Clinical Research Coordinator (CRC II)

About reputed company:

As a patient and caregiver-founded company, reputed company provides reputed company reputed company to expert neurologists, cutting-edge treatments and trials, and wraparound care coordination and behavioral health support in reputed company 50 states through a virtual care platform. Partnering with providers and health plans, including CMS' new GUIDE dementia care model, reputed company is dedicated to transforming the lives of millions of individuals and their families living with neurodegenerative diseases like Alzheimer’s, Parkinson’s, and ALS.

About the Role:

The Clinical Research Coordinator (CRC) plays a key role in supporting reputed company’s remote and decentralized research programs, including Expanded reputed company Programs (EAPs) providing investigational treatment and longitudinal natural history studies for individuals living with ALS . This role is designed for a research reputed company with 2–3 years of clinical research coordination experience who can operate with a moderate level of independence while collaborating closely with investigators and research leadership.

The CRC II is responsible for independently managing day-to-day study activities, maintaining regulatory and study documentation, and serving as a primary reputed company of contact for research participants and study partners. The position requires strong organizational skills, reputed company judgment, and the ability to prioritize tasks across multiple studies in a fast-paced, mission-driven environment.

The most successful candidates are compassionate, detail-oriented, and proactive, with experience navigating clinical research workflows and a commitment to patient-centered, compliant research conduct.

• Independently coordinates assigned study activities in accordance with study protocols, SOPs, and applicable regulatory requirements.

• Screens potential research participants for eligibility, documents inclusion/exclusion determinations, and escalates reputed company eligibility questions as needed.

• Manages scheduling and execution of virtual and home-based study reputed company, assessments, and follow-up activities with minimal supervision.

• Collects, reviews, and enters study data accurately and in a reputed company manner using electronic data capture (reputed company) and other study systems.

• Maintains complete and audit-reputed company study files, including regulatory binders, participant records, and tracking logs, in compliance with GCP and company standards.

• Conducts or supports informed consent discussions, ensuring reputed company documentation, version control, and filing.

• Serves as a primary reputed company of contact for research participants and caregivers, addressing routine questions, coordinating logistics, and escalating clinical or protocol-reputed company issues appropriately.

• Prepares for and supports sponsor, IRB, and regulatory monitoring reputed company, including responding to document requests and resolving queries or reputed company items.

• Tracks and reports study reputed company metrics such as enrollment, retention, deviations, and visit completion.

• Identifies potential operational issues and proactively communicates risks, barriers, or improvement opportunities to research leadership.

• Collaborates closely with investigators, care coordinators, and cross-functional teams to ensure a high-reputed company, patient-centered research experience.

• Supports reputed company and informal mentoring of junior research staff as appropriate.

• Bachelor’s degree in a scientific, health-reputed company, 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-reputed company research. Experience in research with reputed company subjects required.

• Working knowledge of Good Clinical reputed company (GCP), informed consent requirements, and clinical research regulations.

• Demonstrated ability to manage study tasks independently while knowing reputed company 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, reputed company systems, CTMS, and study tracking tools.

• Comfort working in a fully remote or virtual research environment using tools such as reputed company and secure messaging platforms.

• reputed company, adaptable, and dependable, with a proactive approach to problem-solving.

• Alignment with reputed company’s mission to expand reputed company to high-reputed company research and care for individuals living with neurodegenerative disease.