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Part Time Pfizer Clinical Research Jobs (NOW HIRING)

Denali Health

Clinical Research Nurse

Atlanta, GA · On-site

Our commitment to excellence in clinical research operations ensures the highest standards of ... This is a part-time position that requires working one week per month on-site according to the ...

IQVIA

Clinical Research Coordinator

Raleigh, NC · Remote

$35 - $42/hr

On-site Schedule: 24 hours per week (Part-Time) About IQVIA IQVIA is a global leader in advanced analytics, technology solutions, and clinical research services, dedicated to driving healthcare ...

IQVIA

Clinical Research Coordinator

Jefferson City, MO

$35 - $42/hr

Clinical Research Coordinator - Jefferson City, MO Work Set-Up: On-site Schedule Weekly Hours: 24 ... part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of ...

IQVIA

Clinical Research Coordinator

Marietta, GA

$35 - $42/hr

Clinical Research Coordinator - Marietta, GA Work Set-Up: On-site Schedule Weekly Hours: 24 hours ... part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of ...

Main Line Health

Clinical Research Coord II

Wynnewood, PA · Hybrid

$23.25 - $31/hr

This position is eligible for up to $6,000 per year based upon your Full or Part Time status ... Clinical Research Coordinator II Shift: 8am-4:30p and variable, Monday-Friday Flexibility required ...

Main Line Health

Clinical Research Coord I

Wynnewood, PA · On-site

$23.25 - $31/hr

This position is eligible for up to $6,000 per year based upon your Full or Part Time status ... Clinical Research Coordinator I Shift: 8am-4:30p and variable, Monday-Friday Flexibility required ...

Main Line Health

Clinical Research Coord I

Wynnewood, PA · On-site

$23.25 - $31/hr

This position is eligible for up to $6,000 per year based upon your Full or Part Time status ... Clinical Research Coordinator I Shift: 8am-4:30p and variable, Monday-Friday Flexibility required ...

Uofl

$23.25 - $31/hr

This is a part time temporary position scheduled to work 15 hours per week. Essential Duties and Responsibilities: * Facilitates compliance with the research protocol and Good Clinical Practice ...

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All JobsPfizer Clinical Research JobsPart Time Pfizer Clinical Research Jobs

Part Time Pfizer Clinical Research information

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How much do part time pfizer clinical research jobs pay per hour?

As of Aug 14, 2026, the average hourly pay for part time pfizer clinical research in the United States is $34.62, according to ZipRecruiter salary data. Most workers in this role earn between $16.59 and $32.93 per hour, depending on experience, location, and employer.

What cities are hiring for Part Time Pfizer Clinical Research jobs?

Cities with the most Part Time Pfizer Clinical Research job openings:

What are the most commonly searched types of Pfizer Clinical Research jobs?

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Part Time Pfizer Clinical Research jobs near you

Clinical Research Physician - Cardiologist (Part time)

Alcanza Clinical Research

Palmetto Bay, FL

Part-time

Medical, Dental, Vision, Life, Retirement

Re-posted 5 days ago

Job description

Description
Alcanza is a growing multi-site, multi-phase clinical research company with a network of locations in AL, AZ, FL, GA, IL, MA, MI, MO, NV, VA, SC, TN, TX and Puerto Rico. We have established a strong presence across Phase I-IV studies and several therapeutic areas including vaccine, neurology, dermatology, psychiatry, and general medicine. Join us as we continue to grow.
The Principal Investigator conducts and coordinates daily clinical trial activities according to ICH/FDA/GCP guidelines, local regulations, study protocol, and company policies and processes. Working with a local and central team drives clinical oversight and the quality of the assigned studies at the site.

Key Responsibilities
Essential Job Duties:
  • Ensures the medical well-being and safety of the study participants through the safe performance and ethical execution of the clinical trials, in adherence with FDA, ICH, NIH, GCPs & HIPAA guidelines, study protocols, as well as company policies and processes 
  • Overall site leadership with a focus on enhancing efficiencies, patient safety and protocol/GCP /regulatory compliance
  • Evaluates and assesses participants to ensure only eligible participants enroll into the trials.
  • Participates and engages in successful delivery and retention of study participants.
  • Interacts positively and collaboratively with sponsors, clients and team members.
  • Practices attention to detail in recording data and participant information, following protocol guidelines and GCPs.
  • Actively involved in protocol training for staff.
  • Participate in Investigator Meetings (IMs), and continuing education activities in order to maintain current knowledge of recruitment affairs and issues.
  • Perform other duties as assigned, requested, or required based on the needs of the participants, protocols and/or company.


Skills, Knowledge and Expertise
Minimum Qualifications:  MD or DO degree, an active physician license (in good standing) in the state of practice for this role is required.  Board certification is required.
Required Skills: 
  • Clinical skills and clinical procedures based in area of specialty. 
  • Proficiency with computer applications such as MS Office, electronic health records, and web applications, and the ability to type proficiently (40+ wpm). 
  • Must possess strong organizational skills, attention to detail, and math proficiency.
  • Well-developed written and verbal communication skills.  Bi-lingual (English / Spanish) proficiency is highly preferred.
  • Well-developed interpersonal and listening skills and the ability to work well independently as well as with co-workers, employees, subjects, managers and external customers.  
  • Ability to effectively handle multiple tasks and adapt to changes in workloads and priorities.
  • Ability to be professional, respectful of others, self-motivated, and exemplify a strong work ethic.
  • Must possess a high degree of urgency, self-motivation, integrity and dependability.
  • Ability to work independently to identify problems and implement solutions. 
  • Ability to handle highly sensitive information in a confidential and professional manner, and in compliance with HIPAA guidelines.


Benefits
  • Full-time employees regularly scheduled to work at least 30 hours per week are benefits-eligible, with coverage starting on the first day of the month following date of hire. 
  • Medical, dental, vision, life insurance, short and long-term disability insurance, health savings accounts, supplemental insurances, and a 401k plan with a safe harbor match are offered.