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Remote Pfizer Clinical Research Jobs (NOW HIRING)

CRO Strategies

Clinical Research Coordinator

Des Moines, IA · Remote

$23.75 - $31.50/hr

Role Description This is a full-time Clinical Research Coordinator. The Clinical Research ... Ability to work independently in a remote setting and manage multiple priorities * Knowledge of ...

Omada Health

Clinical Research Coordinator

$24.75 - $33/hr

This is a full time position and is remote. Your Impact: * Support Omada's research program by ... Educational exposure to clinical research methods and study design. * Exposure to human-subjects ...

IQVIA

Clinical Research Coordinator

Philadelphia, PA · 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 ...

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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

CRO Strategies

Des Moines, IA • Remote

$23.75 - $31.50/hr

Other

Posted 24 days ago

Job description


Role Description

This is a full-time Clinical Research Coordinator. The Clinical Research Coordinator will be responsible for overseeing and managing clinical research studies, coordinating recruitment and enrollment of study participants, executing informed consent processes, and managing study protocols. Additional tasks include ensuring compliance with applicable regulations, facilitating communication between study teams, maintaining research documentation, and providing support in the execution of high-quality clinical trials.


Qualifications

  • Comprehensive knowledge and experience with Informed Consent processes and Protocol adherence
  • Strong background in Research and Clinical Research Experience
  • Proficiency with Clinical Trials processes and conducting them in compliance with guidelines
  • Strong organizational, communication, and attention-to-detail skills
  • Ability to work independently in a remote setting and manage multiple priorities
  • Knowledge of Good Clinical Practice (GCP) guidelines and applicable regulatory requirements
  • Experience with electronic data capture (EDC) systems is a plus
  • Bachelor's degree in life sciences, healthcare, or a related field preferred

Apply