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INNOVO RESEARCH INC

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Clinical Research Assistant

Open 33d reposted 5× · 2 open copies

JOB SUMMARY

A Clinical Research Assistant is an entry-level research position. This position is responsible for performing a variety of duties including coordinating aspects of clinical trial protocols including but not limited to study initiation, recruitment, study visits, monitor visits, regulatory compliance, and study close-out.

RESPONSIBILITIES

  • Act as a liaison between providers, study representatives, and patients.
  • Maintain case report forms, source documents, and regulatory documents.
  • Maintain stock of supplies needed to carry out protocols.
  • Pack and ship patient labs and review lab results.
  • Provide patient care and collect medical information during visits.
  • Initiate and participate in the informed consent process.
  • Conduct screening of prospective study participants and schedule appointments of patients interested in research studies.
  • Identify potential research participant candidates utilizing various channels including medical records, databases, referrals, and community outreach to identify potential candidates for participation in clinical research studies.
  • Obtain informed consent (if required and appropriately delegated) from eligible participants according to established guidelines and protocols, ensuring comprehension and compliance with ethical standards and regulatory requirements.
  • Conduct thorough remote screenings and assessments to determine initial patient eligibility for participation in clinical trials, coordinating with healthcare professionals as needed to verify medical history and suitability.
  • Maintain detailed and accurate records of patient interactions, recruitment efforts, and consent processes in accordance with regulatory standards and study protocols.
  • Collaborate closely with interdisciplinary team members including investigators, research coordinators, healthcare providers, and administrative staff to facilitate seamless recruitment and enrollment processes.
  • Adhere to all relevant regulatory guidelines, institutional policies, and ethical standards governing the conduct of screening, recruitment, and enrollment in clinical research, prioritizing patient safety, privacy, and confidentiality.
  • Use employee calendars to schedule appointments for patients.
  • Instruct patients regarding study protocols.
  • Arrange for or perform phlebotomy.
  • Perform related work as required.
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