Top 110 authorization representative Jobs in mebane, nc

Clinical Research Coordinator II
Rare Disease Research, LLC —Hillsborough, NC
- $60,000 - $65,000 a year
- 8 hour shift
- Background check
- Vital signs
- Patient monitoring
- Health insurance
- Dental insurance
Quick Apply
Insurance Coordinator
Specialty1 Partners —Mebane, NC
- $21.50 - $25.00 an hour
- Dental office
- Mid-level
- High school diploma or GED
- Health savings account
- Disability insurance
Quick Apply
Customer Service Representative
Cambro Manufacturing Company —Mebane, NC
- Overtime
- Microsoft Word
- Microsoft Excel
- Microsoft Outlook
Revenue Cycle Representative - Patient Accounting
UNC Health —Chapel Hill, NC
- $18.12 - $25.51 an hour
- Full-time
- Remote
- Research
- Mid-level
- High school diploma or GED
6d
Scheduling/Customer Service Representative (Temporary) - UNCH Laboratory Eastowne
UNC Health —Chapel Hill, NC
- $18.84 - $26.77 an hour
- Temporary
- Hospital
- Basic math
- HIPAA
Patient Service Representative (Bilingual)
Piedmont Health Services —Burlington, NC
- $17.66 - $23.74 an hour
- Full-time
- Spanish
- Microsoft Outlook
- HIPAA
- Paid holidays
- Disability insurance
Quick Apply
Patient Service Representative
Piedmont Health Services —Chapel Hill, NC
- $17.66 - $23.74 an hour
- Full-time
- Microsoft Outlook
- Customer service
- HIPAA
- Paid holidays
- Disability insurance
Quick Apply
ELDS Tester- Shift 1
ABB —Mebane, NC
- Full-time
- Computer literacy
- High school diploma or GED
- US work authorization
Medicaid Eligibility Analyst
Duke Health —Durham, NC
- Full-time
- Hybrid work
- Bilingual
- Research
- Mid-level
Master Planner Scheduler
ABB —Mebane, NC
- Full-time
- English
- Mid-level
- US work authorization
Revenue Cycle Financial Representative
UNC Health —Chapel Hill, NC
- $18.84 - $26.77 an hour
- Full-time
- Hybrid work
- Microsoft Word
- Microsoft Outlook
- Mid-level
7d
Accounts Receivable Technician, Part Time
Durham Technical Community College —Durham, NC
- $18.46 an hour
- Part-time
- Office
- Finance
- High school diploma or GED
Manufacturing Quality Tester
ABB —Mebane, NC
- Full-time
- Microsoft Excel
- Mid-level
- US work authorization
Health and Safety Specialist
ABB —Mebane, NC
- Full-time
- Microsoft Office
- Bachelor's degree
- US work authorization
- Paid parental leave
- Health savings account
9d
ELDS MV SWGR Production Operator 1st Shift
ABB —Mebane, NC
- Full-time
- High school diploma or GED
- US work authorization
- 1 year
ELDS Fabrication Machine Operator 1st shift
ABB —Mebane, NC
- Full-time
- High school diploma or GED
- US work authorization
- Data entry
ELDS Warehouse/Internal Logistics Operator 1st shift
ABB —Mebane, NC
- Full-time
- High school diploma or GED
- US work authorization
- Warehouse
ELDS MV SWGR Production Operator- 1st Shift
ABB —Mebane, NC
- Full-time
- High school diploma or GED
- US work authorization
- 1 year
ELSP Logistics Specialist
ABB —Mebane, NC
- Full-time
- High school diploma or GED
- US work authorization
- Data entry
4d
ELDS LIS SWGR- Production Operator- 1st shift
ABB —Mebane, NC
- Full-time
- High school diploma or GED
- US work authorization
- 1 year

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Clinical Research Coordinator II

Rare Disease Research, LLC
Hillsborough, NC

Quick Apply

Job Details

Full-time
$60,000 - $65,000 a year

Benefits

Health insurance
Dental insurance
401(k)
Paid time off
Vision insurance
401(k) matching

Qualifications

Vital signs
Clinical research
Bachelor of Science
Clinical staff training
Bachelor's degree
Clinical training
Team training
Training & development
Clinical trial support in drug product development
Staff development

Full Job Description

About Rare Disease Research:

As an independent clinical research site, we are 100% dedicated to conducting clinical research, accelerating the development of safe and effective treatments and providing rare disease patients with access to innovative investigational therapies. We are a passionate, caring, multi-disciplinary team conducting clinical research with expertise and compassion, and always to the highest ethical standards.

About This Opportunity:

We are looking for a clinical research coordinator who has at least 5 years experience with the conduct of clinical research to join our wonderful team of motivated research professionals. Ideally, the right candidate has prior clinical research experience conducting investigational clinical trials and is already familiar with clinical research workflows, regulatory requirements, and data collection and documentation practices.

* Important Note: Applicants for employment in the United States must have work authorization that does not now or in the future require sponsorship of a visa for employment authorization in the United States and with Rare Disease Research.

Responsibilities:

Assists Principal Investigator (PI) in protection of the rights and welfare of all human research participants involved in research in accordance with federal regulations and university and sponsoring agency policies and procedures.
Assists the PI in development of materials and tools necessary to appropriately train individuals involved in the conduct of the study around issues related to (but not limited to) protocol requirements, schedule of visits, execution of research plan. Maintains documentation of training.
Collaborates with PI and institution to respond to any audit findings and implement approved recommendations.
Reviews and develops a familiarity with the protocol, e.g., study proceedings and timelines, inclusion and exclusion criteria, confidentiality, privacy protections.
Collects documents needed to initiate the study and submit to the sponsor (e.g., Form FDA 1572, CVs, etc.).
Works with the PI to develop and implement recruitment strategies in accordance with HRPO (IRB) requirements and approvals.
Conducts or participates in the informed consent process including interactions with the HRPO (IRB) and discussions with research participants, including answering any questions related to the study. Obtains appropriate signatures and dates on forms in appropriate places. Assures that amended consent forms are appropriately implemented and signed.
Screens subjects for eligibility using protocol specific inclusion and exclusion criteria, documenting each potential participant’s eligibility or exclusion.
Performs safety and efficacy assessments per study protocol.
Collect or coordinate collection of clinical procedures such as vital signs, ECGs, blood draws, IP infusions.
Responsible for timely data entry and query resolutions.
Reports study findings, such as serious adverse events (SAEs) or protocol deviations (PDs) to the applicable department, such as the sponsor or IRB.
Manages participant chart binders and coordinates accurate completion of source with various delegated staff.
Follows participants from the start to end of study participation and escalates safety concerns to appropriate individuals, such as the PI or Medical Monitor.
Prepare study data for interim monitoring visits and meet with study monitor to follow-up on resolving queries/issues.
Communicate with sponsors, CROs, vendors, or other representatives promptly and professionally.
Completes study documentation and maintains study files in accordance with sponsor requirements and University policies and procedures including, but not limited to, consent forms, source documentation, narrative notes if applicable, case report forms, and investigational material accountability forms.
Updates source documents per study protocol amendment.
Coordinate operations with other departments to facilitate completion of procedures during participant visits, includes communications with nurse practitioners, medical assistants, pharmacy, regulatory, and/or physical therapy.
Retains all study records in accordance with sponsor requirements.
Works with the PI and study-specific RAs to manage the day to day activities of the study including problem solving, communication, and protocol management.
Ability to exercise independent judgment and discretion

The above statements are intended only to describe the general nature of the job, and should not be construed as an all-inclusive list of position responsibilities.

Requirements:

BA/BS in a life sciences or related field required.
5 years previous CRC experience at a clinical trial site
2 years experience training/developing RAs and other CRCs
ACRP or SOCRA certification preferred
Must have GCP, IATA, ALCOAC training
BLS/CPR training upon hire date

Job Type: Full-time

Salary: $60,000.00 - $65,000.00 per year

Benefits:

401(k)
401(k) matching
Dental insurance
Health insurance
Paid time off
Vision insurance

Schedule:

8 hour shift
Day shift
Monday to Friday

Ability to commute/relocate:

Reliably commute or planning to relocate before starting work (Required)

Application Question(s):

Have you received the COVID 19 vaccinations or would you be willing to do so before beginning employment?

Work Location: One location, on site and in person

Rare Disease Research is an Equal Opportunity/Affirmative Action employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability, protected Veteran status, or any other characteristic protected by federal, state or local laws.

Notice To Third-Party Agencies:

Rare Disease Research does not accept unsolicited resumes from recruiters or agencies. Any staffing/employment agency, person or entity that submits an unsolicited resume to this site does so with the understanding that the applicant's resume will become the property of Rare Disease Research will have the right to hire that applicant at its discretion and without any fee owed to the submitting staffing/employment agency, person, or entity.

Job Type: Full-time

Pay: $60,000.00 - $65,000.00 per year

Benefits:

401(k)
401(k) matching
Dental insurance
Health insurance
Paid time off
Vision insurance

Work Location: In person

Quick Apply

Refine Your Search

authorization representative jobs in mebane, nc

Clinical Research Coordinator II

Insurance Coordinator

Customer Service Representative

Revenue Cycle Representative - Patient Accounting

Scheduling/Customer Service Representative (Temporary) - UNCH Laboratory Eastowne

Patient Service Representative (Bilingual)

Patient Service Representative

ELDS Tester- Shift 1

Medicaid Eligibility Analyst

Master Planner Scheduler

Revenue Cycle Financial Representative

Accounts Receivable Technician, Part Time

Manufacturing Quality Tester

Health and Safety Specialist

ELDS MV SWGR Production Operator 1st Shift

ELDS Fabrication Machine Operator 1st shift

ELDS Warehouse/Internal Logistics Operator 1st shift

ELDS MV SWGR Production Operator- 1st Shift

ELSP Logistics Specialist

ELDS LIS SWGR- Production Operator- 1st shift

I want to receive the latest job alert for authorization representative in mebane, nc

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