CRA 2/Senior CRA
Durham, NC · On-site
$90K - $175K/yr
IQVIA Biotech is seeking CRA 2 and Sr. CRA 1 candidates with onsite monitoring experience in ... Track and manage study progress, including regulatory approvals, enrollment, and data quality
CRA 2/Senior CRA
Durham, NC · On-site
$90K - $175K/yr
IQVIA Biotech is seeking CRA 2 and Sr. CRA 1 candidates with onsite monitoring experience in ... Track and manage study progress, including regulatory approvals, enrollment, and data quality
CRA 2/Senior CRA
Durham, NC · On-site
$90K - $175K/yr
IQVIA Biotech is seeking CRA 2 and Sr. CRA 1 candidates with onsite monitoring experience in ... Track and manage study progress, including regulatory approvals, enrollment, and data quality
CRA 2/Senior CRA
Durham, NC · On-site
$90K - $175K/yr
IQVIA Biotech is seeking CRA 2 and Sr. CRA 1 candidates with onsite monitoring experience in ... Track and manage study progress, including regulatory approvals, enrollment, and data quality
CRA 2/Senior CRA
Durham, NC · On-site
$90K - $175K/yr
IQVIA Biotech is seeking CRA 2 and Sr. CRA 1 candidates with onsite monitoring experience in ... Track and manage study progress, including regulatory approvals, enrollment, and data quality
CRA 2/Senior CRA
Durham, NC · On-site
$90K - $175K/yr
IQVIA Biotech is seeking CRA 2 and Sr. CRA 1 candidates with onsite monitoring experience in ... Track and manage study progress, including regulatory approvals, enrollment, and data quality
Opportunity for leadership positions/career advancement - Lead CRA, CRA Manager, Clinical Trial Manager, Training and Development Manager; * Customized Fast PACE training program based on your ...
Opportunity for leadership positions/career advancement - Lead CRA, CRA Manager, Clinical Trial Manager, Training and Development Manager; * Customized Fast PACE training program based on your ...
CRA 1, IQVIA Biotech
Durham, NC · On-site
$71K - $119K/yr
The ability to manage multiple tasks, prioritize effectively, and work independently while ... CRA training program considered. * Basic knowledge of clinical research regulations (GCP/ICH)
CRA 1, IQVIA Biotech
Durham, NC · On-site
$71K - $119K/yr
The ability to manage multiple tasks, prioritize effectively, and work independently while ... CRA training program considered. * Basic knowledge of clinical research regulations (GCP/ICH)
CRA 2/Senior CRA
Durham, NC · On-site
$87K - $169K/yr
... CRA) to join our team and play a key role in delivering high-quality clinical trials. In this role ... Track and manage study progress, including regulatory approvals, enrollment, and data quality
CRA 2/Senior CRA
Durham, NC · On-site
$87K - $169K/yr
... CRA) to join our team and play a key role in delivering high-quality clinical trials. In this role ... Track and manage study progress, including regulatory approvals, enrollment, and data quality
CRA 2/Senior CRA
Durham, NC · On-site
$87K - $169K/yr
... CRA) to join our team and play a key role in delivering high-quality clinical trials. In this role ... Track and manage study progress, including regulatory approvals, enrollment, and data quality
CRA 2/Senior CRA
Durham, NC · On-site
$87K - $169K/yr
... CRA) to join our team and play a key role in delivering high-quality clinical trials. In this role ... Track and manage study progress, including regulatory approvals, enrollment, and data quality
CRA 1, IQVIA Biotech
Durham, NC · On-site
$71K - $119K/yr
The ability to manage multiple tasks, prioritize effectively, and work independently while ... CRA training program considered. * Basic knowledge of clinical research regulations (GCP/ICH)
CRA 1, IQVIA Biotech
Durham, NC · On-site
$71K - $119K/yr
The ability to manage multiple tasks, prioritize effectively, and work independently while ... CRA training program considered. * Basic knowledge of clinical research regulations (GCP/ICH)
CRA 2/Senior CRA
Durham, NC · On-site
$87K - $169K/yr
... CRA) to join our team and play a key role in delivering high-quality clinical trials. In this role ... Track and manage study progress, including regulatory approvals, enrollment, and data quality
CRA 2/Senior CRA
Durham, NC · On-site
$87K - $169K/yr
... CRA) to join our team and play a key role in delivering high-quality clinical trials. In this role ... Track and manage study progress, including regulatory approvals, enrollment, and data quality
CRA 1, IQVIA Biotech
Durham, NC · On-site
$71K - $119K/yr
The ability to manage multiple tasks, prioritize effectively, and work independently while ... CRA training program considered. * Basic knowledge of clinical research regulations (GCP/ICH)
CRA 1, IQVIA Biotech
Durham, NC · On-site
$71K - $119K/yr
The ability to manage multiple tasks, prioritize effectively, and work independently while ... CRA training program considered. * Basic knowledge of clinical research regulations (GCP/ICH)
CRA 2/Senior CRA 1
Durham, NC · On-site
$90K - $175K/yr
... CRA) to join our team and play a key role in delivering high-quality clinical trials. In this role ... Track and manage study progress, including regulatory approvals, enrollment, and data quality
CRA 2/Senior CRA 1
Durham, NC · On-site
$90K - $175K/yr
... CRA) to join our team and play a key role in delivering high-quality clinical trials. In this role ... Track and manage study progress, including regulatory approvals, enrollment, and data quality
CRA 2/Senior CRA 1
Durham, NC · On-site
$90K - $175K/yr
... CRA) to join our team and play a key role in delivering high-quality clinical trials. In this role ... Track and manage study progress, including regulatory approvals, enrollment, and data quality
CRA 2/Senior CRA 1
Durham, NC · On-site
$90K - $175K/yr
... CRA) to join our team and play a key role in delivering high-quality clinical trials. In this role ... Track and manage study progress, including regulatory approvals, enrollment, and data quality
CRA 2/Senior CRA 1
$90K - $175K/yr
... CRA) to join our team and play a key role in delivering high-quality clinical trials. In this role ... Track and manage study progress, including regulatory approvals, enrollment, and data quality
CRA 2/Senior CRA 1
$90K - $175K/yr
... CRA) to join our team and play a key role in delivering high-quality clinical trials. In this role ... Track and manage study progress, including regulatory approvals, enrollment, and data quality
CRA 2, Oncology, IQVIA
Durham, NC · On-site
$87K - $145K/yr
Manage the progress of assigned studies by tracking regulatory submissions and approvals ... CRA experience including on-site monitoring. IQVIA is a leading global provider of clinical ...
CRA 2, Oncology, IQVIA
Durham, NC · On-site
$87K - $145K/yr
Manage the progress of assigned studies by tracking regulatory submissions and approvals ... CRA experience including on-site monitoring. IQVIA is a leading global provider of clinical ...
Manage the progress of assigned studies by tracking regulatory submissions and approvals ... Some organizations require completion of CRA training program or prior monitoring experience. Basic ...
Manage the progress of assigned studies by tracking regulatory submissions and approvals ... Some organizations require completion of CRA training program or prior monitoring experience. Basic ...
CRA 2, Oncology, IQVIA
Durham, NC · On-site
$87K - $145K/yr
Manage the progress of assigned studies by tracking regulatory submissions and approvals ... CRA experience including on-site monitoring. IQVIA is a leading global provider of clinical ...
CRA 2, Oncology, IQVIA
Durham, NC · On-site
$87K - $145K/yr
Manage the progress of assigned studies by tracking regulatory submissions and approvals ... CRA experience including on-site monitoring. IQVIA is a leading global provider of clinical ...
Clinical Research Associate (CRA 2), Sponsor Dedicated
Durham, NC · On-site
$71K - $182K/yr
Manage the progress of assigned studies by tracking regulatory submissions and approvals ... Some organizations require completion of CRA training program or prior monitoring experience. Basic ...
Clinical Research Associate (CRA 2), Sponsor Dedicated
Durham, NC · On-site
$71K - $182K/yr
Manage the progress of assigned studies by tracking regulatory submissions and approvals ... Some organizations require completion of CRA training program or prior monitoring experience. Basic ...
CRA 2, Oncology, IQVIA
Durham, NC · On-site
$87K - $145K/yr
Manage the progress of assigned studies by tracking regulatory submissions and approvals ... CRA experience including on-site monitoring. IQVIA is a leading global provider of clinical ...
CRA 2, Oncology, IQVIA
Durham, NC · On-site
$87K - $145K/yr
Manage the progress of assigned studies by tracking regulatory submissions and approvals ... CRA experience including on-site monitoring. IQVIA is a leading global provider of clinical ...
Sr. CRA & CRA II - West Coast - Ophthalmology
Durham, NC · On-site
$105/hr
Responsible for all aspects of site management as prescribed in the project plans * General On-Site ... Ophthalmology experience as a CRA * Open to various hub locations The important thing for us is you ...
Sr. CRA & CRA II - West Coast - Ophthalmology
Durham, NC · On-site
$105/hr
Responsible for all aspects of site management as prescribed in the project plans * General On-Site ... Ophthalmology experience as a CRA * Open to various hub locations The important thing for us is you ...
Meets standards and objectives defined by management for mortgage loan sales and cross-selling objectives. Focuses on selling CRA products and services, targeting low to moderate-income individuals ...
Meets standards and objectives defined by management for mortgage loan sales and cross-selling objectives. Focuses on selling CRA products and services, targeting low to moderate-income individuals ...
Cra Manager information
What is the difference between Cra Manager vs Clinical Research Associate?
| Aspect | Cra Manager | Clinical Research Associate |
|---|---|---|
| Credentials | Bachelor's or higher in life sciences, often with experience in project management | Bachelor's degree in life sciences or related field, often with certification |
| Work Environment | Leads multiple studies, manages teams, oversees project progress | Monitors clinical trials at sites, ensures protocol compliance |
| Employer & Industry | Pharmaceutical companies, CROs, biotech firms | Pharmaceutical companies, CROs, clinical sites |
| Search & Comparison Intent | Higher-level management, overseeing clinical trials | Monitoring and site management roles |
The Cra Manager typically oversees multiple clinical trials, manages teams, and ensures project milestones are met, requiring leadership skills and experience. In contrast, a Clinical Research Associate focuses on monitoring individual trial sites, ensuring compliance with protocols. Both roles are essential in clinical research but differ in scope and responsibilities.
What is a CRA Manager?
A CRA Manager, or Clinical Research Associate Manager, is a professional responsible for overseeing a team of Clinical Research Associates (CRAs) who monitor clinical trials. They ensure that clinical studies are conducted in compliance with regulatory standards, protocols, and company policies. CRA Managers coordinate training, provide performance feedback, and act as a liaison between CRAs, sponsors, and other stakeholders. Their role is critical in maintaining the quality and integrity of clinical research projects.
What are some common challenges a CRA Manager faces when overseeing multiple clinical trial sites?
A CRA Manager often encounters challenges with maintaining consistent quality and compliance across various clinical trial sites, as each site may have unique operational practices and resource limitations. Effective communication and coordination between on-site teams, sponsors, and regulatory bodies are crucial to address issues promptly and ensure study timelines are met. Additionally, balancing the workload among Clinical Research Associates (CRAs) and providing adequate training and support can be demanding, especially when managing geographically dispersed teams.
What are the key skills and qualifications needed to thrive as a CRA Manager, and why are they important?
To thrive as a CRA (Clinical Research Associate) Manager, you need a deep understanding of clinical trial processes, regulatory requirements, and a relevant life sciences degree, often supplemented by experience as a CRA. Familiarity with electronic data capture (EDC) systems, trial management software, and certifications such as ACRP or SOCRA are typically required. Leadership, strong communication, and problem-solving skills help you guide teams and ensure effective collaboration across stakeholders. These skills are crucial for maintaining compliance, ensuring data integrity, and delivering successful clinical trials on time and within budget.
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What are popular job titles related to Cra Manager jobs in Raleigh, NC? For Cra Manager jobs in Raleigh, NC, the most frequently searched job titles are:
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IQVIA rating
8.2
Based on 52 frontline employees who took The Breakroom Quiz
45th of 204 rated it services
Job description
IQVIA Biotech is seeking CRA 2 and Sr. CRA 1 candidates with onsite monitoring experience in oncology.
Join a Team That's Advancing Clinical Research
We're looking for a passionate and driven Clinical Research Associate (CRA) to join our team and play a key role in delivering high-quality clinical trials. In this role, you'll partner with investigative sites and cross-functional teams to ensure studies are executed with excellence, compliance, and patient focus.
What You'll Do- Lead and execute site monitoring visits (selection, initiation, routine, and close-out) in accordance with GCP/ICH guidelines
- Build strong relationships with investigative sites to drive performance, recruitment, and engagement
- Ensure protocol compliance, data integrity, and high-quality study execution
- Proactively identify risks, resolve issues, and escalate when needed
- Track and manage study progress, including regulatory approvals, enrollment, and data quality
- Maintain accurate documentation and contribute to inspection readiness
- Collaborate with cross-functional teams to ensure successful study delivery
- Bachelor's degree in life sciences, healthcare, or related field (or equivalent experience)
- 1+ year of on-site monitoring experience
- Solid understanding of GCP, ICH, and regulatory requirements
- Strong communication, problem-solving, and organizational skills
- Ability to manage multiple priorities in a fast-paced environment
- Make a direct impact on advancing clinical research and improving patient outcomes
- Work alongside experienced, collaborative teams
- Opportunities for growth and career development
- Dynamic, fast-paced environment where your contributions matter
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 accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more athttps://jobs.iqvia.com
IQVIA is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, status as a protected veteran, or any other status protected by applicable law. https://jobs.iqvia.com/eoe
IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.
The potential base pay range for this role, when annualized, is $90,200.00 - $175,100.00. The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered, in addition to a range of health and welfare and/or other benefits.
About IQVIA
Sourced by ZipRecruiter
At IQVIA, we are passionate about helping customers and partners improve results and patient outcomes. Everything we do contributes to this vision for creating a healthier world. In today’s healthcare environment, it’s not only about how much data, information, and technology you have at your fingertips – it’s what you do with it. IQVIA is focused on making intelligent connections for customers across the entire healthcare ecosystem to help you drive healthcare forward. Whether that means partnering with novel technology companies to boost patient engagement, leveraging AI & machine learning to accelerate results, or using decentralized trials to reach the right patients wherever they are – we are always looking for smarter ways to move you forward.
Industry
Health care and social assistance
Company size
10,000+ Employees
Headquarters location
Durham, NC, US