Top 9 Clinical coordinator Jobs in Beaumont, Tx

Clinical Research Coordinator I - Port Arthur, TX
Iterative Health —Port Arthur, TX
- Full-time
- Mid-level
- Bachelor's degree
- Quality control
Clinical Program Coordinator - Forensics Salary Range: $77,349-$82,336 / Annually
SPINDLETOP CENTER —Beaumont, TX
- $77,349 - $82,336 a year
- Full-time
- LMFT
- Management
- Computer literacy
RN Clinical Coordinator
Medical Center SE Texas Port Arthur —Port Arthur, TX
- Full-time
- RN License
- Mid-level
- 3 years
Quick Apply
Palliative Care Clinical Marketer
Harbor Healthcare System —Beaumont, TX
- Online Application
- Sales
- Customer service
- Pass drug screening
- Paid holidays
- Health insurance
Quick Apply
Clinical Psychologist (Drug Abuse Program Coordinator)
US Bureau of Prisons/Federal Prison System —Beaumont, TX
- $89,508 - $116,362 a year
- Online Application
- Management
- Pass drug screening
- Residential
11h
Registered Nurse-Clinical Educator-ICU/CVICU-Days
Baptist Hospitals of Southeast Texas —Beaumont, TX
- Nursing
- RN License
- BLS Certification
- Health insurance
- Dental insurance
Licensed Clinical Psychologist
Josi Health —United States
- Contract
- Remote
- Doctor of Philosophy
- Children
- Psychology
Quick Apply

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Lab Services Coordinator - Clinical Trials Processing Lab
The Ohio State University Wexner Medical Center —Columbus, OH
Participates in data entry and management, quality control, audits and FDA inspections, continuous quality improvement and inventory management of clinical…
Clinical Research Coordinator
OhioHealth —Columbus, OH
This position performs basic day to day activities related to clinical research studies including recruit and screen participants, obtains informed consent,…

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Clinical Research Coordinator I - Port Arthur, TX

Iterative Health -
Port Arthur, TX

Apply Now

Job Details

Full-time

Qualifications

Medication dispensing
Data integrity assurance
Direct patient care
Informed consent
Research ethical considerations
Data validation techniques
EKG
Filing
Care documentation
Phlebotomy specimen handling
Mid-level
Patient safety
Research project coordination
Data integrity and documentation
Schedule management
Bachelor's degree
Research safety & compliance
Health information data integrity
Data quality monitoring
Quality control
Informed consent procedures implementation
Clinical assessment documentation
Health record chart audits
Medical record abstraction
Health information regulatory compliance
Research compliance clinical trial records management
Clinical trial standard operating procedures
Clinical trial patient safety management
Implementing research protocols
Patient recruitment

Full Job Description

Iterative Health is a healthcare technology and services company powering the acceleration of clinical research to transform patient outcomes.

We built a leading performance-driven network of 100+ sites across the US, Europe, India, and Australia, conducting research directly in the communities where care is delivered across gastrointestinal, hepatology, obesity, and cardiology. By combining deep clinical trial expertise with cutting-edge AI, we connect sponsors' scientific ambitions with high-performing research teams that expedite and expand access to novel therapeutics for patients in need. Today, Iterative Health is headquartered in Cambridge, Massachusetts, and New York City with 250+ employees world-wide.

We are seeking a full-time, experienced Clinical Research Coordinator (CRC). The CRC supports, facilitates and coordinates the daily clinical trial activities and plays a critical role in the conduct of the study.

Responsibilities:

Administratively and clinically manage industry-sponsored clinical trials including problem solving, communication and protocol management.
Lead patient recruitment activities, e.g., performing chart reviews, discussing protocols with patients, and verifying the informed consent documentation
Schedule all patient research visits and procedures consistent with protocol requirements
Conduct patient visits as outlined within each study protocol
Dispense study medication, collect vital signs and perform ECGs
Perform blood draws, process and ship specimens per study protocol and IATA regulations
Ensure relevant study and subject specific information is entered into the CTMS system on a regular basis; complete and maintain documentation study files including, but not limited to, consent forms, source documentation, progress notes if applicable, case report forms, and investigational accountability forms.
Act as point of contact for study participants
Adhere to Research SOPs, Good Clinical Practices, and the study protocols
Maintain ongoing communication with the CRO, sponsor, research participants, Site Manager and PI throughout course of the study
Ensure all safety data is reviewed by the PI in a timely manner
Maintain inventory of study equipment and supplies onsite at all times
Participate actively in communication of status and results to management
Assist with routine data verification and quality control, ensuring data integrity and consistency with prescribed study protocol
Schedule and prepare for monitor visits
Assists Study Team in protection of the rights and welfare of all human research participants involved in research in accordance with Federal regulations
Cooperates with site compliance and monitoring efforts regarding the access, use, and disclosure of PHI and reports instances of noncompliance
Complete and maintain case report forms per FDA guidelines, and review them against the patient’s medical record for completeness and accuracy

Iterative Health Expectations

All employees are expected to:

Perform quality work within deadlines with or without direct supervision
Interact professionally with other employees, customers and suppliers
Work effectively as a team contributor on all assignments
Work independently while understanding the necessity for communicating and coordinating work efforts with other employees and organizations

Qualifications

Medical Assistant, LPN, Associates or Bachelor’s degree in a clinical or scientific-related discipline preferred
Minimum 1-2 years of clinical research experience
Able to execute on research tasks with guidance from more experienced staff, PIs, and management
Strong written and verbal communication skils
Ability to read, interpret, and apply clinic policies and research protocols
Ability to use standard office software
Must be able to lift up to 25 pounds

At Iterative Health, we’re actively working towards creating an environment that is representative of the diversity of patients our technology serves. We are focused on building an equitable and inclusive culture, and by extension, hiring process. If you require any accommodations to make the application process or interviewing experience more accessible to you, please contact [email protected].

Apply Now

Refine Your Search

clinical coordinator jobs in beaumont, tx

Clinical Research Coordinator I - Port Arthur, TX

Clinical Program Coordinator - Forensics Salary Range: $77,349-$82,336 / Annually

RN Clinical Coordinator

Palliative Care Clinical Marketer

Clinical Psychologist (Drug Abuse Program Coordinator)

Registered Nurse-Clinical Educator-ICU/CVICU-Days

Licensed Clinical Psychologist

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