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Remote Pfizer Clinical Research Jobs (NOW HIRING)

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 ...

Clinical Research Assistant

Duluth, MN · On-site +1

$18.69 - $27.85/hr

Experience in oncology, clinical research, academic research or similar area. Over 1 year computer ... None FTE: 1 Possible Remote/Hybrid Option: Shift Rotation: Day Rotation (United States of America ...

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

This is an excellent opportunity for an experienced clinical research leader looking to make a significant impact on global healthcare initiatives in a fully remote setting. Accountabilities

The Director of Clinical Research will serve within Hanger's Department of Clinical and Scientific ... Remote: Pay range of $140,000- $150,000 + bonus + benefits. This pay range is posted to comply with ...

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

Job Summary Aptive Resources is seeking a Clinical Research Protocol Manager to support the ... This is a full-time (40 hours/week), 100% remote position. This position is currently funded ...

Job Summary Aptive Resources is seeking a Clinical Research Protocol Manager to support the ... This is a full-time (40 hours/week), 100% remote position. This position is currently funded ...

Showing results 21-40

Remote Pfizer Clinical Research information

See salary details

$36K

$94.3K

$143.5K

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

As of Jul 29, 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:
Infographic showing various Remote Pfizer Clinical Research job openings in the United States as of July 2026, with employment types broken down into 2% As Needed, 73% Full Time, 17% Part Time, and 8% Contract. Highlights an 95% Physical, 1% Hybrid, and 4% Remote job distribution, with an average salary of $94,314 per year, or $45.3 per hour.

Clinical Research Coordinator

IQVIA

Philadelphia, PA • Remote

$35 - $42/hr

Part-time

Medical, Life

This job post has expired today. Applications are no longer accepted.


IQVIA rating

8.1

Company rating: 8.1 out of 10

Based on 53 frontline employees who took The Breakroom Quiz

61st of 230 rated it services


Job description

Clinical Research Coordinator - Philadelphia, PA

Work Setup: On-site
Employment Type: Part-time - 24 Hours per 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 cutting-edge 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 research studies under the direction of a Principal Investigator. This is a hands-on role requiring clinical, operational, and patient-facing expertise to ensure studies are conducted safely, efficiently, and in compliance with regulatory standards.

Key Responsibilities

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

  • Coordinate day-to-day clinical trial activities while ensuring compliance with GCP, protocol, and regulatory requirements

  • Prepare study materials, organize equipment, and support overall site readiness

  • Conduct patient recruitment activities, including chart review, phone screening, and scheduling study visits

  • Perform and manage patient study visits in accordance with protocol requirements

  • Educate and orient participants, ensuring a high standard of patient care and safety

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

  • Resolve data queries in a timely manner and maintain high data quality standards

  • Collaborate with investigators, sponsors, and monitors during site visits and audits

  • Serve as a patient advocate and maintain a safe, compliant clinical environment

Qualifications

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

  • Minimum of 1+ years of clinical research experience in a coordinator or similar role

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

  • Proven ability to conduct patient study visits in accordance with protocol requirements

  • Experience in patient recruitment, including chart review and phone screenings

  • Proficiency with EDC systems, including accurate data entry and query resolution

  • Strong attention to detail, organizational skills, and ability to manage multiple priorities

  • Effective communication skills and ability to build collaborative working relationships

  • Cardiovascular research experience preferred

Why Join IQVIA?

  • Be part of a global organization at the forefront of clinical innovation

  • Collaborate with industry-leading experts and researchers

  • Contribute to advancing treatments that improve patient lives

Note: 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.

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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