Remote Senior Clinical Research Associate - Oncology Trials

Parexel; Pierre (SD); Remote; USD 90,000 - 130,000; Full time

Job summary

Parexel is seeking an experienced Clinical Site Monitor with strong monitoring leadership to oversee trial conduct across oncology and non-oncology studies. The role emphasizes study integrity, regulatory compliance, and timely delivery at investigator sites, with global responsibilities and significant travel.

You will partner with SCP, lead site development and training, coordinate with cross-functional teams, and ensure safety reporting and accurate TMF submissions.

Qualifications

• Strong knowledge of ICH-GCP, FDA regulations, and local country rules.
• Minimum 3 years of clinical site monitoring experience, oncology preferred.
• Experience with global clinical trials and multicenter studies.
• Excellent written and verbal communication in English.
• Willingness to travel 60–80% domestically and internationally.
• Ability to work in a matrix, cross-functional team.

Responsibilities

• Oversee monitoring activities from site activation to database lock.
• Act as primary contact for investigator sites and coordinate with SCP.
• Facilitate information flow among study team, vendors, and sites.
• Provide site development and training to ensure protocol adherence.
• Support enrollment and recruitment initiatives with study team.
• Monitor AEs/SAEs and collaborate with Drug Safety Unit.
• Submit required reports and maintain TMF documentation.

Skills

Clinical trial knowledge

Site monitoring experience

Oncology experience

Global trials

English fluency

Travel 60-80%

Driver’s license & passport

Regulatory knowledge (GCP/ICH/FDA)

Education

Bachelor’s degree in life sciences or equivalent

Job description

Parexel is seeking an experienced Clinical Site Monitor with strong monitoring leadership to oversee trial conduct across oncology and non-oncology studies. The role emphasizes study integrity, regulatory compliance, and timely delivery at investigator sites, with global responsibilities and significant travel.

You will partner with SCP, lead site development and training, coordinate with cross-functional teams, and ensure safety reporting and accurate TMF submissions.