Clinical Research Coordinator Ripley TN

Medovation Clinical Research LLC; Ripley (TN); Presencial; USD 42 000 - 65 000; Tempo integral

Vantagens oferecidas por esta oferta de emprego

Competitive salary

Dental insurance

Health insurance

Paid time off

Training & development

Resumo da oferta

Medovation Clinical Research is seeking a Clinical Research Coordinator (Full Time) to manage and oversee clinical trials at a physician’s practice. The role requires phlebotomy skills and a strong background in medical terminology, data management, and trials coordination, with at least one year ofCRC experience.

On-site work in Ripley, TN, with a collaborative team and opportunities for growth as the company expands its access to clinical research for diverse patient communities.

Qualificações

• Minimum 1 year of experience as a Clinical Research Coordinator (CRC) required.
• Phlebotomy skills required.
• Knowledge of medical terminology relevant to clinical research.
• Proficiency in data entry.
• Patient recruitment experience required.

Responsabilidades

• Manage the day-to-day operations of clinical trials, ensuring adherence to protocols and timelines.
• Analyze data collected during trials and maintain accurate records for compliance management.
• Oversee blood sampling procedures and ensure proper handling and documentation.
• Train on clinical trial protocols and procedures.
• Collaborate with healthcare professionals to ensure participant safety and integrity of data.
• Utilize software for data capture and reporting.
• Maintain knowledge of medical terminology to effectively communicate with team members and stakeholders.
• Ensure compliance with ethical standards and regulatory requirements throughout the research process.

Conhecimentos

Clinical experience

CRC experience

Data entry

Medical terminology

Phlebotomy

Blood sampling

Patient recruitment

Organizational skills

Travel to Ripley TN

Ferramentas

Data capture software

Descrição da oferta de emprego

Benefits:

• Competitive salary
• Dental insurance
• Health insurance
• Paid time off
• Training & development

Clinical Research Coordinator (Full Time)

About Us

We are an Integrated Clinical Research Organization dedicated to expanding access to clinical research and empowering physicians to bring advanced care options closer to diverse patient communities. We pride ourselves on fostering a collaborative and honest work environment where every team member takes ownership of their role.

Role Overview

Here's an opportunity to work for a dynamic and growing clinical research company. We have a fantastic and supportive work environment. The Clinical Research Coordinator plays a pivotal role in managing and overseeing clinical trials, ensuring compliance with regulatory requirements, and facilitating the smooth operation of research studies. This position works on-site at the physician’s practice. This position requires a detail-oriented individual with a strong background in medical terminology, data management, and clinical trials management. The ideal candidate will have at least one year of experience coordinating all aspects of clinical research projects from initiation to completion. Phlebotomy skills required.

Key Responsibilities

• Manage the day-to-day operations of clinical trials, ensuring adherence to protocols and timelines.
• Analyze data collected during trials and maintain accurate records for compliance management.
• Oversee blood sampling procedures and ensure proper handling and documentation.
• Train on clinical trial protocols and procedures.
• Collaborate with healthcare professionals to ensure participant safety and integrity of data.
• Utilize software for data capture and reporting
• Maintain knowledge of medical terminology to effectively communicate with team members and stakeholders.
• Ensure compliance with ethical standards and regulatory requirements throughout the research process.

Required Qualifications

• Clinical experience preferred but not required
• Minimum 1 year of experience as a Clinical Research Coordinator (CRC) required
• Proficiency in data entry
• Knowledge of medical terminology relevant to clinical research
• Phlebotomy and blood sampling techniques is required
• Patient Recruitment experience required
• Excellent organizational skills with attention to detail and the ability to manage multiple tasks simultaneously.
• Travel and work required in Ripley TN

What We Offer

• A mission-driven and collaborative team culture.
• Opportunities for career growth as the company scales.
• The chance to contribute meaningfully to expanding access to clinical research for underserved populations.

If you’re looking for an opportunity to take ownership, build something from the ground up, and make a significant impact, we’d love to hear from you!

Medovation Clinical Research is an Integrated Clinical Research Organization dedicated to expanding access to clinical research and empowering physicians to bring advanced care options closer to diverse patient communities. We pride ourselves on fostering a collaborative and honest work environment where every team member takes ownership of their role. We value impactful work, open collaboration, and a spirit of diversity and inclusion.