Senior Clinical Research Associate - Remote Oncology Trials

Parexel; Jackson (MS); Remote; USD 70,000 - 100,000; Full time

Job summary

Parexel is seeking an experienced Clinical Site Monitor to oversee trial conduct at investigator sites, ensuring adherence to SMP, GCP, and client standards. You will manage site activation through database lock, and collaborate with cross‑functional teams across oncology and non‑oncology programs.

The role requires 3+ years of monitoring experience, oncology exposure preferred, and substantial travel. Strong English fluency and effective communication are essential to support sponsor objectives

Qualifications

• Minimum 3 years relevant experience in clinical research site monitoring
• 2 years oncology experience preferred
• Fluent in English; able to work with global teams
• Willing to travel 60-80% within region and potentially internationally
• Bachelor’s degree in life sciences or equivalent required

Responsibilities

• Ensure proper conduct of clinical trials per SMP, GCP and client standards
• Manage site activation through database lock with timelines and quality deliverables
• Serve as primary contact for investigator sites; coordinate with SCP
• Interface with study team, vendors and sites to enable information flow
• Provide site development, coaching and training on protocol and risks
• Attend investigator meetings and support enrollment and recruitment plans
• Perform onsite and remote monitoring per SMP and SOPs
• Monitor and follow up on AEs/SAEs; collaborate with Drug Safety
• Submit TMF and site documents within required timeframes

Skills

Clinical trial monitoring

Oncology experience

GCP knowledge

English fluency

Excellent communication

Willingness to travel

Driver’s license

Education

Bachelor’s degree in life sciences

Job description

Parexel is seeking an experienced Clinical Site Monitor to oversee trial conduct at investigator sites, ensuring adherence to SMP, GCP, and client standards. You will manage site activation through database lock, and collaborate with cross‑functional teams across oncology and non‑oncology programs.

The role requires 3+ years of monitoring experience, oncology exposure preferred, and substantial travel. Strong English fluency and effective communication are essential to support sponsor objectives