Clinical Research Associate (Oncology)

PRA International; United States; Remote; USD 65,000 - 85,000; Full time

Job summary

PRA International is seeking a Clinical Research Associate to join their team. In this role, you will be responsible for conducting site visits, ensuring protocol compliance, and collaborating with investigators to maintain high-quality clinical data. Ideal candidates will have a Bachelor's degree and at least 2 years of relevant experience in clinical trials.

Qualifications

• Minimum of 2 years of experience as a Clinical Research Associate.
• In-depth knowledge of clinical trial processes and regulations.
• Ability to work independently and collaboratively.

Responsibilities

• Conducting site qualification, initiation, monitoring, and close-out visits for clinical trials.
• Ensuring protocol compliance, data integrity, and patient safety throughout the trial.
• Collaborating with investigators and site staff to facilitate study conduct.

Skills

Organizational skills

Communication skills

Attention to detail

Education

Bachelor's degree in a scientific or healthcare-related field

Job description

Overview

As a CRA you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence.

Responsibilities

What you will be doing

• Conducting site qualification, initiation, monitoring, and close-out visits for clinical trials.
• Ensuring protocol compliance, data integrity, and patient safety throughout the trial process.
• Collaborating with investigators and site staff to facilitate smooth study conduct.
• Performing data review and resolution of queries to maintain high-quality clinical data.
• Contributing to the preparation and review of study documentation, including protocols and clinical study reports

Qualifications

You Are

• Bachelor's degree in a scientific or healthcare-related field.
• Minimum of 2 years of experience as a Clinical Research Associate.
• In-depth knowledge of clinical trial processes, regulations, and ICH-GCP guidelines.
• Strong organizational and communication skills, with attention to detail.
• Ability to work independently and collaboratively in a fast-paced environment.