On-Site Clinical Research Coordinator II | Trial Operations

Kelly Services; Spokane (WA); Sur place; USD 52 000 - 78 000; Plein temps

Avantages offerts par ce poste

Medical benefits

Dental & Vision

Retirement plan

Transit benefit

Paid holidays

Paid sick leave

Résumé du poste

Kelly Science & Clinical seeks a Clinical Research Coordinator II for a Temp-to-Hire role in Spokane, WA. You will independently coordinate trials from startup through close-out, serving as a primary operational contact for participants, investigators, sponsors, CROs, and internal teams, ensuring protocol adherence and data integrity.

Responsibilities include coordinating visits, tracking milestones, maintaining audit-ready source docs, and supporting regulatory processes.

Qualifications

• At least 18 months of direct clinical trial experience in a related role.
• Experience with participant visits, source documentation, EDC data entry, monitoring visits, and protocol compliance.
• Must have or obtain CITI and GCP training before study delegation.
• Strong knowledge of trial operations, informed consent, HIPAA, GCP, ICH guidelines, and source-documentation standards.
• Ability to manage multiple studies, deadlines, participant needs, and sponsor expectations with limited supervision.
• Strong communication, organization, prioritization, and attention-to-detail skills.
• On-site work requirement in Spokane, Washington.

Responsabilités

• Coordinate day-to-day clinical trial activities from startup through close-out.
• Serve as the primary operational contact for study participants, investigators, sponsors, CROs, monitors, and internal teams.
• Prepare for and conduct participant visits per protocol and regulatory requirements.
• Track eligibility, enrollment, visit windows, milestones, and follow-up tasks.
• Maintain accurate, audit-ready source documentation (ALCOA principles).
• Enter data into EDC and sponsor systems; reconcile data and support database-lock readiness.
• Escalate protocol deviations, adverse events, safety concerns, and data integrity issues.
• Support informed-consent processes under PI oversight and educate participants and caregivers.
• Coordinate study supplies, lab kits, specimen processing, and protocol assessments.
• Collaborate with regulatory staff on start-up, amendments, continuing reviews, and safety reporting.

Connaissances

Clinical trials

GCP compliance

Data entry

Communication

Organization

Detail oriented

On-site work

Formation

Bachelor’s degree

CCRC/CRRP certification

Phlebotomy cert/RN/LPN/MA

Outils

EDC systems

CTMS

Sponsor portals

EMR systems

Microsoft Office

Description du poste

Kelly Science & Clinical seeks a Clinical Research Coordinator II for a Temp-to-Hire role in Spokane, WA. You will independently coordinate trials from startup through close-out, serving as a primary operational contact for participants, investigators, sponsors, CROs, and internal teams, ensuring protocol adherence and data integrity.

Responsibilities include coordinating visits, tracking milestones, maintaining audit-ready source docs, and supporting regulatory processes.