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This general interest posting is designed for experienced Clinical Research Coordinators (CRCs) who may not see a current opening that aligns with their location, but want to be considered for future opportunities across our growing network of clinical research sites nationwide. They play a hands-on role in advancing new therapies, supporting patients through clinical trials, and ensuring studies are conducted with the highest level of quality and care.

YEAR

Headlands Research

Clinical Research Coordinator I/Ii/Iii Opportunities - Multiple Locations Nationwide

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The Clinical Research Nurse Coordinator supports clinical research studies by coordinating trial activities, providing patient care, collecting study data, and ensuring compliance with study protocols, FDA regulations, and ICH-GCP guidelines. This role partners with Principal Investigators, research staff, and sponsors to facilitate the successful execution of industry-sponsored and investigator-initiated trials while serving as a strong patient advocate.

Actalent Inc

Clinical Research Nurse Coordinator

Responsibilities may include but are not limited to: Under the direction of the Site Manager/Director and the Principal/Sub Investigators, conducts the following according to study protocol, company processes & procedures, and in compliance with FDA, GCP, ICH regulations and guidelines: Screening of patients for study enrollment; Patient consents; Patient follow-up visits; Documenting in source clinic charts; Entering data in EDC and answers queries; Obtaining vital signs and ECGs; May perform basic lab procedures per protocol, such as: blood specimen collection, centrifuge operation, storing and shipping of lab specimens, accountability of specimens and notification of courier for specimen pick-up; Requesting and tracking medical record requests; Updating and maintaining logs, chart filings; Maintaining & ordering study specific supplies; Scheduling subjects for study visits and conducts appointment reminders; Building/updating source as needed; Conducting monitoring visits and resolves issues as needed in a timely manner; Ensuring study related reports and patient results are reviewed by investigator in a timely manner; o Filing SAE/Deviation reports to Sponsor and IRB as needed; o Documenting and reporting adverse events; o Reporting non-compliance to appropriate staff in timely manner; o Maintaining positive and effective communication with clients and team. Prepare and attend site initiation visits (SIV's) and Investigator Meetings (IMs), as needed; Handles all IRB functions for assigned studies independently, and/or with assigned regulatory team member, as needed; Assist with training of new research assistants and coordinators; Assist with scheduling and planning for visit capacity for assigned studies; May set up, train and maintain all technology needed for studies; May assist with study recruitment, patient enrollment, and tracking as needed; May handle more complex study assignments and volumes; May participate in community outreach / education events; Maintaining confidentiality of patients, customers and company information, and; Performing all other duties as requested or assigned.

Alcanza Clinical Research LLC

Travel Clinical Research Coordinator

Responsibilities may include but are not limited to: Under the direction of the Site Manager/Director and the Principal/Sub Investigators, conducts the following according to study protocol, company processes & procedures, and in compliance with FDA, GCP, ICH regulations and guidelines: Screening of patients for study enrollment; Patient consents; Patient follow-up visits; Documenting in source clinic charts; Entering data in EDC and answers queries; Obtaining vital signs and ECGs; May perform basic lab procedures per protocol, such as: blood specimen collection, centrifuge operation, storing and shipping of lab specimens, accountability of specimens and notification of courier for specimen pick-up; Requesting and tracking medical record requests; Updating and maintaining logs, chart filings; Maintaining & ordering study specific supplies; Scheduling subjects for study visits and conducts appointment reminders; Building/updating source as needed; Conducting monitoring visits and resolves issues as needed in a timely manner; Ensuring study related reports and patient results are reviewed by investigator in a timely manner; o Filing SAE/Deviation reports to Sponsor and IRB as needed; o Documenting and reporting adverse events; o Reporting non-compliance to appropriate staff in timely manner; o Maintaining positive and effective communication with clients and team. Prepare and attend site initiation visits (SIV’s) and Investigator Meetings (IMs), as needed; Handles all IRB functions for assigned studies independently, and/or with assigned regulatory team member, as needed; Assist with training of new research assistants and coordinators; Assist with scheduling and planning for visit capacity for assigned studies; May set up, train and maintain all technology needed for studies; May assist with study recruitment, patient enrollment, and tracking as needed; May handle more complex study assignments and volumes; May participate in community outreach / education events; Maintaining confidentiality of patients, customers and company information, and; Performing all other duties as requested or assigned.

Alcanza Clinical Research

PinpointHQ

Responsibilities: Support the pipelining of candidates to ensure a ready pool of qualified professionals for all clinical levels, including full-time Research Assistants, Clinical Research Coordinators, and Principal/Sub-Investigators, as well as PRN roles such as Registered Nurses, EMTs, and Firefighters across all K2 clinics. This position is designed with a clear growth trajectory: as the individual gains experience and mastery of the role, responsibilities will expand to include conducting initial phone screens, presenting top candidates to hiring teams, and co-leading university outreach and career fairs alongside the Director of Talent.

K2 Medical Research

Talent Coordinator

IRecruitee

Qualifications Qualifications Must meet one of the following: Bachelor's degree in health-related field (i.e., Healthcare Administration, Nursing, Respiratory Therapy, Health & Wellness or Health Information Management); or Associate degree in related field (i.e., Healthcare Administration, Nursing, Respiratory Therapy, Health & Wellness or Health Information Management) and one (1) year of clinical research or healthcare experience (in addition to the requirements listed in the Experience section); or Graduate of an accredited allied health program and one (1) year of clinical research or healthcare experience (in addition to the requirements listed in the Experience section). Qualifications Must meet one of the following: Bachelor's degree in health-related field (i.e., Healthcare Administration, Nursing, Respiratory Therapy, Health & Wellness or Health Information Management); or Associate degree in related field (i.e., Healthcare Administration, Nursing, Respiratory Therapy, Health & Wellness or Health Information Management) and one (1) year of clinical research or healthcare experience (in addition to the requirements listed in the Experience section); or Graduate of an accredited allied health program and one (1) year of clinical research or healthcare experience (in addition to the requirements listed in the Experience section).

Orlando Health Ventures l LLC

Clinical Research Coord - Full Time - Day - Corp

The work environment involves close collaboration with clinical research teams, including clinical study coordinators, data support staff, and cross-functional partners such as Research Services, Study Intake, Portfolio Management, and regulatory offices. The position partners closely with business development teams and Study Intake Program Managers to ensure research projects are high quality, operationally feasible, and responsive to the needs of investigators and patients.

Research Manager

Qualifications Education/Training Must meet one of the following: • Bachelor's degree in health-related field (i.e., Healthcare Administration, Nursing, Respiratory Therapy, Health & Wellness or Health Information Management); or • Associate degree in related field (i.e., Healthcare Administration, Nursing, Respiratory Therapy, Health & Wellness or Health Information Management) and one (1) year of clinical research or healthcare experience (in addition to the requirements listed in the Experience section); or • Graduate of an accredited allied health program and one (1) year of clinical research or healthcare experience (in addition to the requirements listed in the Experience section). Education/Training Must meet one of the following: • Bachelor's degree in health-related field (i.e., Healthcare Administration, Nursing, Respiratory Therapy, Health & Wellness or Health Information Management); or • Associate degree in related field (i.e., Healthcare Administration, Nursing, Respiratory Therapy, Health & Wellness or Health Information Management) and one (1) year of clinical research or healthcare experience (in addition to the requirements listed in the Experience section); or • Graduate of an accredited allied health program and one (1) year of clinical research or healthcare experience (in addition to the requirements listed in the Experience section).

Orlando Health Ventures

Clinical Research Coord - Corp

Summary: The Clinical Research Assistant assists the Clinical Operations Team in a multi-functional capacity to carry out all assigned tasks associated with the collection, documentation, and maintenance of clinical data including phlebotomy/laboratory, data entry and administrative responsibilities. Velocity Clinical Research is an owned and integrated research site organization, providing excellence in patient care, high quality data and fully integrated research sites.

Velocity Clinical Research Inc

Clinical Research Assistant

TEMPORARY

The Clinical Research Assistant assists the Clinical Operations Team in a multi-functional capacity to carry out all assigned tasks associated with the collection, documentation, and maintenance of clinical data including phlebotomy/laboratory, data entry and administrative responsibilities. Overview: Velocity Clinical Research is an owned and integrated research site organization, providing excellence in patient care, high quality data and fully integrated research sites.

Velocity Clinical Research, Inc.

[AW]-iCims

Overseeing resourcing allocations, site assignments and study team members'' output and performance, to ensure study deliverables are on track, identifying risks to delivery or quality, and escalating any risks to clinical trial management deliverables (timeline, quality and budget). Collaborating with other departments (Business Development, Patient Recruitment, Finance, Budgets and Contracts, and Quality) to coordinate delivery expectations, meet expected study milestones (such as site activation targets, enrollment targets, etc.), meet budgets, and delivery quality data to sponsors.

Clinical Research Operations Manager

This general interest posting is designed for Clinical Research Assistants (RAs) who may not see a current opening that aligns with their location, but want to be considered for future opportunities across our growing network of clinical research sites nationwide. We welcome interest from candidates who bring: A bachelor's or master's degree involving 1+ year of laboratory classes, preferably within a scientific or healthcare-related field (e.g., biology, chemistry, psychology, pre-med, or similar) and/or.

Clinical Research Assistant Opportunities - Multiple Locations Nationwide

Overseeing resourcing allocations, site assignments and study team members' output and performance, to ensure study deliverables are on track, identifying risks to delivery or quality, and escalating any risks to clinical trial management deliverables (timeline, quality and budget). Collaborating with other departments (Business Development, Patient Recruitment, Finance, Budgets and Contracts, and Quality) to coordinate delivery expectations, meet expected study milestones (such as site activation targets, enrollment targets, etc.), meet budgets, and delivery quality data to sponsors.

Heartflow is the first AI-driven non-invasive integrated heart care solution across the CCTA pathway that helps clinicians identify stenoses in the coronary arteries (RoadMapAnalysis), assess coronary blood flow (FFRCT Analysis), and characterize and quantify coronary atherosclerosis (Plaque Analysis). The flagship product-an AI-driven, non-invasive cardiac test supported by the ACC/AHA Chest Pain Guidelines called the Heartflow FFRCT Analysis-provides a color-coded, 3D model of a patient's coronary arteries indicating the impact blockages have on blood flow to the heart.

Heartflow Inc

Clinical Trial Manager - East Coast

Ensures teams maintain adequate inventory levels, order approved equipment and supplies, and maintain clinical supply areas. Applicants may review general information about Florida's background screening requirements at the Florida Care Provider Background Screening Clearinghouse: https://info.flclearinghouse.com/ .

AdventHealth

Clinical Research Supervisor

Keywords: Senior Clinical Research Associate, Senior CRA, Clinical Research Associate, CNS Clinical Trials, Neurology Trials, Neuroscience Research, Cardiovascular Clinical Trials, Cardiology Studies, Phase II Clinical Trials, Phase III Clinical Trials, Clinical Monitoring, Independent Monitoring, Site Monitoring, Site Management, Clinical Operations, ICH-GCP, FDA Regulations, GCP Compliance, Clinical Trial Management, Source Data Verification, SDV, Source Data Review, SDR, CRF Review, Case Report Forms, Site Initiation Visits, SIV, Interim Monitoring Visits, IMV, Closeout Visits, COV, Investigative Sites, Patient Enrollment, Subject Recruitment, Clinical Development, Site Oversight, Risk Management, Protocol Compliance, Regulatory Compliance, Data Quality, Inspection Readiness, Sponsor-Facing, CRO, Biotechnology, Pharmaceutical Research, Clinical Study Management, Trial Execution, Clinical Research Operations, Monitoring Visits, Neurology, CNS Disorders, Epilepsy, Parkinson's Disease, Alzheimer's Disease, Multiple Sclerosis, Stroke, Cardiovascular Research, Heart Failure, Hypertension, Coronary Artery Disease, Arrhythmia Studies, Clinical Research Monitoring. This is a full time opportunity that requires regional travel and can be located anywhere in the U.S. Responsibilities for the Senior Clinical Research Associate include: Independently monitoring Phase II-III CNS and Cardiovascular clinical trials to ensure compliance with study protocols, ICH-GCP guidelines, and regulatory requirements.

Zp Group Llc

Senior Clinical Research Associate - CNS/Cardiovascular

The nurse advocates for participants' rights and safety, performs clinical procedures within scope of practice, and collaborates closely with principal investigators, sub-investigators, and the broader research team to collect high-quality data and maintain the integrity of each trial. Promote investigator oversight by promptly advising principal investigators, sub-investigators, supervisors, and clinical operations leadership of protocol deviations, changes in patient status, and any issues affecting trial integrity or participant safety.

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