Clinical Research Coordinator II, Oncology

Syneos Health

. Review assigned protocols and related documentation for accuracy, feasibility, timing, and resources .

Posted 9/23/2026part-timeRemote • SpainJuniorWebsite

Core Competencies

Role fit

Core Competencies

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Demonstrates expertise in managing clinical trials, ensuring compliance with Good Clinical Practices, and coordinating study logistics. Proficient in data collection, regulatory documentation, and participant safety management.

Highest-signal resume keywords

Clinical Research CertificationGood Clinical Practices (GCP)Clinical Trial EDC SoftwareSOP WritingProject Coordination

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Clinical Trial ManagementData CollectionCase Report Form (CRF) CompletionAdverse Event ReportingRegulatory Documentation

Soft Skills

Problem SolvingTime ManagementInterpersonal CommunicationDetail-OrientedMultitasking

Tools & Technologies

Microsoft WordMicrosoft ExcelMicrosoft PowerPoint

Certifications & Qualifications

Registered NurseBachelor of Science Degree

Industry Keywords

ICH GuidelinesClinical ResearchStudy Start-Up ActivitiesParticipant SafetyQuality Control

About the role

Key responsibilities & impact

Review assigned protocols and related documentation for accuracy, feasibility, timing, and resources
Prepare and maintain Investigator Site Files and/or Trial Master Files
Participate in timelines, start-up meetings, Investigator Meetings, Site Initiation Visits, and sponsor discussions
Coordinate study start-up activities, clinic logistics, schedules, team training, source documents, CRFs, laboratory workbooks, staffing, and study supplies
Confirm regulatory and contractual documentation before study start
Support the Principal Investigator with delegation logs, daily task management, visit calendars, and monitor visits
Advertise, recruit, and screen potential study participants
Perform study activities in accordance with Good Clinical Practices
Manage multiple clinical trials simultaneously and protect participant safety
Collect and enter study data; complete Case Report Forms and submit data on time
Coordinate screening and assist with informed consent
Facilitate study-data audits and respond to auditor data-clarification inquiries
Coordinate clinic visits, including admission, dosing, randomization, discharge, and follow-up
Provide on-call support when applicable
Screen eligibility and oversee, coordinate, and/or perform study-drug administration as delegated
Monitor study activities for compliance with protocol, SOPs, and applicable regulations
Manage adverse-event reporting, study logs, trackers, quality control, and monitor findings
Coordinate QC, monitor, CRF, and other findings through resolution
Oversee study close-out documentation, deviation reporting, CRF completion, TMF updates, logs, supply returns, IRB reports, and archiving
Monitor participant compliance and escalate participant or study issues
Prepare for and participate in sponsor, monitor, and QA audits
Provide timely project-status updates to Project Managers and sponsors
Collaborate on process improvement, SOP creation/revision, meetings, and company initiatives
Coordinate and perform regulatory activities, including protocol, consent, amendment, and yearly renewal submissions when requested
Report trial-related adverse events and maintain study files
Perform other assigned work-related duties

Requirements

What you’ll need

Registered Nurse and/or University Degree such as Bachelor of Science Degree required
Clinical Research certification preferred
Minimum of 1 year of experience in clinical research required; 2+ years preferred
Good knowledge of regulations, ICH GCP, privacy, and applicable guidelines
Problem solving, planning, and evaluation skills
Good time management; detail-oriented and able to multitask
Good interpersonal and communication skills with a team focus
Knowledge of SOP writing
Ability to anticipate problems and provide timely solutions
Ability to coordinate multiple clinical research projects with competing deadlines
Proficiency in Word, Excel, and PowerPoint
Proficiency in clinical trial EDC software preferred
Ability to accommodate a flexible schedule, including days, afternoons, nights, and weekends
Travel up to 100%
Equivalent experience, skills, and/or education may be considered

Benefits

Comp & perks

Temporary part-time employment
Remote (Pre-Approved) designation
Flexible schedule accommodating days, afternoons, nights, and weekends