Job Details:-
This is a job posting from company – Deaconess Health System
Employment Type – Full Time
Work Hours: 8
Salary: $20 To $30/An Hour
Location: Indiana, USA
This job is 100% remote.
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Summary
Join our Team
Deaconess Health System is looking for compassionate, caring people to join our talented staff of health care professionals as we continue to grow to be the preferred, regional health care partner in our community.
Benefits
We pride ourselves in retaining our top talent by offering work environments that support professional development and personal success. In addition to our robust healthcare and retirement plans, we offer:
- Onsite children’s care centers (Infant through Pre-K) at various locations
- Tuition reimbursement
- Free access to fitness centers, where health coaches are available to help with workout plans at various locations
- Career advancement opportunities
- Competitive pay, shift and weekend incentives, yearly opportunities for pay increases and bonuses
Job Summary
Completes pre-study activities
Reviews and knows requirements of study protocol thoroughly
Attends investigator meetings locally and/or out of town
Coordinates study related sponsor/CRO visits for site qualification and site initiation meetings
Develops timelines for conducting and completing the clinical trial
Assists in submission of regulatory documents for IRB review
Develops all forms and educational materials needed to efficiently conduct the clinical trial
Coordinates required supplies and resources to efficiently conduct the clinical trial
Implements the procedures of the protocol
Coordinates strategies for recruitment to meet or exceed target enrollment
Participates in the screening of patient charts and recruitment over the telephone
Maintains and, if necessary, develops current patient logs for each clinical trial
Obtains volunteer informed consent according to department SOP’s. Ensures volunteer’s understanding of the informed consent document and his/her participation
Completes all study visit procedures as properly trained or licensed
Monitors enrollment goals and if necessary adjusts enrollment plan and strategies
Accurately records pertinent information in source documentation and ensures transcription is in the case report forms (CRF’s) in a timely fashion
Provides patient education regarding objectives of the protocol
Maintains accurate and current drug dispensation and inventory records for each patient
Assesses adverse events and follows up with the Principal Investigator, patient and sponsor as needed. Reports all serious adverse events (SAE’s) immediately to investigator and within 24 hours to sponsor. Completes required documentation according to sponsor, regulatory, and company policies
Communicates with patient for study-related issues
Ensures all appropriate CRF’s are completed 48 hours prior to monitoring visits
Coordinates, prepares, and attends clinical monitoring visits
Serves as the primary contact person for sponsor or CRO
Resolves queries from sponsors or CRO within required time lines
Efficiently conducts study close-out procedures according to sponsor specifications and company policies, including return of all study product
Assists investigator and/or other staff with patient visits and procedures as per protocol
Provides investigators updates regarding patient status and progress in clinical trial
Provide flexibility with working hours to accommodate patients, sponsor representatives and investigators
Be accessible to patients and investigators via pager during non-working hours
Be willing to travel within a weeks notice
May participate in the supervision of work performed by Clinical Associates
Attends meetings and continuing education seminars for growth and development
Ensures compliance with company standard operating procedures and policies, good clinical practices and FDA regulations in all activities
Education and Experience
At least one year clinical experience preferred.
Phlebotomy skills and preparation of samples for shipping preferred but not required.
Certificates, Licenses, Registrations
Current Indiana license required. Bachelor’s or Associate degree in Nursing, RN or LPN
Certified Clinical Research Coordinator CCRC
Why Choose Deaconess?
Deaconess Health System is the largest employer in the tri-state region, and operates under the direction of a local board, with a local focus. Deaconess is widely recognized for its commitment to excellence. Named the #2 Hospital in Indiana by US News & World Report for the past four years, Deaconess was also named to the Forbes list of America’s Best Employers in 2022. As our organization continues to grow and expand, we welcome skilled, dedicated and compassionate individuals to join us in delivering The Deaconess Difference: putting people at the center of everything we do, making a positive difference in the lives of our patients, families, employees and community.