⏳ Last Date to Apply: Not Disclosed
Parexel Senior Clinical Research Associate Recruitment 2026: Apply Online
Senior Clinical Research Associate / Clinical Research Associate II (FSP)
Job Overview
Parexel is seeking a highly skilled and motivated Senior Clinical Research Associate (Sr. CRA) / Clinical Research Associate II to join their Functional Service Provider (FSP) division. In this role, you will act as a vital link in the clinical trial process, ensuring that life-changing treatments reach patients safely, ethically, and efficiently. As a Sr. CRA, you will be responsible for the comprehensive site management, monitoring, and close-out of assigned clinical trial investigator sites. Your work will directly safeguard patient well-being and ensure the highest quality of study execution in strict accordance with Good Clinical Practices (GCP), ICH guidelines, and local regulatory standards.
Working under the FSP model offers a unique career advantage. You will be fully dedicated to a specific sponsor’s pipeline, allowing you to build deep relationships with investigator sites and gain specialized therapeutic expertise, all while backed by Parexel’s world-class clinical operations support, training, and global network. This role is ideal for clinical research professionals who are passionate about scientific innovation, possess strong analytical skills, and thrive in a dynamic, travel-intensive environment.
Your day-to-day responsibilities will involve conducting onsite and remote monitoring visits, managing investigator relationships, training site staff on protocols, and resolving complex clinical trial issues. You will collaborate closely with Site Care Partners (SCPs), study clinicians, and data management teams to ensure seamless trial execution from site activation through to database lock. If you are a self-starter with a strong background in life sciences and a commitment to putting patients first, Parexel offers an exceptional environment for your professional growth and career advancement.
Key Job Details
| Company Name | Parexel International |
| Job Role | Senior Clinical Research Associate / Clinical Research Associate II (FSP) |
| Experience | Minimum 3 years of clinical research site monitoring experience (preferably 2 years in Oncology). |
| Salary Range | Competitive Industry Standard |
| Job Type | Full-Time |
| Work Mode | Remote / Home-Based (with 60-80% travel) |
| Openings | Multiple |
| Job Location | Texas / Remote (All US Locations) |
Key Responsibilities
- Ensure proper conduct of clinical trials in accordance with the Study Monitoring Plan (SMP), GCP, and Sponsor standards.
- Manage operational aspects of clinical trials at assigned investigator sites from site activation through to database lock.
- Serve as the primary point of contact for assigned investigator sites, facilitating information flow between study teams, vendors, and sites.
- Conduct onsite and remote/electronic monitoring visits for study site initiation, routine monitoring, and site closure.
- Monitor site-level adverse events (AEs) and serious adverse events (SAEs), collaborating with the Drug Safety Unit for timely resolution.
- Identify, track, and resolve investigator site issues, developing corrective and preventative actions (CAPA) to prevent recurrence.
- Ensure adequate oversight of investigational products, including receipt, handling, accounting, storage, and destruction.
- Submit high-quality monitoring reports, follow-up letters, and Trial Master File (TMF) documentation within required timelines.
Requirements & Qualifications
- Minimum of 3 years of active clinical research site monitoring experience.
- Strong preference for at least 2 years of experience monitoring Oncology trials.
- Extensive knowledge of clinical trial methodologies, ICH/GCP guidelines, FDA regulations, and local country laws.
- Ability and willingness to travel between 60% to 80% of the time.
- Must possess a valid driver’s license and a valid passport.
- Fluency in English (both written and verbal) is mandatory.
Required Skills
- Clinical Trial Monitoring
- ICH/GCP Compliance
- Oncology Trial Protocols
- Site Relationship Management
- Problem-Solving & Critical Thinking
- Trial Master File (TMF) Documentation
- Remote & Risk-Based Monitoring
- Effective Communication
About Parexel International
Parexel International is a leading global clinical research organization (CRO) focused on providing a comprehensive range of drug development and clinical trial services. With a patient-first culture, Parexel helps biopharmaceutical and medical device companies bring novel therapies to market faster. The company fosters a highly collaborative, inclusive, and flexible work environment, empowering its global workforce to make a meaningful impact on healthcare.
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