Senior CRA — Remote Oncology Trials Lead

Parexel; Trenton (NJ); Remote; USD 90,000 - 130,000; Full time

Job summary

Parexel in the United States is seeking an experienced Clinical Site Monitoring professional to oversee monitoring responsibilities from site activation through database lock, ensuring adherence to SMP, GCP, and client standards. The role emphasizes oncology and non-oncology trials, with 60-80% travel and collaboration with SCP and study teams.

Applicants should have a life sciences degree and global trial experience, and must be fluent in English.

Qualifications

• Extensive knowledge of clinical trial methodologies, ICH/GCP, FDA regulations and local country requirements.
• Monitoring experience: minimum 3 years in clinical research site monitoring (oncology preferred).
• Therapeutic experience in Oncology, Vaccines, Internal Medicine or Infectious Diseases.
• Global clinical trial experience.
• Fluent in English and in local language(s) of the country they work in.
• Willingness to travel 60-80%; may require international travel.
• Valid driver's license and passport.

Responsibilities

• Oversee monitoring responsibilities from site activation to database lock.
• Serve as primary point of contact for assigned investigator sites.
• Coordinate with SCP and study team to ensure site delivery quality.
• Provide site training and address protocol questions.
• Attend investigator meetings and support recruitment initiatives.
• Ensure timely submission of TMF documents and study reports.
• Manage audits and CAPA development as needed.
• Ensure compliance with Parexel standards and SOPs.

Skills

Clinical trials

Monitoring

Oncology experience

Global trials

English fluency

Travel

Driver's license

Passport

Education

Bachelor's degree in life sciences

Job description

Parexel in the United States is seeking an experienced Clinical Site Monitoring professional to oversee monitoring responsibilities from site activation through database lock, ensuring adherence to SMP, GCP, and client standards. The role emphasizes oncology and non-oncology trials, with 60-80% travel and collaboration with SCP and study teams.

Applicants should have a life sciences degree and global trial experience, and must be fluent in English.