Clinical Research Coordinator

February 17

🐊 Florida – Remote

Although this job is listed in Florida, this company may be open to hiring remote in other states.

⏰ Full Time

🟢 Junior

🟡 Mid-level

🧪 Clinical Research

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Vitalief Inc.

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Vitalief Inc. is a company dedicated to transforming the clinical trial landscape by improving the value and contribution of trial sites throughout the drug development lifecycle. They specialize in offering consulting services, functional service provision (FSP), and workforce solutions to streamline clinical trials, enhance patient outcomes, and deliver value for Sponsors, Contract Research Organizations (CROs), and sites. With a focus on site operations and patient care in the life sciences, Vitalief serves academic sites, community health systems, independent sites, site networks, sponsors, and CROs. Their services address challenges in research and clinical trials, providing end-to-end solutions like strategic planning, resourcing models, training, and operational solutions. Vitalief is committed to delivering more efficient, high-quality clinical trials and driving innovation in the research industry.

51 - 200 employees

🤝 B2B

⚕️ Healthcare Insurance

💊 Pharmaceuticals

💰 $2M Venture Round on 2023-04

📋 Description

• Vitalief is a leading site solutions partner improving clinical trial sites' value and contributions • Seeking a Clinical Research Coordinator (CRC) to support ongoing oncology clinical study • Responsibilities include identifying and screening patients for eligibility in clinical trials • Need to follow-up with patients to ascertain enrollment in specific studies.

🎯 Requirements

• Bachelor’s Degree required, ideally in the healthcare field • Minimum of two (2) years of experience in clinical research as a Clinical Research Coordinator • Experience in patient recruiting/pre-screening/consenting/retention; activation; regulatory compliance, IRB submissions, data management • Experience with collecting, organizing, and handling sensitive research data accurately and securely • At least six (6) months of oncology clinical trials experience required • Must be fluent in EPIC; experience with REDCap preferred • Strong working knowledge of current Code of Federal Regulation and Good Clinical Practice guidelines • Outgoing, friendly and compassionate personality • Self-starter with the ability to demonstrate a “can do” attitude • Capable of independent decision-making

🏖️ Benefits

• 20 PTO (Paid Time Off) days annually • 9 paid Holidays annually • Company paid life insurance • Short / long term disability coverage • 401K retirement program • Robust healthcare plans to choose from