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Part Time Pharmaceutical Research Jobs (NOW HIRING)

Clarivate

Strategic Advisor, Benchmarking - Part-Time

$60K/yr

... pharmaceutical R&D performance measurements. For over 25 years, CMR has worked with the leading ... Hours of Work This is a US based, part-time role at 40 percent, equivalent to approximately two ...

Sinks Pharmacy

Pharmacist - Part-time

Waynesville, MO

$52 - $62.50/hr

We are looking for an efficient, flexible, and highly motivated part-time Pharmacist to join our ... Consults with other health care professionals and conducts research as necessary to ensure that all ...

Vivent Health

Physician (Part-time)

Saint Louis, MO · On-site

**This is a part-time position working up to 20 hours a week** If you are currently employed at ... pharmaceutical, research, and more! * Delivery of quality patient care: Our integrated HIV care and ...

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Part Time Pharmaceutical Research information

What are some common challenges faced in part-time pharmaceutical research positions?

Part-time pharmaceutical research roles often require balancing multiple projects within limited hours, which can be challenging when managing tight deadlines or coordinating with full-time team members. Additionally, adapting quickly to changing research protocols and staying updated on regulatory requirements is crucial. Effective communication and time management are essential, as you may need to collaborate asynchronously with colleagues or attend meetings outside your usual hours. Despite these challenges, part-time positions offer valuable experience and can be a pathway to full-time opportunities or specialized roles within the industry.

What is part time pharmaceutical research?

Part time pharmaceutical research involves working on scientific studies or clinical trials within the pharmaceutical industry, but on a reduced or flexible schedule rather than full time. These roles may include tasks such as data analysis, laboratory work, or supporting research teams with various projects. Part time positions are ideal for students, professionals seeking work-life balance, or those with other commitments who still want to contribute to drug development and medical advances. The responsibilities and required qualifications are similar to full time roles but often offer more flexibility in work hours.

What are the key skills and qualifications needed to thrive as a Part Time Pharmaceutical Researcher, and why are they important?

To thrive as a Part Time Pharmaceutical Researcher, you generally need a background in life sciences, analytical skills, and experience with laboratory techniques, often supported by a degree in pharmacy, biology, or chemistry. Familiarity with laboratory information management systems (LIMS), statistical analysis software, and regulatory compliance certifications like Good Laboratory Practice (GLP) are commonly required. Attention to detail, effective communication, and strong organizational skills help you excel in collaborative, data-driven environments. These competencies are vital for ensuring research accuracy, regulatory compliance, and successful project outcomes in pharmaceutical studies.

What is the difference between Part Time Pharmaceutical Research vs Part Time Pharmaceutical Sales Representative?

AspectPart Time Pharmaceutical ResearchPart Time Pharmaceutical Sales Representative
Required CredentialsTypically requires a degree in pharmacy, biology, or related field; some roles may need certificationOften requires a degree in life sciences or related field; sales experience can be beneficial
Work EnvironmentLaboratories, research facilities, or clinical settingsHospitals, clinics, or direct client interactions in the field
Employer & Industry UsagePharmaceutical companies, research institutions, biotech firmsPharmaceutical companies, medical device firms, healthcare providers

Part Time Pharmaceutical Research focuses on developing and testing new drugs or formulations in lab settings, requiring scientific expertise. In contrast, Part Time Pharmaceutical Sales Representatives promote products to healthcare professionals, emphasizing communication skills and product knowledge. Both roles are essential in the pharmaceutical industry but differ significantly in daily tasks and work environment.

More about Part Time Pharmaceutical Research jobs
What cities are hiring for Part Time Pharmaceutical Research jobs? Cities with the most Part Time Pharmaceutical Research job openings:
What are the most commonly searched types of Pharmaceutical Research jobs? The most popular types of Pharmaceutical Research jobs are:
What states have the most Part Time Pharmaceutical Research jobs? States with the most job openings for Part Time Pharmaceutical Research jobs include:
What job categories do people searching Part Time Pharmaceutical Research jobs look for? The top searched job categories for Part Time Pharmaceutical Research jobs are:
Part Time Pharmaceutical Research jobs near you
Infographic showing various Part Time Pharmaceutical Research job openings in the United States as of June 2026, with employment types broken down into 1% As Needed, 30% Full Time, 68% Part Time, and 1% Temporary. Highlights an 89% Physical, 3% Hybrid, and 8% Remote job distribution.

Remote | Pharmaceutical Research & Development Consultant -- $65-$90/hour

24-MAG

New York, NY • On-site, Remote

$65 - $90/hr

Part-time

Posted 17 days ago

Job description

We are sharing a specialised part-time consulting opportunity for professionals experienced in pharmaceutical research, drug discovery, translational science, clinical development, regulatory documentation, CMC workflows, and structured pharma R&D processes.

This role supports current and upcoming remote consulting opportunities focused on structured pharmaceutical research review, clinical development workflow analysis, regulated R&D documentation, study protocol assessment, biomarker and pharmacology review, regulatory materials, and high-quality project execution. Selected professionals will apply their pharma, biotech, or academic research expertise to review realistic R&D scenarios, evaluate documentation requirements, prepare structured written outputs, and support accurate, evidence-based pharmaceutical research workflow tasks.

Key Responsibilities

Professionals in this role may contribute to:

Drug Discovery & Translational Research Review

  • Review pharmaceutical research scenarios involving target identification, medicinal chemistry, biology workflows, high-throughput screening, DMPK, PK/PD, toxicology, and biomarker analysis
  • Evaluate research materials against source documents, study requirements, experimental rationale, data outputs, and documented scientific criteria
  • Support structured review of pharmacology reports, biomarker analyses, preclinical documentation, translational research materials, and lab workflow records
  • Identify missing assumptions, documentation gaps, scientific inconsistencies, and expected research review outcomes

Clinical Development & Study Documentation

  • Review clinical development scenarios involving study protocols, investigator brochures, Phase I–IV materials, clinical operations workflows, statistical outputs, and study documentation
  • Evaluate clinical materials against required sections, source materials, study objectives, endpoint definitions, and operational requirements
  • Support structured review of DMC briefing documents, clinical study reports, protocol summaries, clinical operations files, and study-related documentation
  • Prepare clear written explanations for clinical development decisions based on source materials and verifiable criteria

Regulatory, CMC & R&D Workflow Support

  • Review regulatory and CMC scenarios involving IND, NDA, BLA, EMA materials, CMC technical reports, quality documentation, safety materials, and submission workflows
  • Support structured review of real-world evidence, HEOR, pharmacovigilance, regulatory affairs, and CMC documentation
  • Work with materials connected to platforms such as Medidata Rave, Oracle Clinical One, Schrödinger Suite, MOE, Benchling, LabArchives, or similar pharma R&D systems
  • Maintain accuracy, consistency, and professional judgment across submitted work

Ideal Profile

Strong candidates may have:

  • 3+ years of experience in pharmaceutical research, biotech research, drug discovery, translational science, clinical development, regulatory affairs, CMC, pharmacovigilance, HEOR, or academic biomedical research
  • Background in one or more areas such as target identification, medicinal chemistry, biology, HTS, DMPK, PK/PD, toxicology, biomarkers, clinical development, biostatistics, clinical operations, regulatory affairs, CMC, real-world evidence, or pharmacovigilance
  • Familiarity with pharma R&D tools and platforms such as Medidata Rave, Oracle Clinical One, Schrödinger Suite, MOE, Benchling, LabArchives, electronic lab notebooks, clinical data systems, or related research systems
  • Comfort reading and preparing pharma research artifacts such as study protocols, investigator brochures, IND/NDA/BLA materials, pharmacology reports, biomarker analyses, CMC reports, DMC briefing documents, and research summaries
  • Strong analytical thinking and written communication skills
  • Ability to translate pharmaceutical R&D workflows into clear, structured task documentation

Educational Background

  • PhD, MD, PharmD, or master's degree in pharmaceutical sciences, biomedical sciences, biology, chemistry, pharmacology, medicine, biostatistics, regulatory affairs, clinical research, or a related field is helpful
  • Equivalent practical experience in pharmaceutical research, clinical development, translational science, regulatory documentation, or biotech R&D workflows is also highly relevant

Nice to Have

  • Experience in pharma, biotech, academic medical centers, clinical research organizations, regulated R&D environments, or major biomedical research programs
  • Familiarity with IND, NDA, BLA, EMA submissions, CMC documentation, clinical trial operations, pharmacovigilance, HEOR, real-world evidence, or DMC materials
  • Experience preparing or reviewing study protocols, investigator brochures, pharmacology reports, biomarker analyses, CMC technical reports, regulatory drafts, or clinical development documentation
  • Industry fellowship training, clinical research certification, regulatory affairs certification, or related specialized training is helpful
  • Strong attention to detail in scientific, regulated, and documentation-heavy research environments

Why This Opportunity

  • Apply pharmaceutical research and clinical development expertise to structured remote project work
  • Contribute to high-quality R&D workflow review, clinical documentation assessment, regulatory materials, and scientific scenario development
  • Work on flexible, project-based assignments aligned with your pharma or biotech background
  • Use your scientific judgment in a focused, detail-oriented research environment
  • Remote structure with competitive hourly compensation

Contract Details

  • Independent contractor role
  • Fully remote with flexible scheduling
  • Part-time commitment depending on project availability
  • Competitive rates between $65–$90 per hour depending on expertise
  • Weekly payments via Stripe or Wise
  • Projects may be extended, shortened, or adjusted depending on scope and performance
  • Work will not involve access to confidential or proprietary information from any employer, client, or institution

About the Platform

This opportunity is available through 24-MAG LLC. We connect experienced professionals with remote consulting opportunities across technical, evaluation, and project-based workstreams.

By submitting this application, you acknowledge that your information may be processed by 24-MAG LLC for recruitment and opportunity matching in accordance with our Privacy Policy: https://www.24-mag.com/privacy-policy.