Oncology Clinical Research Associate - Remote

Parexel; Lincoln (NE); On-site; USD 72,000 - 110,000; 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 oncology monitoring experience to join our Lincoln, NE team. You will manage clinical sites from first contact through closeout, acting as the primary liaison to site staff and ensuring study quality, patient safety, and regulatory compliance.

You will conduct onsite monitoring visits, build strong site relationships, address issues promptly, and support patient enrollment and study delivery.

Qualifications

• At least 18 months of direct onsite monitoring experience as a Clinical Research Associate.
• 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 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 SOPs, 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 with urgency

Client-focused

Flexible learning

Multitasking

Attention to quality

Education

Bachelor's degree or equivalent in biological science, pharmacy, or another 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 oncology monitoring experience to join our Lincoln, NE team. You will manage clinical sites from first contact through closeout, acting as the primary liaison to site staff and ensuring study quality, patient safety, and regulatory compliance.

You will conduct onsite monitoring visits, build strong site relationships, address issues promptly, and support patient enrollment and study delivery.