Clinical Research Coordinator II — Accelerate Trials

Clinical & Support Options Inc; Anderson (SC); On-site; USD 42,000 - 64,000; Full time

Job summary

Velocity Clinical Research in the United States seeks a Clinical Research Coordinator II to conduct and manage multiple clinical trials from start up through close out, in accordance with study protocols, GCP, and Velocity SOPs.

Responsibilities include coordinating start-up, recruitment, visits, data entry, adverse events reporting, and regulatory document submission while ensuring data quality and patient safety.

Qualifications

• Bachelor’s degree with 2 years of life science experience; or an Associate’s with 4 years; or HS diploma with 6 years plus 1 CRC experience.
• Strong knowledge of medical terminology and regulations (GCP/ICH).
• Excellent communication and organizational skills; ability to work in a fast-paced team.

Responsibilities

• Conduct and manage clinical trials in accordance with the study protocol, GCP, ICH Guidelines and Velocity’s SOPs.
• Coordinate start up, vendor management, subject recruitment, visits, and data collection with regulatory documents.
• Apply project management concepts to manage risk and improve quality.
• Develop and implement research and administrative strategies to manage protocols.
• Communicate effectively with coworkers, leadership, sponsors, CROs, and vendors.
• Maintain confidentiality of patient information and sponsor data.
• Ensure data is entered into sponsor data portal and queries resolved timely.
• Create and submit regulatory documents to Sponsors and IRBs as required.
• Evaluate potential subjects for participation via prescreens.
• Collaborate with team to develop quality control strategies.
• Perform clinical duties (drug preparation, phlebotomy, ECG, etc.) within scope.
• Other duties as assigned.

Skills

Medical terminology

Microsoft Office

Attention to detail

Communication skills

Team player

English proficiency

Multi-tasking

Independent planning

Education

Bachelor’s degree + 2 years life science experience

Associate’s degree + 4 years life science experience

High School diploma + 6 years life science experience

Job description

Velocity Clinical Research in the United States seeks a Clinical Research Coordinator II to conduct and manage multiple clinical trials from start up through close out, in accordance with study protocols, GCP, and Velocity SOPs.

Responsibilities include coordinating start-up, recruitment, visits, data entry, adverse events reporting, and regulatory document submission while ensuring data quality and patient safety.