Central Study Coordinator, I

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🔥 0 minutes ago

🇺🇸 United States – Remote

💵 $75k - $95k / year

⏰ Full Time

🟡 Mid-level

🟠 Senior

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CARE

WebsiteLinkedInAll Job Openings

5001 - 10000 employees

Founded 1945

⚕️ Healthcare Insurance

📚 Education

🎯 Recruiter

💰 Grant on 2021-11

Healthcare Insurance • Education • Recruitment

CARE is a boutique provider of high-quality, accredited carers for the Aged Care and Early Learning industries. It specializes in matching experienced professionals, recent graduates, and students with job vacancies in these sectors, facilitating rewarding career placements. CARE aims to support clients and carers by providing effective staffing solutions and contributing to their success in the industry.

📋 Description

• Central Clinical Services enables decentralized and hybrid clinical trials by providing staff who virtually support patients and sites. • The Central Study Coordinator (CSC) position combines clinical research and project management skills into a singular role that delivers a strong customer experience for both patients and sites. • The CSC acts as a virtual extension of the research site and supports one to four sites concurrently across one or more studies. • The CSC is accountable for study delivery at the patient level, including screening, consenting, and conducting protocol mandated study visits, • The CSC also serves as a project manager for their assigned studies with their assigned PIs, helping their sites to stay on top of study deliverables in line with sponsor and CRO expectations. • This role will also manage monitoring visits, data management, and query resolution for their assigned sites, and ensure ongoing inspection readiness.

🎯 Requirements

• Bachelor’s Degree preferred, or equivalent combination of education, training and experience • At least 3 years of relevant clinical research experience • Fluency in Spanish is a bonus • CCRC preferred • Able to navigate and troubleshoot a wide variety of technologies used for clinical research including recruitment platforms, IWRS, EDC, and other clinical trial software, and able to work across multiple platforms at the same time • Proficient with Microsoft Office applications (Word, Outlook, Teams, and Excel) • Demonstrate professionalism in all situations and work effectively with a diverse group of individuals. • Understand when issues require escalation • Strong communication customer service abilities • Proficient in research terminology and basic medical terminology • Understand the overall clinical development paradigm and excellent working knowledge of government regulations, GCP, and ALCOA-C • Strong organization and time management skills • High attention to detail • Ability to work in a fast-paced environment • Critical thinker and problem solver • Ability to work effectively in a remote environment • Proper home office set-up including a private space for participant communication and high-speed internet (at minimum: 100MB up and 15 MB down, 5 GHz router)

🏖️ Benefits

• Paid Time Off (PTO) and Company Paid Holidays • 100% Employer paid medical, dental, and vision insurance plan options • Health Savings Account and Flexible Spending Accounts • Bi-weekly HSA employer contribution • Company paid Short-Term Disability and Long-Term Disability • 401(k) Retirement Plan, with Company Match