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Part Time Biotech Consultant Jobs (NOW HIRING)

... consulting. Medical-Adjacent and Entertainment Messaging, Website, Deck, Campaign and CRM Support ... This is a temporary part-time freelance role expected to run from June through September , with ...

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Part Time Biotech Consultant information

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$10

$41

$87

How much do part time biotech consultant jobs pay per hour?

As of Jun 9, 2026, the average hourly pay for part time biotech consultant in the United States is $41.55, according to ZipRecruiter salary data. Most workers in this role earn between $29.33 and $49.52 per hour, depending on experience, location, and employer.

What is a Part Time Biotech Consultant?

A Part Time Biotech Consultant is a professional who offers specialized advice and expertise to biotechnology companies or organizations on a part-time basis. These consultants typically help with areas such as research and development, regulatory compliance, product commercialization, or business strategy. Working part-time allows them to assist multiple clients or balance consulting with other commitments, such as academic or industry roles. Their work can be project-based or ongoing, depending on client needs, and they often bring extensive experience in life sciences, pharmaceuticals, or biotech startups.

Will AI replace biotechnologists?

AI can assist biotechnologists by automating data analysis, optimizing experiments, and improving research efficiency. However, biotechnologists' expertise in designing experiments, interpreting complex biological data, and making ethical decisions remains essential, making complete replacement unlikely in the near future.

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

To thrive as a Part Time Biotech Consultant, you need a solid background in life sciences or biotechnology, often with an advanced degree and industry experience. Familiarity with laboratory techniques, regulatory compliance systems, and data analysis tools like Excel or specialized biotech software is typically required. Strong communication, problem-solving, and time management skills help consultants effectively advise clients and juggle multiple projects. These skills ensure impactful guidance, efficient project execution, and positive client relationships in a dynamic, evolving sector.

What are the typical responsibilities and expectations for a part-time biotech consultant working with startup teams?

As a part-time biotech consultant, you’ll often advise startups on scientific strategy, regulatory pathways, and product development, typically working remotely or on a flexible schedule. You’ll collaborate closely with founders and technical teams, providing expertise on experimental design, clinical trial planning, or market analysis. Consultants are expected to stay current with industry trends and offer actionable recommendations, sometimes participating in meetings or presentations to investors. Juggling multiple clients and quickly adapting to different organizational needs are common aspects of the role.

Can a consultant be a part-time job?

Yes, a biotech consultant can work part-time, often providing specialized expertise on a flexible schedule. Many consultants choose part-time roles to balance multiple projects or clients, and some positions may require specific certifications or industry experience. Part-time consulting allows for greater flexibility while still contributing valuable knowledge to biotech projects.

What is the difference between Part Time Biotech Consultant vs Part Time Research Associate?

AspectPart Time Biotech ConsultantPart Time Research Associate
CredentialsBiotech degree, industry experienceScience degree, research background
Work EnvironmentClient sites, labs, officesLaboratories, academic or industry settings
Employer & Industry UsageBiotech firms, consulting agenciesResearch institutions, universities, biotech companies
Common Search & ComparisonYesYes

The Part Time Biotech Consultant typically provides strategic advice and project support to biotech companies, leveraging industry experience. In contrast, a Part Time Research Associate focuses on conducting experiments and data analysis within labs. While both roles require scientific credentials, the consultant role emphasizes client interaction and project management, whereas the research associate is more lab-focused. Understanding these differences helps job seekers identify the right position based on their skills and career goals.

What cities are hiring for Part Time Biotech Consultant jobs? Cities with the most Part Time Biotech Consultant job openings:
What are the most commonly searched types of Biotech Consultant jobs? The most popular types of Biotech Consultant jobs are:
What states have the most Part Time Biotech Consultant jobs? States with the most job openings for Part Time Biotech Consultant jobs include:
Infographic showing various Part Time Biotech Consultant job openings in the United States as of June 2026, with employment types broken down into 99% Full Time, and 1% Temporary. Highlights an 82% Physical, 3% Hybrid, and 15% Remote job distribution, with an average salary of $86,430 per year, or $41.6 per hour.
Sr. Manager, Quality Risk Management

Sr. Manager, Quality Risk Management

Astrix Inc

South San Francisco, CA • On-site

$90 - $120/hr

Part-time

Posted 6 days ago


Job description

Sr Manager, Quality Risk Management - PART TIME
We're hiring a Senior Manager, Quality Risk Management to join a rapidly-growing, well-funded biotech building innovative life sciences solutions and scaling its quality systems. This is a hands-on role working in Veeva to build compliant processes from the ground up. Previous GCP experience is required!
Location: Must be local to South San Francisco, CA or Princeton, NJ
Schedule: Part - Time (20-30 hours)
Pay: $90-$120/hr
Role Overview
We are seeking a Senior Manager, Quality Risk Management (QRM) contractor to support the implementation and maturation of risk-based quality management across GxP activities. This role partners closely with Quality, Clinical, CMC, and functional teams to embed practical, inspection-ready QRM and RBQM practices aligned with ICH Q9 (R1) and ICH E6 (R3).
Key Responsibilities
  • Support implementation of a pharma-focused QRM framework aligned with ICH Q9 (R1) and integrated into the QMS
  • Facilitate and support risk assessments across:
    • Clinical development (RBQM per ICH E6 (R3))
    • Tech Ops (CMC)
    • Quality
    • Vendors and outsourced activities
  • Help identify critical-to-quality (CtQ) factors, define risk controls, and ensure traceability to quality processes
  • Coach and guide cross-functional teams in applying risk-based thinking to decision-making
  • Support inspection and audit readiness by helping teams clearly articulate risk rationales and controls
  • Contribute to risk metrics, trending, and continuous improvement activities

Required Qualifications
  • Bachelor's degree in life sciences, pharmacy, engineering, or related field
  • 7+ years of experience in Pharmaceutical Quality, Compliance, Clinical Operations, or related GxP roles
  • Previous coaching or leadership experience within GCP
  • Practical experience supporting Quality Risk Management and/or RBQM activities aligned with ICH Q9 and/or ICH E6 (R3)

Nice to Have
  • Experience spanning clinical development through manufacturing
  • Familiarity with ICH Q10, ISO 31000, or ISO 14971
  • Prior inspection or audit support experience (FDA, EMA)
  • Consulting or contractor experience in pharma

***This job description is a complete list of all desired skills but not all are required. We strongly encourage candidates who have some of the skills to apply. We look forward to a conversation to learn more about you!***
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