Top 1 Senior clinical research coordinator Jobs in Dayton Oh

Senior Clinical Research Coordinator
Iterative Health —Dayton, OH
- 5 years
- HIPAA
- Office
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Senior Clinical Research Coordinator
Iterative Health —Dayton, OH
CCRC® — Certified Clinical Research Coordinator or CCRP® — Certified Clinical Research Professional or equivalent clinical research certification strongly…
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Document site progress and escalate risks or issues to the clinical team. Resolve data queries and drive timely, high-quality data entry.
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Senior Clinical Research Coordinator

Iterative Health -
Dayton, OH

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Job Details

Qualifications

Phlebotomy specimen handling
ECG equipment
Clinical laboratory experience
Blood pressure monitors

Full Job Description

Iterative Health is a healthcare technology and services company powering the acceleration of clinical research to transform patient outcomes.

We built a leading performance-driven network of 100+ sites across the US, Europe, India, and Australia, conducting research directly in the communities where care is delivered across gastrointestinal, hepatology, obesity, and cardiology. By combining deep clinical trial expertise with cutting-edge AI, we connect sponsors' scientific ambitions with high-performing research teams that expedite and expand access to novel therapeutics for patients in need. Today, Iterative Health is headquartered in Cambridge, Massachusetts, and New York City with 250+ employees world-wide.

As a Senior Clinical Research Coordinator (Sr. CRC) at Iterative Health you will serve as a key team member within the clinical research site, overseeing complex studies while supporting staff development, operational performance, and high-quality patient experiences.

This role combines hands-on study coordination with mentorship, process improvement, and cross-functional collaboration to help drive successful study execution, enrollment performance, and regulatory compliance.

Where You'll Drive Impact

Lead and independently manage complex industry-sponsored clinical trials from study start-up through closeout
Coordinate complex study visit schedules and protocol-related activities while ensuring compliance with study timelines and regulatory requirements
Lead patient recruitment and retention initiatives to support enrollment performance and patient engagement goals
Mentor and support junior coordinators and research staff on clinical trial processes, patient interactions, sponsor communication, and operational best practices
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 and timely study documentation including source records, informed consent forms, CTMS updates, and case report forms
Ensure high-quality data entry and timely resolution of sponsor and CRO data queries
Serve as a primary point of contact for study participants, sponsors, CROs, investigators, and site leadership
Build strong relationships with investigators, referring physicians, sponsors, and CRO partners to support study success and patient engagement
Prepare for and support sponsor, CRO, and regulatory monitoring visits, audits, and inspections
Review safety reports and ensure timely investigator review and documentation
Maintain inventory and oversight of study equipment, supplies, and investigational products onsite
Assess operational challenges, identify solutions, and recommend process improvements to enhance site performance and protocol adherence
Support site performance initiatives related to enrollment, screen failures, protocol compliance, and patient retention
Contribute to onboarding, training, and mentorship activities for new research staff
Support the protection of human research participants in compliance with federal regulations, GCP, HIPAA, and institutional policies
Maintain compliance with all site SOPs, privacy standards, and research protocols
Perform job related duties as requested

What You Bring to the Team

Associate's or Bachelor's degree in a scientific, healthcare, or related discipline required
5+ years of clinical research or healthcare experience required
Must be able to perform blood draw, medical review (blood pressure, height, weight etc.) & EKGs, as applicable by state law
CCRC® — Certified Clinical Research Coordinator or CCRP® — Certified Clinical Research Professional or equivalent clinical research certification strongly preferred
Strong understanding of GCP, FDA regulations, and clinical research operations
Demonstrated ability to independently manage complex clinical trials and competing priorities
Experience mentoring or supporting junior research staff
Strong written and verbal communication skills
Strong organizational skills, attention to detail, and problem-solving capabilities
Proficiency with CTMS, EDC systems, and standard office software applications

Physical Requirements

Ability to sit, stand, and move throughout clinical and office environments for extended periods of time
Ability to lift and move up to 25 pounds as needed

At Iterative Health, we're actively working towards creating an environment that is representative of the diversity of patients our technology serves. We are focused on building an equitable and inclusive culture, and by extension, hiring process. If you require any accommodations to make the application process or interviewing experience more accessible to you, please contact [email protected].

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Senior Clinical Research Coordinator

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