Research Study Assistant

1 week ago

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

ABOUT US:

Alliance Clinical LLC is committed to pioneering advancements in medical science and therapeutic technologies through innovative research, dedicated patient support, and robust leadership. Our proactive management team and healthcare professionals are focused on expediting clinical trials to introduce transformative medications to the market more swiftly; our research personnel possess extensive hands-on experience in conducting Phase 1-4 clinical trials. Each project is aimed at combating diseases 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 vital role in the daily operations of clinical research initiatives.

KEY RESPONSIBILITIES: The following duties are essential. 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 current 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 with study protocols.
  9. Conduct assessments for Adverse Events (A/E) and Serious Adverse Events (SAE).
  10. Perform EKGs, monitor vital signs, and execute protocol-specific procedures.
  11. Collect, process, and dispatch biological samples including blood, urine, and tissue.
  12. Assist in the upkeep of 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 role, an individual must effectively perform each essential duty. The qualifications listed below represent the knowledge, skills, and abilities required. Reasonable accommodations may be made to enable individuals with disabilities to fulfill essential functions.

EDUCATION AND EXPERIENCE:

  1. Bachelor's degree in Biology or a related discipline is required.
  2. Proficient in computer usage and data collection; expertise in Microsoft Office is required.
  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. Experience with EKGs and other technical skills as required by protocol is preferred.
  8. Familiarity with medical terminology is beneficial.
  9. Ability to operate with minimal supervision.
  10. Strong problem-solving skills and quick learning ability.
  11. Excellent verbal and written communication skills are essential.
  12. Outstanding customer service skills with both internal and external stakeholders.
  13. Proven ability to manage multiple tasks in a dynamic environment.

BENEFITS:

401k Plan with employer matching

Medical, Dental, and Vision coverage

Paid Time Off (PTO) and paid holidays

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