Senior Clinical Research Associate - Remote Oncology Trials

Parexel; Annapolis (MD); Remote; USD 90,000 - 130,000; Full time

Job summary

Parexel is seeking a Clinical Site Monitor to oversee monitoring activities and study conduct across oncology and non-oncology trials. The role requires coordinating site activation, monitoring visits, and study deliverables with the SCP and study team.

The candidate will drive QA remediation, ensure patient safety, and manage timelines while traveling 60–80% within the region and potentially international. Fluency in English is required.

Qualifications

• Extensive knowledge of clinical trial methodologies, ICH/GCP, FDA regulations and local country rules.
• 3+ years monitoring experience in clinical research site monitoring (Oncology preferred).
• Ability to work in a global, matrix environment and communicate with diverse teams.

Responsibilities

• Oversee monitoring responsibilities and study conduct to meet SMP, timelines and quality.
• Manage operational aspects from site activation to database lock.
• Serve as main contact for investigator sites and coordinate with SCP and study team.
• Interface with study team, vendors, and sites to ensure information flow.

Skills

Clinical trial monitoring

Oncology experience

GCP familiarity

Study coordination

Travel readiness

Fluent in English

Education

Bachelor’s degree in life sciences

Job description

Parexel is seeking a Clinical Site Monitor to oversee monitoring activities and study conduct across oncology and non-oncology trials. The role requires coordinating site activation, monitoring visits, and study deliverables with the SCP and study team.

The candidate will drive QA remediation, ensure patient safety, and manage timelines while traveling 60–80% within the region and potentially international. Fluency in English is required.