$25 - $30/hr
NC Retina Associates is looking for a Research Assistant to join our team! The research assistant ... Prepare visit-specific documentation and charts for Clinical Research Coordinator. * Observe ...
Quick apply
Clinical Research Assistant
Wake Forest, NC · On-site
$25 - $30/hr
NC Retina Associates is looking for a Research Assistant to join our team! The research assistant ... Prepare visit-specific documentation and charts for Clinical Research Coordinator. * Observe ...
Clinical Research Associate (CRA 2), Sponsor Dedicated
Durham, NC · On-site
$71K - $182K/yr
IQVIA is hiring Clinical Research Associates (CRA) at the CRA 2 level. Ideal candidates will have 1-2 years of onsite monitoring experience with expertise in Cardiovascular/Renal/Metabolic, Oncology ...
Clinical Research Associate (CRA 2), Sponsor Dedicated
Durham, NC · On-site
$71K - $182K/yr
IQVIA is hiring Clinical Research Associates (CRA) at the CRA 2 level. Ideal candidates will have 1-2 years of onsite monitoring experience with expertise in Cardiovascular/Renal/Metabolic, Oncology ...
Clinical Research Coordinator
Durham, NC · On-site
$23.50 - $31.25/hr
Completion of an Associate's degree Experience * Work requires a minimum of two years of relevant research experience. Completion of the DOCR North Carolina state approved Clinical Research ...
Clinical Research Coordinator
Durham, NC · On-site
$23.50 - $31.25/hr
Completion of an Associate's degree Experience * Work requires a minimum of two years of relevant research experience. Completion of the DOCR North Carolina state approved Clinical Research ...
FSP Clinical Research Associate 2 - West Region
Durham, NC · Remote
$100/hr
... clinical research standards. Responsibilities : * Responsible for all aspects of study site monitoring including routine monitoring and close-out of clinical sites, maintenance of study files ...
FSP Clinical Research Associate 2 - West Region
Durham, NC · Remote
$100/hr
... clinical research standards. Responsibilities : * Responsible for all aspects of study site monitoring including routine monitoring and close-out of clinical sites, maintenance of study files ...
Clinical Research Associate information
See Roxboro, NC salary details
$10.57 - $15.19
0% of jobs
$15.19 - $19.80
8% of jobs
$19.80 - $24.42
13% of jobs
$25.65 is the 25th percentile. Wages below this are outliers.
$24.42 - $29.03
15% of jobs
$29.03 - $33.64
13% of jobs
The median wage is $34.33 / hr.
$33.64 - $38.26
11% of jobs
$38.26 - $42.87
12% of jobs
$44.50 is the 75th percentile. Wages above this are outliers.
$42.87 - $47.48
13% of jobs
$47.48 - $52.10
14% of jobs
$52.10 - $56.71
2% of jobs
$56.71 - $61.33
1% of jobs
$10
$36
$61
How much do clinical research associate jobs pay per hour?
What is a clinical research associate?
What are the key skills and qualifications needed to thrive as a clinical research associate?
What are some common challenges clinical research associates face when monitoring clinical trial sites?
What is the difference between Clinical Research Associate vs Clinical Trial Coordinator?
| Aspect | Clinical Research Associate | Clinical Trial Coordinator |
|---|---|---|
| Credentials | Bachelor's degree, often with clinical research certifications | Bachelor's degree, often with clinical research or healthcare certifications |
| Work Environment | Monitors clinical sites, reviews data, ensures compliance | Coordinates trial activities, manages schedules, and communicates with sites |
| Employer & Industry | Pharmaceutical companies, CROs, biotech firms | Hospitals, research institutions, CROs |
Both roles are essential in clinical trials, with CRAs focusing on site monitoring and compliance, while Clinical Trial Coordinators handle day-to-day trial management. They often collaborate but have distinct responsibilities within the clinical research process.
Is being a clinical research associate worth it?
Is it hard to get a clinical research associate job?
What are the most commonly searched types of Clinical Research jobs in Roxboro, NC?
The most popular types of Clinical Research jobs in Roxboro, NC are:
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For Clinical Research Associate jobs in Roxboro, NC, the most frequently searched job titles are:
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The top searched job categories for Clinical Research Associate jobs in Roxboro, NC are:
What cities near Roxboro, NC are hiring for Clinical Research Associate jobs?
Cities near Roxboro, NC with the most Clinical Research Associate job openings:

Clinical Research Associate II - Oncology - United States (Remote)
Durham, NC • On-site, Remote
Full-time
Re-posted 23 days ago
Key responsibilities
Perform on-site and remote monitoring visits in accordance with protocol, GCP, ICH guidelines, and company SOPs
Build strong relationships with investigative sites and serve as a trusted partner
Review source documents, verify data accuracy, and support site activation, enrollment, maintenance, and closeout activities
Job description
Who we are
We're a global, midsize CRO that pushes boundaries, innovates and invents because the path to a cure for the world's most persistent diseases is not paved by those who play it safe. It is built by those who take pioneering, creative approaches and implement them with quality and excellence.
We are Worldwide Clinical Trials, and we are a global team of over 3,500+ experts, bright thinkers, dreamers and doers and, together, we are changing the way the world experiences CROs - in the best possible way.
Our mission is to work with passion and purpose every day to improve lives and we are looking for others who value this same pursuit.
Why Worldwide
We believe everyone plays an important role in making a world of difference for patients and their caregivers. From our hands-on, accessible leaders, to our cohesive and supportive teams, we are committed to enabling professionals from all backgrounds and experiences to succeed. We prioritize cultivating a diverse and inclusive environment that continues to promote collaboration and creativity. We are proud to be a workplace where people thrive by being themselves and are inspired to do their best work every day.Join us!
What Clinical Operations does at Worldwide
At Worldwide Clinical Trials, we invite you to embark on a rewarding journey within Clinical Operations, where your contributions will leave a profound impact on the lives of patients.
Are you a motivated Clinical Research Associate with 2-3 years of monitoring experience who is looking for more than just your next job? Are you seeking a company that will invest in your development, provide meaningful career progression, and give you the opportunity to work alongside experienced clinical research professionals?
If so, we'd love to hear from you.
We are looking for a CRA II who is eager to expand their monitoring expertise, build strong site relationships, and grow into a senior clinical operations role. This position is ideal for someone who has established a solid foundation in site monitoring and is ready to accelerate their career within a supportive, collaborative, and quality-focused organization.
What you will do
As a CRA II, you will play a critical role in ensuring the successful execution of clinical trials by:
Performing on-site and remote monitoring visits in accordance with protocol, GCP, ICH guidelines, and company SOPs
Building strong relationships with investigative sites and serving as a trusted partner
Reviewing source documents and verifying data accuracy
Identifying risks, issues, and trends at sites and proactively driving resolution
Supporting site activation, enrollment, maintenance, and closeout activities
Ensuring patient safety, data integrity, and protocol compliance
Preparing detailed monitoring reports and follow-up letters
Collaborating cross-functionally with CTMs, project teams, and site personnel
What you will bring to the role
Excellent interpersonal, oral, and written communication skills in English
Superior organizational skills with attention to detail
Ability to work with little or no supervision
Proficiency in Microsoft Office, CTMS, and EDC Systems
Your experience
Required Qualifications
2 - 3 years of experience as a regional, traveling Clinical Research Associate
4-year universitydegree OR Nursing Degree
Knowledge of ICH-GCP guidelines and regulatory requirements
Experience conducting monitoring visits across multiple sites
Strong organizational, communication, and problem-solving skills
Ability to manage priorities in a fast-paced environment
Experience in Oncology is required
Willingness to travel regionally required
Preferred Qualifications
Experience in a CRO environment
Exposure to multiple therapeutic areas
Experience with decentralized or hybrid trial models
Desire to take on increasing responsibility and grow within Clinical Operations
At Worldwide Clinical Trials, we are committed to fostering an inclusive and equitable workplace by providing transparent compensation.
The salary range for this position is annually (For hourly paid positions, the stated salary range reflects hourly rates):
United States of America - $79,500.00 - $158,500.00
The salary range provided is intended to give candidates an understanding of potential earnings. Compensation will fall within the provided range, and it not a guarantee of exact salary. The final salary will be determined based on relevant experience, performance, education, and internal equity. In addition to base salary, we offer a competitive benefits package depending on location. We ensure pay equity and transparency and comply with all applicable labor laws. Salary information will be discussed during the interview process, and we encourage candidates to inquire about compensation at any stage.
We love knowing that someone is going to have a better life because of the work we do.
To view our other roles, check out our careers page at Discover a world of difference at Worldwide!For more information on Worldwide, visit www.Worldwide.com or connect with us on LinkedIn.
About Worldwide Clinical Trials
Sourced by ZipRecruiter
Industry
Scientific research and development services
Company size
10,000+ Employees
Headquarters location
Durham, NC, US
Year founded
1986