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Clinical Scientist

Avenio Corporation

United States

Remote

USD 70,000 - 130,000

Part time

Yesterday
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Job summary

Avenio Corporation seeks a Clinical Scientist (Product Manager) for their AI-powered platform. This role involves translating clinical workflows and regulatory requirements into product specifications while collaborating with engineering teams. Ideal candidates have a bachelor's degree in biosciences with a strong background in clinical trials and regulatory compliance. This is a remote part-time position offering flexibility and the chance to impact biopharma innovation.

Benefits

Flexible remote schedule
Opportunity to shape a transformative AI product

Qualifications

  • 3+ years of experience in clinical development or trial management.
  • Familiarity with regulatory documentation and operational strategies.
  • Experience working with digital tools for clinical operations.

Responsibilities

  • Translate clinical workflows into product specifications.
  • Conduct interviews with clinical trial professionals for feedback.
  • Ensure compliance with scientific accuracy and regulatory frameworks.

Skills

Communication
Domain Expertise
Regulatory Compliance
Analytical Skills

Education

Bachelor’s degree in Biosciences
Master’s or PhD preferred

Tools

CTMS
EDC

Job description

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Job Title: Clinical Scientist (Product Manager) – AvenioGPT (https://gpt.avenio.ai/avenio)

Location: Remote (Part-Time)

Experience Required: 3+ years in Clinical Trial Operations or Clinical Development

Education: Bachelor’s degree in Biosciences or related field (advanced degrees preferred)

Employment Type: Contract / Part-Time

About AvenioGPT

AvenioGPT (https://gpt.avenio.ai/avenio) is a next-generation generative AI agent built for Biopharma R&D. Purpose-built for clinical researchers, medical scientists, and regulatory professionals, it transforms how research and reasoning are conducted across clinical development workflows.

We are now seeking a Clinical Scientist to join our team as a Product Manager, bringing domain expertise in clinical trial management and helping shape an intelligent, assistant-like product that meets the real-world needs of Biopharma teams.

Role Summary

As a Clinical Scientist (Product Manager), you will serve as the critical link between clinical trial users and our AI product team. You will help define the product roadmap for AvenioGPT by ensuring it reflects the complexity of clinical trial design, conduct, and regulatory compliance. Your deep understanding of the clinical development process and your ability to think critically and reason through scientific and operational contexts will directly shape the product's capabilities.

Responsibilities

  • Translate clinical workflows, use cases, and regulatory requirements into product specifications
  • Prioritize product features that align with real-world clinical trial pain points
  • Partner with engineering and design to build intuitive, science-aware user experiences
  • Domain Expertise & Research Reasoning
  • Bring subject matter expertise in ICH-GCP, regulatory submission pathways (IND, NDA/BLA), and trial lifecycle processes
  • Guide the development of reasoning tasks the AI should support, such as feasibility assessments, protocol reviews, and risk mitigation planning
  • User Collaboration
  • Conduct interviews and feedback sessions with clinical trial professionals
  • Identify and champion high-value workflows that AvenioGPT should automate or augment
  • Compliance & Scientific Rigor
  • Ensure that the product adheres to scientific accuracy, ethical considerations, and evolving clinical guidelines
  • Collaborate with compliance teams to interpret and adapt to regulatory frameworks

Qualifications

  • Bachelor’s degree in Life Sciences, Biomedical Engineering, Nursing, Pharmacy, or a related discipline (Master’s or PhD a plus)
  • 3+ years of experience in clinical development, trial management, or regulatory affairs within Biopharma or CRO environments
  • Familiarity with protocol design, operational strategy, and regulatory documentation
  • Demonstrated ability to reason through complex clinical scenarios and design decision trees or logical frameworks
  • Experience working with digital tools for clinical operations or documentation (e.g., CTMS, EDC, eTMF, Medidata, Veeva, etc.)
  • Excellent communication skills; ability to interface with both scientific and technical teams

Nice to Have

  • Experience with AI, machine learning, or decision-support tools in healthcare or pharma
  • Prior experience as a clinical study manager, CRA, or regulatory writer
  • Exposure to or curiosity about working in a product development environment

Why Join Us?

  • Help shape a transformative AI product from the ground up
  • Work with a cross-functional team of engineers, AI scientists, and domain experts
  • Flexible remote schedule with the opportunity to influence high-impact Biopharma innovation
Seniority level
  • Seniority level
    Mid-Senior level
Employment type
  • Employment type
    Part-time
Job function
  • Job function
    Research, Analyst, and Information Technology
  • Industries
    Technology, Information and Internet

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