Clinical Trial Research Coordinator
Oakland, CAFull-time
55K–90K a year
Behavioral Health Market Context
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Job Description
edications 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.
Kaiser Permanente is an Equal Opportunity Employer. We celebrate diversity and are committed to creating an inclusive environment for all employees. We do not discriminate based upon race, religion, color, national origin, sex, sexual orientation, gender identity, age, status as a protected veteran, status as an individual with a disability, or other applicable legally protected characteristics.
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.
Kaiser Permanente is an Equal Opportunity Employer. We celebrate diversity and are committed to creating an inclusive environment for all employees. We do not discriminate based upon race, religion, color, national origin, sex, sexual orientation, gender identity, age, status as a protected veteran, status as an individual with a disability, or other applicable legally protected characteristics.
Qualifications
Benefits
Responsibilities
- •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
- •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
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