Clinical Research Assistant

3 months ago

Plymouth Meeting, United States SQRL Full time

Highlights

  • Play a key role in helping patients get involved in clinical trials
  • up to $19 - $23 an hour+ full benefits
  • Monday - Friday; no weekends
  • Growth opportunities to CRC, Sr. CRC, and more
  • Great stepping stone into research, or a way to get more experience


As an entry-level Clinical Research Assistant, you will be integral to the success of our research endeavors, providing essential support throughout all phases of clinical trials. Key responsibilities include:

  • Assist in Start-up and Implementation Activities: Collaborate with the research team to facilitate the initiation of new studies, including protocol development and regulatory submissions.
  • Completion and Submission of Clinical Trials Amendments: Ensure timely completion and accurate submission of all amendments to the Institutional Review Board (IRB), adhering to regulatory guidelines and protocols.
  • Editing Informed Consent Documents: Review and edit informed consent documents to ensure clarity, accuracy, and compliance with regulatory standards.
  • Correspondence with Stakeholders: Serve as a primary point of contact for communication with the IRB, investigators, and sponsors throughout the clinical trial process, maintaining open lines of communication and addressing inquiries promptly.
  • Preparation of Annual Progress Reports: Compile and prepare comprehensive progress reports for IRB renewal of ongoing studies, summarizing key findings and milestones achieved.
  • Collection and Submission of Regulatory Documents: Facilitate the collection, completion, and submission of regulatory documents to various regulatory entities, ensuring compliance with regulatory requirements.
  • Maintenance of Regulatory Binders: Establish and maintain regulatory binders and other relevant files, organizing documentation meticulously during the review, approval, and activation process for clinical trials.
  • Coordination of Safety Reports: Coordinate the review and processing of safety reports to the IRB, ensuring prompt reporting and appropriate follow-up actions as required.


Qualifications:

  • Bachelor's degree in a relevant field (e.g., life sciences, healthcare administration, or related discipline) preferred.
  • Prior experience in clinical research or healthcare administration is preferred.
  • Experience with Phlebotomy, EKG, taking Vitals, etc. REQUIRED
  • Strong attention to detail and organizational skills.
  • Excellent written and verbal communication abilities.
  • Familiarity with regulatory requirements governing clinical research (e.g., FDA regulations, ICH-GCP guidelines) is desirable.

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