Remote Oncology Clinical Research Associate

Parexel; Cheyenne (WY); On-site; USD 65,000 - 90,000; Full time

Benefits offered by this job

Health Insurance

Vision Insurance

Dental Insurance

Tuition Reimbursement

Vacation/Holidays/Sick Time

Flexible Spending Account

Health Savings Account

Work/Life Balance

401(k) Matching

Pet Insurance

Job summary

Parexel is seeking a Clinical Research Associate (CRA) with oncology monitoring experience to join our team. You will manage clinical sites from initiation through closeout, serving as the primary contact for site teams and ensuring study quality, patient safety, and regulatory compliance.

You will conduct onsite monitoring visits, build productive site relationships, address issues, and support enrollment and study delivery using Parexel technology and training.

Qualifications

• 18+ months of direct onsite monitoring experience.
• Oncology clinical trial monitoring experience.
• 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 CTMS, EDMS, 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 sites, and prepare timely visit reports.
• Manage site quality and delivery from site identification through closeout.
• Serve as the primary point of contact for assigned sites and resolve issues to support study execution.
• Oversee study integrity and build relationships with investigators and site staff.
• Review trial performance and safeguard rights, safety, and wellbeing of participants per protocol.
• Develop patient recruitment strategies with sites to support enrollment timelines.
• Ensure compliance with SOPs, protocols, amendments, GCP, and regulatory requirements.
• Evaluate data quality and site performance; ensure accountability of investigational products.
• Monitor completeness and quality of regulatory documentation and perform site document verification.

Skills

Site relationship management

Problem-solving

Communication

Independent work

Client-focused

Adaptability

Multitasking

Attention to quality

Team collaboration

Education

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

Tools

CTMS

EDMS

Microsoft Office

Excel

Word

Job description

Parexel is seeking a Clinical Research Associate (CRA) with oncology monitoring experience to join our team. You will manage clinical sites from initiation through closeout, serving as the primary contact for site teams and ensuring study quality, patient safety, and regulatory compliance.

You will conduct onsite monitoring visits, build productive site relationships, address issues, and support enrollment and study delivery using Parexel technology and training.