Clinical Research Assistant - Falls Church, United States - Virginia Heart

Virginia Heart
Virginia Heart
Verified Company
Falls Church, United States

4 weeks ago

Mark Lane

Posted by:

Mark Lane

beBee recruiter
Description

Location:
Fairfax


Position type:
Full-time /Non-Exempt

$ $25.00/hr.


The Clinical Research Assistant plays a pivotal role in ensuring the smooth execution of clinical trials conducted at our site.

As a vital member of our research team, you will assist in the coordination and management of clinical research studies, ensuring adherence to protocols and regulatory requirements


Roles and Responsibilities:

  • Collaborate with the Clinical Research Coordinator to oversee the planning, implementation, and completion of clinical research studies.
  • Assist in the recruitment, screening, and enrollment of study participants, ensuring compliance with eligibility criteria.
  • Maintain accurate and complete study documentation, including regulatory documents, study protocols, and participant records.
  • Coordinate study visits and procedures, including scheduling participant appointments, arranging studyrelated tests and assessments, and ensuring timely completion of study activities.
  • Communicate with study participants, healthcare providers, and other research staff to provide support and ensure study procedures are carried out effectively.
  • Assist in the collection, entry, and management of study data, ensuring data integrity and confidentiality.
  • Assist in the preparation and submission of regulatory documents to regulatory authorities and institutional review boards (IRBs).
  • Participate in study team meetings, training sessions, and quality assurance activities as required.
  • Maintain current knowledge of Good Clinical Practice (GCP) guidelines and regulatory requirements governing clinical research.

Skill Requirements and Qualifications:

  • Bachelor's degree in a relevant field (e.g., life sciences, health sciences, nursing) preferred.
  • Prior experience in clinical research or healthcarerelated field is advantageous.
  • Strong organizational skills and attention to detail.
  • Excellent interpersonal and communication skills, with the ability to interact effectively with diverse stakeholders.
  • Ability to work independently and collaboratively in a dynamic and fastpaced environment.
  • Knowledge of regulatory requirements and guidelines governing clinical research (e.g., ICH-GCP, FDA regulations) is desirable.
  • EMR experience, (EPIC a plus) and Microsoft Excel, Word, and Outlook.
  • Detailed oriented, excellent written and verbal communication skills.
  • Excellent time management skills, team player with the ability to work independently.
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