
Clinical Trial Research Coordinator
Are you passionate about making a difference in healthcare? Do you have experience in clinical research and a strong attention to detail? If so, Kaiser Permanente is seeking a dedicated and driven individual to join our team as a Clinical Trial Research Coordinator. In this role, you will play a crucial part in the development and execution of clinical trials, helping to bring new treatments and medications to our patients. We are looking for someone who is organized, proactive, and able to work independently. If you have a background in healthcare and a desire to contribute to groundbreaking research, we encourage you to apply for this exciting opportunity.
- Coordinate and manage all aspects of clinical trials, including recruitment and enrollment of participants, scheduling appointments, and maintaining accurate records.
- Communicate with research team members, healthcare providers, and study participants to ensure smooth execution of clinical trials.
- Keep up-to-date with all relevant research protocols, regulations, and ethical guidelines.
- Review and maintain study documents, such as informed consent forms, study protocols, and case report forms.
- Collaborate with the research team to develop and implement study procedures and ensure compliance with study protocols.
- Conduct data collection, entry, and analysis, and assist with the preparation of study reports.
- Ensure the safety and well-being of study participants by monitoring adverse events and following up with appropriate actions.
- Maintain strict confidentiality of all study-related information and ensure compliance with HIPAA regulations.
- Participate in training and professional development opportunities to enhance knowledge and skills related to clinical research.
- Serve as a liaison between the research team and external agencies, such as regulatory bodies and institutional review boards.
- Contribute to the development of new research initiatives and assist with grant writing and funding applications.
- Stay informed about current healthcare trends, advancements, and regulations to identify potential opportunities for research collaborations.
- Act as a mentor and resource for other members of the research team, providing guidance and support as needed.
- Represent Kaiser Permanente in a professional manner and maintain positive relationships with colleagues, study participants, and other stakeholders.
Bachelor's Degree In A Relevant Field Such As Nursing, Public Health, Or Clinical Research.
Minimum Of 2 Years Experience In Clinical Research Coordination, Preferably In A Healthcare Setting.
Knowledge Of Fda Regulations, Good Clinical Practice (Gcp) Guidelines, And Institutional Review Board (Irb) Processes.
Strong Organizational And Project Management Skills, With The Ability To Handle Multiple Tasks And Prioritize Effectively.
Excellent Communication And Interpersonal Skills, With The Ability To Work Collaboratively With A Diverse Team Of Healthcare Professionals And Research Participants.
Budgeting
Communication
Time Management
Attention to detail
Data Management
Teamwork
Regulatory compliance
Electronic
Patient Recruitment
Informed Consent
Study Coordination
Protocol Adherence
Communication
Conflict Resolution
Emotional Intelligence
Leadership
Time management
creativity
Teamwork
Adaptability
Problem-Solving
Decision-making
According to JobzMall, the average salary range for a Clinical Trial Research Coordinator in Oakland, CA, USA is $55,000 - $90,000 per year. This range can vary depending on factors such as experience, qualifications, and the specific company or institution the coordinator is working for.
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Kaiser Permanente is an American integrated managed care consortium, based in Oakland, California, United States, founded in 1945 by industrialist Henry J. Kaiser and physician Sidney Garfield.

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