Conduct study initiation visits (SIVs) * While most of the site management efforts will be ... a Clinical Research Associate * 4-year universitydegree OR Nursing Degree * Experience in ...
Conduct study initiation visits (SIVs) * While most of the site management efforts will be ... a Clinical Research Associate * 4-year universitydegree OR Nursing Degree * Experience in ...
Conduct study initiation visits (SIVs) * While most of the site management efforts will be ... a Clinical Research Associate * 4-year university degree OR Nursing Degree * Experience in ...
Conduct study initiation visits (SIVs) * While most of the site management efforts will be ... a Clinical Research Associate * 4-year university degree OR Nursing Degree * Experience in ...
... Research Associates (CRAs) play a vital role in ensuring our clinical research programs are ... Manage monitoring deliverables to achieve the study budget and identify out-of-scope activities ...
... Research Associates (CRAs) play a vital role in ensuring our clinical research programs are ... Manage monitoring deliverables to achieve the study budget and identify out-of-scope activities ...
Clinical Trial Associate
$31.25 - $42.75/hr
The Clinical Trial Associate supports the Clinical Trials team(s) in the overall management and ... The primary responsibility is to independently manage clinical study tasks on behalf of the team in ...
Quick apply
Clinical Trial Associate
$31.25 - $42.75/hr
The Clinical Trial Associate supports the Clinical Trials team(s) in the overall management and ... The primary responsibility is to independently manage clinical study tasks on behalf of the team in ...
Clinical Research Coordinator I
$23.50 - $31.25/hr
Participate in study start-up activities such as putting together charts, pulling patient charts ... Certified Ophthalmic Associate or Certified Ophthalmic Technician certifications is strongly ...
Quick apply
Clinical Research Coordinator I
$23.50 - $31.25/hr
Participate in study start-up activities such as putting together charts, pulling patient charts ... Certified Ophthalmic Associate or Certified Ophthalmic Technician certifications is strongly ...
May act as primary liaison with study site personnel, or in collaboration with Central Monitoring Associate. Ensures all assigned sites and project-specific site team members are trained and ...
May act as primary liaison with study site personnel, or in collaboration with Central Monitoring Associate. Ensures all assigned sites and project-specific site team members are trained and ...
Clinical Research Coordinator - Duke Cancer Institute
$23.50 - $31.25/hr
Associate's degree required * Minimum of two years of relevant clinical research experience ... Ability to manage and oversee multiple concurrent clinical trials and study teams * Strong ...
Clinical Research Coordinator - Duke Cancer Institute
$23.50 - $31.25/hr
Associate's degree required * Minimum of two years of relevant clinical research experience ... Ability to manage and oversee multiple concurrent clinical trials and study teams * Strong ...
Clinical Research Coordinator - Duke Cancer Institute
Durham, NC · On-site
$23.50 - $31.25/hr
Associate's degree required * Minimum of two years of relevant clinical research experience ... Ability to manage and oversee multiple concurrent clinical trials and study teams * Strong ...
Clinical Research Coordinator - Duke Cancer Institute
Durham, NC · On-site
$23.50 - $31.25/hr
Associate's degree required * Minimum of two years of relevant clinical research experience ... Ability to manage and oversee multiple concurrent clinical trials and study teams * Strong ...
Clinical Studies RN II, Surgery Trauma
Wake Forest, NC · On-site
$38.20 - $57.30/hr
EDUCATION/EXPERIENCE An associate's degree in Nursing from an accredited School of Nursing with one ... James Holmes IV and the Study Investigators. Also receives supervision and mentoring from the Study ...
Clinical Studies RN II, Surgery Trauma
Wake Forest, NC · On-site
$38.20 - $57.30/hr
EDUCATION/EXPERIENCE An associate's degree in Nursing from an accredited School of Nursing with one ... James Holmes IV and the Study Investigators. Also receives supervision and mentoring from the Study ...
Study Start-Up Clinical Research Associate, Sponsor Dedicated
$71.90K - $145.30K/yr
IQVIA is seeking Study Start-Up Clinical Research Associates to join our Sponsor Dedicated teams. Ideal candidates will have experience in Study Start-Up and at least 6 months of on-site or in-house ...
Study Start-Up Clinical Research Associate, Sponsor Dedicated
$71.90K - $145.30K/yr
IQVIA is seeking Study Start-Up Clinical Research Associates to join our Sponsor Dedicated teams. Ideal candidates will have experience in Study Start-Up and at least 6 months of on-site or in-house ...
Study Start-Up Clinical Research Associate, Sponsor Dedicated
$71.90K - $145.30K/yr
IQVIA is seeking Study Start-Up Clinical Research Associates to join our Sponsor Dedicated teams. Ideal candidates will have experience in Study Start-Up and at least 6 months of on-site or in-house ...
Study Start-Up Clinical Research Associate, Sponsor Dedicated
$71.90K - $145.30K/yr
IQVIA is seeking Study Start-Up Clinical Research Associates to join our Sponsor Dedicated teams. Ideal candidates will have experience in Study Start-Up and at least 6 months of on-site or in-house ...
Study Start-Up Clinical Research Associate, Sponsor Dedicated
Durham, NC · On-site
$71.90K - $145.30K/yr
IQVIA is seeking Study Start-Up Clinical Research Associates to join our Sponsor Dedicated teams. Ideal candidates will have experience in Study Start-Up and at least 6 months of on-site or in-house ...
Study Start-Up Clinical Research Associate, Sponsor Dedicated
Durham, NC · On-site
$71.90K - $145.30K/yr
IQVIA is seeking Study Start-Up Clinical Research Associates to join our Sponsor Dedicated teams. Ideal candidates will have experience in Study Start-Up and at least 6 months of on-site or in-house ...
Clinical Research Associate 2, IQVIA
Durham, NC · On-site
$71.90K - $189K/yr
Clinical Research Associate 2 IQVIA is hiring a Clinical Research Associate 2 with on-site ... Administer protocol and related study training to assigned sites and establish regular lines of ...
Clinical Research Associate 2, IQVIA
Durham, NC · On-site
$71.90K - $189K/yr
Clinical Research Associate 2 IQVIA is hiring a Clinical Research Associate 2 with on-site ... Administer protocol and related study training to assigned sites and establish regular lines of ...
May act as primary liaison with study site personnel, or in collaboration with Central Monitoring Associate. Ensures all assigned sites and project-specific site team members are trained and ...
May act as primary liaison with study site personnel, or in collaboration with Central Monitoring Associate. Ensures all assigned sites and project-specific site team members are trained and ...
Completion of an Associate's degree * A minimum of two years of relevant clinical or research ... Be Bold. Clinical Trial Operations, Study, and Site Management * Provide leadership and ...
Completion of an Associate's degree * A minimum of two years of relevant clinical or research ... Be Bold. Clinical Trial Operations, Study, and Site Management * Provide leadership and ...
Completion of an Associate's degree * A minimum of two years of relevant clinical or research ... Be Bold. Clinical Trial Operations, Study, and Site Management * Provide leadership and ...
Completion of an Associate's degree * A minimum of two years of relevant clinical or research ... Be Bold. Clinical Trial Operations, Study, and Site Management * Provide leadership and ...
CLINICAL RESEARCH COORDINATOR, SR
Durham, NC · On-site
$23.50 - $31.25/hr
Your work will directly support complex clinical studies, multidisciplinary investigations, and ... Minimum QualificationsEducation Work requires an Associate's degree Experience Work requires a ...
CLINICAL RESEARCH COORDINATOR, SR
Durham, NC · On-site
$23.50 - $31.25/hr
Your work will directly support complex clinical studies, multidisciplinary investigations, and ... Minimum QualificationsEducation Work requires an Associate's degree Experience Work requires a ...
CLINICAL RESEARCH COORDINATOR, SR
Durham, NC · On-site
$23.50 - $31.25/hr
Your work will directly support complex clinical studies, multidisciplinary investigations, and ... Minimum Qualifications Education Work requires an Associate's degree Experience Work requires a ...
CLINICAL RESEARCH COORDINATOR, SR
Durham, NC · On-site
$23.50 - $31.25/hr
Your work will directly support complex clinical studies, multidisciplinary investigations, and ... Minimum Qualifications Education Work requires an Associate's degree Experience Work requires a ...
Clinical Research Coordinator II
$21.50 - $28.50/hr
Conduct and manage clinical trials in accordance with the study protocol, GCP, ICH Guidelines and ... Associate's degree with 4 years relevant experience in the life science industry OR * High School ...
Clinical Research Coordinator II
$21.50 - $28.50/hr
Conduct and manage clinical trials in accordance with the study protocol, GCP, ICH Guidelines and ... Associate's degree with 4 years relevant experience in the life science industry OR * High School ...
Clinical Research Coordinator II
Raleigh, NC · On-site
$21.50 - $28.50/hr
Conduct and manage clinical trials in accordance with the study protocol, GCP, ICH Guidelines and ... Associate's degree with 4 years relevant experience in the life science industry OR * High School ...
Clinical Research Coordinator II
Raleigh, NC · On-site
$21.50 - $28.50/hr
Conduct and manage clinical trials in accordance with the study protocol, GCP, ICH Guidelines and ... Associate's degree with 4 years relevant experience in the life science industry OR * High School ...
Clinical Study 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 - $42.47
8% of jobs
$42.47 - $46.23
6% of jobs
$46.23 - $49.99
6% of jobs
$49.99 - $53.75
3% of jobs
$12
$30
$53
How much do clinical study associate jobs pay per hour?
What are the key skills and qualifications needed to thrive as a Clinical Study Associate, and why are they important?
What are some common challenges Clinical Study Associates face when managing multiple clinical trials simultaneously?
What are Clinical Study Associates?
What is the difference between Clinical Study Associate vs Clinical Research Coordinator?
| Aspect | Clinical Study Associate | Clinical Research Coordinator |
|---|---|---|
| Credentials | Bachelor's degree, often in life sciences; certifications like CCRP or CCRA beneficial | Bachelor's degree in health sciences or related field; certifications like CCRP advantageous |
| Work Environment | Pharmaceutical companies, CROs, clinical trial sites | Hospitals, clinics, research centers |
| Job Focus | Monitoring clinical trials, ensuring protocol compliance, data accuracy | Managing daily trial activities, patient recruitment, data collection |
| Employer & Industry Usage | Commonly employed in pharma and CROs | Primarily in healthcare and academic research settings |
Both roles involve clinical trial oversight but differ in focus: Clinical Study Associates primarily monitor and ensure compliance during trials, while Clinical Research Coordinators manage daily trial operations and patient interactions. Understanding these distinctions helps in choosing the right career path or job search focus.
Senior Clinical Research Associate, Psychiatry - Southeast - Remote
Worldwide Clinical TrialsDurham, NC
Full-time
Posted 2 days ago
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.
As a Clinical Research Associate (CRA) at Worldwide, you will find yourself working alongside brilliant minds across diverse therapeutic areas, including Cardiovascular, Metabolic, Neuroscience, Oncology, and Rare Diseases. Collaboration with top-tier colleagues from various backgrounds and specialties is not just encouraged; it's ingrained in our culture. Our commitment to advancing clinical research is nurtured within a supportive and team-oriented environment. In a CRA role, you'll receive extensive support through regulatory submissions, TMF management, and in-house CRAs for projects with heavy site management needs.
Through regular touchpoints and coaching conversations with your Line Manager, we ensure that your professional development remains a top priority. We offer a clear career path and development that can lead to Clinical Trial Manager roles. We take pride in our accessible Executive Leadership team, who are equally committed to advancing science and surmounting obstacles to make a difference in the lives of patients around the world.
We offer an unparalleled experience, where you can drive remarkable scientific breakthroughs and be at the very core of every successful clinical trial. Experience a world of difference with us at Worldwide!
What you will do
Responsible for managing the research activities at sites participating in Worldwide's clinical research projects
Typically involved in all stages of the clinical study, including identifying potential sites to participate in the research effort, performing various study start-up activities such as working with sites to collect appropriate regulatory documents and supporting the negotiation of contracts and budgets, training the sites to collect data properly and report any potential safety-related events, managing the site's activities during study maintenance, and closing down research activities at the sites once the study has concluded
Conduct study initiation visits (SIVs)
While most of the site management efforts will be performed remotely, you will be required to ensure compliance with obtaining informed consent, reporting potential safety-related events, and adhering to all applicable regulatory requirements
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
5+ years of experience as a Clinical Research Associate
4-year universitydegree OR Nursing Degree
Experience in Psychiatry is required
Candidates must reside in the Southeast, preferably the Atlanta area
Willingness to travel regionally required
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.
Worldwide is an equal opportunity employer that is committed to enabling professionals from all backgrounds and experiences to succeed and, to that end, we prioritize attracting diverse talent and cultivating an inclusive environment that encourages collaboration and creativity. We know that when our employees feel appreciated and included, they can be more creative,innovative,and successful. We'reon a mission to hire thevery bestand are committed to creating exceptional employee experiences where everyone is respected and has access to equal opportunity. We provide equal employment opportunities to all employees and applicants regardless of race, color, ethnicity, ancestry, religion, national origin, gender, sex, gender identity or expression, sexual orientation, age, citizenship, marital or parental status, disability, military status, or other class protected by applicable law.
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