Clinical Research Coordinator I - India

requirements and institutional policies. Process, prepare, and ship laboratory specimens according to protocol

requirements and laboratory guidelines. Maintain accurate, complete, and timely source documentation, regulatory documentation, CTMS updates, and electronic Case Report Forms (eCRFs). Enter study data into EDC systems and assist with timely resolution of data queries. Coordinate investigational product accountability and study supply management. Serve as the primary point of contact for study participants throughout study participation. Collaborate with investigators, sponsors, CROs, central laboratories, and internal teams to ensure successful study execution. Support study startup, site activation, document collection, and ongoing maintenance of essential study documentation across assigned research sites. Review study documentation for completeness, accuracy, and protocol compliance while supporting data quality and inspection readiness. Prepare for and support sponsor monitoring visits, audits, and regulatory inspections. Maintain study regulatory files and essential documents throughout the study lifecycle. Ensure compliance with applicable regulations, institutional policies, privacy

requirements, and Good Clinical Practice (ICH-GCP). Participate in ongoing training and quality improvement initiatives. Willingness to travel to other sites in India upon request. Perform other duties as assigned. What You Bring to

the Team Bachelor's or Master's degree in Life Sciences, Pharmacy (B.Pharm/PharmD), Nursing, Biotechnology, Allied Health Sciences, or a related scientific discipline. 1–3 years of clinical research, healthcare, or hospital experience. Working knowledge of ICH-GCP guidelines and Indian clinical research regulations. Experience supporting multiple clinical research sites or working in a centralized clinical operations environment is preferred. Strong understanding of clinical trial documentation and research workflows. Excellent organizational skills with strong attention to detail. Ability to manage multiple studies and competing priorities in a fast-paced environment. Effective verbal and written communication skills in English. Strong interpersonal skills with the ability to build relationships with participants, investigators, sponsors, and internal stakeholders. Proficiency with Microsoft Office applications. Familiarity with clinical research technologies, including CTMS, EDC, eSource, EMR/EHR, or similar systems preferred Physical

Requirements Ability to sit, stand, and move throughout clinical and office environments for extended periods of time Ability to lift and move up to 10 kilograms (22 pounds) as needed At Iterative Health, we’re actively working towards creating an environment that is representative of the diversity of patients our technology serves. We are focused on building an equitable and inclusive culture, and by extension, hiring process. If you require any accommodations to make the application process or interviewing experience more accessible to you, please contact [email protected].

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