ZipRecruiter

Log In

1

Clinical Investigator Jobs in Raleigh, NC (NOW HIRING)

Fujifilm

Investigator 2, Manufacturing

Durham, NC · On-site

Position Overview Investigator 2, Manufacturing is responsible to perform investigation for Cell ... Demonstrated knowledge of cGDPs and cGMPs and the requirements to operate in a clinical and ...

Duke University

Clinical Research Coordinator

Durham, NC · On-site

$23.50 - $31.25/hr

Clinical Research Coordinator - Neurosurgery Research Be You. At Duke, we celebrate individuality ... Manage investigational products, including receipt, storage, accountability, tracking, and ...

Duke University

Clinical Research Coordinator

Durham, NC · On-site

$23.50 - $31.25/hr

Clinical Research Coordinator - Neurosurgery Research Be You. At Duke, we celebrate individuality ... Manage investigational products, including receipt, storage, accountability, tracking, and ...

next page

Showing results 1-20

All JobsClinical Investigator JobsClinical Investigator Jobs in Raleigh, NC

Clinical Investigator information

See Raleigh, NC salary details

$31.1K

$73.2K

$127.3K

How much do clinical investigator jobs pay per year?

As of Aug 31, 2026, the average yearly pay for clinical investigator in Raleigh, NC is $73,217.00, according to ZipRecruiter salary data. Most workers in this role earn between $51,000.00 and $95,700.00 per year, depending on experience, location, and employer.

What is a clinical investigator?

A Clinical Investigator is a medical or scientific professional responsible for conducting clinical trials to evaluate the safety and effectiveness of new drugs, treatments, or medical devices. They design study protocols, ensure compliance with regulatory guidelines, oversee patient participation, and analyze trial data. Clinical Investigators often work in pharmaceutical companies, research institutions, or healthcare settings, collaborating with regulatory agencies like the FDA. Their role is critical in advancing medical science and bringing new treatments to market.

What are the typical responsibilities of a clinical investigator during a clinical trial?

As a Clinical Investigator, you will be responsible for overseeing the design, conduct, and documentation of clinical trials, ensuring they adhere to study protocols and regulatory requirements. This includes recruiting and monitoring participants, managing informed consent, interpreting results, and maintaining high-quality study records. You will work closely with research coordinators, regulatory agencies, sponsors, and other healthcare professionals to support the integrity and progress of clinical research. Ensuring patient safety and compliance throughout the process is also a key part of your daily work. This role offers a dynamic environment with opportunities to develop expertise in clinical research methodologies and regulatory affairs.

What are the key skills and qualifications needed to thrive as a clinical investigator, and why are they important?

To thrive as a Clinical Investigator, you need a robust background in clinical research, data analysis, and regulatory compliance, often supported by an advanced healthcare degree and GCP (Good Clinical Practice) certification. Familiarity with clinical trial management systems (CTMS), electronic data capture (EDC) platforms, and relevant regulatory guidelines is essential. Excellent attention to detail, critical thinking, and strong communication skills are vital for effectively managing studies and collaborating across multidisciplinary teams. These competencies ensure that clinical investigations are conducted ethically, safely, and in alignment with regulatory and scientific standards.

How do you become a clinical investigator?

To become a clinical investigator, typically one needs a medical or scientific degree such as MD or PhD, along with experience in clinical research. Many pursue additional training or certifications in Good Clinical Practice (GCP) and gain experience by working on clinical trials or research projects. Strong analytical skills, knowledge of regulatory requirements, and familiarity with research protocols are also important.

How much does a clinical investigator make?

The average salary for a clinical investigator ranges from $70,000 to $130,000 annually, depending on experience, location, and the complexity of trials. Senior investigators or those with specialized skills can earn higher compensation, often supplemented by benefits and research stipends.

What are the most commonly searched types of Clinical Investigator jobs in Raleigh, NC?

The most popular types of Clinical Investigator jobs in Raleigh, NC are:

What are popular job titles related to Clinical Investigator jobs in Raleigh, NC?

For Clinical Investigator jobs in Raleigh, NC, the most frequently searched job titles are:

What job categories do people searching Clinical Investigator jobs in Raleigh, NC look for?

The top searched job categories for Clinical Investigator jobs in Raleigh, NC are:

Clinical Investigator jobs near you
Infographic showing various Clinical Investigator job openings in Raleigh, NC as of August 2026, with employment types broken down into 3% As Needed, 72% Full Time, 17% Part Time, and 8% Contract. Highlights an 94% Physical, 1% Hybrid, and 5% Remote job distribution, with an average salary of $73,217 per year, or $35.2 per hour.

Principal Investigator (MD/DO) - Clinical Research - Durham, NC

Durham, NC • On-site

The IMA Group
Health Care and Social Assistance • 201 - 500 employees
Learn more about The IMA Groupexternal

$44K - $45K/yr

Part-time

Posted 7 days ago

Job description

Description
Principal Investigator - Durham, NC
IMA Clinical Research New Site Launch
IMA Clinical Research is expanding into Durham, NC and seeking a Principal Investigator for our newest clinical research site. This is an opportunity to support a new site launch while working within IMA's established research infrastructure, operational processes, and support model. Both full-time and part-time schedules may be considered.
What You'll Do
  • Serve as the Principal Investigator of record for assigned clinical trials
  • Conduct study-related medical evaluations and procedures in accordance with approved protocols
  • Monitor participant safety throughout study participation
  • Review protocols, informed consent materials, participant records, and relevant regulatory documentation
  • Assess participant eligibility and review clinically significant findings
  • Complete required study documentation accurately and within established timelines
  • Communicate with sponsors, CROs, IRBs, and internal research teams as required
  • Help establish relationships with local healthcare providers and community organizations
  • Follow established IMA workflows, standard operating procedures, and regulatory requirements

What You Bring
  • MD, DO, or equivalent clinical degree with an active, unrestricted state medical license
  • Experience as a Principal Investigator or Sub-Investigator on clinical trials
  • Current GCP certification or willingness to obtain it before starting
  • Strong knowledge of ICH-GCP guidelines and FDA regulatory standards
  • A collaborative approach and comfort working within an established, team-based research environment

Why Durham, NC
You'll have the opportunity to support the launch and growth of a new research site while benefiting from IMA's established workflows, experienced research teams, and clinical research infrastructure.
Schedule
Full-time or part-time, based on site and study needs.
The IMA Group is an Affirmative Action/Equal Opportunity Employer
Our Government Services Division supports local, state, and federal agencies and delivers professional and objective medical and psychological examinations as well as ancillary services. Our Payer Services Division meets the evaluation and screening needs of Carriers, TPAs, Public Entities and Employers and includes behavioral health and physical medicine specialty services, working with a wide range of organizations within the workers' compensation, disability, liability, and auto markets. Our Clinical Research Division performs all types of Phase II-IV clinical trials in multiple therapeutic areas through a flexible nationwide network of site locations and virtual capabilities.
#LI-RC1 #LI-ONSITE
IMA Group logo

About IMA Group

Sourced by ZipRecruiter

IMA Group is a prominent player in the healthcare sector headquartered in Tarrytown, NY, USA. The company is known for offering a range of comprehensive health assessments, disability evaluations, as well as related services. It has been providing these services for over three decades, having been established back in the late 1980s. IMA Group is driven by a core mission – to assist individuals and families through challenging times of their lives with their health and disability-related services. The company believes in delivering personalized, professional, and compassionate service.

Industry

Health care and social assistance

Company size

201 - 500 Employees

Headquarters location

Tarrytown, NY, US

Year founded

1990

Social media

FacebookTwitter

View All IMA Group Jobs

Apply