2 Clinical Research Associate Ii Remote jobs in whatjobs
Clinical Research Associate II (Remote)
Posted 14 days ago
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Job Description
Our client, a leading pharmaceutical company, is seeking a dedicated and experienced Clinical Research Associate II (CRA II) to join their dynamic, fully remote clinical operations team. In this critical role, you will play an integral part in ensuring the successful execution of clinical trials according to Good Clinical Practice (GCP) guidelines, regulatory requirements, and study protocols. Your primary responsibilities will include remote site monitoring, conducting pre-study, initiation, interim, and close-out visits (where applicable, via remote means or at local sites if needed and permitted). You will be responsible for verifying data accuracy and integrity, ensuring source data verification (SDV), and managing essential study documents. The CRA II will serve as the primary point of contact for assigned investigational sites, building strong relationships with investigators and site staff. You will provide training and ongoing support to site personnel, address protocol-related questions, and ensure timely resolution of site issues. This role requires meticulous attention to detail, excellent organizational skills, and the ability to manage multiple studies and sites concurrently. The ideal candidate will possess strong analytical and problem-solving abilities, coupled with exceptional written and verbal communication skills. Proficiency in clinical trial management systems (CTMS), electronic data capture (EDC) systems, and other relevant clinical trial software is essential. As this is a remote position, you must be a self-starter, highly motivated, and capable of working autonomously with minimal supervision. We are looking for individuals with a proven track record in clinical research monitoring and a commitment to patient safety and data quality. This opportunity offers a significant chance to contribute to the development of life-saving pharmaceuticals while enjoying the flexibility of a remote work arrangement. Your dedication to excellence will directly impact the success of our clinical development programs. The role is essential for ensuring compliance and operational efficiency in drug development.
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Clinical Research Associate II (Remote)
Posted 8 days ago
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Job Description
Our client is a leading global contract research organization (CRO) looking for a dedicated and detail-oriented Clinical Research Associate II (CRA II) to join our expanding, fully remote clinical operations team. This position offers the exciting opportunity to contribute to groundbreaking clinical trials across various therapeutic areas, all managed from your remote workspace. As a CRA II, you will be instrumental in ensuring the quality, integrity, and timely execution of clinical research studies by monitoring study sites, verifying data, and ensuring compliance with Good Clinical Practice (GCP) guidelines and regulatory requirements. Your responsibilities will include site initiation visits, routine monitoring visits, and site closure visits, all conducted virtually or with occasional travel as required by specific study protocols. You will serve as the primary point of contact for assigned clinical sites, building strong relationships with investigators and site staff to facilitate smooth study conduct. This role demands exceptional organizational skills, meticulous attention to detail, and the ability to manage multiple tasks and priorities effectively in a remote setting. You will be responsible for reviewing source documents, Case Report Forms (CRFs), and other study-related documentation to ensure accuracy and completeness. Furthermore, you will identify, track, and resolve site issues, escalate protocol deviations, and contribute to study close-out activities. The ideal candidate will possess a Bachelor's degree in a life science, nursing, or a related field, with a minimum of 2-3 years of direct CRA experience. Proven experience in clinical trial monitoring, understanding of ICH-GCP and relevant regulatory guidelines, and proficiency in clinical trial management systems (CTMS) and electronic data capture (EDC) systems are essential. Excellent communication and interpersonal skills are vital for successful remote collaboration and site management. This role is a fully remote position, offering flexibility and autonomy. While the official location is tied to Ongata Rongai, Kajiado, KE , you will be working from home. Our client provides a supportive and collaborative virtual environment, competitive compensation, and opportunities for professional growth within the clinical research field. If you are a results-driven CRA seeking a challenging and rewarding remote opportunity, we encourage you to apply.
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