Senior Clinical Research Associate

This is a fully remote position, open to applicants in United States.

📋 Description

• Ensure the proper execution of clinical trials in alignment with the Study Monitoring Plan (SMP), relevant laws, Good Clinical Practice (GCP), and the Sponsor's standards to meet project objectives, timelines, and quality.

• Oversee the operational components for the execution of clinical trial activities at designated investigator sites, from site activation to database lock, ensuring that timelines and quality deliverables are adhered to.

• Act as the primary liaison for assigned investigator sites.

• Collaborate with and/or escalate issues to the SCP to guarantee the quality of site performance.

• Monitor site-level adverse events (AEs) and serious adverse events (SAEs), working together with the Drug Safety Unit and following up with investigator sites.

⛳️ Requirements

• At least 3 years of relevant experience in clinical research site monitoring, with a preference for 2 years in Oncology.

• Preferred therapeutic experience in Oncology, Vaccines, Internal Medicine, or Infectious Diseases.

• Proficiency in English and the native language(s) of the country in which they will be working is essential.

• Willingness to travel 60-80% of the time.

• A valid driver’s license and passport are required.

• A Bachelor’s degree in life sciences or a professional degree in life sciences, such as nursing, pharmacy, medical background, or an equivalent qualification.

🏝️ Benefits

• Equal opportunity employer