Remote Senior Clinical Research Associate — Oncology

Parexel; Columbus (OH); Remote; USD 90,000 - 120,000; Full time

Job summary

Parexel is seeking a Clinical Research Associate with oncology experience to oversee monitoring activities, ensuring compliant conduct of trials per SMP and GCP standards. The role involves site activation through database lock, coordinating with study teams, and ensuring high-quality site performance.

The candidate will travel extensively (60-80%), work in a matrix team, and mentor junior staff while maintaining strong regulatory, safety, and data integrity practices across global studies.

Qualifications

• Thorough knowledge of clinical trial methodologies and regulatory requirements (GCP/ICH).
• Experience monitoring clinical trials at site level, preferably oncology.
• Fluency in English and local language of posting country.

Responsibilities

• Oversee monitoring responsibilities and study conduct per SMP and SOPs.
• Manage site activation through database lock, ensuring timelines and quality.
• Serve as main contact for investigator sites and collaborate with SCP for site delivery.

Skills

ICH-GCP knowledge

English fluent

Study monitoring

Clinical trials

Site management

Trial safety

Excellent communication

Travel 60-80%

Regulatory understanding

Quality management

Education

Bachelor’s degree in life sciences or related field

Tools

NONE

Job description

Parexel is seeking a Clinical Research Associate with oncology experience to oversee monitoring activities, ensuring compliant conduct of trials per SMP and GCP standards. The role involves site activation through database lock, coordinating with study teams, and ensuring high-quality site performance.

The candidate will travel extensively (60-80%), work in a matrix team, and mentor junior staff while maintaining strong regulatory, safety, and data integrity practices across global studies.