Remote Biotech research and development Jobs · Clinical Research

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$140,000–$150,000/yr

  • Set strategic direction and lead large clinical trials and data collection efforts.
  • Manage clinical research operations, including site selection, budgets, and regulatory compliance.
  • Author publications and represent the company at major annual conferences.

Hanger is the world's premier provider of orthotic and prosthetic services and products, offering advanced solutions and clinical programs. With 160 years of history, the company operates nationwide clinics and employs thousands, focusing on empowering human potential through superior patient care.

US 3w PTO

  • Lead and evolve guideline methodology, including AI-enabled approaches, to ensure consistency and rigor across AHA/ACC clinical guidelines.
  • Oversee comprehensive methodological review of recommendations, evidence grading, and compliance with industry relationships.
  • Supervise staff and develop training programs for writing committee members on evidence evaluation and guideline development.

The American Heart Association is a nonprofit organization dedicated to fighting cardiovascular disease and stroke, having cut related deaths in half since 1924. The Association employs thousands and fosters a culture of work-life harmonization and employee growth through resources like Heart U and Employee Resource Groups.

  • Co-own Tiny Health's clinical evidence roadmap and define study objectives aligned with product and regulatory goals.
  • Lead the design and publication of observational, interventional, and real-world evidence studies, including protocol development and statistical analysis plans.
  • Partner with cross-functional teams to ensure analytical rigor, translate findings into defensible claims, and present results to internal and external audiences.

Tiny Health advances lifelong health through precision microbiome science, addressing chronic disease from the first 1,000 days to the last. Founded in 2020 by microbiome scientists and physicians, the company is a remote-first team of about 30-50 employees with a culture of high standards, transparency, and continuous learning.

$16–$16/hr

  • Perform chart abstraction from electronic medical records and enter data into databases.
  • Call research participants to schedule visits and support clinical trials.
  • Conduct literature reviews and assist with special projects.

OHSU is Oregon's only public academic health center, leading groundbreaking research and training healthcare professionals. As Portland's largest employer, it is committed to becoming an anti-racist institution and welcomes people of all backgrounds.

  • Lead and mentor a high-performing team of Clinical Research Associates, ensuring operational excellence and efficient resource utilization.
  • Manage hiring, onboarding, performance management, and professional development activities for CRA staff.
  • Collaborate with Project Managers and cross-functional teams to support successful delivery of clinical trials.

PSI is a leading Contract Research Organization with more than 30 years in the industry, offering a balance between stability and innovation. They focus on delivering quality and on-time services across various therapeutic indications.

$75,000–$142,500/yr

  • Acts as primary point of contact for investigative sites, providing training and support to ensure compliance with protocols and regulations.
  • Conducts site evaluation, monitoring, and closure activities while managing recruitment and retention plans based on patient journey.
  • Collaborates with central monitoring to assess risks and ensure data quality, safety reporting, and audit readiness at assigned sites.

AbbVie discovers and delivers innovative medicines and solutions addressing serious health issues in immunology, oncology, and neuroscience. It is a large pharmaceutical company with a global presence and a culture focused on remarkable impact.

  • Serves as clinical trial lead, overseeing study planning, conduct, and oversight per protocol and regulations.
  • Develops study documents, manages site feasibility, and drives recruitment strategies.
  • Leads internal clinical team meetings and ensures quality deliverables through metric reporting.

Precision Medicine Group is a life sciences company that supports clinical research and development. The company is large enough to offer a range of benefits and emphasizes a collaborative, ethical culture focused on quality and compliance.

  • Act as primary clinical point of contact with clients and lead planning, execution, and oversight of clinical studies across Latin America.
  • Develop country-level recruitment strategies, guide monitoring and quality strategies, and mentor CRAs and partners.
  • Collaborate with project managers on budgets, vendor management, and ensure compliance with ICH-GCP and regulatory requirements.

Precision Medicine Group is a precision medicine company that provides clinical research and commercialization services. The company is an Equal Opportunity Employer with a focus on expanding clinical operations across Latin America.

  • Provides study-level oversight and leadership for global clinical trials from inception through closure, managing vendors, recruitment, and cross-functional teams.
  • Develops and manages study materials including protocols, regulatory submissions, and budgets while ensuring compliance with quality standards and inspection readiness.
  • Contributes to system management like EDC, IRT, and eTMF, and supports process improvement initiatives or serves as a mentor.

AbbVie discovers and delivers innovative medicines and solutions to address serious health issues in immunology, oncology, neuroscience, and aesthetics. As a global biopharmaceutical company with a robust pipeline, they emphasize integrity and innovation, serving patients worldwide with a dedicated team.

  • Serve as the primary point of contact and partner with investigative sites to ensure high-quality clinical trial conduct.
  • Conduct site evaluation, training, monitoring, and closure activities in compliance with regulations, GCPs, and SOPs.
  • Utilize risk-based monitoring and site engagement strategies to improve data integrity, compliance, and study performance.

AbbVie discovers and delivers innovative medicines and solutions across immunology, oncology, neuroscience, and aesthetics. A large global biopharmaceutical company, AbbVie fosters a culture of innovation and integrity to transform patients' lives.