Clinical Research Associate: Site Monitoring & Study Delivery

Parexel; Santa Fe (NM); On-site; USD 65,000 - 90,000; 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 is seeking a Clinical Research Associate (CRA) with at least 1 year of onsite monitoring experience to join our team in the United States. You will manage clinical sites from start-up through closeout, ensuring study quality, patient safety, regulatory compliance, and accurate data collection.

You will conduct site visits, build strong site relationships, support enrollment, and ensure timely study delivery.

Qualifications

• Minimum 12 months of direct onsite monitoring experience as a CRA.
• Bachelor's degree or equivalent in biological science, pharmacy, or health-related discipline.
• Knowledge of GCP, regulatory requirements, and trial processes.
• Experience using a CTMS, EDMS, and MS Office including Excel and Word.
• Strong interpersonal, written, verbal, organizational, and problem-solving skills.
• Oncology, Ophthalmology, CAR-T, and/or MASH 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

Onsite monitoring

Site relationship management

Regulatory compliance

Documentation & reporting

Problem-solving

Communication

Education

Bachelor's degree in biological sciences or health-related discipline

Tools

Clinical Trial Management System

Electronic Document Management System

Microsoft Office (Excel/Word)

Job description

Parexel is seeking a Clinical Research Associate (CRA) with at least 1 year of onsite monitoring experience to join our team in the United States. You will manage clinical sites from start-up through closeout, ensuring study quality, patient safety, regulatory compliance, and accurate data collection.

You will conduct site visits, build strong site relationships, support enrollment, and ensure timely study delivery.