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Associate Clinical Project Manager Jobs in Garner, NC

IQVIA, Inc.

RWE Clinical Project Manager (FSP)

Durham, NC · On-site

$93K - $232K/yr

In this role, the clinical project manager will be responsible for end-to-end project delivery of real-world observational studies within the oncology therapeutic area. It is important for this ...

IQVIA

RWE Clinical Project Manager (FSP)

Durham, NC · On-site

$93K - $232K/yr

In this role, the clinical project manager will be responsible for end-to-end project delivery of real-world observational studies within the oncology therapeutic area. It is important for this ...

IQVIA

Clinical Project Manager, Immuno-Oncology

Durham, NC · On-site

$93K - $232K/yr

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 ...

IQVIA

Senior Clinical Project Manager- CNS

Durham, NC · On-site

Clinical Project Management is focused on project delivery, productivity and quality resulting in strong financial performance and customer satisfaction. Clinical Project leads run their own studies.

IQVIA

Clinical Project Manager- IVD

Durham, NC · On-site

$93K - $232K/yr

... project management experience. * Conceptual and practical knowledge of Product Development and basic knowledge of Clinical Operations or related areas. IQVIA is a leading global provider of clinical ...

IQVIA

Clinical Project Manager- IVD

Durham, NC · On-site

$93K - $232K/yr

... project management experience. * Conceptual and practical knowledge of Product Development and basic knowledge of Clinical Operations or related areas. IQVIA is a leading global provider of clinical ...

STI

Epic Clinical Project Manager :: NC

Durham, NC · On-site

CANDIDATE MUST BE CERTIFIED IN AT LEAST ONE CLINICAL APPLICATION The North Carolina Department of Health and Human Services requires the services of an EXPERT Epic Clinical project manager to manage ...

IQVIA

Senior Clinical Project Manager- CNS

Durham, NC · On-site

Clinical Project Management is focused on project delivery, productivity and quality resulting in strong financial performance and customer satisfaction. Clinical Project leads run their own studies.

IQVIA, Inc.

Clinical Project Manager- IVD

Durham, NC · On-site

$93K - $232K/yr

... project management experience. * Conceptual and practical knowledge of Product Development and basic knowledge of Clinical Operations or related areas. IQVIA is a leading global provider of clinical ...

IQVIA

Associate Director, Study Operations

Durham, NC · Remote

$102K - $285K/yr

Home-based in USA/Canada Job Overview Associate Clinical Project Management Directors supervise, manage and provide oversight to assigned Clinical Project Management staff who manage or support ...

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All JobsAssociate Clinical Project JobsAssociate Clinical Project Manager JobsAssociate Clinical Project Manager Jobs in Garner, NC

Associate Clinical Project Manager information

See Garner, NC salary details

$14

$34

$53

How much do associate clinical project manager jobs pay per hour?

As of Sep 4, 2026, the average hourly pay for associate clinical project manager in Garner, NC is $34.54, according to ZipRecruiter salary data. Most workers in this role earn between $26.59 and $40.05 per hour, depending on experience, location, and employer.

What is an associate clinical project manager?

An Associate Clinical Project Manager (ACPM) is an entry- to mid-level professional who assists in planning, coordinating, and overseeing clinical trials and research projects within pharmaceutical, biotech, or clinical research organizations. They work closely with project managers and cross-functional teams to ensure studies are conducted according to protocol, regulatory requirements, and timelines. ACPMs may handle tasks such as tracking project progress, supporting site management, preparing documentation, and communicating with stakeholders. Their role helps ensure the smooth execution and delivery of clinical research projects.

What are the key skills and qualifications needed to thrive as an associate clinical project manager?

To thrive as an Associate Clinical Project Manager, you need a solid understanding of clinical research processes, project management principles, and typically a degree in life sciences or a related field. Familiarity with clinical trial management systems (CTMS), electronic data capture (EDC) tools, and Good Clinical Practice (GCP) certification is often required. Exceptional organizational skills, attention to detail, and strong communication abilities help you coordinate teams and timelines effectively. These competencies are crucial for ensuring clinical trials run smoothly, meet regulatory standards, and deliver reliable results on schedule.

What are the common challenges faced by an associate clinical project manager and how can they be addressed?

Associate Clinical Project Managers often encounter challenges such as balancing multiple study timelines, coordinating cross-functional teams, and ensuring regulatory compliance. Managing communication between sponsors, vendors, and internal teams can also be complex. To address these challenges, it's important to prioritize tasks, maintain clear documentation, and foster strong relationships with stakeholders. Leveraging project management tools and regularly reviewing project milestones can help ensure studies stay on track and issues are promptly resolved.

What is the difference between Associate Clinical Project Manager vs Clinical Project Coordinator?

AspectAssociate Clinical Project ManagerClinical Project Coordinator
CredentialsBachelor's degree, often some project management or clinical research experienceBachelor's degree, entry-level in clinical research
Work EnvironmentSupports project managers, involved in planning and oversightAssists with daily tasks, data collection, and site communication
Employer & Industry UsagePharmaceutical, biotech, clinical research organizationsClinical research sites, CROs, pharma companies

The Associate Clinical Project Manager typically has more responsibility in project planning and oversight compared to the Clinical Project Coordinator, who mainly supports data collection and site coordination. Both roles are essential in clinical research teams, with the associate role often serving as a stepping stone to more senior project management positions.

What job categories do people searching Associate Clinical Project Manager jobs in Garner, NC look for?

The top searched job categories for Associate Clinical Project Manager jobs in Garner, NC are:

What cities near Garner, NC are hiring for Associate Clinical Project Manager jobs?

Cities near Garner, NC with the most Associate Clinical Project Manager job openings:

Associate Clinical Project Manager jobs near you
Infographic showing various Associate Clinical Project Manager job openings in Garner, NC as of August 2026, with employment types broken down into 83% Full Time, 16% Part Time, and 1% Contract. Highlights an 81% Physical, 2% Hybrid, and 17% Remote job distribution, with an average salary of $71,842 per year, or $34.5 per hour.

RWE Clinical Project Manager (FSP)

IQVIA, Inc.

Durham, NC • On-site

$93K - $232K/yr

Full-time

Re-posted 16 days ago

IQVIA rating

8.1

Company rating: 8.1 out of 10

Based on 53 frontline employees who took The Breakroom Quiz

62nd of 226 rated it services

Job description

Job Overview
IQVIA is hiring a clinical project manager to expand our dedicated Real World Evidence (RWE) FSP team, working fully within the environment of a prominent pharma company. In this role, the clinical project manager will be responsible for end-to-end project delivery of real-world observational studies within the oncology therapeutic area. It is important for this individual to have experience working in observational research across primary and secondary data collection study designs as well as leading clinical studies independently.
Who do you work with?
  • Epidemiologists, data science, and clinical leads to deliver project specific goals and timelines
  • Vendors to communicate status of deliverables and workflow
  • Program and business leads to manage full portfolio of projects

What are you great at?
  • Independently executing observational and real-world studies while balancing speed, quality, and cost
  • Leading cross-functional teams to achieve milestones and resolve study issues
  • Proactively identifying risks and implementing mitigation plans
  • Communicating clearly with stakeholders, including preparing and presenting project updates to leadership
  • Good understanding of project financials including experience managing, contractual obligations and implications
  • Driving operational excellence and strategic partnership with clients
  • Managing vendors effectively across different sourcing models (in-house, hybrid, outsourced)
  • Bringing clarity to complex or ambiguous situations and making informed decisions
  • Results-oriented approach to work towards delivery and output
  • Strong organizational, prioritization, and time management skills
  • Ability to operate effectively in a matrixed, fast-paced, and evolving environment

Your responsibilities may include:
  • Leading global, cross-functional observational study teams and owning delivery of contracted scope, timelines, and quality
  • Developing study documentation, including project management plans
  • Ensuring consistent use of study tools, training materials, and compliance with SOPs, policies, and procedures
  • Monitoring study progress and financial performance; supporting forecasting and change control as needed
  • Lead project vendor management related activities and communications per project requirements
  • Anticipating operational and quality risks, responding to issues raised by the project team and planning/implementing appropriate corrective or preventative actions
  • Generating project- or program-level metrics and reports for senior management
  • Capturing lessons learned and contributing to continuous improvement and best practices

Required knowledge, skills, and abilities
  • Bachelor's degree in life sciences or related field
  • Minimum 4-6 years of experience in project management and/or clinical operations within pharma, CRO, or RWE environment (or equivalent combination of education, training, and experience)
  • Demonstrated experience leading observational or real-world evidence studies
  • Strong understanding of RWE study designs and clinical research conduct and skill in applying applicable clinical research regulatory requirements
  • Experience with primary and secondary data study designs

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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