Clinical Research Associate / Senior Clinical Research Associate

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

📋 Description

• Oversee the management, monitoring, and completion of designated clinical trials at various sites.

• Prioritize patient safety and ensure high-quality execution of the study.

• Foster relationships with investigator sites to facilitate the successful delivery of clinical trials.

• Maintain the integrity of investigator sites, focusing on patient safety and adherence to GCP standards.

• Address and resolve all protocol-related concerns for the assigned investigator sites.

• Collaborate closely with the Site Care Partner and other team members involved in the study.

⛳️ Requirements

• At least 1 year of relevant experience in monitoring and managing clinical research sites.

• Familiarity with clinical trial methodologies, ICH/GCP guidelines, FDA regulations, and local laws.

• Preferred background in therapeutic areas such as Oncology, Vaccines, Internal Medicine, or Infectious Diseases.

• Global experience in clinical trials is a plus.

• Proficiency in English as well as the local language(s) of the country of employment is required.

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

• Proven understanding of clinical research and development processes.

• Capability to function effectively within a matrix team environment.

• Strong verbal and written communication skills are essential.

🏝️ Benefits

• Comprehensive benefits package.

• Sick leave.

• 401K retirement plan.

• Paid holidays.

• Paid time off.