healthcare
Posted 1 hour agoSenior Clinical Research Coordinator - Southaven, MS
Southaven, United StatesOn-site
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Responsibilities
- 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
- 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
- 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
- Support the protection of human research participants in compliance with federal regulations, GCP, HIPAA, and institutional policies
- Perform job related duties as requested
Requirements
- By combining deep expertise in clinical trials with cutting-edge AI, we empower research teams and study sponsors to expand and expedite access to novel therapeutics for patients in need.
- 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.
- requirements and applicable IATA regulations
- Associate’s or Bachelor’s degree in a scientific, healthcare, or related discipline preferred
- Experience in [gastroenterology, hepatology, cardiology] therapeutic areas preferred
- CCRC® — Certified Clinical Research Coordinator or CCRP® — Certified Clinical Research Professional or equivalent clinical research certification preferred
- Strong understanding of GCP, FDA regulations, and clinical research operations
- Demonstrated ability to independently manage complex clinical trials and competing priorities •
- 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
Experience
- 5+ years of clinical research or healthcare experience •
Contact
- experience more accessible to you, please contact CandidateAccommodations@iterative.health.
Additional details
- Iterative Health is a healthcare technology and services company powering the acceleration of clinical research to transform patient outcomes.
- The Iterative Health Site Network is a premier network of 100+ clinical research sites across the US and Europe, accelerating the path to market for novel therapies.
- 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.
- Today, Iterative Health is headquartered in Cambridge, Massachusetts, and New York City with 250+ employees world-wide.
- At Iterative Health, you’ll have the opportunity to help shape the future of clinical research while working alongside a collaborative, mission-driven team.
- We believe research changes lives, and every team member plays a critical role in improving patient access to innovative therapies.
- 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.
- Serve as a primary point of contact for study participants, sponsors, CROs, investigators, and site leadership
- Contribute to onboarding, training, and mentorship activities for new research staff