Oncology Clinical Site Monitor
Are you passionate about making a difference in the field of oncology? Do you have experience in clinical site monitoring? If so, Atrium Health is seeking a dedicated and detail-oriented Oncology Clinical Site Monitor to join our team. In this role, you will play a pivotal role in ensuring the success of our oncology clinical trials and contribute to advancing cancer care. We are looking for a highly motivated individual with a strong background in oncology research and a commitment to upholding ethical standards. Join us in our mission to improve the lives of cancer patients and make a positive impact on the healthcare industry.
- Conduct regular site visits to monitor and evaluate the progress of oncology clinical trials.
- Ensure compliance with study protocols, regulations, and institutional policies.
- Review and verify accuracy of study data and source documents.
- Identify and address any issues or discrepancies found during site visits.
- Communicate effectively with study coordinators, investigators, and other healthcare professionals.
- Maintain accurate and thorough documentation of site visits and findings.
- Collaborate with the study team to develop and implement strategies for improving study performance.
- Assist with the development and review of study protocols and informed consent documents.
- Stay up-to-date on industry trends and regulatory changes related to oncology clinical trials.
- Uphold ethical standards and promote patient safety throughout the clinical trial process.
- Provide guidance and support to site staff on study procedures and requirements.
- Assist with site selection and qualification processes.
- Participate in study meetings and trainings as needed.
- Maintain confidentiality of study data and patient information.
- Contribute to the overall success of the oncology clinical trials and the advancement of cancer care.
Bachelor's Degree In Nursing Or A Related Healthcare Field, With A Strong Understanding Of Oncology Treatments And Protocols.
Minimum Of 3-5 Years Of Experience In Clinical Research, Preferably In Oncology Clinical Trials.
Knowledge Of Fda Regulations And Good Clinical Practice (Gcp) Guidelines For Clinical Trials.
Excellent Communication And Interpersonal Skills, With The Ability To Effectively Communicate With Physicians, Study Coordinators, And Other Healthcare Professionals.
Strong Attention To Detail And Ability To Manage Multiple Tasks And Priorities, With A Focus On Ensuring Accuracy And Compliance In Data Collection And Documentation.
Communication Skills
Data Analysis
Time Management
Clinical Research
Attention to detail
Risk assessment
Regulatory compliance
Problem-Solving
Patient Recruitment
Protocol Compliance
Oncology Knowledge
Communication
Conflict Resolution
Leadership
Time management
Organization
Critical thinking
Teamwork
Adaptability
Problem-Solving
Empathy
According to JobzMall, the average salary range for a Oncology Clinical Site Monitor in Charlotte, NC, USA is $65,000 - $90,000 per year. However, this can vary depending on factors such as years of experience, level of education, and specific job responsibilities.
Apply with Video Cover Letter Add a warm greeting to your application and stand out!
Atrium Health, formerly Carolinas HealthCare System, is a not for profit hospital network which operates hospitals, freestanding emergency departments, urgent care centers, and medical practices in the American states of North Carolina, South Carolina and Georgia.
Get interviewed today!
JobzMall is the world‘ s largest video talent marketplace.It‘s ultrafast, fun, and human.
Get Started