Top 202 Clinical research Jobs in Raleigh Durham 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
Clinical Trial Manager
Experis —Chapel Hill, NC
- $58.26 - $64.00 an hour
- Contract
- Microsoft Outlook
- 5 years
- English
- Health savings account
- Disability insurance
Quick Apply
16h
Clinical Trial Manager
Experis —Chapel Hill, NC
- $58.26 - $64.00 an hour
- Contract
- 5 years
- English
- Bachelor's degree
- Health savings account
- Disability insurance
Quick Apply
16h
Clinical Study Manager
Kaztronix —Durham, NC
- Contract
- Office
- Bachelor's degree
- Contracts
Quick Apply
8d
Principal Clinical Trial Coordinator - FSP
Thermo Fisher Scientific —North Carolina
- Full-time
- Remote
- Office
- Bachelor's degree
- Team management
13d
Clinical Research Coordinator - Raleigh, NC
IQVIA —Raleigh, NC
- $35 - $42 an hour
- Part-time
- Vital signs
- Office
- Bachelor's degree
CRA 1, IQVIA Biotech
IQVIA —Durham, NC
- $71,900 - $145,300 a year
- Full-time
- Bachelor's degree
- Travel
- Communication skills
Clinical Research Associate, IQVIA Biotech
IQVIA —Durham, NC
- $71,900 - $169,300 a year
- Full-time
- Bachelor's degree
- Travel
- Experience equivalent to degree accepted
Clinical Research Coordinator
ClinTrial Research, INC —Raleigh, NC
- $55,000 - $75,000 a year
- Full-time
- HIPAA
- Continuous improvement
- Senior level
- Health savings account
- Health insurance
Quick Apply
4d
Clinical Research Assistant
University of North Carolina at Chapel Hill —Chapel Hill, NC
- $40,864 - $48,000 a year
- Overtime
- Clinic experience
- Mid-level
- Clinic
- Health insurance
- Retirement plan
10d
UTS - Temporary Research Assistant at UNC Chapel Hill
North Carolina State University —Chapel Hill, NC
- $23 an hour
- Temporary
- University
- Leadership
- Entry level
Clinical Project Manager (US)
Alimentiv —Raleigh-Durham, NC
- $95,500 - $159,000 a year
- Full-time
- Remote
- English
- Mid-level
- Bachelor's degree
Quick Apply
Clinical Research Assistant
Velocity Clinical Research, Inc. —Durham, NC
- Full-time
- Vital signs
- English
- High school diploma or GED
- Paid holidays
- Health insurance
Quick Apply
3d
Lead Clinical Research Coordinator
University of North Carolina at Chapel Hill —Chapel Hill, NC
- $70,973 - $86,509 a year
- Full-time
- Microsoft Excel
- Microsoft Outlook
- University
- Health insurance
- Retirement plan
10d
Clinical Research Associate 2, IQVIA
IQVIA —Durham, NC
- $71,900 - $189,000 a year
- Full-time
- Microsoft Excel
- Computer literacy
- English
Clinical Lead- CVRM
IQVIA —Durham, NC
- $93,100 - $232,800 a year
- Full-time
- Remote
- Microsoft Excel
- 5 years
- English
- Work from home
Senior Clinical Research Associate (level dependent on experience)
CTI Clinical Trial Services, Inc —Raleigh, NC
- Hybrid work
- Nursing
- Mid-level
- Master's degree
- Paid parental leave
- Tuition reimbursement
Quick Apply
Clinical Research Coordinator
Revival Research Institute, LLC —Cary, NC
- Full-time
- Microsoft Excel
- Microsoft Outlook
- BLS Certification
Quick Apply
Manager, Clinical Operations
IQVIA —Durham, NC
- $86,500 - $216,000 a year
- Full-time
- Remote
- Microsoft Excel
- English
- Mid-level
- Work from home
Data Coordinator
University of North Carolina at Chapel Hill —Chapel Hill, NC
- $55,886 - $65,000 a year
- Overtime
- Mid-level
- Clinic
- Bachelor's degree
- Health insurance
- Retirement plan
12h

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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

clinical research jobs in raleigh durham nc

Clinical Research Coordinator II

Clinical Trial Manager

Clinical Trial Manager

Clinical Study Manager

Principal Clinical Trial Coordinator - FSP

Clinical Research Coordinator - Raleigh, NC

CRA 1, IQVIA Biotech

Clinical Research Associate, IQVIA Biotech

Clinical Research Coordinator

Clinical Research Assistant

UTS - Temporary Research Assistant at UNC Chapel Hill

Clinical Project Manager (US)

Clinical Research Assistant

Lead Clinical Research Coordinator

Clinical Research Associate 2, IQVIA

Clinical Lead- CVRM

Senior Clinical Research Associate (level dependent on experience)

Clinical Research Coordinator

Manager, Clinical Operations

Data Coordinator

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