Sr. Clinical Research Associate - Remote (West Coast)

Parexel; Austin (TX); Remote; USD 90,000 - 130,000; Full time

Job summary

Parexel is seeking a highly experienced Clinical Site Monitor to oversee monitoring activities for oncology and non-oncology trials. You will manage site activation through database lock, ensuring adherence to the SMP and client standards while coordinating with cross-functional teams.

The role requires extensive travel (60-80%), fluency in English, and a strong background in GMP/ICH-GCP. A life sciences degree and driving license are required.

Qualifications

• Extensive knowledge of clinical trial methodologies, ICH/GCP, FDA and local country regulations.
• Monitoring Experience: Minimum 3 years relevant experience in clinical research site monitoring (preferably 2 years in Oncology).
• Preferred therapeutic experience in Oncology, Vaccines, Internal Medicine or Infectious Diseases.
• Global clinical trial experience.
• Must be fluent in English and in the native language(s) of the country they will work in.
• Significant travel (60-80%) within area is required. May require some international travel and some weekend travel.
• Valid driver’s license and passport required.

Responsibilities

• Oversee monitoring responsibilities and study conduct per SMP and applicable laws.
• Manage site activation through database lock with timelines and quality deliverables.
• Serve as primary contact for investigator sites and coordinate with SCP for site delivery quality.
• Interface with study team to facilitate information flow between members, vendors and sites.
• Provide site development, coaching and training to ensure protocol adherence and patient safeguarding.

Skills

ICH/GCP knowledge

Monitoring experience

Oncology experience

Global clinical trials

English fluency

Travel readiness

Driver's license & passport

Education

Bachelor’s degree in life sciences

Job description

Parexel is seeking a highly experienced Clinical Site Monitor to oversee monitoring activities for oncology and non-oncology trials. You will manage site activation through database lock, ensuring adherence to the SMP and client standards while coordinating with cross-functional teams.

The role requires extensive travel (60-80%), fluency in English, and a strong background in GMP/ICH-GCP. A life sciences degree and driving license are required.