Clinical Research Coordinator II (CRC II)

1 month, 1 week ago
Full-time
Junior
Project and Program Management
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

Description

  • Independently coordinate assigned study activities in compliance with protocols, SOPs, GCP, and regulatory requirements.
  • Screen and evaluate potential research participants for eligibility and document inclusion/exclusion criteria.
  • 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 using EDC systems and study tools.
  • Maintain complete, accurate, and audit-ready study documentation, including regulatory binders, participant records, and tracking logs.
  • Conduct or support informed consent discussions and ensure proper documentation and version control.
  • Serve as a primary point of contact for research participants and caregivers, answering routine questions and coordinating logistics.
  • Prepare for and support sponsor, IRB, and regulatory monitoring visits and respond to document requests.
  • Track and report study metrics such as enrollment, retention, deviations, and visit completion.
  • Identify operational risks or inefficiencies and communicate improvement opportunities to research leadership.
  • Collaborate with investigators, care coordinators, and cross-functional teams to support a high-quality research experience.
  • Support onboarding and informal mentoring of junior research staff as appropriate.

Requirements

  • Bachelor’s degree in a scientific, health-related, or behavioral field preferred.
  • 2–3 years of experience as a Clinical Research Coordinator or in an equivalent role.
  • Experience with human subjects research required; neurology, ALS, or decentralized trial experience preferred.
  • Working knowledge of GCP, informed consent requirements, and clinical research regulations.
  • Ability to manage study responsibilities 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 EDC systems, CTMS, electronic health records, and study tracking tools.
  • Comfort working in a fully remote research environment using virtual communication platforms.
  • Collaborative, adaptable, and dependable, with alignment to Synapticure’s mission and values.

Benefits

  • Remote-first work environment.
  • Opportunity to contribute to research for neurodegenerative diseases, including ALS and dementia-related care.
  • Work on remote and decentralized clinical trials and Expanded Access Programs.
  • Mission-driven culture centered on patients and caregivers.

Interested in this position?

Apply directly on the company website

Apply Now

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