Clinical Research Coordinator II - Tacoma WA

Iterative Health•Tacoma, WA

About The Position

As a Clinical Research Coordinator II (CRC II) at Iterative Health, you will independently coordinate daily clinical-trial activities and help ensure compliance with study protocols, regulatory standards, and patient-safety guidelines. You will manage complex studies with minimal oversight, working closely with patients, investigators, sponsors, CROs, and internal teams to support high-quality study execution and successful enrollment. The role spans study start-up through closeout and includes coordinating study visits, recruiting and retaining participants, conducting protocol-required assessments and procedures, processing specimens, maintaining study records and data, and supporting monitoring visits, audits, and inspections. You will also help maintain onsite study supplies and equipment, contribute to process improvements, and may support onboarding and mentoring junior research staff.

Requirements

Associate’s or Bachelor’s degree in a scientific, healthcare, or related discipline.
3–5 years of clinical research or healthcare experience.
Strong organizational skills and attention to detail.
Ability to manage competing priorities in a fast-paced environment.
Ability to read, interpret, and apply research protocols and clinic policies.
Proficiency with CTMS, EDC systems, and standard office software applications.
Ability to sit, stand, and move throughout clinical and office environments for extended periods.
Ability to lift and move up to 25 pounds as needed.

Nice To Haves

Experience in gastroenterology, hepatology, or cardiology therapeutic areas.
CCRC® (Certified Clinical Research Coordinator), CCRP® (Certified Clinical Research Professional), or equivalent clinical research certification.
Familiarity with CTMS or EDC systems.

Responsibilities

Independently coordinate and manage industry-sponsored clinical trials from study start-up through closeout with minimal supervision.
Manage complex study visit schedules and protocol-related activities while adhering to study timelines and requirements.
Lead patient recruitment and retention efforts, including chart review, patient outreach, informed consent discussions, and enrollment tracking.
Conduct protocol-required patient visits and assessments in accordance with study protocols, GCP guidelines, and site SOPs.
Perform protocol-required clinical procedures, including vital signs, ECGs, specimen collection, investigational product accountability, and phlebotomy, as permitted by applicable regulations, training, and organizational policy.
Process laboratory specimens and prepare shipments in accordance with protocol requirements and applicable IATA regulations.
Maintain accurate, complete, and timely study documentation, including source records, informed consent forms, CTMS updates, and case report forms.
Enter high-quality study data and resolve data queries in a timely manner according to sponsor expectations and established timelines.
Serve as a primary point of contact for study participants throughout their participation.
Communicate with sponsors, CROs, investigators, site leadership, and internal teams to proactively resolve study-related issues.
Prepare for and support sponsor, CRO, and regulatory monitoring visits, audits, and inspections.
Review safety reports and ensure timely investigator review and documentation.
Maintain the inventory and organization of onsite study equipment, supplies, and investigational products.
Contribute to process improvement initiatives that enhance site performance, operational efficiency, and patient experience.
Protect human research participants in compliance with federal regulations, GCP, HIPAA, and institutional policies.
Maintain compliance with site SOPs, privacy standards, and research protocols.
May support onboarding and mentorship of junior research staff and coordinators.
Perform job-related duties as requested.