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Clinical Research Coordinator (CRC II)

3 weeks, 3 days ago
Anywhere
Full-time
Junior
Project Coordinator
Project and Program Management
Apply Now
Synapticure

Synapticure

Synapticure provides personalized virtual care to individuals living with neurodegenerative diseases such as Alzheimer’s, Parkinson’s, and ALS. Their expert team offers 24/7 support via telehealth, focusing on proactive care to improve outcomes and sim...

Health Care Providers & Services
11-50
Founded 2019
View All Jobs 8

Description

  • Independently coordinate assigned study activities in accordance with study protocols, SOPs, and regulatory requirements.
  • Screen potential research participants for eligibility and document inclusion and exclusion determinations.
  • Manage scheduling and execution of virtual and home-based study visits, assessments, and follow-up activities.
  • Collect, review, and enter study data accurately and on time in electronic data capture and other study systems.
  • Maintain complete, audit-ready study files, including regulatory binders, participant records, and tracking logs.
  • Conduct or support informed consent discussions and ensure proper documentation and filing.
  • Serve as a primary point of contact for research participants and caregivers, coordinating logistics and escalating issues as needed.
  • Prepare for and support sponsor, IRB, and regulatory monitoring visits, including resolving document requests and queries.
  • Track and report study progress metrics such as enrollment, retention, deviations, and visit completion.
  • Identify operational issues and communicate risks or improvement opportunities to research leadership.

Requirements

  • Bachelor’s degree in a scientific, health-related, or behavioral field preferred.
  • 2–3 years of experience as a Clinical Research Coordinator or equivalent role, preferably in interventional studies, decentralized trials, or neurology-related research.
  • Experience in research with human subjects required.
  • Working knowledge of Good Clinical Practice (GCP), informed consent requirements, and clinical research regulations.
  • Ability to manage study tasks independently and know when to escalate issues.
  • Strong organizational skills with the ability to prioritize across multiple studies and deadlines.
  • Excellent written and verbal communication skills, including comfort working directly with patients and caregivers.
  • Experience using electronic health records, EDC systems, CTMS, and study tracking tools.
  • Comfort working in a fully remote or virtual research environment using tools such as Zoom and secure messaging platforms.
  • Collaborative, adaptable, and dependable with a proactive approach to problem-solving.

Interested in this position?

Apply directly on the company website

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