Job Summary We are seeking a highly motivated, organized, and detail-oriented Study Coordinator to join our Clinical Research team. This position is ideal for a recent graduate or an individual with up to one year of relevant experience who is interested in pursuing a career in clinical research. The Study Coordinator will support the planning, coordination, and execution of clinical research studies while ensuring compliance with study protocols, regulatory requirements, institutional policies, and Good Clinical Practice (GCP) standards. The successful candidate will work closely with Principal Investigators, research staff, study participants, laboratory personnel, and other stakeholders to ensure the accurate and timely completion of study activities. Key Responsibilities Coordinate and support day-to-day clinical research activities in accordance with approved study protocols. Assist with participant recruitment, screening, enrollment, scheduling, and follow-up activities. Maintain accurate and complete study documentation, source records, regulatory files, and study logs. Assist with the collection, entry, review, and maintenance of clinical research data. Ensure study activities are conducted in accordance with FDA regulations, ICH GCP guidelines, applicable drug regulations, and institutional policies. Support preparation for monitoring visits, audits, regulatory reviews, and other study-related activities. Communicate and collaborate effectively with investigators, research staff, laboratory personnel, and external stakeholders. Assist in tracking study milestones, participant visits, required documentation, and study supplies. Identify and communicate protocol deviations, data discrepancies, and other study-related issues to the appropriate team members. Maintain confidentiality and safeguard participant information in accordance with applicable privacy requirements. Assist with research administration, study reporting, and other clinical research activities as assigned. Participate in required training and continuously develop knowledge of clinical research processes and regulatory requirements. Required Qualifications Bachelor's degree in Life Sciences, Pharmacy, Nursing, Biotechnology, Microbiology, Healthcare, or a related field. Fresh graduates are encouraged to apply. Candidates with up to 1 year of relevant clinical research experience are also welcome. Valid ICH GCP certification or an equivalent recognized GCP certification is mandatory. Basic understanding of clinical research principles and processes. Strong written and verbal communication skills. Excellent organizational skills and attention to detail. Ability to maintain accurate and confidential records. Proficiency in Microsoft Office Suite, including Word, Excel, and PowerPoint. Ability to work effectively both independently and as part of a multidisciplinary team. Strong time-management skills and the ability to prioritize multiple responsibilities. Preferred Qualifications Clinical research internship, academic research, or related practical experience. Familiarity with FDA regulations and ICH GCP requirements. Exposure to clinical trial documentation, research databases, or electronic data capture (EDC) systems. Knowledge of research data management and documentation practices. Interest in developing a long-term career in clinical research. Why Join Us? This is an excellent opportunity for an entry-level professional to gain practical experience in clinical research, study coordination, data management, regulatory compliance, and research documentation while working in a collaborative and professional research environment. If you are a motivated recent graduate or an early-career professional with a valid GCP certification and a strong interest in clinical research, we encourage you to apply.

Pay:

$20.00 - $24.00 per hour

Benefits:

401(k) Paid time off

Work Location:

In person