Data Research Coordinator - Charlotte, NC

We are seeking a Clinical Research Coordinator to join our Trauma & Acute Care Surgery Research team. As a key member of our team, you will be responsible for coordinating clinical trials and ensuring the safety of patients and quality of clinical trial data. · ...

Manages protocols to ensure the safety of patients and quality of clinical trial data. · Determines protocol-related needs to conduct the trial and order supplies and equipment. · Recruits and screens potential patients and obtains informed consent. · ...

As a Clinical Research Coordinator on our Trauma Acute Care Surgery Research team, you'll contribute to research that saves lives and sets new standards in trauma acute care medicine. · ...

Manages protocols to ensure the safety of patients and quality of clinical trial data. · Bachelors Degree and research experience required. · ...

· Calls caregivers and subjects to obtain missing information on questionnaires. · Performs medical record chart abstractions. · Tracks lost subjects. · ...

Are you passionate about making a real difference in patients' lives? As a Clinical Research Coordinator, you'll be at the forefront of groundbreaking studies that shape the future of critical care. · ...

We are seeking an experienced Clinical Research Coordinator to join our Trauma & Acute Care Surgery Research team. This role will be responsible for managing clinical trials and ensuring patient safety. · Prior experience in clinical trials is required. · ...

The OrthoCarolina Research Institute is looking for a Clinical Research Coordinator to join their team. · The role involves completing clinical trial assignments in a timely manner under close supervision. · Attention to detail · Excellent written and verbal communication skills ...

The OrthoCarolina Research Institute (OCRI) is an independent, non-profit 501(c)3 uniquely positioned as both an academic research center and clinical research site servicing industry research. · If you have the desire to work for an organization that is dedicated to raising the ...

Manages protocols to ensure the safety of patients and quality of clinical trial data. · ...

The job involves managing protocols to ensure patient safety and quality of clinical trial data. The candidate prepares and submits Institutional Review Board paperwork and maintains regulatory document submissions. The role requires close personal contact with patients, handling ...

We are recruiting for a CRC role at an early-stage site operator building a scalable Phase II–IV clinical trial engine in North Carolina. · This is a build-and-execute role: helping stand up workflows and templates, then running studies with monitor-ready documentation and reliab ...

The Data Research Coordinator role serves a dual function in providing administrative and program management support to the Urban Institute and Data Trust.The position assists with monitoring and tracking of research projects, governance documents, and procedures. · ...

+The Clinical Research Coordinator will serve as a hands-on operator across startup, regulatory, participant visits, data quality, and sponsor/CRO coordination. · +Own study startup and regulatory execution (essential documents, training documentation) · Create and maintain inves ...

We are looking for an experienced Clinical Research Coordinator for a busy and growing clinical research site. · A clinical research coordinator coordinates clinical studies adhering to ICH/Good Clinical Practice principles. This includes collecting medical history from patients, ...

+Job Summary · Full time experienced clinical trials research nurse coordinators to staff various COVID research studies throughout inpatient and ambulatory facilities. · +Skills:Recruits, interviews and obtains informed consent from prospective subjects for entrance into clinica ...

A non-exempt position responsible for managing clinical trials excluding regulatory binder management conducting operation components of clinical trials access patient population up to twenty five thousand opportunity serve seven office locations forty five dialysis units work di ...

Hawthorne Health is seeking an experienced Clinical Research Coordinator (CRC) to join our Concord site. · Conduct and coordinate all aspects of clinical trial activities at the site. · Perform phlebotomy on patients following proper clinical and safety protocols. · ...

Hawthorne Health is seeking an experienced Clinical Research Coordinator (CRC) to join our Concord, NC site. · This individual will work closely with investigators, patients, and sponsor representatives to ensure successful execution of clinical trials in compliance with all regu ...

As a Clinical Research Coordinator at Monroe Biomedical Research you will play a critical role in the execution of clinical trials by managing patient interactions performing study procedures and ensuring the accuracy and integrity of collected data. · ...