Indianapolis, IN · On-site
$87K - $145K/yr
Work with sites to adapt, drive, and track subject recruitment plan in line with project needs to ... Manage the progress of assigned studies by tracking regulatory submissions and approvals ...
Indianapolis, IN · On-site
$87K - $145K/yr
Work with sites to adapt, drive, and track subject recruitment plan in line with project needs to ... Manage the progress of assigned studies by tracking regulatory submissions and approvals ...
$87K - $145K/yr
Work with sites to adapt, drive, and track subject recruitment plan in line with project needs to ... Manage the progress of assigned studies by tracking regulatory submissions and approvals ...
$87K - $145K/yr
Work with sites to adapt, drive, and track subject recruitment plan in line with project needs to ... Manage the progress of assigned studies by tracking regulatory submissions and approvals ...
Chicago, IL · On-site
$87K - $145K/yr
Work with sites to adapt, drive, and track subject recruitment plan in line with project needs to ... Manage the progress of assigned studies by tracking regulatory submissions and approvals ...
Chicago, IL · On-site
$87K - $145K/yr
Work with sites to adapt, drive, and track subject recruitment plan in line with project needs to ... Manage the progress of assigned studies by tracking regulatory submissions and approvals ...
$87K - $145K/yr
Work with sites to adapt, drive, and track subject recruitment plan in line with project needs to ... Manage the progress of assigned studies by tracking regulatory submissions and approvals ...
$87K - $145K/yr
Work with sites to adapt, drive, and track subject recruitment plan in line with project needs to ... Manage the progress of assigned studies by tracking regulatory submissions and approvals ...
Columbus, OH · On-site
$87K - $145K/yr
Work with sites to adapt, drive, and track subject recruitment plan in line with project needs to ... Manage the progress of assigned studies by tracking regulatory submissions and approvals ...
Columbus, OH · On-site
$87K - $145K/yr
Work with sites to adapt, drive, and track subject recruitment plan in line with project needs to ... Manage the progress of assigned studies by tracking regulatory submissions and approvals ...
$87K - $145K/yr
Work with sites to adapt, drive, and track subject recruitment plan in line with project needs to ... Manage the progress of assigned studies by tracking regulatory submissions and approvals ...
$87K - $145K/yr
Work with sites to adapt, drive, and track subject recruitment plan in line with project needs to ... Manage the progress of assigned studies by tracking regulatory submissions and approvals ...
Kansas City, MO · On-site
$87K - $145K/yr
Work with sites to adapt, drive, and track subject recruitment plan in line with project needs to ... Manage the progress of assigned studies by tracking regulatory submissions and approvals ...
Kansas City, MO · On-site
$87K - $145K/yr
Work with sites to adapt, drive, and track subject recruitment plan in line with project needs to ... Manage the progress of assigned studies by tracking regulatory submissions and approvals ...
$87K - $145K/yr
Work with sites to adapt, drive, and track subject recruitment plan in line with project needs to ... Manage the progress of assigned studies by tracking regulatory submissions and approvals ...
$87K - $145K/yr
Work with sites to adapt, drive, and track subject recruitment plan in line with project needs to ... Manage the progress of assigned studies by tracking regulatory submissions and approvals ...
Philadelphia, PA · On-site
$87K - $145K/yr
Work with sites to adapt, drive, and track subject recruitment plan in line with project needs to ... Manage the progress of assigned studies by tracking regulatory submissions and approvals ...
Philadelphia, PA · On-site
$87K - $145K/yr
Work with sites to adapt, drive, and track subject recruitment plan in line with project needs to ... Manage the progress of assigned studies by tracking regulatory submissions and approvals ...
$87K - $145K/yr
Work with sites to adapt, drive, and track subject recruitment plan in line with project needs to ... Manage the progress of assigned studies by tracking regulatory submissions and approvals ...
$87K - $145K/yr
Work with sites to adapt, drive, and track subject recruitment plan in line with project needs to ... Manage the progress of assigned studies by tracking regulatory submissions and approvals ...
$87K - $145K/yr
Work with sites to adapt, drive, and track subject recruitment plan in line with project needs to ... Manage the progress of assigned studies by tracking regulatory submissions and approvals ...
$87K - $145K/yr
Work with sites to adapt, drive, and track subject recruitment plan in line with project needs to ... Manage the progress of assigned studies by tracking regulatory submissions and approvals ...
Indianapolis, IN · On-site
$87K - $145K/yr
Work with sites to adapt, drive, and track subject recruitment plan in line with project needs to ... Manage the progress of assigned studies by tracking regulatory submissions and approvals ...
Indianapolis, IN · On-site
$87K - $145K/yr
Work with sites to adapt, drive, and track subject recruitment plan in line with project needs to ... Manage the progress of assigned studies by tracking regulatory submissions and approvals ...
Durham, NC · On-site
$87K - $145K/yr
Work with sites to adapt, drive, and track subject recruitment plan in line with project needs to ... Manage the progress of assigned studies by tracking regulatory submissions and approvals ...
Durham, NC · On-site
$87K - $145K/yr
Work with sites to adapt, drive, and track subject recruitment plan in line with project needs to ... Manage the progress of assigned studies by tracking regulatory submissions and approvals ...
$87K - $145K/yr
Work with sites to adapt, drive, and track subject recruitment plan in line with project needs to ... Manage the progress of assigned studies by tracking regulatory submissions and approvals ...
$87K - $145K/yr
Work with sites to adapt, drive, and track subject recruitment plan in line with project needs to ... Manage the progress of assigned studies by tracking regulatory submissions and approvals ...
Collegeville, PA · On-site
$87K - $145K/yr
Work with sites to adapt, drive, and track subject recruitment plan in line with project needs to ... Manage the progress of assigned studies by tracking regulatory submissions and approvals ...
Collegeville, PA · On-site
$87K - $145K/yr
Work with sites to adapt, drive, and track subject recruitment plan in line with project needs to ... Manage the progress of assigned studies by tracking regulatory submissions and approvals ...
Chicago, IL · On-site
$87K - $145K/yr
Work with sites to adapt, drive, and track subject recruitment plan in line with project needs to ... Manage the progress of assigned studies by tracking regulatory submissions and approvals ...
Chicago, IL · On-site
$87K - $145K/yr
Work with sites to adapt, drive, and track subject recruitment plan in line with project needs to ... Manage the progress of assigned studies by tracking regulatory submissions and approvals ...
Durham, NC · On-site
$87K - $145K/yr
Work with sites to adapt, drive, and track subject recruitment plan in line with project needs to ... Manage the progress of assigned studies by tracking regulatory submissions and approvals ...
Durham, NC · On-site
$87K - $145K/yr
Work with sites to adapt, drive, and track subject recruitment plan in line with project needs to ... Manage the progress of assigned studies by tracking regulatory submissions and approvals ...
Parsippany, NJ · On-site
$87K - $145K/yr
Work with sites to adapt, drive, and track subject recruitment plan in line with project needs to ... Manage the progress of assigned studies by tracking regulatory submissions and approvals ...
Parsippany, NJ · On-site
$87K - $145K/yr
Work with sites to adapt, drive, and track subject recruitment plan in line with project needs to ... Manage the progress of assigned studies by tracking regulatory submissions and approvals ...
$87K - $145K/yr
Work with sites to adapt, drive, and track subject recruitment plan in line with project needs to ... Manage the progress of assigned studies by tracking regulatory submissions and approvals ...
$87K - $145K/yr
Work with sites to adapt, drive, and track subject recruitment plan in line with project needs to ... Manage the progress of assigned studies by tracking regulatory submissions and approvals ...
$87K - $145K/yr
Work with sites to adapt, drive, and track subject recruitment plan in line with project needs to ... Manage the progress of assigned studies by tracking regulatory submissions and approvals ...
$87K - $145K/yr
Work with sites to adapt, drive, and track subject recruitment plan in line with project needs to ... Manage the progress of assigned studies by tracking regulatory submissions and approvals ...
$20.5K - $32.5K
13% of jobs
$41.5K is the 25th percentile. Wages below this are outliers.
$32.5K - $44.5K
16% of jobs
$44.5K - $56.5K
13% of jobs
The median wage is $64.7K / yr.
$56.5K - $68.5K
12% of jobs
$68.5K - $80.5K
9% of jobs
$80.5K - $92.5K
8% of jobs
$100.6K is the 75th percentile. Wages above this are outliers.
$92.5K - $104.5K
8% of jobs
$104.5K - $116.5K
6% of jobs
$116.5K - $128.5K
6% of jobs
$128.5K - $140.5K
6% of jobs
$140.5K - $152.5K
3% of jobs
$20.5K
$78.4K
$152.5K
| Aspect | Cra Line Manager | Clinical Research Associate |
|---|---|---|
| Credentials | Typically requires a degree in life sciences, plus experience in clinical trials | Requires a degree in life sciences or related field, often with certification in clinical research |
| Work Environment | Manages teams, oversees multiple trials, involved in project planning | Conducts site visits, monitors trial progress, ensures compliance at trial sites |
| Employer & Industry Usage | Used in pharmaceutical companies, CROs, biotech firms | Commonly employed in clinical trial sites, CROs, pharmaceutical companies |
The Cra Line Manager focuses on overseeing clinical trial teams and project management, while the Clinical Research Associate primarily monitors trial sites and ensures compliance. Both roles require relevant scientific credentials and are integral to clinical research operations, but they differ in scope and responsibilities.
8.1
Based on 51 frontline employees who took The Breakroom Quiz
53rd of 203 rated it services
IQVIA is seeking a CRA 2 with a minimum of 1.5 years of on-site oncology monitoring experience:
Essential Functions
Perform site monitoring visits (selection, initiation, monitoring and close-out visits) in accordance with contracted scope of work and regulatory requirements, i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines.
Work with sites to adapt, drive, and track subject recruitment plan in line with project needs to enhance predictability.
Administer protocol and related study training to assigned sites and establish regular lines of communication with sites to manage ongoing project expectations and issues.
Evaluate the quality and integrity of study site practices related to the proper conduct of the protocol and adherence to applicable regulations. Escalate quality issues as appropriate.
Manage the progress of assigned studies by tracking regulatory submissions and approvals, recruitment and enrollment, case report form (CRF) completion and submission, and data query generation and resolution. May support start-up phase.
Ensure copies/originals (as required) site documents are available for filing in the Trial Master File (TMF) and verify that the Investigator's Site File (ISF) is maintained in accordance with GCP and local regulatory requirements.
Create and maintain appropriate documentation regarding site management, monitoring visit findings and action plans by submitting regular visit reports, generating follow-up letters and other required study documentation.
Collaborate and liaise with study team members for project execution support as appropriate.
If applicable, may be accountable for supporting development of project subject recruitment plan on a per site basis.
If applicable, may be accountable for site financial management according to executed clinical trial agreement and retrieve invoices according to local requirement.
Education: Bachelor's Degree (Degree in scientific discipline or health care preferred)
Experience: 1.5 to 2 years of relevant CRA experience including on-site monitoring.
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 $87,200.00 - $145,300.00. 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.
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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.
Health care and social assistance
10,000+ Employees
Durham, NC, US
