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Responsible for managing and coordinating clinical trials and research studies conducted in various healthcare settings. Their job description includes various tasks such as: Study Planning: Collaborate with research teams to design and develop study protocols, including determining eligibility criteria, data collection methods, and study timelines. Participant Recruitment: Identify and screen potential study participants, ensuring they meet the necessary criteria, and obtain informed consent from those who are interested in participating. Data Collection and Management: Collect and record accurate and complete data from study participants, ensuring compliance with regulatory guidelines and protocols. They also maintain and organize study documentation and