Top 13 Clinical research associate 2 Jobs in Raleigh Nc

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
Clinical Research Associate 2
Grifols —Durham, NC
- Full-time
- Writing skills
- Mid-level
- Office
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
Clinical Research Associate II - Psychiatry - United States (Remote)
Worldwide Clinical Trials —Durham, NC
- $79,500 - $158,500 a year
- Full-time
- Remote
- Nursing
- Psychiatry
- English
Clinical Research Coordinator II (On-site)
Wake Research —Raleigh, NC
- Full-time
- HIPAA
- Mid-level
- Team management
- Disability insurance
- Health insurance
Quick Apply
FSP Sr. Clinical Research Associate II - NYC Metro or PHL - Onc
Fortrea —Durham, NC
- $125,000 - $140,000 a year
- Full-time
- Up to 50% travel
- 5 years
- Office
Clinical Project Manager II – Inflammation/ Phase 2b (Sponsor Dedicated/ Remote; Hybrid Foster City, CA Preferred)
サイネオス・ヘルス —Morrisville, NC
- $95,000 - $175,700 a year
- Remote
- Nursing
- Medicine
- Bachelor's degree
- Employee stock purchase plan
- Health insurance
Site Management Associate II
PSI CRO —Durham, NC
- Full-time
- Hybrid work
- Microsoft Outlook
- English
- Mid-level
Quick Apply
CRC II (Onsite) - Marietta, GA
サイネオス・ヘルス —Morrisville, NC
- $67,700 - $115,100 a year
- Weekends as needed
- Nursing
- RN License
- Word processing
- Employee stock purchase plan
- Health insurance
FSP CRA II/ Sr CRA I - Oncology & Gen Med - East Coast/West Coast
Thermo Fisher Scientific —Cary, NC
- $85,000 - $120,000 a year
- Full-time
- Background check
- Nursing
- RN License
- Commuter assistance
- Paid parental leave

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Clinical Research Associate, IQVIA Biotech
IQVIA —Durham, NC
Bachelor’s degree in life sciences or health-related field (or equivalent experience). Monitor study progress by tracking regulatory submissions, subject…
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Clinical Research Associate 2, IQVIA

IQVIA -
Durham, NC

Apply Now

Job Details

Full-time
$71,900 - $189,000 a year

Qualifications

Computer literacy
Employee relationship building

Full Job Description

Durham, United States of America | Full time | Field-based | R1538099

IQVIA is hiring a Clinical Research Associate 2 with on-site monitoring experience in IM/GI, MASH/NASH, dermatology and/or asthma/respiratory clinical trials. Women's Health experience is a plus!

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) and verify that the Investigator's Site File (ISF) is maintained in accordance with GCP 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 in scientific discipline or health care preferred. Req
Requires at least 1 year of on-site monitoring experience. Req
Equivalent combination of education, training and experience may be accepted in lieu of degree. Req
Good 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 $71,900.00 - $189,000.00. 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.

Where you'll work

Field-based

You’ll work where the action is — out in the field, directly engaging with our customers, sites or partners. Field-based roles offer the opportunity to build relationships face-to-face, gain real-world insights and make a tangible impact.

Culture

Culture at IQVIA is built on a shared belief: that when people are empowered with better data, smarter technology and deeper expertise, they can change what’s possible for patients. Across every team and every corner of the globe, you’ll find colleagues who genuinely care — about the mission and about each other. That’s what makes this a place where people tend to stay, grow and do the best work of their careers.

Apply Now

Refine Your Search

clinical research associate 2 jobs in raleigh nc

Clinical Research Associate 2, IQVIA

Clinical Research Associate II/III - US

Clinical Research Associate 2

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

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

Clinical Research Coordinator II (On-site)

FSP Sr. Clinical Research Associate II - NYC Metro or PHL - Onc

Clinical Project Manager II – Inflammation/ Phase 2b (Sponsor Dedicated/ Remote; Hybrid Foster City, CA Preferred)

Site Management Associate II

CRC II (Onsite) - Marietta, GA

FSP CRA II/ Sr CRA I - Oncology & Gen Med - East Coast/West Coast

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