Current jobs related to Clinical Research Coordinator - Santa Monica, California - Maximus Health, Inc.


  • Santa Ana, California, United States Clemente Clinical Research Full time

    Job Title: Clinical Research Coordinator ManagerWe are seeking an experienced Clinical Research Coordinator Manager to join our team at Clemente Clinical Research. As a key member of our team, you will be responsible for overseeing our team of clinical research coordinators, working closely with renowned doctors and researchers, and coordinating and...


  • Santa Ana, California, United States Clemente Clinical Research Full time

    Job OverviewClemente Clinical Research is seeking an experienced Clinical Research Coordinator Manager to oversee our team of clinical research coordinators. As a key member of our team, you will work closely with renowned doctors and researchers to coordinate and attend monitor site visits and prepare site visit documentation.The ideal candidate will have...


  • Santa Monica, California, United States Ampcus Full time

    Job Title: Clinical Research Coordinator Job Summary: We are seeking a highly organized and detail-oriented Clinical Research Coordinator to join our team at Ampcus. The successful candidate will be responsible for the operational management of clinical research/trial/study activities from design, set up, conduct, through closeout. Key...


  • Santa Monica, California, United States Compu-Vision Consulting Full time

    Job Title: Clinical Research CoordinatorCompu-Vision Consulting is seeking a highly organized and detail-oriented Clinical Research Coordinator to join our team. As a key member of our research operations team, you will be responsible for the implementation of research activities for one or more studies.Key Responsibilities:Plan and organize necessary tasks...


  • Santa Monica, California, United States Providence Health & Services Full time

    Job SummaryThe Clinical Research Coordinator is responsible for overseeing the day-to-day functions of multiple clinical research studies. This role involves interfacing with the Principal Investigator, patients, sponsors, and the Institutional Review Board (IRB). The Coordinator ensures that all documentation is timely and accurate, working closely with the...


  • Santa Monica, California, United States Compu-Vision Consulting Full time

    Clinical Research Coordinator Job DescriptionCompu-Vision Consulting is seeking a highly organized and detail-oriented Clinical Research Coordinator to join our team. As a Clinical Research Coordinator, you will play a critical role in the operational management of clinical research/trial/study activities from design, set up, conduct, through closeout.Key...


  • Santa Monica, California, United States University of California Full time

    Job SummaryThe University of California seeks a highly skilled Senior Clinical Research Coordinator to play a critical role in the operational management of clinical research activities. This position requires a technical leader who can ensure the accurate, safe, and timely completion of study protocols and procedures.Key ResponsibilitiesImplement research...


  • Santa Barbara, California, United States Sansum Diabetes Research Institute Full time

    Job DescriptionJob Summary: We are seeking a highly motivated and detail-oriented Clinical Research Coordinator to join our team at the Sansum Diabetes Research Institute. The successful candidate will be responsible for coordinating and managing clinical research trials, ensuring the integrity and quality of the research process.Key...

  • Research Coordinator

    2 weeks ago


    Santa Monica, California, United States Compu-Vision Consulting Full time

    Clinical Research CoordinatorCompu-Vision Consulting is seeking a highly skilled Clinical Research Coordinator to contribute to the operational management of clinical research/trial/study activities from design, set up, conduct, through closeout.Key Responsibilities:Implement research activities for one or more studies, ensuring adherence to the study...


  • Santa Monica, California, United States Providence Service Full time

    Job Summary:The Clinical Research Coordinator is responsible for overseeing the day-to-day functions of multiple clinical research studies. This role involves interfacing with the Principal Investigator, patients, sponsors, and the Institutional Review Board (IRB) to ensure timely and accurate documentation and strict compliance to study protocols...


  • Santa Barbara, California, United States Sansum Diabetes Research Institute Full time

    Job SummaryWe are seeking a highly skilled and experienced Clinical Research Nurse Coordinator to join our team at the Sansum Diabetes Research Institute. The successful candidate will be responsible for coordinating and conducting clinical research studies, ensuring compliance with federal, state, and local regulations, and maintaining the highest standards...


  • Santa Monica, California, United States Maximus Health, Inc. Full time

    Job Title: Clinical Research CoordinatorMaximus Health, Inc. is seeking a highly skilled Clinical Research Coordinator to join our team. As a key member of our clinical trials team, you will play a crucial role in ensuring the successful execution of our research studies.Job SummaryThe Clinical Research Coordinator will be responsible for managing various...


  • Santa Monica, California, United States Providence Health & Service Full time

    About the RoleThe Clinical Research Nurse has a working knowledge of clinical research activities and is responsible for the coordination of clinical research protocols, ensuring compliance with federal regulations, good clinical practice (GCP), Institutional Review Board (IRB) guidelines, and department standard work.This role requires a strong...


  • Santa Monica, California, United States Providence Full time

    About the RoleWe are seeking a highly skilled Clinical Research Nurse to join our team at Providence. As a Clinical Research Nurse, you will play a critical role in the coordination of clinical research protocols, ensuring compliance with federal regulations, good clinical practice (GCP), and Institutional Review Board (IRB) guidelines.Key...


  • Santa Monica, California, United States Providence Health & Service Full time

    Job SummaryWe are seeking a highly skilled Clinical Research Nurse to join our team at Providence Saint John's Medical Foundation. As a Clinical Research Nurse, you will play a critical role in the coordination of clinical research protocols, ensuring compliance with federal regulations, good clinical practice (GCP), and Institutional Review Board (IRB)...


  • Santa Monica, California, United States Providence Full time

    Job SummaryWe are seeking a highly skilled Clinical Research Nurse to join our team at Providence. As a Clinical Research Nurse, you will play a critical role in the coordination of clinical research protocols, ensuring compliance with federal regulations, good clinical practice (GCP), and Institutional Review Board (IRB) guidelines.Key...


  • Santa Monica, California, United States Providence Full time

    About the RoleThe Clinical Research Nurse will be responsible for coordinating clinical research protocols, ensuring compliance with federal regulations, good clinical practice (GCP), and Institutional Review Board (IRB) guidelines. This role requires a working knowledge of clinical research activities and the ability to work within their scope of...


  • Santa Monica, California, United States Providence Full time

    Job SummaryProvidence is seeking a highly skilled Clinical Research Nurse to join our team. As a key member of our research team, you will be responsible for coordinating clinical research protocols, ensuring compliance with federal regulations, and providing exceptional patient care.Key ResponsibilitiesCoordinate clinical research protocols, ensuring...


  • Santa Monica, California, United States Providence Service Full time

    The Clinical Research Coordinator plays a vital role in overseeing the day-to-day functions of multiple clinical research studies at Providence Saint John's Medical Foundation. This position requires a strong understanding of patient-focused, whole-person care and a commitment to delivering exceptional results.Key Responsibilities:Oversee the day-to-day...


  • Santa Barbara, California, United States Sansum Diabetes Research Institute Full time

    Job SummaryThe Clinical Research Nurse Coordinator I will serve as a Registered Nurse on various clinical research studies, ensuring the integrity and quality of clinical trials are maintained and conducted in accordance with federal, state, local, Institutional Review Board (IRB), and organizational regulations.Key Responsibilities Work with the principal...

Clinical Research Coordinator

2 months ago


Santa Monica, California, United States Maximus Health, Inc. Full time
Job Summary

We are seeking a highly skilled Clinical Research Coordinator to join our team at Maximus Health, Inc. as a key member of our clinical trials team. The successful candidate will play a crucial role in the management and coordination of clinical trials, ensuring the timely and accurate delivery of tasks.

Key Responsibilities
  • Patient Recruitment and Enrollment: Lead the recruitment and enrollment of patients for clinical trials, ensuring that all necessary protocols are followed.
  • Clinical and Lab Procedures: Conduct clinical and lab procedures, including remote phlebotomy and lab processing, to ensure high-quality data.
  • Protocol Management and Adherence: Ensure that all clinical trials are conducted in accordance with established protocols and regulatory requirements.
  • Data Management and Quality: Maintain high data quality standards, ensuring that all data is accurate and complete.
  • Training and Mentoring: Train and mentor junior research staff to ensure that they have the necessary skills and knowledge to perform their roles effectively.
Requirements
  • Strong Attention to Detail: Possess strong attention to detail and organizational skills to ensure that all tasks are completed accurately and efficiently.
  • Excellent Communication Skills: Demonstrate excellent communication skills, both verbal and written, to effectively interact with patients, investigators, and team members.
  • Data Management and Query Resolution: Possess proficiency in data management and query resolution to ensure that all data is accurate and complete.
  • Clinical Trial Protocols and Regulatory Requirements: Have experience with or willingness to learn clinical trial protocols and regulatory requirements.
  • Technical Procedures: Possess the ability to perform technical procedures such as remote phlebotomy and lab processing.
  • Interpersonal Skills: Demonstrate strong interpersonal skills to build relationships with patients, investigators, and team members.
  • Adaptability and Problem-Solving: Possess adaptability and problem-solving skills to navigate the dynamic research environment.
  • Patient Education and Informed Consent: Demonstrate a commitment to patient education and the informed consent process.
  • GSuite/Sheets and Electronic Medical Records: Possess expertise in using GSuite/Sheets and Electronic Medical Records.
  • Project Timelines and Status Reports: Possess the ability to create and maintain project timelines and status reports.
  • Study Medication Dispensing and Prescription Management: Have experience in or willingness to learn about study medication dispensing and prescription management.
  • Regulatory Compliance: Demonstrate a strong sense of ethics and commitment to regulatory compliance.
  • Teamwork and Self-Awareness: Possess a teamwork mentality and self-awareness to effectively work with team members.
  • Empathy and Patient Experience: Demonstrate empathy and dedication to creating an exceptional patient and provider experience.
Preferred Qualifications
  • Bachelor's Degree in a Related Field: Possess a Bachelor's degree in a related field, such as Nursing, Life Sciences, or Public Health.
  • Previous Experience in Clinical Research Coordination: Have previous experience in clinical research coordination, preferably in a similar role.
  • Certification as a Clinical Research Coordinator: Possess certification as a Clinical Research Coordinator (CCRC).
Company Culture

At Maximus Health, Inc., we value intellectual diversity and celebrate individuality. We are committed to creating a work environment that is inclusive, respectful, and supportive of all employees. We believe that our employees are our greatest asset and are committed to providing them with the resources and opportunities they need to succeed.

Benefits
  • Premium Health Insurance: Offer premium health insurance plans, including Blue Shield Platinum PPO and HMO plans.
  • Full Suite of Benefits: Provide a full suite of benefits, including medical, dental, vision, and life insurance.
  • Best-in-Class 401K Options: Offer best-in-class 401K options to help employees save for their future.
  • Flexible Vacation/Time-Off Policies: Provide flexible vacation/time-off policies to ensure that employees have the time they need to recharge and pursue their interests.
  • Liquidity of Options: Offer liquidity of options to employees, allowing them to exercise their options at their convenience.
  • Extended Options Exercise Window: Provide an extended options exercise window for loyal employees, allowing them to exercise their options over a longer period of time.