Clinical Research Coordinator — Protocols & Site Ops
Dm Clinical Research Group
Dm Clinical Research Group is seeking a Clinical Research Coordinator III in Houston, Texas. This role involves ensuring quality research is conducted at investigative sites, adhering to sponsor protocols, FDA regulations, and guidelines. The successful candidate will oversee study subject visits and ensure data quality. Responsibilities include conducting training, maintaining regulatory standards, and enhancing subject recruitment. Strong communication skills and a background in clinical research are essential. #J-18808-Ljbffr Dm Clinical Research Group
$49.61k - $87.28k
...8.00 - $87,276.80Position SummaryThe Clinical Research Coordinator functions as an integral part of the... ...AreasKPA 1 – Study Start-Up, Regulatory & Site InitiationResponsible for supporting... ...activities to ensure compliance with protocols, regulatory requirements, and...Website- Jimmy Jazz in Houston is looking for a Clinical Research Coordinator II. The role involves overseeing the management of clinical trials, ensuring compliance with protocols, and liaising with laboratories. This position is critical for the successful execution of research...Suggested
- ...Position Clinical Research Coordinator II Location Juno Research, Houston, TX Department Study Operations... ..., and clinical staff to maintain protocol compliance, uphold regulatory and documentation... ...skills. This position reports to the Site Manager or Site Director. Key...WebsiteWork experience placement
$19.66 - $34.59 per hour
...for the performance of the research study under the medical supervision... ...Investigator. The Clinical Research Coordinator I (non-RN) is responsible for... ...and procedures. KPA 1 - Protocol Comprehension and Implementation... ...and complete feasibility/site assessment questionnaires...WebsiteContract workRemote workMonday to Friday- Johnson County Clin Trials (JCCT) in Houston, Texas is seeking a Clinical Research Coordinator II (Bilingual English/Spanish) to manage multiple clinical trials and ensure protocol compliance. This role requires a minimum of three years experience in clinical research and...Website
- ...an alternative application process. Clinical Research Coordinator (CRC)-FT Full Time HDR Memorial Hermann... ...the Principal Investigator and the Site Director. They maintain accurate, confidential... ...of all components of each study protocol through review and analysis of study...WebsiteFull timeWork at office
- ...Employee Type: Non-Exempt - FT Job Title: Clinical Research Coordinator II FSLA Classification: Non-Exempt Reports to: Site Operations Manager Job Summary / Objective... ...laboratories. Monitor study compliance with protocols and ethical standards. Ensure adherence to...WebsiteWork at officeMonday to Friday
- ...Clinical Research Coordinator I Position is on-site Monday - Friday in South Houston, Texas Renal Specialists of Houston 3333 Bayshore Blvd, Ste. 270... ...Coordinator I will perform delegated duties such as protocol required visit procedures, administering questionnaires...WebsiteContract workLocal areaMonday to FridayNight shift
- Job Details Job Location: CyFair - Houston, TX 77065 The Clinical Research Coordinator III will ensure that quality research is conducted at assigned investigative sites in accordance with the sponsor protocol, FDA Regulations, and ICH/GCP guidelines and to provide the...Website
- ...Clinical Research Coordinator II - Houston, TX Houston, TX Iterative Health is a healthcare technology... ...performance-driven network of 100+ sites across the US, Europe, India, and... ...activities and ensuring compliance with protocol requirements, regulatory standards,...WebsiteWork at office
- ...Senior Clinical Research Coordinator Are you passionate about the patient experience? At HCA Healthcare... ...for coordinating multiple research protocols; serving as a liaison with local investigators... ..., and training necessary to maintain site compliance and patient safety....WebsiteTemporary workLocal areaFlexible hours
- ...following certifications: CCRC - Certified Clinical Research Coordinator (ACRP) or CCRP - Certified Clinical... ...testing procedures required by study protocol (medical history interview, vital... ...timely timecard approval, etc.). Monitors site visits pre-study, at study initiation...WebsiteImmediate startFlexible hours
$130k - $150k
...cancers. Our cutting-edge science and robust clinical pipeline form the broadest PRAME... ...Clinical Operations team. The CTM will oversee site management, monitoring oversight, and... ...report review and training supportManage protocol and GCP deviations and contribute to continuous...WebsiteTemporary workWork at officeImmediate start- Baylor College of Medicine in Houston is seeking a Research Coordinator I to oversee day-to-day activities of IBD clinical trials. This full-time, on-site position collaborates with a team and principal investigators to ensure regulatory compliance and successful study...WebsiteFull time
- ...powering the acceleration of clinical research to transform patient... ...performance-driven network of 100+ sites across the US, Europe, India... ...As a Clinical Research Coordinator II (CRC II) at Iterative Health... ...and ensuring compliance with protocol requirements, regulatory standards...WebsiteWork at office
- ...Description Job Description Summary: The Clinical Research Coordinator will manage the day-to-day operations... ...pre-established work scope, study protocol, and regulatory requirements are... ..., Operations Manager, and Site Director or Regional Director Maintain...WebsiteTemporary workWork at officeLocal areaFlexible hours
$20 - $25 per hour
...Clinical Research Data Coordinator - Oncology Onsite Contract Required Qualifications MUST HAVE 3 years of clinical research data coordination... ...quality reviews to ensure accuracy, completeness, and protocol compliance Generate, track, and resolve data queries...Contract workTemporary work- ...Mental Health and IDD as a Clinical Project Manager, Health Analytics and Research. The Clinical Project... ...outcome research protocols to ensure productivity... ...meetings and provide on‑site leadership for the project... ...it serves. Ability to coordinate diverse project components...WebsiteTraineeshipLocal area
- A leading healthcare provider in Houston is seeking a Clinical Research Coordinator to oversee clinical research personnel and manage study protocols. The ideal candidate will have a Bachelor's degree and at least five years of clinical research experience, along with the...
- University of Texas MD Anderson Cancer Center seeks a Research Data Coordinator to provide administrative and patient care services for coordinating... .... You will collect and manage patient data, coordinate protocol administration, and ensure regulatory compliance within a...
- At Houston Methodist, the Research Coordinator position is responsible for coordinating the day-to‑day activities of research protocols as well as assessing and determining qualification... ...language principles. Sufficient clinical and research data entry skills. Capability...
- Houston Methodist is looking for a Research Coordinator in Houston, Texas. The successful candidate will coordinate daily activities of research protocols, assess patient qualifications for studies, and ensure data accuracy and safety of research participants. Qualified...
- Houston Methodist is seeking a Research Coordinator to manage day-to-day activities of research protocols, assess patient eligibility, and ensure accurate data collection... ...communication to support compliant, efficient clinical studies. Strong attention to detail and...
- Houston Methodist is seeking a Research Coordinator II responsible for coordinating day-to-day research activities and ensuring patient qualification... ..., and supporting administrative duties within research protocols. The ideal candidate will hold a Bachelor’s degree, have...
- ...The purpose of this position is to coordinate assigned projects from initiation through completion... ...Degree or higher required PMP required Clinical licensure or relevant clinical... ...all hospital locations as required; be on‑site at hospitals at pivotal times during process...WebsiteTemporary work
- ...target cities including Chicago, Minneapolis, Dallas, Houston, and Austin. Responsibilities Participate in clinical research activities at the study and site levels, including documentation, vendor management, and project management tasks. Develop trial timelines, enrollment...Website
- Immatics US, Inc. is seeking a Clinical Trial Manager to support the U.S. Clinical Operations team. The role focuses on overseeing clinical... ...regulatory requirements. You will work closely with clinical sites to drive operational excellence in trials. Candidates should...WebsiteRemote job
- ...A prominent healthcare institution in Houston is looking for a Research Assistant to evaluate patient eligibility for studies. Candidates... ...and analytical skills. Responsibilities include maintaining clinical study records, scheduling patient appointments, and ensuring regulatory...
- Houston Methodist is seeking a Research Coordinator III in Houston, Texas. This role involves coordinating clinical research projects, gathering patient data, and supporting Principal Investigators. Candidates must have a Bachelor’s degree and five years of clinical research...
- Houston Methodist is seeking a Research Coordinator to coordinate day-to-day research activities, ensuring accurate data collection and participant safety. The successful candidate will evaluate patient qualifications for research studies and contribute to a collaborative...
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