Clinical Research Coordinator

1 week 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 our clinical trials, ensuring the timely and accurate delivery of tasks.

Key Responsibilities
  • Patient Recruitment and Enrollment: Lead the recruitment and enrollment of patients for our 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 the highest level of data quality.
  • Protocol Management and Adherence: Ensure that all clinical trials are conducted in accordance with established protocols and regulatory requirements.
  • Data Management and Query Resolution: Maintain high data quality standards and resolve any queries or issues that may arise during the trial.
  • 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 and Organizational Skills: The ability to maintain accurate records and ensure that all tasks are completed on time.
  • Excellent Communication Abilities: Strong verbal and written communication skills, with the ability to build relationships with patients, investigators, and team members.
  • Proficiency in Data Management and Query Resolution: Experience with data management systems and the ability to resolve queries and issues.
  • Experience with Clinical Trial Protocols and Regulatory Requirements: Knowledge of clinical trial protocols and regulatory requirements, with the ability to ensure compliance.
  • Ability to Perform Technical Procedures: The ability to perform technical procedures, including remote phlebotomy and lab processing.
  • Strong Interpersonal Skills: The ability to build relationships with patients, investigators, and team members.
  • Adaptability and Problem-Solving Skills: The ability to adapt to changing circumstances and resolve problems effectively.
  • Commitment to Patient Education and Informed Consent: A commitment to patient education and informed consent, with the ability to ensure that patients are fully informed and involved in the trial.
  • Expertise in Using GSuite/Sheets and Electronic Medical Records: Experience with GSuite/Sheets and electronic medical records, with the ability to create and maintain project timelines and status reports.
  • Ability to Create and Maintain Project Timelines and Status Reports: The ability to create and maintain project timelines and status reports, with the ability to track progress and identify areas for improvement.
  • Experience in or Willingness to Learn About Study Medication Dispensing and Prescription Management: Experience with study medication dispensing and prescription management, or a willingness to learn.
  • Strong Sense of Ethics and Commitment to Regulatory Compliance: A strong sense of ethics and a commitment to regulatory compliance, with the ability to ensure that all clinical trials are conducted in accordance with established protocols and regulatory requirements.
  • Teamwork Mentality and Self-Awareness: A teamwork mentality and self-awareness, with the ability to work effectively with others and identify areas for personal growth and development.
  • Empathy and Dedication to Creating an Exceptional Patient and Provider Experience: Empathy and a dedication to creating an exceptional patient and provider experience, with the ability to ensure that patients are fully informed and involved in the trial.
Preferred Qualifications
  • Bachelor's Degree in a Related Field: A bachelor's degree in a related field, such as nursing, life sciences, or public health.
  • Previous Experience in Clinical Research Coordination: Previous experience in clinical research coordination, with a strong understanding of clinical trial protocols and regulatory requirements.
  • Certification as a Clinical Research Coordinator (CCRC): Certification as a clinical research coordinator (CCRC), with a strong understanding of clinical trial protocols and regulatory requirements.
Benefits
  • Premium Blue Shield Platinum PPO & HMO Plans: Premium Blue Shield Platinum PPO & HMO plans, with up to 80% coverage.
  • Full Suite: Medical, Dental, Vision, Life Insurance: A full suite of medical, dental, vision, and life insurance benefits.
  • Best-in-class 401K Options: Best-in-class 401K options, with a strong focus on employee retirement savings.
  • Flexible Vacation/Time-Off Policies: Flexible vacation/time-off policies, with a strong focus on work-life balance.
  • Liquidity of Options Whenever Available: Liquidity of options whenever available, with a strong focus on employee stock ownership.
  • Extended Options Exercise Window for Loyal Employees: An extended options exercise window for loyal employees, with a strong focus on employee retention.

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