Top 121 Research Associate Jobs in Raleigh, NC

Clinical Research Associate, Full Service
5PY IQVIA RDS Inc. —Durham, NC
- $47,400 - $169,300 a year
- Full-time
- Microsoft Excel
- Computer literacy
- English
10d
Social/Clinical Research Assistant
University of North Carolina at Chapel Hill —Chapel Hill, NC
- $36,320 - $62,096 a year
- Full-time
- Spanish
- Surgery
- English
- Health insurance
- Retirement plan
5d
Research Associate I
Asklepios BioPharmaceutical —Durham, NC
- Full-time
- Microsoft Excel
- Microsoft Outlook
- Research
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
Temporary Research Associate
North Carolina State University —Raleigh, NC
- $25 - $30 an hour
- Temporary
- University
- Entry level
Clinical Research Associate 2, IQVIA
IQVIA —Durham, NC
- $71,900 - $189,000 a year
- Full-time
- Microsoft Excel
- Computer literacy
- English
Clinical Research Associate II/III - US
Optimapharm d.o.o. —Raleigh, NC
- $75,000 - $100,000 a year
- Full-time
- Remote
- Nursing
- Computer literacy
- Mid-level
- Dental insurance
- Paid time off
4d
Senior Clinical Research Associate - US
Optimapharm d.o.o. —Raleigh, NC
- $100,000 - $130,000 a year
- Full-time
- Remote
- Nursing
- 5 years
- Computer literacy
- Dental insurance
- Paid time off
4d
Temporary Research Assistant
North Carolina State University —Raleigh, NC
- $28.48 an hour
- Temporary
- Entry level
7d
Clinical Research Associate II - Oncology - United States (Remote)
Worldwide Clinical Trials —Durham, NC
- $79,500 - $158,500 a year
- Full-time
- Remote
- Nursing
- English
- Mid-level
FSP - Clinical Research Associate 2 - CRA 2 / Sr. CRA 1- Northeast or Central - Oncology
Fortrea —Durham, NC
- $100,000 - $115,000 a year
- Full-time
- Mid-level
- Office
- Travel
5d
Research Associate/Chemist (multiple level available)
Synoligo Biotechnologies, Inc —Morrisville, NC
- Full-time
- Bachelor of Science
- Bachelor's degree
- In-person
- Health savings account
- Relocation assistance
Quick Apply
4d
Associate Scientist - Upstream Cell Culture
Novartis —Durham, NC
- $73,500 - $136,500 a year
- Full-time
- Mid-level
- Communication skills
- Commercial
- Health insurance
- 401(k) matching
11d
Clinical Research Associate 2
Grifols —Durham, NC
- Full-time
- Writing skills
- Mid-level
- Office
In Process Research Associate
KBI Biopharma —Durham, NC
- $19.23 - $26.44 an hour
- Full-time
- Bachelor of Science
- Writing skills
- Analysis skills
- Paid holidays
- Health insurance
Associate Clinical Research Coordinator
University of North Carolina at Chapel Hill —Chapel Hill, NC
- $50,312 - $57,000 a year
- Full-time
- Mid-level
- University
- Bachelor's degree
- Health insurance
- Retirement plan
6d
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
Temporary Cotton Breeding Research Associate
North Carolina State University —Raleigh, NC
- $24 - $29 an hour
- Temporary
- Entry level
14d
Senior Research Associate
KBI Biopharma —Durham, NC
- Full-time
- Bachelor of Science
- Mid-level
- Master's degree
Research Assistant
University of North Carolina at Chapel Hill —Chapel Hill, NC
- $25 - $35 an hour
- Temporary
- University
- Bachelor's degree
- Experience equivalent to degree accepted
5d

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Clinical Research Associate, Full Service

5PY IQVIA RDS Inc. -
Durham, NC

Apply Now

Job Details

Full-time
$47,400 - $169,300 a year
10 days ago

Qualifications

Computer literacy
Employee relationship building

Full Job Description

Job Overview
Perform monitoring and site management work to ensure that sites are conducting the study(ies) and reporting study data as required by the study protocol, applicable regulations and guidelines, and sponsor requirements.

Essential Functions

Perform site monitoring visits (selection, initiation, monitoring and close-out visits) in accordance with contracted scope of work and regulatory requirements, i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines.
Work with sites to adapt, drive and track subject recruitment plan in line with project needs to enhance predictability.
Administer protocol and related study training to assigned sites and establish regular lines of communication with sites to manage ongoing project expectations and issues.
Evaluate the quality and integrity of study site practices related to the proper conduct of the protocol and adherence to applicable regulations. Escalate quality issues as appropriate.
Manage the progress of assigned studies by tracking regulatory submissions and approvals, recruitment and enrollment, case report form (CRF) completion and submission, and data query generation and resolution. May support start-up phase.
Ensure copies/originals (as required) site documents are available for filing in the Trial Master File (TMF) verify that the Investigator's Site File (ISF) is maintained in accordance with GCP / ICH and local regulatory requirements.
Create and maintain appropriate documentation regarding site management, monitoring visit findings and action plans by submitting regular visit reports, generating follow-up letters and other required study documentation.
Collaborate and liaise with study team members for project execution support as appropriate.
If applicable, may be accountable for supporting development of project subject recruitment plan on a per site basis.
If applicable, may be accountable for site financial management according to executed clinical trial agreement and retrieve invoices according to local requirement.

Qualifications

Bachelor's Degree Degree in scientific discipline or health care preferred. Req
Equivalent combination of education, training and experience may be accepted in lieu of degree.
Some organizations require completion of CRA training program or prior monitoring experience.
Basic knowledge of, and skill in applying, applicable clinical research regulatory requirements (i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines).
Good therapeutic and protocol knowledge as provided in company training.
Computer skills including proficiency in use of Microsoft Word, Excel and PowerPoint and use of a laptop computer and iPhone and iPad (where applicable).
Written and verbal communication skills including good command of English language.
Organizational and problem-solving skills.
Effective time and financial management skills.
Ability to establish and maintain effective working relationships with coworkers, managers, and clients.

IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com

IQVIA is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, status as a protected veteran, or any other status protected by applicable law. https://jobs.iqvia.com/eoe

IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

The potential base pay range for this role, when annualized, is $47,400.00 - $169,300.00. The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered, in addition to a range of health and welfare and/or other benefits.

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Refine Your Search

Research Associate jobs in Raleigh, NC

Clinical Research Associate, Full Service

Social/Clinical Research Assistant

Research Associate I

Clinical Research Associate, IQVIA Biotech

Temporary Research Associate

Clinical Research Associate 2, IQVIA

Clinical Research Associate II/III - US

Senior Clinical Research Associate - US

Temporary Research Assistant

Clinical Research Associate II - Oncology - United States (Remote)

FSP - Clinical Research Associate 2 - CRA 2 / Sr. CRA 1- Northeast or Central - Oncology

Research Associate/Chemist (multiple level available)

Associate Scientist - Upstream Cell Culture

Clinical Research Associate 2

In Process Research Associate

Associate Clinical Research Coordinator

Senior Clinical Research Associate (level dependent on experience)

Temporary Cotton Breeding Research Associate

Senior Research Associate

Research Assistant

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