Lead cross‑functional project teams to deliver Phase IV clinical trials, ensuring quality, cost, and schedule targets while managing stakeholder expectations and regulatory compliance.
Responsibilities
Serve as primary contact between sponsor and organization at project level
Ensure escalation pathways adhered to internally and externally
Define responsibilities and communication pathways for secondary project leads
Accountable for overall delivery of cross‑functional project (time, cost, quality)
Lead a high-performing team of clinical application analysts and technical specialists to implement, support, and enhance clinical research application suite, primarily Epic Research and CTMS, within Stanford Medicine.
Compensation
Base Pay Scale: Generally starting at $79.21 - $104.97 per hour
Responsibilities
Lead, coach, and mentor a team of application analysts
Own end-to-end service delivery and SLA performance for Epic Research, CTMS, and related research applications
Lead day-to-day clinical research operations, ensuring study conduct aligns with START standards, applicable regulatory requirements, and high-quality patient care.
Compensation
competitive compensation package—based on experience—along with comprehensive benefits designed to support you both personally and professionally
Responsibilities
Provide proactive leadership and day-to-day oversight to the Clinical Research Coordinator team
Train, coach, and assess staff competency for assigned job responsibilities
Ensure timely and accurate study documentation and communication with monitors and auditors
Maintain compliance with GCP, applicable SOPs, and required training documentation
Support study acquisition and activation in partnership with Shared Services
Requirements
Associate’s degree in health administration, nursing or other related field
Nice to have: Bachelor's/Master’s degree in health administration, nursing or other related field
Nice to have: specialty certification in research or associated field
Nice to have: conference attendance, poster presentations, conference presenter/coordinator
Lead day-to-day clinical research operations, ensuring study conduct aligns with START standards, applicable regulatory requirements, and high-quality patient care.
Locations (2)
Grand Rapids, Michigan, United States
5800 Foremost Dr SE, Michigan, United States
Compensation
competitive compensation package—based on experience—along with comprehensive benefits designed to support you both personally and professionally
Responsibilities
Provide proactive leadership and day-to-day oversight to the Clinical Research Coordinator team
Train, coach, and assess staff competency for assigned job responsibilities
Ensure timely and accurate study documentation and communication with monitors and auditors
Maintain compliance with GCP, applicable SOPs, and required training documentation
Support study acquisition and activation in partnership with Shared Services
Manages the conduct, development, and promotion of clinical research at Saint Francis Medical Center.
Compensation
Expected pay for this position is $39.49 - $52.31/hour. Actual pay will be determined by experience, skills and internal equity. This is a Salaried position.
Responsibilities
Lead a Clinical Research team on a Phase I Clinical Oncology trial
Collaborate with interdisciplinary team on research
Shape future of oncology care
Assure compliance and prioritize clinical research activities
Provide oversight to clinical research at Saint Francis Medical Center and faculty of UICOMP
Requirements
Bachelor’s degree (scientific discipline)
Nice to have: Master’s degree
Nice to have: Oncology clinical trial experience
Nice to have: Current Research Certification (ACRP, Socra, HCCA, CIP, etc)
Nice to have: RN licensure or 5+ years clinical experience
Intermediate Clinical Research Nurse (CRN) advocates for patient safety and protocol integrity, adheres to patient care standards, and communicates effectively to ensure effective conduct of clinical trials and quality patient care.
Responsibilities
Advocates for patient safety and protocol integrity
Adheres to patient care standards
Communicates effectively to ensure effective conduct of clinical trials
Play a critical role in the successful execution of clinical trials by independently coordinating daily study activities and ensuring compliance with protocol requirements, regulatory standards, and patient safety guidelines.
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 ensuring adherence to study timelines and requirements
Lead patient recruitment and retention efforts including chart review, patient outreach, informed consent discussions, and enrollment tracking to support study enrollment goals
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
Requirements
Associate’s or Bachelor’s degree in a scientific, healthcare, or related discipline
Nice to have: gastroenterology
Nice to have: hepatology
Nice to have: cardiology
Nice to have: CCRC® — Certified Clinical Research Coordinator
The Clinical Trial Manager will oversee the day-to-day conduct of active clinical studies, ensuring compliance with GCP, FDA regulations, and HIPAA. The role involves study start-up, site oversight, regulatory management, and team leadership.
Responsibilities
Evaluate new studies with the Principal Investigator (PI)
Assess protocol feasibility, patient population, staffing, equipment, and space
Complete Sponsor and CRO feasibility questionnaires
Take part in pre-study and site qualification visits
Prepare and submit IRB applications, informed consent forms, amendments, continuing reviews, and safety reports
comprehensive benefit plans – including wellbeing support, retirement and financial protection benefits, and insurance offerings (medical, dental, vision, life and disability)
Clinical Research SupervisorNewSTART Center for Cancer Research · West Valley City, US
CTO Clinical Research Nurse - IntermediateNewUT Health San Antonio Staff Positions · San Antonio, US
Clinical Research Coordinator IINewIterative Health · Chesterfield, US