Chicago, IL · On-site
$25 - $33.25/hr
Position SummaryThe Clinical Research Coordinator manages and directs the coordination and timely ... Coordinates comprehensive patient protocol treatment schedules to maintain compliance to protocol ...
Chicago, IL · On-site
$25 - $33.25/hr
Position SummaryThe Clinical Research Coordinator manages and directs the coordination and timely ... Coordinates comprehensive patient protocol treatment schedules to maintain compliance to protocol ...
Collect study data as required by the protocol, e.g., interviews, surveys, clinical procedures, etc ... Oral and Written Communications - Awareness * Organizational Skills - Awareness The core technical ...
Collect study data as required by the protocol, e.g., interviews, surveys, clinical procedures, etc ... Oral and Written Communications - Awareness * Organizational Skills - Awareness The core technical ...
Celerion is seeking a Full-time overnight Clinical Research Nurse to assist with our clinical ... You will be responsible for performing scheduled events according to the study protocol. * You will ...
Celerion is seeking a Full-time overnight Clinical Research Nurse to assist with our clinical ... You will be responsible for performing scheduled events according to the study protocol. * You will ...
Specific Duties & Responsibilities Collect study data as required by the protocol, e.g., interviews ... Written Communications - Awareness Organizational Skills - Awareness The core technical skills ...
Specific Duties & Responsibilities Collect study data as required by the protocol, e.g., interviews ... Written Communications - Awareness Organizational Skills - Awareness The core technical skills ...
Flint, MI · On-site
$23.50 - $31.25/hr
... research protocol to the medical and nursing staff; evaluating the eligibility of potential ... Essential Functions and Responsibilities : 1. Evaluates eligibility of candidates for clinical ...
Flint, MI · On-site
$23.50 - $31.25/hr
... research protocol to the medical and nursing staff; evaluating the eligibility of potential ... Essential Functions and Responsibilities : 1. Evaluates eligibility of candidates for clinical ...
Portsmouth, VA · On-site
$23.50 - $31.25/hr
Culmen International, LLC is hiring a Clinical Research Coordinator to assist the Naval Medical ... each protocol in accordance with written policies and procedures as set forth in Title 21 of the ...
Portsmouth, VA · On-site
$23.50 - $31.25/hr
Culmen International, LLC is hiring a Clinical Research Coordinator to assist the Naval Medical ... each protocol in accordance with written policies and procedures as set forth in Title 21 of the ...
Cincinnati, OH · On-site
$23.25 - $31/hr
Determines protocol feasibility and some budgetary issues. Adheres to the standard operating ... Acts as the point person for audit staff coming into institution for a review prepares a written ...
Cincinnati, OH · On-site
$23.25 - $31/hr
Determines protocol feasibility and some budgetary issues. Adheres to the standard operating ... Acts as the point person for audit staff coming into institution for a review prepares a written ...
Celerion is seeking a Full-time overnight Clinical Research Nurse to assist with our clinical ... You will be responsible for performing scheduled events according to the study protocol. * You will ...
Celerion is seeking a Full-time overnight Clinical Research Nurse to assist with our clinical ... You will be responsible for performing scheduled events according to the study protocol. * You will ...
$23.25 - $31/hr
Determines protocol feasibility and some budgetary issues. Adheres to the standard operating ... Acts as the point person for audit staff coming into institution for a review prepares a written ...
$23.25 - $31/hr
Determines protocol feasibility and some budgetary issues. Adheres to the standard operating ... Acts as the point person for audit staff coming into institution for a review prepares a written ...
Cincinnati, OH · On-site
$23.25 - $31/hr
Determines protocol feasibility and some budgetary issues. Adheres to the standard operating ... Acts as the point person for audit staff coming into institution for a review prepares a written ...
Cincinnati, OH · On-site
$23.25 - $31/hr
Determines protocol feasibility and some budgetary issues. Adheres to the standard operating ... Acts as the point person for audit staff coming into institution for a review prepares a written ...
Flint, MI · On-site
$23.50 - $31.25/hr
... research protocol to the medical and nursing staff; evaluating the eligibility of potential ... Essential Functions and Responsibilities : 1. Evaluates eligibility of candidates for clinical ...
Flint, MI · On-site
$23.50 - $31.25/hr
... research protocol to the medical and nursing staff; evaluating the eligibility of potential ... Essential Functions and Responsibilities : 1. Evaluates eligibility of candidates for clinical ...
Coordinate development of research protocols and treatment plans with physicians, pharmacists ... CCRP, CRN-BC, OCN) Effective problem-solving abilities Effective communication and writing skills ...
Coordinate development of research protocols and treatment plans with physicians, pharmacists ... CCRP, CRN-BC, OCN) Effective problem-solving abilities Effective communication and writing skills ...
The Woodlands, TX · On-site
$21.75 - $28.75/hr
Company Description Renovatio Clinical is a network of community-based clinical research centers ... We adhere to the highest standards of protocol compliance, teamwork, and data accuracy to deliver ...
The Woodlands, TX · On-site
$21.75 - $28.75/hr
Company Description Renovatio Clinical is a network of community-based clinical research centers ... We adhere to the highest standards of protocol compliance, teamwork, and data accuracy to deliver ...
Coordinate development of research protocols and treatment plans with physicians, pharmacists ... CCRP, CRN-BC, OCN) • Effective problem-solving abilities • Effective communication and writing ...
Coordinate development of research protocols and treatment plans with physicians, pharmacists ... CCRP, CRN-BC, OCN) • Effective problem-solving abilities • Effective communication and writing ...
Madison, WI · On-site
$70 - $100/hr
* Direct planning and implementation of clinical research protocols within K-12 settings * Ensure ... Strong written and verbal communication skills * Master's degree required * Preferred degree in ...
Madison, WI · On-site
$70 - $100/hr
* Direct planning and implementation of clinical research protocols within K-12 settings * Ensure ... Strong written and verbal communication skills * Master's degree required * Preferred degree in ...
Cincinnati, OH · On-site
$23.25 - $31/hr
Determines protocol feasibility and some budgetary issues. Adheres to the standard operating ... Acts as the point person for audit staff coming into institution for a review prepares a written ...
Cincinnati, OH · On-site
$23.25 - $31/hr
Determines protocol feasibility and some budgetary issues. Adheres to the standard operating ... Acts as the point person for audit staff coming into institution for a review prepares a written ...
Coordinate development of research protocols and treatment plans with physicians, pharmacists ... CCRP, CRN-BC, OCN) Effective problem-solving abilities Effective communication and writing skills ...
Coordinate development of research protocols and treatment plans with physicians, pharmacists ... CCRP, CRN-BC, OCN) Effective problem-solving abilities Effective communication and writing skills ...
Flint, MI · On-site
$23.50 - $31.25/hr
... research protocol to the medical and nursing staff; evaluating the eligibility of potential ... Essential Functions and Responsibilities : 1. Evaluates eligibility of candidates for clinical ...
Flint, MI · On-site
$23.50 - $31.25/hr
... research protocol to the medical and nursing staff; evaluating the eligibility of potential ... Essential Functions and Responsibilities : 1. Evaluates eligibility of candidates for clinical ...
Demonstrates the ability to develop processes to facilitate implementation of the research protocol ... Acts as the point person for audit staff coming into institution for a review prepares a written ...
Demonstrates the ability to develop processes to facilitate implementation of the research protocol ... Acts as the point person for audit staff coming into institution for a review prepares a written ...
Cincinnati, OH · On-site
Demonstrates the ability to develop processes to facilitate implementation of the research protocol ... Acts as the point person for audit staff coming into institution for a review prepares a written ...
Cincinnati, OH · On-site
Demonstrates the ability to develop processes to facilitate implementation of the research protocol ... Acts as the point person for audit staff coming into institution for a review prepares a written ...
$25 - $30.31
10% of jobs
$30.31 - $35.62
9% of jobs
$39.07 is the 25th percentile. Wages below this are outliers.
$35.62 - $40.93
11% of jobs
$40.93 - $46.24
2% of jobs
$46.24 - $51.55
1% of jobs
The median wage is $55.31 / hr.
$51.55 - $56.86
26% of jobs
$56.86 - $62.17
15% of jobs
$63.28 is the 75th percentile. Wages above this are outliers.
$62.17 - $67.48
13% of jobs
$67.48 - $72.79
10% of jobs
$72.79 - $78.10
4% of jobs
$78.10 - $83.41
1% of jobs
$25
$54
$83
Cities with the most Overnight Clinical Research Protocol Writer job openings:
The most popular types of Clinical Research Protocol Writer jobs are:
States with the most job openings for Overnight Clinical Research Protocol Writer jobs include:
Chicago, IL • On-site
$25 - $33.25/hr
Full-time
This job post has expired 1 day ago. Applications are no longer accepted.
Position SummaryThe Clinical Research Coordinator manages and directs the coordination and timely handling of all components of clinical research protocols in and outside of the clinical setting. This position will develop and implement standards for research protocol management, policies, and procedures. Responsible for the implementation and conduct of multiple research projects.
Coordinates comprehensive patient protocol treatment schedules to maintain compliance to protocol requirements. Develops and implements effective patient recruitment strategies, research budgets, and related fiscal planningDuties & Responsibilities RESEARCH, Clinical Trials, DATA & PROTOCOL MANAGEMENT Lead within the department to improve clinical research practices and operations across studies and serve as a resource to others. Oversee and participate in coordinating and conducting complex clinical research studies, ensuring compliance with federal and institutional regulations.
Take initiative in establishing and coordinating the implementation of clinical research protocol priorities and organizational structure based on study needs, identifying areas for improvement. Execute project goals and tasks as outlined in the project plan by actively assuming responsibility for components necessary for timely completion. Lead protocol changes, assessing and coordinating with various departments to implement changes.
Coordinate the activation and maintenance of clinical protocols, including review and completion of submissions, amendments, and adverse event reports as required by the UIC Institutional Review Board (IRB), Protocol Review Committee and grant sponsors. Review laboratory and clinical procedures and evaluations regularly to ensure protocol compliance. Act as liaison between physicians, clinical staff and the UIC IRB office, grant sponsors and regulatory agencies to ensure priorities are clearly communicated and resources are allocated appropriately across multiple ongoing projects.
Execute informed consent process and monitors patient status; Enroll participants into programs, explaining the research protocols to the clients and supporting family/friends, and obtain appropriate consent forms. Maintain working knowledge of current protocols and internal Standard Operating Procedures (SOPs) and disseminate information on any changes to all stakeholders. Collaborate with the Principal Investigator (PI), department, sponsor, and institution to support and guide the administration of compliance, financial, personnel, and other related aspects of clinical studies.
Prepare, submit, and assist Investigators with multiple levels of research documentation, including educational materials, reports, grant renewal reports, and study forms. Prepare and evaluate protocols, manuscripts, reports, and dissemination tools. Lead team efforts in collaboration with the Assistant Director of Compliance to complete all activities and ensure regulatory compliance, including leading on all Protocol Deviations (PDs), Adverse Events (AEs), and Notes to File (NTFs).
Collaborate with other research personnel with reports to regulatory agencies such as the IRB, FDA, and Data and Safety Review Committee. Ensure validity of research results through timely, accurate, and complete data submission, query resolution, and reporting of deviations. Solve complex problems related to data management and the analysis of large administrative datasets.
Independently develop, manage, and report on key data, ensuring timeliness of data and reporting submissions from multiple investigators. Develop and implement procedures, maintain records, track progress, and conduct quality assurance on collected data. Actively collaborate with research call center agents to support efficient scheduling of research participants.
Delegate tasks to team members within the study program.
