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Clinical Research Coordinator 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 Nurse Coordinator
By Lightship At , Concord $50 - $65 an hour
Required knowledge, skills, and abilities
Knowledge of medical terminology, drug calculation skills, and clinical medicine
Bachelor of Nursing or another Science degree preferred, or requisite combination of education, training, and experience
Administering investigational medications or providing patient education regarding administration, as necessary
Documenting study data in patient records (paper and electronic, as applicable) to capture protocol requirements
Participating in recruitment and selection of study patients by interviewing and documenting medical history / medication history per protocol requirements
Clinical Research Coordinator I
By Emory University At , Atlanta, 30322
Maintains data pertaining to research projects, completes source documents/case report forms, and performs data entry.
Performs related approved responsibilities as required.
(1.) High School Diploma or GED and three years of administrative support experience OR
(3.) Licensed as a practical nurse (LPN) and one year admin support or one year of licensed practical nursing experience OR
Handles or assists with administrative activities generally associated with the conduct of clinical trials.
Assists with patient recruitment. Attends study meetings.
Clinical Research Coordinator I
By The Geneva Foundation At , San Antonio, 78234 $43,800 - $58,800 a year
Computer skills including at least intermediate level experience with Excel and other Microsoft Office Software
Bachelors degree or equivalent work experience required
2-4 years experience in clinical research preferred
2-4 years non-profit, research, or healthcare experience desired
Knowledge of CFR, GCP and ICH guidelines
Promote safety and confidentiality of research participants at all times
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 Data Coordinator
By Sarah Cannon At Girlstown USA, TX, United States
Experience using EMR and strong computer skills preferred.
You will maintain working knowledge of protocols and eCRF completion guidelines for assigned projects.
You will regularly review protocol, amendments or clarifications, and revisions for eDC data entry.
You will support non-treatment studies. You will abstract and analyze data from necessary sources to complete the EDC and resolve queries.
A strong understanding of research protocols and implementation.
Attention to details and accuracy
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 ...

Coordinator, Clinical Studies - Translational Research Training Program
By MD Anderson Cancer Center At , Houston, 77030, Tx
Follows patients on study and maintains knowledge of adverse events
Collaborates with physicians, mid-level practitioners, research nurse and data managers to document patient care
Coordinates reports for the study manager for submitting grant data in a timely manner
Provides study related coordination including protocol maintenance
Develops and maintains a processing and tracking system for all protocol related documents
Develops patient care methodology for protocols, including criteria for patient participation
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 I
By Morehouse School Of Medicine At , Atlanta, 30310, Ga
Improve the health and well-being of individuals and communities;
Increase the diversity of the health professional and scientific workforce;
You will find a fulfilling career at
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:

Are you looking for an exciting opportunity to make a difference in the medical field? We are seeking a Clinical Research Coordinator to join our team and help us advance medical research. You will be responsible for managing clinical trials, coordinating patient visits, and ensuring compliance with regulatory standards. If you have a passion for helping others and a commitment to excellence, this could be the perfect job for you!

A Clinical Research Coordinator (CRC) is responsible for the coordination and management of clinical trials and research studies. They are responsible for ensuring that the research is conducted in accordance with the protocol, applicable regulations, and Good Clinical Practice (GCP).

What is Clinical Research Coordinator Skills Required?

• Excellent organizational and communication skills
• Ability to work independently and as part of a team
• Knowledge of medical terminology
• Knowledge of clinical research regulations and guidelines
• Proficiency in computer applications
• Ability to manage multiple tasks and prioritize
• Ability to work in a fast-paced environment

What is Clinical Research Coordinator Qualifications?

• Bachelor’s degree in a health-related field
• Certification in clinical research (CCRC)
• Previous experience in clinical research

What is Clinical Research Coordinator Knowledge?

• Knowledge of clinical research protocols
• Knowledge of clinical trial design and data management
• Knowledge of medical terminology
• Knowledge of Good Clinical Practice (GCP)

What is Clinical Research Coordinator Experience?

• Previous experience in clinical research
• Previous experience in data management
• Previous experience in clinical trial design

What is Clinical Research Coordinator Responsibilities?

• Develop and implement clinical research protocols
• Monitor clinical trial progress and data
• Ensure compliance with applicable regulations and GCP
• Prepare and submit regulatory