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Cra Project Manager Jobs (NOW HIRING)

IQVIA Holdings

CRA 2, Oncology, IQVIA

Wayne, PA

$87K - $145K/yr

... manage ongoing project expectations and issues. Evaluate the quality and integrity of study site ... CRA experience including on-site monitoring. IQVIA is a leading global provider of clinical ...

IQVIA Holdings

CRA 2, Oncology, IQVIA

Chicago, IL · On-site

$87K - $145K/yr

... manage ongoing project expectations and issues. Evaluate the quality and integrity of study site ... CRA experience including on-site monitoring. IQVIA is a leading global provider of clinical ...

IQVIA Holdings

CRA 2, Oncology, IQVIA

Indianapolis, IN · On-site

$87K - $145K/yr

... manage ongoing project expectations and issues. Evaluate the quality and integrity of study site ... CRA experience including on-site monitoring. IQVIA is a leading global provider of clinical ...

MSD

Sr. CRA - Clinical Research Associate

Guaynabo, PR · On-site

Performs clinical study site management/monitoring activities in compliance with ICH-GCP, Sponsor ... Demonstrates and projects professional demeanor and communication consistent with organizational ...

Alto Neuroscience, Inc.

Clinical Research Associate

$80/hr

The CRA assists the Clinical Trial Manager and/or Clinical Project Manager by managing their assigned clinical sites to ensure enrollment, timely review of data, identification of site issues, and ...

Tigermed America

Clinical Research Associate

Denver, CO · Remote

... CRA responsible sites, and assessing overall status of the project; * Develop the project management plan, monitoring plan etc as required for the study; * Develop study specific tools/forms, study ...

IQVIA

CRA 2, Oncology, IQVIA

Wayne, PA

$87K - $145K/yr

... manage ongoing project expectations and issues. Evaluate the quality and integrity of study site ... CRA experience including on-site monitoring. IQVIA is a leading global provider of clinical ...

IQVIA

CRA 2, Oncology, IQVIA

Boston, MA

$87K - $145K/yr

... manage ongoing project expectations and issues. Evaluate the quality and integrity of study site ... CRA experience including on-site monitoring. IQVIA is a leading global provider of clinical ...

IQVIA

CRA 2, Oncology, IQVIA

Chicago, IL

$87K - $145K/yr

... manage ongoing project expectations and issues. Evaluate the quality and integrity of study site ... CRA experience including on-site monitoring. IQVIA is a leading global provider of clinical ...

IQVIA

CRA 2, Oncology, IQVIA

Indianapolis, IN

$87K - $145K/yr

... manage ongoing project expectations and issues. Evaluate the quality and integrity of study site ... CRA experience including on-site monitoring. IQVIA is a leading global provider of clinical ...

IQVIA

CRA 2, Oncology, IQVIA

Indianapolis, IN

$87K - $145K/yr

... manage ongoing project expectations and issues. Evaluate the quality and integrity of study site ... CRA experience including on-site monitoring. IQVIA is a leading global provider of clinical ...

IQVIA, Inc.

CRA 2, Oncology, IQVIA

Durham, NC · On-site

$87K - $145K/yr

... manage ongoing project expectations and issues. Evaluate the quality and integrity of study site ... CRA experience including on-site monitoring. IQVIA is a leading global provider of clinical ...

Tigermed America

Clinical Research Associate

Denver, CO · Remote

... CRA responsible sites, and assessing overall status of the project; * Develop the project management plan, monitoring plan etc as required for the study; * Develop study specific tools/forms, study ...

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Cra Project Manager information

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$48.5K

$92.9K

$159K

How much do cra project manager jobs pay per year?

As of Sep 10, 2026, the average yearly pay for cra project manager in the United States is $92,933.00, according to ZipRecruiter salary data. Most workers in this role earn between $65,500.00 and $115,500.00 per year, depending on experience, location, and employer.

What is a CRA Project Manager?

A CRA Project Manager is a professional who oversees and coordinates clinical research projects, often within pharmaceutical or biotechnology companies or contract research organizations (CROs). They are responsible for planning, executing, and closing clinical trials in compliance with regulatory guidelines. Their duties include managing budgets, timelines, and resources, communicating with stakeholders, and ensuring the quality and integrity of the research data. CRA Project Managers also supervise clinical research associates (CRAs) and ensure that all trial activities adhere to protocols and Good Clinical Practice (GCP) standards.

What are the key skills and qualifications needed to thrive as a CRA Project Manager?

To thrive as a CRA Project Manager, you need a solid background in clinical research, project management expertise, and typically a degree in life sciences or a related field. Familiarity with clinical trial management systems (CTMS), regulatory compliance (such as GCP), and often a project management certification like PMP are highly beneficial. Strong leadership, problem-solving, and communication skills set exceptional candidates apart, especially when managing diverse teams and stakeholders. These skills ensure successful project delivery, regulatory adherence, and effective coordination of clinical research activities.

What are some common challenges faced by a CRA Project Manager when coordinating multi-site clinical trials?

CRA Project Managers often encounter challenges such as ensuring consistent communication across diverse research sites, maintaining regulatory compliance, and managing tight project timelines. They must address site-specific issues quickly while balancing the needs of sponsors, investigators, and regulatory bodies. Success in this role requires strong organizational skills, adaptability, and a proactive approach to problem-solving, as well as the ability to foster collaboration among cross-functional teams.

What is the difference between Cra Project Manager vs Clinical Research Associate?

AspectCra Project ManagerClinical Research Associate
CredentialsBachelor's degree, often advanced degrees, project management certificationsBachelor's degree in life sciences or related field, clinical research certifications
Work EnvironmentOversees multiple projects, manages teams, coordinates with sponsorsMonitors clinical trials at sites, ensures protocol compliance
Employer & Industry UsagePharmaceutical companies, CROs, biotech firmsPharmaceutical companies, CROs, clinical trial sites

The Cra Project Manager focuses on overseeing entire clinical projects, managing teams, and ensuring timely delivery. In contrast, a Clinical Research Associate primarily monitors clinical trial sites to ensure compliance with protocols. Both roles require related certifications and work within the clinical research industry, but their responsibilities and scope differ significantly.

What cities are hiring for Cra Project Manager jobs?

Cities with the most Cra Project Manager job openings:

What states have the most Cra Project Manager jobs?

States with the most job openings for Cra Project Manager jobs include:

What are popular job titles related to Cra Project Manager jobs?

For Cra Project Manager jobs, the most frequently searched job titles are:

Cra Project Manager jobs near you

CRA 2, Oncology, IQVIA

Wayne, PA

IQVIA Holdings
Health Care and Social Assistance • 10K+ employees
Learn more about IQVIA Holdingsexternal

$87K - $145K/yr

Full-time, Part-time

Posted 12 days ago

IQVIA rating

8.1

Company rating: 8.1 out of 10

Based on 53 frontline employees who took The Breakroom Quiz

Job description

CRA 2 Position

IQVIA is seeking a CRA 2 with a minimum of 1.5 years of on-site oncology monitoring experience:

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.

Education: Bachelor's Degree (Degree in scientific discipline or health care preferred)

Experience: 1.5 to 2 years of relevant CRA experience including on-site monitoring.

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.

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.

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 $87,200.00 - $145,300.00. 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

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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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