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Remote Pfizer Clinical Research Jobs (NOW HIRING)

IQVIA

Clinical Research Coordinator

Raleigh, NC · Remote

$35 - $42/hr

This position is not eligible for visa sponsorship #LI-CES and #LI-DNP #LI-HCP #remote IQVIA is a leading global provider of clinical research services, commercial insights and healthcare ...

Emmes

Senior Clinical Research Associate

Rockville, MD · On-site +1

Overview Senior Clinical Research Associate US Remote Emmes Group: Building a better future for us all. Emmes Group is transforming the future of clinical research, bringing the promise of new ...

Pfizer

Oncology Field Medical Director

OR · Remote

Cultivate research and therapeutic area expertise, including familiarity with latest congress data ... Represent Pfizer Medical Affairs leadership with clinical/professional associations and/or ...

Pfizer

Cultivate research and therapeutic area expertise, including familiarity with latest congress data ... Represent Pfizer Medical Affairs leadership with clinical/professional associations and/or ...

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$36K

$94.3K

$143.5K

How much do remote pfizer clinical research jobs pay per year?

As of Jun 11, 2026, the average yearly pay for remote pfizer clinical research in the United States is $94,314.00, according to ZipRecruiter salary data. Most workers in this role earn between $62,500.00 and $128,000.00 per year, depending on experience, location, and employer.

What are remote Pfizer clinical research jobs?

Remote Pfizer clinical research jobs involve supporting or conducting clinical trials and research studies for Pfizer while working from a location outside of a traditional office or clinical site. These roles can encompass tasks such as data management, clinical monitoring, regulatory documentation, and coordinating trial activities virtually. Remote positions offer flexibility and the ability to collaborate with global teams, while still ensuring adherence to regulatory standards and study protocols. Candidates typically need experience in clinical research and strong communication and organizational skills.

What is the difference between Remote Pfizer Clinical Research vs Remote Clinical Data Coordinator?

AspectRemote Pfizer Clinical ResearchRemote Clinical Data Coordinator
Required CredentialsBachelor's degree in health sciences, clinical research certification often preferredBachelor's degree in health or related field, data management training
Work EnvironmentRemote, within pharmaceutical or clinical research settingsRemote, focused on data entry and management
Employer & IndustryPfizer, pharmaceutical/biotech industryHealthcare organizations, research sites, or CROs
Common Search & ComparisonYesYes

Remote Pfizer Clinical Research roles involve overseeing clinical trials, ensuring compliance, and working within pharmaceutical companies. Remote Clinical Data Coordinators focus on managing and entering clinical trial data, often within research sites or CROs. Both roles require related certifications and work in the clinical research industry, but they differ in responsibilities and daily tasks.

What are the key skills and qualifications needed to thrive as a Remote Pfizer Clinical Research professional, and why are they important?

To thrive as a Remote Pfizer Clinical Research professional, you need a background in life sciences or a related field, experience in clinical research, and often a relevant certification such as CCRA or SOCRA. Familiarity with electronic data capture (EDC) systems, clinical trial management systems (CTMS), and Good Clinical Practice (GCP) guidelines is typically required. Strong analytical thinking, attention to detail, and excellent written and verbal communication skills set top candidates apart. These skills ensure the integrity, compliance, and effectiveness of clinical trials conducted remotely to advance medical research.

What are some common challenges faced by remote Pfizer clinical research professionals, and how can they be managed?

Remote Pfizer clinical research professionals often encounter challenges related to communication and coordination with cross-functional teams, as research projects typically involve colleagues from multiple departments and time zones. Maintaining data integrity and ensuring compliance with regulatory standards can also be more complex when working remotely. To manage these challenges, it's important to leverage collaborative digital platforms, establish clear communication protocols, and participate in regular virtual meetings. Additionally, staying up-to-date with company training and guidelines helps ensure that all research activities align with Pfizer’s high standards and regulatory requirements.
More about Remote Pfizer Clinical Research jobs
What cities are hiring for Remote Pfizer Clinical Research jobs? Cities with the most Remote Pfizer Clinical Research job openings:
What are the most commonly searched types of Pfizer Clinical Research jobs? The most popular types of Pfizer Clinical Research jobs are:
What states have the most Remote Pfizer Clinical Research jobs? States with the most job openings for Remote Pfizer Clinical Research jobs include:
What job categories do people searching Remote Pfizer Clinical Research jobs look for? The top searched job categories for Remote Pfizer Clinical Research jobs are:
Remote Pfizer Clinical Research jobs near you
Infographic showing various Remote Pfizer Clinical Research job openings in the United States as of June 2026, with employment types broken down into 62% Full Time, 25% Part Time, and 13% Contract. Highlights an 100% Remote job distribution, with an average salary of $94,314 per year, or $45.3 per hour.
Clinical Research Coordinator

Clinical Research Coordinator

IQVIA

Raleigh, NC • Remote

$35 - $42/hr

Part-time

Medical, Life

Posted 25 days ago

IQVIA rating

8.2

Company rating: 8.2 out of 10

Based on 52 frontline employees who took The Breakroom Quiz

46th of 204 rated it services

Job description

Clinical Research Coordinator - Raleigh, NC

Work Setup: On-site
Employment Type: Part-Time, 24 Hours/Week

About IQVIA

IQVIA is a global leader in advanced analytics, technology solutions, and clinical research services, dedicated to driving healthcare forward. We partner with leading pharmaceutical, biotechnology, and medical device organizations to improve patient outcomes and accelerate innovation. By combining deep scientific expertise with advanced technology, we deliver high-quality data and insights that shape the future of clinical trials.

Position Overview

We are seeking a Clinical Research Coordinator (CRC) to support the successful execution of clinical trials under the supervision of a Principal Investigator. This role requires a detail-oriented, patient-focused professional who can manage clinical, operational, and data-related responsibilities while ensuring compliance with regulatory and protocol requirements.

Key Responsibilities

  • Perform clinical procedures including ECGs, vital signs, and biological sample collection in accordance with study protocols

  • Coordinate daily clinical trial activities while ensuring compliance with GCP, study protocols, and regulatory guidelines

  • Prepare study materials, maintain equipment, and support site readiness for study visits

  • Conduct patient recruitment and pre-screening activities, including chart review and phone screenings

  • Schedule and conduct patient study visits, ensuring protocol adherence and participant safety

  • Educate, consent, and orient study participants throughout the clinical trial process

  • Accurately collect, document, and enter clinical data into EDC systems and case report forms (CRFs)

  • Perform data review and resolve queries to maintain high-quality, audit-ready datasets

  • Collaborate with investigators, sponsors, and monitors, including support during monitoring visits and audits

  • Maintain a safe clinical environment and serve as a patient advocate in accordance with health and safety standards

Qualifications

  • Bachelor's degree preferred or equivalent combination of education and relevant experience

  • Minimum of 1+ year of clinical research experience, including hands-on coordinating responsibilities

  • Demonstrated experience conducting study visits, patient recruitment, and pre-screening activities

  • Proficiency in clinical data entry, including use of EDC systems and query resolution

  • Working knowledge of clinical trial processes, GCP guidelines, and medical terminology

  • Strong attention to detail with the ability to manage multiple priorities in a fast-paced environment

  • Effective communication and interpersonal skills with the ability to collaborate cross-functionally

Additional Information

  • This position is not eligible for visa sponsorship

#LI-CES and #LI-DNP #LI-HCP #remote

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 is $35.00-$42.00 per hour. 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

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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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