Clinical Research Coordinator

Northwest Clinical Trials is seeking a motivated and detail-oriented Clinical Research Coordinator to join our team. As a leading research organization in the pharmaceutical research industry, we are dedicated to improving patient care through clinical trials. In this role, you will have the opportunity to work on groundbreaking research projects and contribute to medical advancements. If you have a strong passion for healthcare, attention to detail, and excellent organizational skills, we want to hear from you!

As a Clinical Research Coordinator, you will be responsible for managing all aspects of clinical trials, from planning to execution. You will work closely with physicians, nurses, patients, and other research staff to ensure the smooth operation of trials and the collection of accurate data. Your exceptional communication skills will be essential as you will act as the point of contact for study participants, providing them with detailed information about the trials...

A multi-year Clinical Research Coordinator (CRC) position is available at our research site in Plano, TX with an initial focus on an active pulmonary study from a major pharmaceutical sponsor. Working independently under the Research Program Manager, the CRC will be responsible for carrying out clinical research studies, including but not limited to participant recruitment and enrollment, scheduling study visits, carrying out study procedures, data collection and transfer to data repositories, and maintaining study records. The CRC must be able to work in a medical clinic setting supporting the principal investigator (PI) with protocol requirements, display a high degree of initiative, and have excellent interpersonal, organizational, and time management skills.

The company is hiring full-time and part-time positions.

Interested candidates should send a current resume and introductory cover letter to s.mcauley@empowerclinics.com

May perform some or all the...

Are you a driven and detail-oriented individual with a passion for clinical research? Look no further! EPW Curesearch LLC is seeking a Clinical Research Coordinator (CRC) to join our dedicated team in Los Angeles County, CA

In this multi-year position, you will have the opportunity to work on an active pulmonary study conducted by a major pharmaceutical sponsor. As a CRC, you will be responsible for various aspects of clinical research including participant recruitment and enrollment, scheduling study visits, carrying out study procedures, data collection and transfer to data repositories, and maintaining study records. You will work closely with the Research Program Manager and support the principal investigator (PI) in meeting protocol requirements.

We are looking for someone who can thrive in a medical clinic setting, exhibit a high degree of initiative, and possess excellent interpersonal, organizational, and time management skills.

We are currently hiring for...

The Senior Clinical Research Coordinator (CRC) is a specialized research professional working with and under the direction of the clinical Principal Investigator (PI). While the Principal Investigator is primarily responsible for the overall design, conduct, and management of the clinical trial, the CRC supports, facilitates and coordinates the daily clinical trial activities and plays a critical role in the conduct of the study. By performing these duties, the CRC works with the PI and internal teams to support and provide guidance on the administration of the compliance, financial, personnel and other related aspects of the clinical study.

The Senior Clinical Research Coordinator will coordinate all research-related activities, including the initial set-up of the study, study participant recruitment and retention, delivery of the intervention, data collection, entry, and quality control activities, protocol compliance and patient safety. He/She will also work on monitoring...

Company Description

LVIS Corporation is on a mission to revolutionize the entire continuum of neurological care by developing AI driven software tools to help physicians accelerate patient throughput and improve patient diagnostic and treatment outcomes. We have an international team with our headquarters located in Palo Alto, California, USA, and we have an office in Gangnam, Seoul, South Korea. We are looking for talented individuals to join us in our mission to transform the neurology health care industry.

Key responsibilities:

• You’ll be responsible for the collection, validation, and organization of LVIS’ clinical data in compliance with regulatory requirements.
• Collaborating with other team members to ensure accuracy and timely data delivery.
• Clinical database management, ensuring data integrity, consistency, and compliance.
• Preparation and management of clinical trial-related...