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Description
Company Description Acceltrials is dedicated to optimizing clinical trial processes and advancing medical research. We partner with research sites—including physician practices and specialized research centers—to boost operational efficiency and enhance patient outcomes. Our comprehensive range of services includes: - Patient recruitment and retention strategies - Regulatory compliance and document preparation - Data management and quality assurance - Staff training and development With expertise in various therapeutic areas, such as psychiatric, orthopedic, dermatology, ophthalmology, oncology, cardiology, and neurology, we empower sites to undertake complex studies and effectively meet sponsor requirements. Based in Ahmedabad, we act as a crucial bridge between sponsors and research sites, fostering innovation in clinical research. Together, we're advancing healthcare solutions. Role Description: Clinical Research Coordinator (On-site, Contract-Based) Location: Ahmedabad, India Type: Contract-Based | On-Site Role We are seeking a detail-oriented and proactive Clinical Research Coordinator to join our team on a contract basis. In this role, you will be responsible for overseeing the daily operations of clinical research studies, ensuring strict adherence to study protocols, regulatory guidelines, and Good Clinical Practice (GCP) standards. You will play a critical role in supporting investigators, engaging with study participants, managing data collection and analysis, and ensuring the overall integrity and success of research activities. Key Responsibilities: Coordinate and manage day-to-day activities of clinical research studies. Ensure compliance with study protocols, ICH-GCP guidelines, and applicable regulatory requirements. Facilitate the informed consent process and maintain participant engagement throughout the study. Collect, enter, and verify clinical data accurately and in a timely manner. Assist investigators in preparing study documentation and reports. Maintain regulatory and ethics committee documentation. Liaise with sponsors, CROs, and other stakeholders as needed. Ensure proper storage, handling, and documentation of study materials and investigational products. Qualifications & Skills: Strong understanding of regulatory guidelines, including ICH-GCP and ethical standards. Proficiency in clinical data collection, entry, and basic analysis. Excellent organizational and documentation skills with attention to detail. Effective communication and interpersonal skills to interact with participants and research teams. Ability to work collaboratively in a fast-paced, multidisciplinary environment. Bachelor’s degree in Life Sciences, Nursing, Pharmacy, or a related field (Master’s degree or certification in Clinical Research is a plus). If you’re passionate about advancing healthcare through clinical research and meet the above criteria, we invite you to apply and be part of our impactful research journey. Show more Show less
