Remote Clinical Research Associate – Oncology Trials

Parexel; Cheyenne (WY); 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 experience in Oncology, Ophthalmology, Metabolic, Hematology, or CAR-T to monitor sites from identification through closeout. You will ensure study quality, patient safety and data integrity while serving as the primary contact for site teams.

You will conduct onsite visits, build strong site relationships, address issues promptly, and support enrollment goals.

Qualifications

• At least 18 months of direct onsite monitoring experience.
• Oncology, Ophthalmology, Metabolic, Hematology or CAR-T clinical trial monitoring experience required.
• Bachelor's degree or equivalent in biological science, pharmacy, or another health-related discipline.
• Knowledge of Good Clinical Practice, applicable 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.

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

Problem-solving

Communication skills

Independent worker

Time management

Education

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

Tools

Clinical Trial Management System

Electronic Document Management System

Microsoft Excel

Microsoft Word

Job description

Parexel is seeking a Clinical Research Associate (CRA) with experience in Oncology, Ophthalmology, Metabolic, Hematology, or CAR-T to monitor sites from identification through closeout. You will ensure study quality, patient safety and data integrity while serving as the primary contact for site teams.

You will conduct onsite visits, build strong site relationships, address issues promptly, and support enrollment goals.