Clinical Research Coordinator supporting pediatric research initiatives at Shriners Children's in Pasadena. Ensuring compliance with protocols and managing research data collection.
About the role
- Clinical Research Coordinator independently managing key aspects of clinical trials. Overseeing data management and ensuring compliance with study protocols and regulations.
Responsibilities
- Independently manages significant and key aspects of a large clinical trial or all aspects of one or more small trials, or research projects.
- Trains and provides guidance to less experienced staff.
- Oversees data management for research projects.
- Interfaces with research participants and resolves issues related to study protocols.
- Authorizes purchases for supplies and equipment maintenance.
- Determines effective strategies for promoting/recruiting research participants and retaining participants in long term clinical trials.
- Periodically audits operations including laboratory procedures to ensure compliance with applicable regulations; provides leadership in identifying and implementing corrective actions/processes.
- Monitors IRB submissions and responds to requests and questions.
- Interfaces with study sponsors, monitors and reports SAEs; resolves study queries.
- Provides leadership in determining, recommending, and implementing improvements to policies/processes.
- Assists in developing grant proposals and protocols.
- With appropriate credentialing and training may perform phlebotomy, specimens collection or diagnostics.
- May perform some supervisory duties.
- Performs related approved responsibilities as required.
Requirements
- High School Diploma or GED and seven years of clinical research experience.
- Two years of college in a scientific, health related or business administration program and five years of clinical research experience.
- Licensed as a Practical Nurse (LPN) and four years of clinical research experience.
- Bachelor's degree in a scientific, health related or business administration program and three years clinical research experience.
- Master's degree, MD or PhD in a scientific, health related or business administration program and one year of clinical research experience.
- Certified Research Administrator (CRA) or Clinical Research Coordinator (CRC) preferred.
Benefits
- Health insurance
- Flexible work arrangements
- Professional development opportunities
Job title
Job type
Experience level
Salary
Not specified
Degree requirement
Location requirements
Associate Clinical Research Director providing medical expertise to clinical studies and supporting development activities in a global biopharmaceutical company. Collaborating with stakeholders to ensure optimal study execution.
Clinical Research Coordinator, Sr advancing federally funded and industry - sponsored neonatal and perinatal research at Duke. Overseeing regulatory compliance and mentoring research staff in a medical center.
Clinical Research Specialist collaborating with CRMS to oversee clinical studies in Japan. Responsible for managing relationships and ensuring compliance in clinical trials.
Clinical Research Coordinator managing screening, enrollment, and retention of study participants for USF. Ensuring quality of data and implementing research procedures under supervision.
Director, Global Clinical Scientist Lead at CSL Behring overseeing clinical development activities for a team of clinical scientists. Collaborating cross - functionally to drive strategic clinical programs.
Clinical Research Coordinator in Orthopaedic Sports Medicine at Mass General Brigham. Responsibilities include developing research hypotheses, data analysis, and patient enrollment for studies.
Senior Clinical Trial Manager leading global clinical trials for Disc Medicine. Focused on project management and vendor oversight within a hybrid work environment.
Manager overseeing Project Management team in Clinical Research at Sanford Health. Collaborating with Clinical Research Managers and guiding strategic research initiatives.
Overseeing and administering clinical research studies and managing study budgets for military health research. Coordinating project planning and ensuring compliance with regulatory requirements.