Senior Clinical Research Associate – Remote, Oncology Trials

Parexel; Bismarck (ND); Remote; USD 90,000 - 120,000; Full time

Job summary

Parexel is seeking a Clinical Site Monitoring professional with oncology exposure to oversee trial conduct across investigator sites. You will manage site activation through database lock, while ensuring quality and adherence to SMP, GCP, and client standards.

Travel is extensive and you will train site staff and support recruitment. You will collaborate with the SCP and study team, conduct onsite and remote monitoring, and handle AE/SAE follow-up in partnership with Drug Safety.

Qualifications

• Bachelor’s degree in life sciences or equivalent.
• Minimum 3 years monitoring experience in clinical research ( Oncology preferred).
• Fluent in English and local country language where you’ll work.
• Willingness to travel 60–80% within the area; some international travel may be required.

Responsibilities

• Ensure proper conduct of clinical trials per SMP, GCP, laws and client standards.
• Manage operational aspects from site activation to database lock.
• Serve as primary site contact; collaborate with SCP for site quality.
• Interface with study team, vendors and sites to enable information flow.
• Develop and train investigator sites; provide protocol training.
• Attend investigator meetings; support enrollment and recruitment initiatives.
• Conduct onsite/remote monitoring per SMP and SOPs.
• Monitor AEs/SAEs; coordinate with Drug Safety for resolution of SAE reports.
• Submit TMF docs, site reports, deviations and progress metrics.

Skills

Clinical trial methodologies

Monitoring experience

Oncology background

Global clinical trials

English fluency

High travel willingness

Driver's license & passport

Education

Bachelor’s degree in life sciences

Job description

Parexel is seeking a Clinical Site Monitoring professional with oncology exposure to oversee trial conduct across investigator sites. You will manage site activation through database lock, while ensuring quality and adherence to SMP, GCP, and client standards.

Travel is extensive and you will train site staff and support recruitment. You will collaborate with the SCP and study team, conduct onsite and remote monitoring, and handle AE/SAE follow-up in partnership with Drug Safety.