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Clinical Research Coordinator 229228 Jobs in Ellis, Texas

Junior Clinical Research Coordinator
By Axiom Resource Management At , Nellis Afb, 89191
Coordinate with study auditors, regulatory agencies, collaborators, and sponsors in management of research studies.
Must have current Basic Life Support (BLS) certification within 15 days of hire.
Superb organization skills with a high level of attention to detail.
Refined interpersonal and communication skills.
Experience working within the Military Healthcare System preferred.
Send resume and salary requirements to:
Account Coordinator/Manager, Clinical Research
By Clinitiative Health Research At Dallas, TX, United States
Works on client clinical trial pipeline to secure study award
Persists to locate appropriate contacts for trial updates and outreach
Demonstrates basic understanding of clinical research
Acts on behalf of sites to sponsors to ensure consideration for feasibility and award
Communicates study updates to sites and other staff members
Completes multiple competing tasks in expected timelines
Clinical Research Coordinator - Manager
By Medix™ At San Antonio, Texas Metropolitan Area, United States
Clearly and concisely document patient assessments, observations, test results and other study related information per federal regulations, protocol requirements and GCPs;
Obtain patient informed consent according to federal regulations, GCPs and IRB requirements;
Schedule and conduct patient visits according to protocol requirements and timelines;
Read, understand and is able to accomplish protocol specified patient visits and procedures;
Maintain accurate and complete written source documentation of patient visits and protocol related activities;
Accurately complete case report forms (CRFs &/or eCRFs) and/or worksheets generated by the sponsor;
Clinical Research Coordinator Jobs
By University of Washington At , Seattle, 98195 $4,554 - $6,100 a month
Data & Patient Management – 40%
As a UW employee, you will enjoy generous benefits and work/life programs.
Prior experience working with patients and/or the public or healthcare providers in a healthcare setting.
Prior experience with industry-sponsored clinical trials preferred.
Experience with diabetes technologies including pump and CGM preferred.
Seattle - South Lake Union
Clinical Research Coordinator Jobs
By Medix™ At Houston, TX, United States
Coordinates patient care in compliance with protocol requirements
Disburses investigational drug and provide patient teaching regarding administration and other patient educational needs
Screens potential patients for protocol eligibility
Presents trial concepts and details to the patients, participates in the informed consent process, and enrolls patients on clinical trials
Responsible for review of consents to ensure proper execution of the informed consent process for study subjects
Oversees the preparation of orders by physicians to assure that protocol compliance is maintained
Clinical Research Coordinator Jobs
By Complete Health & Wellness At Missouri City, TX, United States
Prepare and manage research budgets.
Record any adverse events or side effects experienced by patients.
Prior experience, at least one year (preferred).
Provide ongoing information to patients about treatments.
Maintains records on the database about patients' treatment plans and outcomes.
Monitor patients to ensure they adhere to treatment plans.
Sr. Clinical Research Coordinator
By Stryde Research At Dallas-Fort Worth Metroplex, United States
Work with management to plan and oversight studies and staff
Use clinical trial management systems or similar programs to manage subject visit data and other research activity
Perform site study start-up activities to ensure compliance with sponsor, IRB, and other regulatory requirements
Must have 4+ years of experience in clinical research, specifically in industry sponsored trialsas a cordinator
Strong teamwork skills and willingness to take on a variety of clinical and non-clinical duties
Huge Room for Growth- For right candidate potential to be site director in the future
Clinical Research Coordinator Jobs
By Eurofins Lancaster Laboratories At Austin, TX, United States
Act as project manager on studies as directed by department manager
Provide a professional experience to test subjects, and answer all inquiries, as appropriate
Perform data entry and data review to ensure study quality
Efficiently time manage multiple projects
Succinctly communicate day to day project details to both department manager and Principal Investigator
Record observations, measurements, and test results, as required
Clinical Research Coordinator Jobs
By New England Baptist Hospital At , Boston, 02120, Ma

When you join the growing BILH team, you're not just taking a job, you’re making a difference in people’s lives. Job Type: Regular Scheduled Hours: 40 Work Shift: Day (United States ...

Clinical Research Coordinator - Cantor Center
By Dana-Farber Cancer Institute At , Boston, 02215, Ma

Job ID: 34839 Location: 450 Brookline Ave, Boston, MA 02215 Category: Clinical Research Employment Type: Full time Work Location: PTL Remote: 2-3 days remote/wk Overview The Clinical ...

Coordinator, Clinical Research Program - Leukemia
By MD Anderson Cancer Center At , Houston, 77030, Tx
Systematically review and report on individual faculty assistant compliance with protocol-related job duties
Develops and maintains a processing and tracking system for all protocol related paperwork
Establishes and participates in information systems for the development of research programs including writing, processing, submission and maintenance of protocols
Provides protocol and protocol-related data and information for grant applications in collaboration within the department
Undertake and oversee clinical trial-related grant applications through public and private sector mechanisms
Collaborate on larger departmental grant applications as preparation and production specialist
Clinical Research Coordinator 1 Jobs
By Baylor Scott & White Health At , Dallas, 75226, Tx
Implements various protocols for assigned research projects with appropriate departments throughout the organization by interacting with PIs, clinical managers and supervisors.
Obtains knowledge of departmental functions through reading literature, attending workshops, seminars and conferences and participating in professional organizations.
Research certification or other certifications per specialty area preferred.
Proven written and oral communication skills.
Exceptional computer skills, including Microsoft Office.
Ability to manage time reactive projects in order to meet deadlines.
Clinical Research Coordinator Jobs
By HCA Healthcare At Fort Worth, TX, United States
Education assistance (tuition, student loan, certification support, dependent scholarships)
Family support through fertility and family building benefits with Progyny and adoption assistance.
Employee Health Assistance Fund that offers free employee-only coverage to full-time and part-time colleagues based on income.
You will ensure the protection of study patients by verifying informed consent procedures and adhering to protocol requirements/compliance
You will ensure timely adherence to protocol requirements
You will communicate all protocol-related issues to appropriate study colleagues or manager
Clinical Research Coordinator Jobs
By Dana-Farber Cancer Institute At , Boston, 02215, Ma

KNOWLEDGE, SKILLS, AND ABILITIES REQUIRED:

Clinical Research Coordinator 1 Jobs
By Massachusetts General Hospital(MGH) At , Boston, 02114, Ma
Strong organizational and time management skills
. Bachelor’s degree, with an academic record demonstrating experience and skills in analytical thinking and/or quantitative methods
Strong communication skills including proficiency in written and spoken English
Ability to work both independently and as part of a team, and to collaborate with team members located remotely
Participate in all phases of research projects, from conception and design of studies through proofing manuscripts for submission to academic journals
Monitor study activities for compliance with all applicable regulations and facilitate trainings for study personnel as needed
Clinical Research Coordinator Jobs
By SBR Scientific At Plano, TX, United States
Ability to work autonomously, remotely, in dynamic fast-paced environments, using problem solving skills to adapt to changing demands.
Excellent interpersonal skills, openness to feedback, and a desire to learn and improve skills.
BS, MS, MD, nursing degree or relevant clinical research experience in a related discipline
1-3 years of clinical research experience preferred
·Maintain constant communication with Principal Investigator and Research Manager regarding patient care issues.
Basic understanding of statistical data analysis and interpretation.
Clinical Research Coordinator Jobs
By RAOOF MD Dermatology At , Encino, 91436, Ca

Facilitate and coordinate the daily clinical trial activities. Responsible for recruitment, patient screening, and enrollment for clinical studies. Schedule and attend study participant ...

Clinical Research Coordinator Jobs
By Piedmont Healthcare At , Atlanta, Ga

Forbes named Piedmont one of Georgia’s 10 best employers and the highest-ranked healthcare provider.

Clinical Research Coordinator Jobs
By Vitalief Inc. At Bryan, TX, United States
Any exposure to EPIC (Electronic Health Records system) and/or OnCore (Clinical Trials Management System) is a plus.
Manage eligibility check lists, perform patient screening/consenting (informed consent), patient activation and managing patient care (patient retention).
Any experience in Oncology and/or working on complex clinical trials is a plus.
Must possess excellent interpersonal skills to interact with patients in a clear and confident manner.
Experience in preparation of documents for submission to the Institutional Review Board (IRB), continuing reviews, and submission of amendments and modifications.
Must have strong Microsoft Office skills.
Clinical Research Coordinator - Houston
By Healthwaze At Bellaire, TX, United States
Manages the inventory of equipment and supplies related to the study.
Responsible for ensuring study compliance with local and federal laws and regulations.
Facilitate regulatory start up-documentation and filings, including central IRB submissions.
Recruits and prescreens potential study participants and may perform intake assessments.
Schedule and coordinate protocol-specified study visits.
Creates and/or maintains all documents and records related to the study.