Travel Oncology Clinical Research Coordinator

Travel Oncology Clinical Research Coordinator (Temporary Assignment – Mobile, AL)Location: Mobile, ALEmployment Type: Full-Time / Temporary AssignmentAssignment Duration: 3–6 MonthsTravel Requirement: Relocation to assignment location for project durationPosition OverviewWe are seeking an experienced Travel Oncology Clinical Research Coordinator (CRC) for a temporary assignment supporting oncology clinical trial operations in Mobile, AL. This role is ideal for clinical research professionals who are open to traveling to a designated assignment location and remaining on-site for the full assignment duration of approximately 3–6 months.The Travel Oncology CRC will provide hands-on operational support to oncology research sites requiring additional coverage, study startup assistance, enrollment support, or interim staffing. Candidates should be comfortable temporarily relocating to the assignment area while working closely with local site teams, investigators, sponsors, and sponsors.Key ResponsibilitiesTemporarily relocate to Mobile for the duration of the assignment (approximately 3–6 months)Coordinate and manage oncology clinical trials from startup through closeoutSupport sites experiencing staffing gaps, increased enrollment, or high study volumeScreen, recruit, consent, and schedule study participantsCoordinate protocol-required visits, procedures, and follow-up appointmentsMaintain accurate source documentation, regulatory binders, and study recordsCollect, review, and enter study data into EDC systemsEnsure compliance with ICH-GCP guidelines, FDA regulations, sponsor requirements, and site SOPsAssist with monitoring visits, audits, and study startup activitiesTrack and report adverse events, protocol deviations, and study-related issuesCollaborate closely with investigators, research nurses, pharmacists, and sponsorsProvide workflow support and training to local site staff when neededQualificationsRequiredMinimum 2–3 years of clinical research coordination experienceMinimum 1–2 years of oncology clinical research experienceStrong knowledge of ICH-GCP, FDA regulations, and oncology protocolsExperience with EDC systems, CTMS platforms, and regulatory documentationWillingness to temporarily relocate to assignment locations for 3–6 month periodsStrong organizational, communication, and problem-solving skillsAbility to work independently and adapt quickly to new clinical environmentsPreferredBachelor’s degree in Life Sciences, Healthcare, Nursing, or related fieldACRP or SOCRA certification (CCRC, CCRP, or equivalent)Experience supporting Phase I–IV oncology studiesAcademic medical center or CRO experienceExperience with biospecimen collection and central lab processingWhat We OfferCompetitive compensationHousing assistance and travel reimbursementMedical, dental, and vision benefitsOpportunity to support leading oncology research programsExposure to innovative oncology therapies and clinical trialsWhy Join UsThis position offers the opportunity to make a direct impact on oncology research while working in a collaborative, patient-focused environment. If you enjoy project-based assignments, adapting to new teams, and contributing to cutting-edge cancer research, we encourage you to apply.