1

Clinical Study Manager Jobs in Raleigh, NC (NOW HIRING)

Data Management leadership on studies and take responsibility for the development of the project ... The Senior Clinical Data Manager will work with the leadership team to provide guidance, mentoring ...

Data Management leadership on studies and take responsibility for the development of the project ... The Senior Clinical Data Manager will work with the leadership team to provide guidance, mentoring ...

New

The Clinical Trial Manager (CTM) is responsible for managing various aspects of clinical trials including study start-up, site management and monitoring activities. This includes vendor management ...

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 ...

Ensures the contracted services and expectations of a clinical study are carried out by the Company ... Works in the role of a project manager on assigned project(s), which may range from single service ...

Ensures the contracted services and expectations of a clinical study are carried out by the Company ... Works in the role of a project manager on assigned project(s), which may range from single service ...

Clinical Project Manager

Durham, NC · On-site

$85K - $120K/yr

Whether it involves preventive health care, at-home tests, or access to lifesaving clinical studies ... As a Clinical Project Manager, you will play a critical role in leading cross-functional teams ...

Showing results 41-60

Clinical Study Manager information

See Raleigh, NC salary details

$28

$60

$93

How much do clinical study manager jobs pay per hour?

As of Aug 13, 2026, the average hourly pay for clinical study manager in Raleigh, NC is $60.77, according to ZipRecruiter salary data. Most workers in this role earn between $49.28 and $68.46 per hour, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive as a clinical study manager?

To thrive as a Clinical Study Manager, you need a strong background in clinical research, project management, and regulatory compliance, typically supported by a degree in life sciences and experience in clinical trials. Familiarity with clinical trial management systems (CTMS), electronic data capture (EDC) platforms, and certifications like GCP (Good Clinical Practice) are highly valued. Strong organizational, leadership, and communication skills help manage cross-functional teams and ensure study timelines are met. These skills are crucial for maintaining study quality, ensuring regulatory adherence, and delivering successful trial outcomes.

What are some common challenges faced by clinical study managers, and how can they be addressed?

Clinical Study Managers often encounter challenges such as coordinating multiple stakeholders, ensuring regulatory compliance, and managing tight timelines across study sites. Effective communication and proactive planning are essential to address these issues, as well as staying up to date with changing industry regulations. Building strong relationships with site staff and fostering a collaborative team environment can also help mitigate delays and ensure study milestones are met successfully.
What are the most commonly searched types of Clinical Study jobs in Raleigh, NC? The most popular types of Clinical Study jobs in Raleigh, NC are:
What are popular job titles related to Clinical Study Manager jobs in Raleigh, NC? For Clinical Study Manager jobs in Raleigh, NC, the most frequently searched job titles are:
What cities near Raleigh, NC are hiring for Clinical Study Manager jobs? Cities near Raleigh, NC with the most Clinical Study Manager job openings:
Infographic showing various Clinical Study Manager job openings in Raleigh, NC as of August 2026, with employment types broken down into 33% Full Time, and 67% Contract. Highlights an 67% In-person, and 33% Remote job distribution, with an average salary of $126,397 per year, or $60.8 per hour.

Clinical Project Manager, Immuno-Oncology

IQVIA

Durham, NC

$93K - $232K/yr

Full-time

Re-posted 29 days ago


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 Clinical Project Manager with proven experience in Immuno-oncology and Cell & Gene Therapy clinical trials to join IQVIA Biotech.

Overview

As a Clinical Project Manager, you'll play an essential role in accelerating clinical trial delivery and improving patient lives by helping bring new therapies to market faster. You will serve as a key member of the core project team, ensuring the successful execution of clinical studies in alignment with contractual requirements, SOPs, and regulatory standards. This role blends strategic leadership, operational excellence, financial oversight, and customer partnership to drive highquality outcomes across regional and global studies.

Key Responsibilities

  • Participate in bid defense presentations and contribute to study strategy development; may lead presentations for smaller or regional studies.

  • Develop and implement integrated study management plans alongside the core project team.

  • Lead the planning and execution of smaller or less complex regional clinical studies, optimizing speed, quality, and cost.

  • Serve as a primary or backup point of contact for clients, fostering strong, collaborative customer relationships.

  • Build, manage, and guide crossfunctional project teams, ensuring effective communication and milestone achievement.

  • Monitor study progress, proactively manage risks, and drive timely issue resolution.

  • Ensure adherence to ICH GCP, applicable local regulations, standard processes, and company policies.

  • Manage project financials, including forecasting, scope management, revenue optimization, and identification of acceleration opportunities.

  • Oversee vendor management activities when assigned.

  • Support team development by mentoring less experienced project team members and contributing to a culture of continuous improvement.

Qualifications

  • Bachelor's degree in Life Sciences or a related field.

  • 5+ years of relevant clinical research experience, including at least 1 year of project management experience.

  • Broad protocol and therapeutic knowledge; familiarity with the competitive landscape and ability to articulate the value of IQVIA solutions.

  • Excellent communication and presentation skills

  • Proven leadership capabilities, including decisionmaking, performance management, and crossfunctional collaboration.

  • Strong problemsolving, planning, organizational, and prioritization skills.

  • Ability to manage conflicting priorities while maintaining quality and accuracy.

  • Proficiency in MS Office applications (Word, Excel, PowerPoint).

  • Understanding of project financials, including budgets, forecasting, and contractual obligations.

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 athttps://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.

What IQVIA employees say

Pay

Benefits

Hours and flexibility

Workplace

Get the full story on Breakroom


IQVIA logo

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