Senior Clinical Research Associate - Oncology (Remote/West Coast)

Parexel; Hartford (CT); Remote; USD 90,000 - 140,000; Full time

Job summary

Parexel is seeking a Clinical Site Monitoring professional to oversee trial conduct meeting SMP and GCP standards. You will manage site activation through database lock, ensuring timelines and high quality deliverables while collaborating with the SCP and study team.

The role requires oncology exposure or related therapeutic experience, strong regulatory knowledge, and frequent travel (60–80%). A life sciences degree is required, with fluency in English and local languages as needed.

Qualifications

• Extensive knowledge of clinical trial methodologies, ICH/GCP, FDA and local regulations.
• Minimum 3 years of site monitoring experience in clinical research.
• Oncology exposure preferred (or related therapeutic areas).
• Willingness to travel 60–80% and some international travel.
• Bachelor-level degree in life sciences or equivalent.

Responsibilities

• Oversee monitoring responsibilities and study conduct per SMP and GCP to meet timelines and quality.
• Manage operational aspects from site activation to database lock with quality deliverables.
• Act as primary contact for investigator sites and coordinate with SCP and study team.
• Coordinate information flow between study team, vendors and sites.
• Provide site personnel training and protocol guidance to ensure patient safety and protocol adherence.
• Support enrollment and recruitment initiatives at the site level.

Skills

Clinical trial methodologies & GCP

Site monitoring experience

Oncology exposure

Global clinical trials

English & local language fluency

Travel availability (60-80%)

Driver’s license & passport

Education

Bachelor’s degree in life sciences or equivalent

Job description

Parexel is seeking a Clinical Site Monitoring professional to oversee trial conduct meeting SMP and GCP standards. You will manage site activation through database lock, ensuring timelines and high quality deliverables while collaborating with the SCP and study team.

The role requires oncology exposure or related therapeutic experience, strong regulatory knowledge, and frequent travel (60–80%). A life sciences degree is required, with fluency in English and local languages as needed.