Senior Clinical Research Coordinator

OverviewThe Senior Clinical Research Coordinator is responsible for supporting the day-to-day execution and management of clinical research studies, including operational, regulatory, and patient-facing activities.This role involves collaboration with internal teams and external study stakeholders to ensure studies are conducted in compliance with protocol requirements, regulatory standards, and organizational procedures.The individual may also assist with training and mentoring junior team members while contributing to a professional, collaborative, and quality-focused environment.Key ResponsibilitiesCoordinate assigned clinical research studies from startup through closeoutSupport patient recruitment and enrollment initiativesCollaborate with internal teams on study operations and participant engagement strategiesEducate study participants and caregivers on study procedures and requirementsEnsure compliance with study protocols, regulatory guidelines, and operational proceduresMaintain accurate and audit-ready study documentation and recordsCoordinate and manage study visits according to protocol requirementsComplete and maintain source documentation in a timely and accurate mannerEnter and manage study data within electronic data capture systemsMaintain study materials and inventory to support trial executionParticipate in study meetings and site initiation activities as neededPerform protocol-related clinical procedures where applicableCommunicate study updates and findings with appropriate stakeholdersAssist with adverse event documentation and reporting processesMaintain study logs and essential trial documentationSupport audit readiness and ongoing compliance initiativesEnsure confidentiality and secure handling of participant and study dataAssist with training and mentorship of junior staff membersPerform additional responsibilities as neededRequired Skills & QualificationsPrior experience supporting multiple clinical research studies preferredAbility to work independently and collaboratively within a team settingStrong communication and interpersonal skillsStrong organizational and problem-solving abilitiesFamiliarity with medical terminology and clinical research processes preferredLeadership or mentoring experience preferredWillingness to travel occasionally to support operational needsEducation & ExperienceHigh school diploma or equivalent required; additional education or training preferred2–5 years of clinical research or related healthcare experience preferredRelevant certifications preferred where applicable