Clinical Research Associate (Senior)

Join a team advancing clinical research as a Clinical Research Associate (CRA). Responsibilities Include Leading and executing site monitoring visits in accordance with GCP/ICH guidelinesBuilding strong relationships with investigative sites to enhance performance and engagementEnsuring protocol compliance, data integrity, and high-quality study executionIdentifying risks, resolving issues, and escalating when necessaryManaging study progress, including regulatory approvals, enrollment, and data qualityMaintaining accurate documentation and supporting inspection readinessCollaborating with cross-functional teams for successful study delivery Qualifications And Skills Bachelor’s degree in life sciences, healthcare, or related field (or equivalent experience)At least 1.5 years of on-site monitoring experienceStrong knowledge of GCP, ICH, and regulatory standardsExcellent communication, problem-solving, and organizational skillsAbility to manage multiple priorities in a fast-paced environment Benefits Of The Role Impact on clinical research and patient outcomesCollaborative and experienced teamsOpportunities for growth and career developmentDynamic work environment where contributions matter