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Clinical Research Laboratory Assistant

Rovia Clinical Research
Posted a month ago, valid for 2 days
Location

St. Charles, MO, US

Salary

Competitive

Contract type

Part Time

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Sonic Summary

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  • The Clinical Research Assistant coordinates and executes clinical trials in line with study protocols and regulatory guidelines.
  • Candidates should have a high school diploma, with a bachelor's degree preferred, and 0-1 years of clinical research experience.
  • The role involves conducting patient visits, performing clinical tasks, and ensuring informed consent is obtained and documented.
  • Strong knowledge of medical terminology, excellent organizational skills, and proficiency in Microsoft Office are essential for this position.
  • The position requires availability to start at 6:00 AM, and the salary is competitive based on experience.

Position Summary:

The Clinical Research Laboratory Assistant is responsible for coordinating and executing clinical trials in accordance with study protocols, ICH/GCP guidelines, sponsor requirements, and Rovia SOPs. This role partners closely with site teams to support study startup, enrollment, data quality, and overall study success.

 

Key Responsibilities:

  • Conduct and coordinate patient visits in accordance with study protocols.
  • Perform clinical tasks such as vital signs, ECGs, specimen collection/processing, and phlebotomy (as applicable).
  • Ensure informed consent is properly obtained and documented.
  • Educate and guide participants throughout the study, ensuring a positive patient experience.
  • Monitor subject safety, report adverse events, and escalate concerns as appropriate.
  • Complete timely and accurate source documentation and EDC data entry.
  • Resolve data queries and ensure data integrity.
  • Maintain investigational product accountability and proper storage/handling.
  • Prepare for and support monitoring visits, audits, and inspections.
  • Collaborate with site staff and investigators to ensure protocol adherence and efficient visit flow.
  • Perform other duties as assigned.

Skills/Abilities:

  • Strong knowledge of medical terminology and clinical procedures.
  • Understanding of ICH/GCP and regulatory requirements.
  • Excellent organizational skills and attention to detail.
  • Strong interpersonal and patient-facing communication skills.
  • Ability to multitask and manage competing priorities in a fast-paced environment.
  • Proficiency in Microsoft Office, EDC, and CTMS applications.
  • Ability to work both independently and collaboratively.
  • High level of professionalism and commitment to patient confidentiality.

Education/Experience:

  • High school diploma required, bachelor’s degree in related field preferred.
  • 0-1 years of clinical research experience.
  • Experience with patient-facing activities (phlebotomy, vital signs, EKGs, lab processing, etc.) required.
  • Phlebotomy or Medical Assistant certification preferred.
  • Current IATA certification preferred.

Position will require availability to start at 6:00AM.




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