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TravelNurseSource is working with Adelphi Healthcare to find a qualified Other RN in Asheville, North Carolina, 28801! Coordinate and manage clinical research studies and protocols.

TravelNurseSource is working with Adelphi Healthcare to find a qualified Other RN in Asheville, North Carolina, 28801! Summary: <ul><li>Ref #: M-RN-296257</li><li>Profession: Registered Nurse</li><li>Specialty: Clinical Research Coordinator</li><li>Job Type: Full-time</li><li>Start Date: ASAP</li><li>Location: Asheville, NC</li><li>Shift Type: Days</li><li>Rate:</li></ul> Requirements: <ul><li>Active RN license</li><li>Graduate of accredited nursing program</li><li>BLS required</li><li>Previous clinical research experience preferred</li><li>Knowledge of GCP, FDA, and research regulations preferred</li><li>Strong organizational, communication, and documentation skills</li></ul> Responsibilities: <ul><li>Coordinate and manage clinical research studies and protocols</li><li>Screen, enroll, and educate research participants</li><li>Obtain informed consent and maintain study documentation</li><li>Collect and record clinical data and study results</li><li>Monitor patient safety and protocol compliance</li><li>Coordinate study visits, labs, and follow-up appointments</li><li>Collaborate with investigators, sponsors, and care teams</li><li>Ensure compliance with regulatory and ethical standards</li></ul>

TravelNurseSource

Travel Nurse RN in Asheville, NC

Clinical Data Collection

Clinical Outcomes

Clinical Research

Communication Skills

Documentation

FDA Requirements

GCP (Good Clinical Practices)

Healthcare

Informed Consent

Maintain Compliance

Medical Records

Nursing Credentials

Organizational Skills

Patient Safety

Registered Nurse (RN)

Regulatory Compliance

Safety Compliance

TravelNurseSource.com

FEED

This is a high-enrolling study requiring strong patient-facing skills, organizational abilities, and project management experience. A leading healthcare research organization is seeking a Clinical Research Coordinator to support trials in the Asheville area.

Job Title: Clinical Research Coordinator Location: Asheville, NC 100% Onsite Schedule: Monday–Friday Type: Contract- 6 months with the possibility of extensionA leading healthcare research organization is seeking a Clinical Research Coordinator to support trials in the Asheville area. This is a high-enrolling study requiring strong patient-facing skills, organizational abilities, and project management experience. If you have a background in clinical research and enjoy patient interaction, this is an excellent opportunity to contribute to impactful maternal health research. Apply today for immediate consideration. <h3> Responsibilities</h3><ul><li>Screen, consent, and enroll patients into the study.</li><li>Ensure protocol compliance and patient safety through accurate informed consent.</li><li>Collect, review, and enter study data into electronic case report forms (EDC).</li><li>Maintain study documentation and create source tools as needed.</li><li>Support clinical procedures, such as ECGs, phlebotomy, and specimen processing/shipping.</li></ul><h3>Requirements</h3><ul><li>Bachelor’s degree required.</li><li>1+ years of clinical research experience (any therapeutic area).</li><li>Prior patient-facing role with informed consent experience.</li><li>Experience with research project management or high-volume study enrollment.</li><li>Phlebotomy or specimen-handling experience required.</li><li>Certified Clinical Research Coordinator (CCRC) credential a plus.</li></ul> Ref: #568-Clinical

Every day, System One focuses on services and solutions that require a high degree of specialization, in-demand technical skills, and large-scale operational expertise. We are essential partners to those on the front lines of our nation’s most critical infrastructure, technology, and life sciences initiatives. 
Founded more than 40 years ago as a staffing partner to the engineering industry, today System One is a diversified organization operating in over 50 locations and putting more than 9,000 people to work in the United States, Canada, and the United Kingdom.

System One

Clinical Research Coordinator

Case Report Form (CRF)

Certified Clinical Research Coordinator (CCRC)

Clinical Support

Data Entry

Electrocardiogram

Electronic Data Capture (EDC)

Phlebotomy

Project/Program Management

Research Skills

Sample/Specimen Processing

Volume Planning

Snaphop

Strong analysis & critical thinking skills including problem solving, decision-making, planning, time management, and organizational ability.  Preferred experience with EMR systems, clinical trial data entry (EDC), and clinical trial management systems (CTMS).

YEAR

Medical Edge Recruitment has an immediate opening for an RN Clinical Research Coordinator for a Direct Hire opportunity in Asheville, NC. SALARY RANGE: $72,000.00 to $93,000.00 SCHEDULE: Day Shift <hr/>MINIMUM EDUCATION & EXPERIENCE REQUIREMENTS:  High school education required 
 ASN or BSN required 
 Registered Nurse (RN) license required 
 25 years nursing experience required, oncology preferred <hr/>KNOWLEDGE, SKILLS & ABILITIES:  Strong analysis & critical thinking skills including problem solving, decision-making, planning, time management, and organizational ability 
 Detail-oriented with ability to exercise independent judgment 
 Strong interpersonal effectiveness including emotional intelligence, diplomacy, tact, conflict management, delegation, and diversity awareness 
 Ability to work effectively with sensitive, confidential, and emotionally charged situations 
 Strong communication skills (oral, written, presentation) with ability to actively listen and provide balanced feedback 
 Strong customer service orientation with ability to build a culture of quality, performance, and operational excellence 
 Ability to collaborate effectively with employees, physicians, and community partners 
 Self-motivated with ability to work independently with limited supervision 
 Ability to manage competing priorities in a fast-paced, multi-site environment 
 Strong time management, stress management, and organizational skills 
 Proficiency in MS Office (Word, Excel, PowerPoint, Outlook) 
 Preferred experience with EMR systems, clinical trial data entry (EDC), and clinical trial management systems (CTMS) <hr/>SPECIAL REQUIREMENTS:  Registered Nurse license in the state of practice 
 Valid state Drivers License required (travel to satellite offices and offsite meetings) 
 Must comply with company Driver Safety Operations and Motor Vehicle Records Check Policy 
 Must be able to work in multi-site and potentially remote environments as needed 
 Oncology experience preferred but not required 
#indeed

Medical Edge Recruitment

RN Clinical Research Coordinator

Analysis Skills

Clinical Data

Clinical Information Systems

Clinical Trial

Clinical Trial Management

Conflict Resolution

Customer Support/Service

Detail Oriented

Diversity

Driver's License

Electronic Medical Records

Interpersonal Skills

Microsoft Excel

Microsoft Office

Microsoft Outlook

Microsoft PowerPoint

Microsoft Word

Nursing

Oncology

Presentation/Verbal Skills

Problem Solving Skills

Safety/Work Safety

Team Player

Time Management

Willing to Travel

Writing Skills

HaleyMarketing

The ideal candidate will play a critical role in the conduct of clinical trials by serving as a Principal Investigator (PI) or Sub-Investigator, while continuing to provide high-quality medical care to adult patients within a clinical research setting. Elite Clinical Network (ECN) is seeking a dedicated and research-oriented Physician – Family Medicine to join our expanding team of clinical professionals.

Position OverviewElite Clinical Network (ECN) is seeking a dedicated and research-oriented Physician – Family Medicine to join our expanding team of clinical professionals. The ideal candidate will play a critical role in the conduct of clinical trials by serving as a Principal Investigator (PI) or Sub-Investigator, while continuing to provide high-quality medical care to adult patients within a clinical research setting. This is a part time/per diem position with a unique opportunity to contribute to the advancement of medicine through clinical studies.Key Responsibilities<ul><li>Serve as Principal Investigator or Sub-Investigator on multiple Phase I–IV clinical trials.</li><li>Perform comprehensive physical exams and clinical assessments for protocol screening and enrollment.</li><li>Evaluate patient eligibility based on inclusion/exclusion criteria of clinical protocols.</li><li>Provide medical oversight for clinical trial participants, including safety assessments, adverse event evaluations, and ongoing care.</li><li>Collaborate closely with Clinical Research Coordinators, Sponsors, and Monitors to ensure protocol compliance and data integrity.</li><li>Review and sign off on source documents, case report forms (CRFs), and regulatory documentation.</li><li>Maintain detailed and accurate clinical trial documentation in compliance with ICH-GCP, FDA, and sponsor requirements.</li><li>Participate in Site Initiation Visits (SIVs), Monitoring Visits, and Audits as needed.</li><li>Manage chronic and acute conditions among study participants in alignment with standard care and protocol guidelines.</li><li>Educate and counsel patients on study procedures, informed consent, and potential side effects.</li><li>Support recruitment efforts and promote patient retention in trials.</li></ul>Qualifications<ul><li>MD or DO degree from an accredited medical school.</li><li>Valid, unrestricted medical license in the state of employment.</li><li>Board Certified or Board Eligible (BC/BE) in Internal or Family Medicine.</li><li>BC/BE in Family Medicine or Geriatric Medicine will also be considered.</li><li>Current Good Clinical Practice (GCP) certification or willingness to obtain prior to start.</li><li>Minimum of 1 year of experience in clinical practice; prior clinical research experience preferred but not required.</li></ul>Preferred Skills<ul><li>Familiarity with FDA, ICH-GCP, and clinical trial protocols.</li><li>Experience managing or participating in industry-sponsored clinical trials.</li><li>Strong attention to detail and ability to document accurately.</li><li>Excellent interpersonal and communication skills for patient interaction and sponsor collaboration.</li><li>Ability to work collaboratively with a cross-functional team in a fast-paced research environment.</li><li>Comfortable using electronic medical records (EMRs) and clinical trial management systems (CTMS).</li><li>DEA license (preferred).</li></ul>

Research Jobs in Asheville, NC

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Research Jobs in Asheville, NC

Travel Nurse RN in Asheville, NC TravelNurseSource

Clinical Research Coordinator System One

RN Clinical Research Coordinator Medical Edge Recruitment

Physician - Family Medicine ECN Operating LLC

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