Senior Clinical Research Coordinator
Providence St. Patrick Hospital
Anchorage, AKFull-time
71K–90K a year
Behavioral Health Market Context
Apply Nowvia JobzMall
Job Description
s, ensuring that they are conducted in compliance with all relevant regulations and protocols. You will work closely with physicians, nurses, and other healthcare professionals to ensure the smooth and efficient execution of research projects.To be successful in this role, you must have a Bachelor's degree in a health-related field and at least 3 years of experience in clinical research coordination. You should also have excellent communication and interpersonal skills, as well as a strong understanding of regulatory requirements and good clinical practices.If you are a self-motivated and driven individual with a strong commitment to patient care and advancing medical knowledge, we encourage you to apply for this exciting opportunity. Join us in making a difference in the lives of patients and contributing to the future of healthcare at Providence St. Patrick Hospital.
Manage and coordinate all aspects of clinical trials and studies in accordance with protocols and regulatory requirements.
Ensure compliance with all relevant regulations, guidelines, and ethical standards.
Work closely with physicians, nurses, and other healthcare professionals to ensure the smooth and efficient execution of research projects.
Develop and maintain study timelines, budgets, and resources.
Monitor and track study progress and report any deviations or issues to the appropriate parties.
Coordinate and participate in the recruitment and screening of study participants.
Collect and maintain accurate and complete study data and documentation.
Maintain study records and files in accordance with regulatory requirements.
Communicate with study sponsors, investigators, and study team members to provide updates and ensure study objectives are met.
Develop and implement strategies to improve patient recruitment and retention.
Train and mentor junior research coordinators and provide guidance and support as needed.
Stay current with industry trends, regulations, and best practices in clinical research.
Facilitate and participate in study-related meetings, conference calls, and presentations.
Collaborate with various departments and stakeholders to ensure seamless execution of research projects.
Uphold a high level of confidentiality and ethical standards in all aspects of work.
Providence St. Patrick Hospital 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.
Manage and coordinate all aspects of clinical trials and studies in accordance with protocols and regulatory requirements.
Ensure compliance with all relevant regulations, guidelines, and ethical standards.
Work closely with physicians, nurses, and other healthcare professionals to ensure the smooth and efficient execution of research projects.
Develop and maintain study timelines, budgets, and resources.
Monitor and track study progress and report any deviations or issues to the appropriate parties.
Coordinate and participate in the recruitment and screening of study participants.
Collect and maintain accurate and complete study data and documentation.
Maintain study records and files in accordance with regulatory requirements.
Communicate with study sponsors, investigators, and study team members to provide updates and ensure study objectives are met.
Develop and implement strategies to improve patient recruitment and retention.
Train and mentor junior research coordinators and provide guidance and support as needed.
Stay current with industry trends, regulations, and best practices in clinical research.
Facilitate and participate in study-related meetings, conference calls, and presentations.
Collaborate with various departments and stakeholders to ensure seamless execution of research projects.
Uphold a high level of confidentiality and ethical standards in all aspects of work.
Providence St. Patrick Hospital 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
- •You will work closely with physicians, nurses, and other healthcare professionals to ensure the smooth and efficient execution of research projects.To be successful in this role, you must have a Bachelor's degree in a health-related field and at least 3 years of experience in clinical research coordination
- •You should also have excellent communication and interpersonal skills, as well as a strong understanding of regulatory requirements and good clinical practices.If you are a self-motivated and driven individual with a strong commitment to patient care and advancing medical knowledge, we encourage you to apply for this exciting opportunity
Benefits
Responsibilities
- •If so, we have an exciting opportunity for you to join our team as a Senior Clinical Research Coordinator at Providence St. Patrick Hospital.As a Senior Clinical Research Coordinator, you will play a crucial role in managing and coordinating clinical trials and studies, ensuring that they are conducted in compliance with all relevant regulations and protocols
- •Manage and coordinate all aspects of clinical trials and studies in accordance with protocols and regulatory requirements
- •Ensure compliance with all relevant regulations, guidelines, and ethical standards
- •Work closely with physicians, nurses, and other healthcare professionals to ensure the smooth and efficient execution of research projects
- •Develop and maintain study timelines, budgets, and resources
- •Monitor and track study progress and report any deviations or issues to the appropriate parties
- •Coordinate and participate in the recruitment and screening of study participants
- •Collect and maintain accurate and complete study data and documentation
- •Maintain study records and files in accordance with regulatory requirements
- •Communicate with study sponsors, investigators, and study team members to provide updates and ensure study objectives are met
- •Develop and implement strategies to improve patient recruitment and retention
- •Train and mentor junior research coordinators and provide guidance and support as needed
- •Stay current with industry trends, regulations, and best practices in clinical research
- •Facilitate and participate in study-related meetings, conference calls, and presentations
- •Collaborate with various departments and stakeholders to ensure seamless execution of research projects
- •Uphold a high level of confidentiality and ethical standards in all aspects of work
More Jobs
- Clinical Director - BCBA at Discover Hope Behavioral Solutions Fremont, CAat Discover Hope Behavioral Solutions
- Speech Therapist-9at Raze Therapeutics
- RBT Applied Behavior Analyst Therapistat Guiding River ABA
- ABA Therapist at Kids First Services Queens, NYat Kids First Services
- Behavior Technician - Working with Childrenat Attain ABA Therapy
- IM Research Program Coordinator - Clinical Trials Opsat Texas Tech University Health Sciences Center
- School Speech and Language Pathologist | Marana, Arizonaat ProCare Therapy
- RBT/Behavioral Tech – Clinic ABA, Paid Trainingat Behavioral Innovations
- Director of Clinical Research and Real World Evidenceat Virta Health
- Behavior Technicianat Imagination ABA Therapy