Clinical Research Associate — Site Lead & Growth Path

Parexel; Phoenix (AZ); On-site; USD 75,000 - 95,000; Full time

Benefits offered by this job

Health, Vision & Dental Insurance

Tuition Reimbursement

Vacation/Holiday/Sick Time

Flexible Spending & Health Savings

Work/Life Balance

401(k) with Company match

Pet Insurance

Job summary

Parexel, a leading global clinical development partner, is seeking a Clinical Research Associate with at least 12 months onsite monitoring experience to join our team. You will manage clinical sites from identification through closeout, act as primary contact for site teams, ensure study quality and regulatory compliance, and support patient safety.

You will conduct onsite monitoring, build site relationships, support enrollment, and ensure data integrity.

Qualifications

• At least 12 months of direct onsite monitoring experience as a Clinical Research Associate.
• Bachelor’s degree or equivalent in biological science, pharmacy, or another health-related discipline.
• Knowledge of Good Clinical Practice, regulatory requirements, and clinical trial processes.
• Experience using a Clinical Trial Management System, an Electronic Document Management System, and Microsoft Office applications, including Excel and Word.
• Strong interpersonal, written, verbal, organizational, and problem-solving skills.
• Oncology, Ophthalmology, CAR-T, and/or MASH clinical trial monitoring experience preferred.

Responsibilities

• Conduct qualification visits (QV), site initiation visits (SIV), monitoring visits (MV), and termination visits (TV) at assigned clinical sites, and prepare timely visit and contact reports.
• Manage site quality and delivery from site identification through closeout.
• Serve as the primary point of contact for assigned clinical sites, addressing questions and resolving issues to support successful study execution.
• Oversee study integrity and build effective relationships with investigators and site staff.
• Review trial performance at designated sites and help safeguard the rights, safety, and well-being of study participants in accordance with the protocol.
• Develop patient recruitment strategies with clinical sites to support enrollment timelines.
• Ensure compliance with approved standard operating procedures, study protocols and amendments, Good Clinical Practice, and applicable regulatory requirements.
• Evaluate the quality and integrity of reported data, site performance, and investigational product accountability.
• Monitor the completeness and quality of regulatory documentation and perform site document verification.

Skills

Site relationship management

Communication

Independent work

Client focus

Multi-tasking

Quality focus

Education

Bachelor’s degree in biological science or health-related discipline

Tools

CTMS

EDMS

Microsoft Office (Excel, Word)

Job description

Parexel, a leading global clinical development partner, is seeking a Clinical Research Associate with at least 12 months onsite monitoring experience to join our team. You will manage clinical sites from identification through closeout, act as primary contact for site teams, ensure study quality and regulatory compliance, and support patient safety.

You will conduct onsite monitoring, build site relationships, support enrollment, and ensure data integrity.