Lead a team of Clinical Scientists and Medical Writers in Oncology Early Clinical Development at Roche. Focus on innovative trials and regulatory excellence in drug development.
About the role
- Clinical Research Coordinator managing clinical trials with oversight of research data and participant compliance at Emory University. Training and guiding staff while ensuring adherence to protocols and regulations.
Responsibilities
- Independently manages significant aspects of clinical trials
- Trains and provides guidance to staff
- Oversees data management for research projects
- Interfaces with research participants and resolves study protocol issues
- Authorizes purchases for supplies and equipment maintenance
- Determines strategies for promoting/recruiting research participants
- Periodically audits operations for compliance
- Monitors IRB submissions and responds to requests
- Interfaces with study sponsors and resolves study queries
- Provides leadership in recommending and implementing improvements
- Assists in developing grant proposals and protocols
- May perform phlebotomy, specimens collection, or diagnostics
Requirements
- High School Diploma or GED with 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) with 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
- Clinical research support
- In-person and potential remote work days
Job title
Job type
Experience level
Salary
Not specified
Degree requirement
Location requirements
Clinical Research Nurse enhancing pediatric oncology care at Monash Children's Hospital. Collaborating with medical staff and managing patient flow for effective cancer treatment.
Senior Clinical Trial Manager overseeing site management and monitoring for biopharmaceutical solutions organization. Responsible for clinical monitoring, patient safety, and regulatory compliance in South Africa.
Associate HR Partner supporting employee operations at CPS Clinical Research Units. Providing HR guidance and managing employee relations in a clinical environment with on - site presence.
Clinical Research Study Assistant involved in Alzheimer's disease research collecting samples and data. Participating in study protocols and maintaining participant interactions.
Oncology Clinical Research Coordinator at WVU managing clinical trials and ensuring protocol compliance. Collaborating with research staff and healthcare providers while advocating for ethical participant care.
Clinical Research Coordinator supporting clinical research for pediatric care at Shriners Children’s. Ensuring compliance with research protocols and collaborating with clinical teams in Pasadena.
Clinical Research Coordinator managing aspects of clinical trials at Winship Cancer Institute. Handling data management, participant interface, and overseeing trial compliance in Atlanta.
Feasibility Manager at Novo Nordisk optimizing clinical trials through data analysis and strategic partnerships across South Africa. Driving site selection and operational readiness for impactful clinical development.
Clinical Research Coordinator managing overall coordination and implementation of clinical trials. Collaborating with investigators to ensure compliance with study protocols and maintaining accurate subject records.