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Clinical Research Coordinator Jobs
Company | HCA Healthcare |
Address | Fort Worth, TX, United States |
Employment type | FULL_TIME |
Salary | |
Category | Hospitals and Health Care |
Expires | 2023-06-19 |
Posted at | 11 months ago |
Description
- Employee Stock Purchase Plan with 10% off HCA Healthcare stock
- Free counseling services and resources for emotional, physical and financial wellbeing
- Employee Health Assistance Fund that offers free employee-only coverage to full-time and part-time colleagues based on income.
- Time Away From Work Program (paid time off, paid family leave, long- and short-term disability coverage and leaves of absence)
- Education assistance (tuition, student loan, certification support, dependent scholarships)
- Comprehensive medical coverage that covers many common services at no cost or for a low copay. Plans include prescription drug and behavioral health coverage as well as free telemedicine services and free AirMed medical transportation.
- 401(k) Plan with a 100% match on 3% to 9% of pay (based on years of service)
- Colleague recognition program
- Referral services for child, elder and pet care, home and auto repair, event planning and more
- Additional options for dental and vision benefits, life and disability coverage, flexible spending accounts, supplemental health protection plans (accident, critical illness, hospital indemnity), auto and home insurance, identity theft protection, legal counseling, long-term care coverage, moving assistance, pet insurance and more.
- Consumer discounts through Abenity and Consumer Discounts
- Family support through fertility and family building benefits with Progyny and adoption assistance.
- Retirement readiness, rollover assistance services and preferred banking partnerships
- You will implement study-specific communications
- You will assist sponsor and US FDA audit teams
- You will be responsible for working with the principal investigator to meet or exceed study enrollment.
- You will support enrolling patients onto clinical trials through recruitment, screening, enrollment and follow up of eligible subjects according to protocol requirements
- You will create study specific tools for source documentation when not provided by sponsor
- You will review and respond to any monitoring and auditing findings and escalates issues defined by Regional Site Manager
- You will be responsible for completion of all required documentation according to site works guidelines
- You will report and follow up on serious adverse events as necessary
- You will communicate all protocol-related issues to appropriate study colleagues or manager
- You will track and report adverse events, serious adverse events, protocol waivers, deviations, and violations
- 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 review the study design and inclusion/exclusion criteria with physician and patient
- You will apprise the principal investigator, Research Operations Director and Regional Site Manager of all study specific medical issues for guidance
- You will ensure timely and accurate data completion
- You will collect, complete, and enter data into study specific case report forms or electronic data capture systems
- You will ensure the integrity of the data submitted on Case Report Forms or other data collection tools by careful source document review; monitors data for missing or implausible data
- You will attend study specific on site meetings, investigator meetings, conference calls and monthly CRC meetings as required or asked to do so
- You will generate and track drug shipments, device shipments, and supplies as needed
- You will maintain accurate and complete records including regulatory documents when applicable, signed informed consent forms, source documentation, drug dispensing logs, device utilization logs, subject logs and study-related communications
- Excellent interpersonal skills
- The ability to work independently in a fast pace environment with minimal supervision at off-site facilities
- Organizational and prioritizing capabilities
- Computer skills including use of clinical trial database, electronic data capture, and MS Word or Excel
- The ability to communicate and work effectively with a diverse team of professionals
- Knowledge of federal regulations, good clinical practices (GCP)
- Excellent Verbal and written communication skills
- Nursing experience is preferred
- Knowledge of medical and research terminology
- At least one year of experience as a Clinical Research Coordinator
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