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Clinical Research Coordinator

2 months ago

Inglewood, California, United States ALLIANCE CLINICAL LLC Full time
Job Overview

ABOUT US:

Alliance Clinical LLC is committed to fostering medical advancements and innovative healing solutions through pioneering research, dedicated patient support, and robust management practices. Our proactive management team and clinical personnel are focused on conducting efficient trials that expedite the availability of transformative medications; our research team possesses extensive experience in executing Phase 1-4 clinical investigations. Each project is aimed at combating illness and enhancing the quality of life for individuals.

WORK ENVIRONMENT: Onsite

POSITION SUMMARY: The Clinical Research Assistant, under the guidance and continuous oversight of the Principal Investigator, plays a crucial role in the daily operations of clinical research initiatives.

KEY RESPONSIBILITIES: The following duties are essential to this role. Additional responsibilities may be assigned:

  1. Adhere to all organizational policies, procedures, and ethical standards.
  2. Maintain strict confidentiality and compliance with regulatory standards.
  3. Engage effectively and courteously with study participants.
  4. Gather patient medical histories and health conditions.
  5. Facilitate the collection of Informed Consent Forms.
  6. Manage study drug distribution and accountability.
  7. Collect and assess concomitant medications.
  8. Review medical records for compliance purposes.
  9. Conduct assessments for Adverse Events (A/E) and Serious Adverse Events (SAE).
  10. Perform EKGs, vital signs monitoring, and protocol-specific procedures.
  11. Collect, process, and dispatch biological samples such as blood, urine, and tissue.
  12. Assist in maintaining regulatory documentation for the office site.
  13. Ensure the accuracy of collected data.
  14. Support the documentation of temperature records for investigational products stored on-site.
  15. Work directly with patients who have tested positive for COVID-19.
  16. Oversee all necessary study initiation documentation, training, and timelines for assigned protocols.
  17. Fulfill all study protocol requirements and deadlines.

QUALIFICATIONS: To excel in this position, candidates must demonstrate the ability to perform each essential duty effectively. The qualifications listed below are representative of the knowledge, skills, and abilities required. Reasonable accommodations may be made to enable individuals with disabilities to perform essential functions.

EDUCATION AND EXPERIENCE:

  1. Bachelor's degree in Biology or a related discipline is required.
  2. Proficiency in computer skills and data collection; expertise in Microsoft Office is essential.
  3. Willingness to travel between site locations for clinical research activities is required.
  4. Prior research experience is preferred but not mandatory.
  5. Certification as a Medical Assistant is preferred.
  6. 1-2 years of Phlebotomy experience is required.
  7. Knowledge of EKG and other technical skills as dictated by protocol is preferred.
  8. Familiarity with medical terminology is advantageous.
  9. Ability to operate with minimal supervision.
  10. Strong problem-solving skills and a quick learning aptitude are essential.
  11. Excellent verbal and written communication skills are a must.
  12. Outstanding customer service abilities with both internal and external stakeholders.
  13. A proven capacity to manage multiple tasks in a dynamic environment.

BENEFITS:

401k Plan with employer matching

Medical, Dental, and Vision coverage

Paid Time Off (PTO) and holidays