Remote Oncology Clinical Research Associate

Parexel; Helena (MT); On-site; USD 65,000 - 90,000; Full time

Benefits offered by this job

Health Insurance

Vision Insurance

Dental Insurance

Tuition Reimbursement

Vacation/Holiday/Sick Time

Flexible Spending Account

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 (CRA) with oncology monitoring experience to join our team. You will manage clinical sites from identification through closeout, serving as the primary contact for site teams and helping ensure study quality, patient safety, and data integrity.

You will conduct onsite monitoring visits, build relationships with investigators, support enrollment and study delivery, and ensure adherence to GCP,

Qualifications

• At least 18 months of direct onsite monitoring experience as a CRA.
• Oncology clinical trial monitoring experience.
• Bachelor's degree or equivalent in biological science, pharmacy, or another health-related discipline.
• Knowledge of GCP, regulatory requirements, and clinical trial processes.
• Experience using a Clinical Trial Management System and EDMS, plus MS Office.
• Strong interpersonal, written, verbal, organizational, and problem-solving skills.

Responsibilities

• Conduct qualification visits, site initiation visits, monitoring visits, and termination visits at assigned sites and prepare reports.
• Manage site quality and delivery from site identification through closeout.
• Serve as the primary contact for assigned sites and resolve questions to support study execution.
• Oversee study integrity and build relationships with investigators and site staff.
• Review trial performance and safeguard the rights, safety, and well-being of participants.
• Develop patient recruitment strategies with clinical sites to support enrollment timelines.
• Ensure compliance with SOPs, protocols, Good Clinical Practice, and regulations.
• Evaluate data quality, site performance, and investigational product accountability.
• Monitor completeness and quality of regulatory documentation and perform site document verification.

Skills

Onsite monitoring experience

Oncology monitoring

GCP knowledge

CTMS experience

MS Office (Excel/Word)

Education

Bachelor's degree in biological sciences or related health field

Tools

Clinical Trial Management System

Electronic Document Management System

Job description

Parexel, a leading global clinical development partner, is seeking a Clinical Research Associate (CRA) with oncology monitoring experience to join our team. You will manage clinical sites from identification through closeout, serving as the primary contact for site teams and helping ensure study quality, patient safety, and data integrity.

You will conduct onsite monitoring visits, build relationships with investigators, support enrollment and study delivery, and ensure adherence to GCP,