Clinical Research Associate (Remote)

About the Role Our client is a renowned pharmaceutical company seeking a dedicated Clinical Research Associate (CRA) to join their expanding team. This position is a fully remote opportunity, allowing you to contribute significantly to our clinical trial operations without the need for physical office presence. You will play a crucial role in ensuring the smooth execution of clinical studies by monitoring trial sites, verifying data integrity, and upholding regulatory compliance. This role is essential for bringing life‑saving therapies to patients and offers a chance to be part of a dedicated, distributed team committed to excellence. We champion a remote‑first culture, empowering our employees with flexibility while maintaining the highest standards of professional conduct and scientific integrity. Your expertise will be vital in managing multiple studies and ensuring they meet all ethical and regulatory requirements, making a tangible difference in the advancement of healthcare. Join us in our mission to improve patient lives through rigorous clinical research conducted by a talented, globally dispersed team. Key Responsibilities Conduct site visits (initiation, monitoring, close‑out) according to protocol and regulatory requirements, primarily remotely through virtual tools. Verify the accuracy, completeness, and compliance of clinical trial data by reviewing source documents and electronic data capture (EDC) systems. Ensure adherence to Good Clinical Practice (GCP) guidelines, Standard Operating Procedures (SOPs), and study protocols. Serve as the primary point of contact for assigned clinical trial sites, addressing questions and resolving issues promptly. Manage study site recruitment and enrollment activities, working closely with investigators and site staff. Prepare and submit essential study documents to the appropriate regulatory authorities and Institutional Review Boards (IRBs)/Ethics Committees. Monitor subject safety and report adverse events (AEs) and serious adverse events (SAEs) according to protocol and regulatory standards. Oversee study drug accountability and management at clinical sites. Communicate effectively with internal project teams, including study managers, data managers, and investigators. Requirements Bachelor's degree in a life science, nursing, or related discipline. Minimum of 3 years of direct experience as a Clinical Research Associate. In-depth knowledge of clinical trial processes, GCP, ICH guidelines, and regulatory requirements. Proof of proven ability to manage multiple clinical trials and sites simultaneously. Excellent organizational, analytical, and problem‑solving skills. Proficiency in using EDC systems, CTMS (Clinical Trial Management Systems), and other clinical research software. Strong interpersonal and communication skills, essential for remote team collaboration and site interactions. Ability to work independently and proactively in a remote setting. Willingness to travel occasionally for essential site visits or team meetings, as needed. Benefits Competitive salary and performance‑based bonuses. Comprehensive medical, dental, and vision coverage. Retirement savings plan. Generous annual leave and public holiday entitlement. Continuous training and professional development opportunities. Home office equipment allowance. Flexible work schedule options. #J-18808-Ljbffr Placements24