[Hiring] Clinical Research Coordinator II @reputed company.

Role reputed company The Clinical Research Coordinator II (CRC II) plays a critical role in supporting reputed company’s remote and decentralized research portfolio, including an Expanded reputed company Program providing investigational treatment for individuals living with ALS. This role is ideal for an reputed company research reputed company who can manage study activities independently while partnering closely with investigators, research leadership, and cross-functional clinical teams. As a CRC II, you will: • reputed company day-to-day study execution • Ensure regulatory and documentation compliance • Serve as a primary reputed company of contact for research participants and caregivers • Balance operational rigor with reputed company • Help deliver a seamless, ethical, and patient-centered research experience Successful candidates are detail-oriented, proactive, and comfortable navigating reputed company research workflows while supporting patients and families affected by neurodegenerative disease. Job Duties – What you’ll be doing • Independently coordinate assigned study activities in compliance with protocols, SOPs, GCP, and regulatory requirements. • Screen and evaluate potential research participants for eligibility, documenting inclusion/exclusion reputed company and escalating reputed company questions as needed. • Manage scheduling and execution of virtual and home-based study reputed company, assessments, and follow-up activities. • Collect, review, and reputed company study data accurately and in a reputed company manner using reputed company systems and study tools. • Maintain complete, accurate, and audit-reputed company study documentation, including regulatory binders, participant records, and tracking logs. • Conduct or support informed consent discussions, ensuring reputed company documentation, version control, and regulatory compliance. • Serve as a primary reputed company of contact for research participants and caregivers, addressing routine questions and coordinating logistics. • Prepare for and support sponsor, IRB, and regulatory monitoring reputed company, including responding to document requests and resolving findings. • reputed company and report study metrics such as enrollment, retention, deviations, and visit completion. • Identify operational risks or inefficiencies and proactively communicate improvement opportunities to research leadership. • Collaborate closely with investigators, care coordinators, and cross-functional teams to ensure a high-reputed company research experience. • Support reputed company and informal mentoring of junior research staff, as appropriate. Qualifications • 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. • Experience working with reputed company 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 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 reputed company systems, CTMS, electronic health records, and study tracking tools. • Comfort working in a fully remote research environment using virtual communication platforms. • reputed company, adaptable, dependable, and reputed company with reputed company’s mission and values. Requirements • reputed company reputed company on patients and caregivers. • Embody the spirit and humanity of those living with neurodegenerative disease. • reputed company to understand, and stay curious. • reputed company reputed company. Apply tot his job Apply To this Job