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Clinical research professional with solid experience in managing and monitoring clinical trials. Strong focus on team collaboration and achieving results, adaptable to changing needs. Skilled in data analysis, protocol adherence, regulatory compliance, and patient interaction. Reliable and prepared to make impactful contribution to clinical research initiatives.

Detail-oriented and highly organized Clinical Research Associate (CRA) with [X] years of experience in monitoring and managing clinical trials across multiple therapeutic areas. Skilled in ensuring compliance with ICH-GCP, FDA, EMA, and other regulatory guidelines, conducting site visits, and maintaining high-quality data integrity. Adept at site initiation, monitoring, and close-out activities, ensuring patient safety, and collaborating with investigators and site staff. Proficient in using electronic data capture (EDC) systems and resolving protocol deviations efficiently. Strong communication, problem-solving, and analytical skills, committed to delivering high-quality clinical research outcomes.

As a detail-oriented Clinical Research Professional, I am well-versed in coordinating clinical trials, managing clinical sites, and drafting comprehensive reports. I am skilled in action planning, database management, and adherence to standard operating procedures (SOPs). I am seeking a clinical research role where I can apply my expertise in clinical monitoring, site and project management, and investigational product (IP) accountability.
I am committed to leveraging my skills to drive impactful clinical trials globally, while remaining open to learning new techniques and advancing my knowledge. I also play an integral role in participant recruitment , and screening to ensure research objectives are met. I am highly effective at handling multiple tasks in fast-paced environments. I am proactive in identifying and addressing issues, with a focus on process optimization and supporting team objectives.
Lastly, I manage the coordination of lab samples to ensure accurate and detailed data collection. I am diligent in executing studies aligned with good clinical practices (GCP), study-specific requirements, and clinical monitoring plans, with a strong understanding of regulatory requirements, quality standards, and company procedures.

Accomplished Clinical Research Associate with 3 years of experience performing and documenting pre-study site evaluations, regulatory document collection, interim monitoring and study close-out visits of phase II, III and IV clinical trials. Diligent in performing studies aligned with good clinical practices, study-specific requirements and clinical monitoring plans. In-depth knowledge of company procedures, regulatory requirements and quality standards.
Analytical, result-driven and proactive individual who is adept at prioritizing tasks and completing these in a timely fashion thus producing positive results.

RACHEL SEBASTIAN

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Clinical Research Associate

Clinical Research Project Coordinator

Laboratory Technologist

Laboratory Technician

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Bachelor of Arts - Zoology

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Clinical Research Associate

Clinical Research Project Coordinator

Laboratory Technologist

Laboratory Technician

Bachelor of Arts - Zoology

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