- BSN with minimum of two years clinical experience
- Bachelors (BA or BS) and two years' experience in clinical research with human subjects
- Associate Degree Nursing (ADN), RN, with minimum of four years clinical experience
- Current certification in clinical research (SOCRA-CCRP, ACRP-CCRC or ACRP-CP) with three years clinical research experience with human subjects
- See above
- Current South Carolina RN license (for nurse applicants only)
- Master's in a Heath Related field
- One (1) year oncology experience
- Clinical research experience
- Phlebotomy experience
- Certification in research (CCRC, CCRP)
- Membership in a Clinical Research Professional organization (ACRP, SoCRA, etc...) within 1 year of hire or as eligible based on research experience.
- Must be able to work as a team member with other Research staff, doctors, departments, community, and other components.
- Must have own transportation to other hospitals and doctors' offices.
- Must be flexible in responsibilities and work schedule.
- Travel required to attend NCI meetings.
- Must be meticulous with detail.
- Must be able to read, write, and speak English fluently.
- Must have good communication skills.
- Must be able to respond calmly and efficiently in high stress situations.
- Must be able to sit for long periods of time, filling out paperwork.
- Must be self-directed and able to work without supervisor.
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Clinical Research Coordinator
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Clinical Research Coordinator
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Clinical Research Coordinator
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Spartanburg Regional Healthcare System Spartanburg, United States Full timeSummary · Position Summary · Clinical Research Coordinator assumes responsibility for the overall coordination of oncology research trials from all aspects. This position will be responsible for identifying clinical trials, feasibility reviews and study activation. Screens for p ...
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Bilingual Patient Service Rep
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Resource Coordinator
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Environmental Consultants (ECI) Spartanburg, United StatesWe are currently seeking a **Resource Coordinator** to join our team. We are looking for energetic professionals who enjoy working outdoors and value the freedom of working independently. If you enjoy a fast-paced environment and the challenges of a rewarding profession, consider ...
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Patient Services Rep
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Program Coordinator-Research, FT
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Prisma Health Greenville, United StatesInspire health. Serve with compassion. Be the difference. · Job Summary · Supports the Office of Research Services in the planning, implementation and analysis of efforts to improve the quality and efficiency of processes critical to conducting clinical research, implements techn ...
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Prisma Health Greenville, United States Full timeInspire health. Serve with compassion. Be the difference. · Job Summary · Responsible for the implementation, management and oversight of clinical trial research studies including the education of research staff, healthcare team member, participants and their caregivers. Register ...
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Clinical Research Coordinator, Full-Time, Days
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Prisma Health Greenville, United States Full timeInspire health. Serve with compassion. Be the difference. · Job Summary · Under minimal supervision, assists with screening, consents, enrollment and maintaining research subjects as well as maintain compliance to research protocols. Acts as the liaison between monitors, investig ...
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Edward Via College of Osteopathic Medicine Spartanburg, United StatesThe position of Director for International and Appalachian Outreach Programs provides coordination of VCOM's international and Appalachian outreach activities on the Carolinas campus, reporting to the Vice Provost for International and Appalachian Outreach, and, in some instances ...
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Sr. Manager Financial Systems
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Dell Simpsonville, United States Full timeSenior Manager, Financial Systems · Location: The position can be fully remote with a preference of Atlanta, GA based. · Secureworks (NASDAQ: SCWX) is a global cybersecurity leader that secures human progress with Secureworks TaegisTM, a SaaS-based, open XDR platform built on 20 ...
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Sales Representative
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SYSCO Greenville, United States Full timeCompany: · US1166 FreshPoint Charlotte, Division of FreshPoint North Carolina, Inc.Zip Code: · 28269Employment Type: · Full TimeTravel Percentage: · Up to 50%COMPENSATION INFORMATION: · The pay range provided is not indicative of Sysco's actual pay range but is merely algorithm ...
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Grant Writer
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Navigator-Precision Medicine
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AmeriCorps Program Director
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Environmental Health and Safety Specialist
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Spartanburg Steel Products Spartanburg, United StatesCompany Description · Spartanburg Steel Products is a major supplier of metal stampings and welded sub-assemblies for automotive, lawn & garden, agricultural, and construction equipment OEMs throughout the United States: · * Motivated, experienced, and stable team, ready to execu ...
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Administrative Secretary
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Guy Roofing Spartanburg, United States· * Assist the VP with daily administrative duties and completes a broad variety of administrative tasks that include managing an active calendar of appointments; completing expense reports; composing and preparing correspondence; arranging complex and detailed travel plans, iti ...
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Administrative Secretary
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Tax Processing Associate
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Security Finance Spartanburg, United States· As Tax Associate, you will: · * Assist with developing training for field operations and seasonal support team: · * Coordinate with tax processing supervisors and LMS administrator to develop/update multiple types of training, including but not limited to; online, webinar and ...
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Spartanburg Regional Medical Center Spartanburg, United StatesPosition Summary # The Acute Care Registered Nurse (RN) provides inpatient nursing care to patients in compliance with the SC Nurse Practice Act and organization protocols, policies, procedures, and guidelines. The RN demonstrates clinical competency utilizing evidence-based prac ...
Clinical Research Coordinator - Spartanburg, United States - Spartanburg Regional Medical Center
Description
Position Summary Clinical Research Coordinator assumes responsibility for the overall coordination of oncology research trials from all aspects.# This position will be responsible for identifying clinical trials, feasibility reviews and study activation.#
Screens for potential patients for clinical trial opportunities, educating patients and families about research and, obtaining and developing research data, and monitoring compliance with research protocols.
##Responsible for oncology study coordination and study implementation in collaboration with the participating physicians, their staff, regulatory staff and study sponsor.
## Maintains strong communication with physicians, nurses, pharmacy and other key persons regarding available protocols.# Maintains protocol integrity through adherence of protocol requirements.Responsible for data management as required per protocol.# Must be self-starter/motivated, detail-oriented, willing to develop the clinical research service line within the oncology programs.
Knowledge of oncology nursing practices preferred. Willing to learn and train on required clinical research database and clinical trial management system.# Minimum Requirements Education########### BSN with minimum of two years clinical experience OR Bachelors (BA or BS) and two years# experience in clinical research with human subjects OR Associate Degree Nursing (ADN), RN, with minimum of four years clinical experience OR Current certification in clinical research (SOCRA-CCRP, ACRP-CCRC or ACRP-CP) with three years clinical research experience with human subjects Experience######## See above License/Registration/Certifications####### Current South Carolina RN license (for nurse applicants only) # Preferred Requirements Preferred Education###### Master#s in a Heath Related field Preferred Experience### One (1) year oncology experience Clinical research experience Phlebotomy experience Preferred License/Registration/Certifications### Certification in research (CCRC, CCRP) # Core Job Responsibilities Membership in a Clinical Research Professional organization (ACRP, SoCRA, etc#) within 1 year of hire or as eligible based on research experience.
Must be able to work as a team member with other Research staff, doctors, departments, community, and other components. Must have own transportation to other hospitals and doctors# offices. Must be flexible in responsibilities and work schedule. Travel required to attend NCI meetings. Must be meticulous with detail. Must be able to read, write, and speak English fluently. Must have good communication skills. Must be able to respond calmly and efficiently in high stress situations. Must be able to sit for long periods of time, filling out paperwork. Must be self-directed and able to work without supervisor. #Position Summary
Clinical Research Coordinator assumes responsibility for the overall coordination of oncology research trials from all aspects. This position will be responsible for identifying clinical trials, feasibility reviews and study activation.
Screens for potential patients for clinical trial opportunities, educating patients and families about research and, obtaining and developing research data, and monitoring compliance with research protocols.
Responsible for oncology study coordination and study implementation in collaboration with the participating physicians, their staff, regulatory staff and study sponsor.
Maintains strong communication with physicians, nurses, pharmacy and other key persons regarding available protocols. Maintains protocol integrity through adherence of protocol requirements. Responsible for data management as required per protocol. Must be self-starter/motivated, detail-oriented, willing to develop the clinical research service line within the oncology programs. Knowledge of oncology nursing practices preferred. Willing to learn and train on required clinical research database and clinical trial management system.Minimum Requirements
Education
Preferred Education
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