CHILD CONTENT-SINGLE LOADED
⏳ Last Date to Apply: Ongoing
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Parexel
Parexel Clinical Research Associate (CRA II/Senior) Recruitment 2026: Apply Online
Clinical Research Associate (CRA II / Senior)
Experience Required
18+ Months Direct Onsite Monitoring Experience
Salary / Package
Competitive & Industry Standard
Work Mode
Remote
Openings
Multiple
Job Overview
- Conduct qualification visits, site initiation visits, monitoring visits, and termination visits at assigned clinical trial locations.
- Ensure that all clinical trials are conducted in accordance with approved standard operating procedures and Good Clinical Practice.
- Serve as the primary point of contact for clinical sites, actively addressing operational challenges and resolving issues promptly.
- Evaluate trial performance, data quality, and investigational product accountability across designated study sites.
- Collaborate with cross-functional global teams to support patient recruitment strategies and meet strict project delivery timelines.
Key Job Details
| Company Name | Parexel |
| Job Role | Clinical Research Associate (CRA II / Senior) |
| Experience | 18+ Months Direct Onsite Monitoring Experience |
| Salary Range | Competitive & Industry Standard |
| Job Type | Full-Time |
| Work Mode | Remote |
| Openings | Multiple |
| Job Location | United States (Remote / Any Region) |
Key Responsibilities
- Perform rigorous onsite and remote monitoring visits ensuring absolute adherence to clinical protocols.
- Verify source data integrity and maintain complete, accurate regulatory documentation.
- Support clinical trial sites from initial startup phase through formal closeout.
- Maintain effective communication channels between sponsors, investigators, and site personnel.
Requirements & Qualifications
- Minimum of 18 months of active onsite monitoring experience as a Clinical Research Associate.
- Specialized monitoring background in Metabolic, MASH, or Obesity clinical trials.
- Bachelor’s degree in Biological Science, Pharmacy, or related health discipline.
- Strong working knowledge of regulatory frameworks and clinical trial workflows.
Required Skills
- Site Relationship Management
- Problem-Solving & Analytical Thinking
- Attention to Detail & Data Quality
- Independent Work Ethic & Time Management
- Clinical Trial Management Systems (CTMS)
About Parexel
Parexel is a leading global clinical development partner helping life sciences and biopharmaceutical clients deliver innovative treatments to patients faster. Driven by a patient-centric culture and a commitment to working With Heart, Parexel combines clinical expertise, advanced technology, and global reach to shape the future of healthcare research.
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Frequently Asked Questions
Q: What is the primary role of a Clinical Research Associate at Parexel?
A: A CRA manages clinical trial sites from setup to closeout, ensuring protocol compliance, data accuracy, and patient safety.
Q: What are the core educational requirements for this role?
A: Applicants need a Bachelor’s degree in a biological science, pharmacy, or a related health-oriented discipline.
Q: How much prior experience is required?
A: Candidates must possess at least 18 months of direct onsite clinical monitoring experience.
Q: Is this a remote work opportunity?
A: Yes, this position is offered on a remote basis for candidates residing anywhere in the United States.
Q: What therapeutic experience is needed?
A: Experience monitoring clinical trials in Metabolic, MASH, or Obesity indications is required.
Q: How can I submit my application?
A: Applications can be submitted online through the direct Workday application link provided on the official recruitment page.
Disclaimer: This job post is prepared by collecting data from the official career page of Parexel. We are not direct recruiters or representatives. Candidates should carefully review the requirements and policies on the company’s portal before initiating an application.