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Remote Pfizer Clinical Research Jobs in Decatur, GA

Alimentiv

Consulting Statistician

Atlanta, GA · On-site +1

$110.50K - $184K/yr

... remote based, Canada or USA) Statistical Consulting Services * Communicates with clients and ... Reviews literature related to clinical research, assigned therapy areas and in the areas of clients ...

Corcym

Clinical Field Specialist

Atlanta, GA · Remote

... OR with a remote Proctor. * Must be able to provide/facilitate field-based product training ... Build relationships with leading experts in clinical practice or research relevant to the products ...

Integrated Resources INC

Case Manager

Alpharetta, GA · Remote

$19.50 - $25.25/hr

Information Technology (IT), Clinical Research, Rehabilitation Therapy and Nursing. Education Level ... The Alpharetta, GA candidate will also have the ability to work remote. This is an inbound ...

Actalent

Remote Pharmacy Technician

Atlanta, GA · Remote

$18 - $20/hr

Remote Pharmacy Technician We are seeking a dedicated Pharmacy Technician to join our dynamic team ... Research and resolve questions or issues related to pharmacy operations. Consult with Clinical ...

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Remote Pfizer Clinical Research information

See Decatur, GA salary details

$35.1K

$92.1K

$140.1K

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

As of May 30, 2026, the average yearly pay for remote pfizer clinical research in Decatur, GA is $92,082.00, according to ZipRecruiter salary data. Most workers in this role earn between $61,000.00 and $125,000.00 per year, depending on experience, location, and employer.

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.

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 popular job titles related to Remote Pfizer Clinical Research jobs in Decatur, GA? For Remote Pfizer Clinical Research jobs in Decatur, GA, the most frequently searched job titles are:
What job categories do people searching Remote Pfizer Clinical Research jobs in Decatur, GA look for? The top searched job categories for Remote Pfizer Clinical Research jobs in Decatur, GA are:
What cities near Decatur, GA are hiring for Remote Pfizer Clinical Research jobs? Cities near Decatur, GA with the most Remote Pfizer Clinical Research job openings:
Remote Pfizer Clinical Research jobs near you
Infographic showing various Remote Pfizer Clinical Research job openings in Decatur, GA as of May 2026, with employment types broken down into 1% As Needed, 67% Full Time, 24% Part Time, and 8% Contract. Highlights an 73% Physical, and 27% Remote job distribution, with an average salary of $92,082 per year, or $44.3 per hour.

Consulting Statistician

Alimentiv

Atlanta, GA • On-site, Remote

$110.50K - $184K/yr

Full-time

Posted 7 days ago

Job description

As a member of Alimentiv's Statistical Center of Excellence, the Consulting Statistician is responsible for the research, development, and application of innovative biostatistical methods to support clients in clinical study design and implementation. This role advises internal and external clients on statistical planning, study design, data analyses, reporting and interpretation in accordance with project, regulatory and Alimentiv quality standards. Maintains contemporaneous knowledge of statistical methods, industry standards, and regulatory requirements in assigned therapy areas. Provides statistical education and communicates abstract statistical concepts in a manner such that non-statistical colleagues and clients can make informed decisions. Demonstrates thought leadership though contributions to website content and scientific publications and by delivering presentations at conferences or via webinar. Contributes to business development opportunities by meeting with potential clients and contributing to study proposals and capabilities presentations
 
Positions available: 1 (remote based, Canada or USA)
Statistical Consulting Services
  • Communicates with clients and internal stakeholders to understand their statistical and clinical needs. Provides recommendations, guidance, and education on statistical concepts. Creates supplementary materials such as slides or reports to assist in communication and understanding of recommendations and concepts.  Provides critique of and recommendations for study design after investigating innovative methods, accepted industry standards, and regulatory requirements.
  • Prepares statistical analysis plans and oversee project data collection, management, and analysis, with input from the project team, incorporating details regarding the type of information collected, sample size, randomization procedures, table and listing shells, project statistical policies, protocols, and methodology to be used to appropriately translate scientific questions into statistical hypotheses.
  • Reviews, edits, and assists in preparing statistical sections of study synopses, protocols, reports, publications, or presentations in collaboration with clients and internal stakeholders ensuring statistical analyses adhere to trial, sponsor, organizational and regulatory requirements, and best practices.
  • Advises and consults with various departments internally ensuring that strategies include critical project success factors.
  • Oversees and supports project teams in relevant studies; analyzes implementation gaps and works with relevant stakeholders to close them.
Professional Development and Thought Leadership
  • Stays up to date on new innovations in statistical methods, especially in study design relating to chosen or assigned areas of focus.
  • Reviews statistical research papers, learning new statistical techniques and methodologies, and maintaining subject matter expertise.
  • Reviews literature related to clinical research, assigned therapy areas and in the areas of clients' studies to pair with statistical knowledge to provide guidance that is innovative and in line with the needs and standards.
  • Represents Alimentiv at relevant scientific meetings and congresses and attends trainings relating to statistics, clinical research, and medical areas of interest to continue knowledge growth and expertise.
Business Development Support
  • Working in conjunction with the Statistics and Medical Research and Development teams, develops and presents new and novel clinical trial designs and processes and statistical methodologies into publishable and promotable scientific operations and results.
  • Creates materials such as white papers, case studies, and statistical education materials for presentation and posting on Alimentiv websites to foster client relationship development and attract new clients.
  • Leads or supports strategy discussions and development of proposals for Statistical Center of Excellence projects.
  • Provides the proposal lead and functional leads with information necessary to prepare an accurate proposal that meets the strategy parameters. 
  • Involved in frequent client meetings/presentations and responsible for transferring knowledge to applicable project team members regarding the proposal/study strategy at the time of a bid defense.
Qualifications
  • Candidates should posses a Master's degree and a minimum of 4-6 years of related experience. Advanced degrees in Statistics/Biostats is considered an asset.
  • The ability to communicate abstract concepts
  • Highly refined oral and written communication skills
  • High level of presentation skills
$110,500 - $184,000 a year
Stay Alert to Recruitment Scams
We have been made aware of individuals posing as our recruiters and contacting candidates with fraudulent opportunities. Our hiring process always includes direct engagement with a recruiter or hiring manager, and we will never ask for sensitive personal information early in the process. Official communication will only come from our company email domains. If something doesn't feel right, we encourage you to verify before responding.
We may use artificial intelligence (AI) tools to support parts of the hiring process, such as reviewing applications, analyzing resumes, or assessing responses. These tools assist our recruitment team but do not replace human judgment. Final hiring decisions are ultimately made by humans. If you would like more information about how your data is processed, please contact us.
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