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Clinical Studies Jobs in Raleigh, NC (NOW HIRING)

IQVIA

Senior Global Clinical Study Manager

Durham, NC · On-site

... studies. This role ensures successful site selection, activation, monitoring oversight, and ... Ensure clinical monitoring processes meet study needs and timelines * Partner with CRAs to optimize ...

AskBio

VP, GDNF Clinical Development

Durham, NC · On-site +1

This individual will be responsible for the analysis, interpretation and reporting of clinical studies to support BLA/MAA filings and global product launch. As SME they will work closely with medical ...

AskBio

VP, GDNF Clinical Development

Durham, NC

This individual will be responsible for the analysis, interpretation and reporting of clinical studies to support BLA/MAA filings and global product launch. As SME they will work closely with medical ...

Adecco

Clinical Trials Manager- Remote

Chapel Hill, NC · Remote

$62 - $64.73/hr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

Manage clinical operational and quality activities for assigned studies in compliance with ICH/GCP and applicable regulations . * Develop and maintain clinical tools, monitoring plans, guidelines ...

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Clinical Studies information

See Raleigh, NC salary details

$14

$33

$87

How much do clinical studies jobs pay per hour?

As of Aug 14, 2026, the average hourly pay for clinical studies in Raleigh, NC is $33.65, according to ZipRecruiter salary data. Most workers in this role earn between $16.11 and $32.02 per hour, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive in clinical studies, and why are they important?

To excel in Clinical Studies, a background in life sciences, strong analytical skills, and familiarity with clinical research methodologies are essential, often complemented by degrees such as a BSc or MSc in a relevant field. Proficiency in clinical trial management systems (CTMS), electronic data capture (EDC) platforms, and knowledge of Good Clinical Practice (GCP) guidelines or certifications are typically required. Attention to detail, organization, and effective communication are vital soft skills for coordinating studies and collaborating with diverse teams. These competencies ensure the integrity, regulatory compliance, and successful execution of clinical trials.

What are some common challenges clinical studies professionals face when coordinating multi-site trials?

Clinical studies professionals often encounter challenges such as ensuring consistent protocol adherence across multiple sites, managing timely data collection, and maintaining clear communication among diverse research teams. Navigating regulatory requirements and addressing unexpected issues like patient recruitment delays or logistical hurdles are also common. Successful coordination relies on strong project management skills, proactive problem-solving, and effective collaboration with site investigators, sponsors, and regulatory bodies.

What are clinical studies?

Clinical studies are research investigations involving human participants, designed to answer specific questions about the safety and effectiveness of medical treatments, interventions, or devices. They are a critical part of medical research, helping to develop new treatments and improve patient care. Clinical studies can include clinical trials, which test new drugs or therapies, as well as observational studies that monitor health outcomes in different populations. These studies follow strict ethical and regulatory guidelines to protect participants and ensure reliable results.

What can I do with a clinical studies degree?

A clinical studies degree prepares individuals for roles such as clinical research coordinator, clinical data manager, or clinical research associate. These positions involve managing and monitoring clinical trials, ensuring compliance with regulations, and collecting and analyzing data, often requiring knowledge of Good Clinical Practice (GCP) and familiarity with trial management software.

What is the difference between Clinical Studies vs Clinical Research Coordinator?

AspectClinical StudiesClinical Research Coordinator
CredentialsTypically requires a degree in health sciences, nursing, or related fields; certifications like CCRP are commonOften requires similar degrees; certifications like CCRP or CRC are advantageous
Work EnvironmentConducted in hospitals, clinics, or research facilities; involves overseeing clinical trialsWorks directly with research teams, managing daily trial activities at sites
Employer & IndustryPharmaceutical companies, hospitals, research institutionsResearch sites, hospitals, academic institutions

While both roles are integral to clinical research, Clinical Studies generally refers to the broader process of conducting clinical trials, whereas a Clinical Research Coordinator manages the day-to-day operations of these trials at research sites. Both require similar credentials and work in related environments, but their specific responsibilities differ.

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

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

What cities near Raleigh, NC are hiring for Clinical Studies jobs?

Cities near Raleigh, NC with the most Clinical Studies job openings:

Clinical Studies jobs near you
Infographic showing various Clinical Studies job openings in Raleigh, NC as of August 2026, with employment types broken down into 2% As Needed, 72% Full Time, 19% Part Time, and 7% Contract. Highlights an 94% Physical, 1% Hybrid, and 5% Remote job distribution, with an average salary of $69,992 per year, or $33.6 per hour.

Senior Clinical Project Manager, CNS - IQVIA Biotech

IQVIA, Inc.

Durham, NC • On-site

$93K - $232K/yr

Full-time

Re-posted yesterday

IQVIA rating

8.1

Company rating: 8.1 out of 10

Based on 53 frontline employees who took The Breakroom Quiz

61st of 223 rated it services

Job description

IQVIA Biotech is a full-service CRO purpose-built to serve biotech sponsors. With over 25 years of experience, we offer agile, therapeutically aligned solutions and trusted partnerships that help bring breakthrough treatments to patients faster.
We are seeking a US-based Senior Clinical Project Manager with proven experience in Central Nervous System (CNS) clinical trials to join IQVIA Biotech. This role is ideal for a seasoned project management professional who thrives in a fast-paced environment and is passionate about advancing therapies in the CNS space. You will leverage your expertise to lead complex, multi-regional studies and ensure operational excellence while building strong client relationships.
Overview
As a Senior Clinical Project Manager at IQVIA Biotech, you'll play a critical role in accelerating the delivery of clinical trials and improving patient lives by bringing new therapies to market faster. You will lead core project teams, ensuring successful execution of clinical studies in alignment with contractual requirements, SOPs, and regulatory standards. This role combines strategic leadership, operational excellence, and customer engagement to deliver high-quality results.
Key Responsibilities
  • Lead bid defense presentations and contribute to study strategy development.
  • Develop and implement integrated study management plans.
  • Oversee planning and execution of medium to large, multi-regional clinical studies, ensuring speed, quality, and cost optimization.
  • Serve as the primary point of contact for clients, fostering strong relationships and customer satisfaction.
  • Build and lead cross-functional teams, driving collaboration and milestone achievement.
  • Monitor project progress, manage risks, and resolve issues proactively.
  • Ensure compliance with ICH GCP, local regulations, and company processes.
  • Manage project financials, including forecasting, scope changes, and revenue acceleration opportunities.
  • Mentor and support team members, promoting continuous improvement and knowledge sharing.

Qualifications
  • Bachelor's degree in Life Sciences or related field.
  • 7+ years of clinical research experience, including 4+ years in project management.
  • Strong knowledge of clinical trial conduct, regulatory requirements, and therapeutic areas.
  • Excellent leadership, communication, and negotiation skills.
  • Proven ability to manage complex projects across geographies and functions.
  • Proficiency in MS Office and project management tools.

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 $93,100.00 - $232,800.00. 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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About IQVIA

Sourced by ZipRecruiter

At IQVIA, we are passionate about helping customers and partners improve results and patient outcomes. Everything we do contributes to this vision for creating a healthier world. In today’s healthcare environment, it’s not only about how much data, information, and technology you have at your fingertips – it’s what you do with it. IQVIA is focused on making intelligent connections for customers across the entire healthcare ecosystem to help you drive healthcare forward. Whether that means partnering with novel technology companies to boost patient engagement, leveraging AI & machine learning to accelerate results, or using decentralized trials to reach the right patients wherever they are – we are always looking for smarter ways to move you forward.

Industry

Health care and social assistance

Company size

10,000+ Employees

Headquarters location

Durham, NC, US

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