Medical Assistant

3 weeks ago

Plymouth Meeting, United States SQRL Full time
Job DescriptionJob Description

Opportunity to join one of the fastest-growing Clinical Research site networks in the US Your daily work contributes to the development of life-saving and life-improving treatment options for millions.

The Plymouth Meeting clinical research site is well-known as a major contributor to Alzheimer's Disease research

Highlights

  • Play a major role in advancing medicine with a team dedicated to the patient experience
  • Full Benefits (Health, Dental, Vision, 401k w/ 4% Match, 15 days of PTO, 10 Paid Holidays)
  • Competitive Base Salary ($20-$24/hr)
  • Gain experience in the fast-growing world of clinical research and develop skills that are in high demand
  • Monday - Friday 8:30 AM - 5 PM
  • The company is invested in growth, providing employees with unique opportunities for career advancement
  • Join a dedicated team at a large site with opportunities for advancement at the site and site network level.

Position

The Clinical Research Assistant plays a critical role in supporting the Clinical Research Coordinators and the research team in providing an impeccable patient experience in every single interaction. Your role will include a variety of tasks, from patient recruitment, source documentation, data entry, and direct patient interaction during site visits. This position will also be responsible for performing phlebotomy or other clinical procedures during patient visits.

Responsibilities

  • Assist in the recruitment, screening, and enrollment of study participants.
  • Coordinate and manage the scheduling of trials and maintain communication with participants.
  • Collect, organize, and process clinical data from trials.
  • Maintain source documentation from patient visits and protocol activities
  • Work alongside Clinical Research Coordinators in conducting patient visits.
  • Perform phlebotomy, EKGs, and/or other diagnostic procedures as needed
  • Learn, understand, and comply with rules and regulations governing medical ethics, IRB, GCP, and ICH guidelines
  • Provide administrative support to research staff by organizing meetings, preparing reports, and maintaining records.

Company

Our client is a Clinical Research site network with over 17 research sites across the United States. Their sites conduct Phase I-IV trials in therapeutic areas like cardiology, metabolic disorders, renal, CNS, pulmonology, women's health, and vaccines. They are a fast-growing site network with plans to grow from 17 sites to over 30 sites in 2024 alone.

Qualifications

  • Phlebotomy experience is required; EKG or other patient labs/process experience preferred
  • Clinical research experience is a plus, but not required
  • Impeccable organizational skills and attention to detail
  • Excellent communication and interpersonal skills to effectively interact with the Principal Investigator, research team, Study Sponsor/CROs, potential subjects, and referral sources
  • An ethical compass that compels the candidate to be honest, detail-oriented, and self-driven
  • High-level critical thinking skills
  • Working knowledge of medical terminology and lab collection/processing/storage procedures
  • Proficiency with computers and Microsoft Office Suite

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