Remote Biotech research and development Jobs

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  • Provide clinical, scientific, and strategic expertise to drug development programs from lead compound identification to launch.
  • Lead execution of clinical development plans, including trial documents, regulatory interactions, and cross-functional alignment.
  • Establish and maintain relationships with external medical experts and represent Ipsen at investigator meetings and scientific conferences.

Ipsen is a mid-sized global biopharmaceutical company focused on transformative medicines in Oncology, Rare Disease and Neuroscience. With teams in more than 40 countries, it champions human-centric leadership and fosters a culture of collaboration, excellence and impact.

UK 5w PTO

  • Lead Numan's clinical research function as Principal Investigator across interventional and real-world evidence studies.
  • Build the infrastructure, partnerships, and pipeline to establish Numan as a credible clinical research organisation.
  • Develop external research relationships with pharmaceutical partners, academic institutions, and funding organisations.

Numan is a digital healthcare platform that integrates diagnostics, medication, supplements, digital programs, and doctor consultations to help people manage their health. Founded in 2018, the company has grown to a remote team of over 300 employees across the globe, driven by a mission to empower people to take control of their health.

  • Work on the frontline of communication with project stakeholders, ensuring timelines, targets, and standards.
  • Build and maintain relationships with clinical sites and investigators, focusing on subjects' rights, safety, and well-being.
  • Conduct and report all types of onsite monitoring visits, including CRF reviews and source document verification.

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

US 3w PTO

  • Guide and partner with science volunteers to create scientific statements, clinical practice guidelines, and educational programs.
  • Serve as in-house science expert, consulting on programs, press releases, and professional content across the Association.
  • Synthesize and explain current cardiovascular science and medicine to staff, volunteers, and the public.

The American Heart Association is a nonprofit organization dedicated to reducing cardiovascular disease and stroke, advancing science and public health. Since 1924, it has built a large national community with a collaborative culture, offering professional development and work-life harmonization for employees.

  • Execute systematic literature reviews according to PRISMA methods and Cochrane guidelines using designated systematic review tools.
  • Perform meta-analyses using statistical analysis tools such as R software and conduct real-world evidence studies.
  • Present data clearly to stakeholders and prepare scientific manuscripts, abstracts, posters, and presentations for peer-reviewed journals.

Intuitive is a global leader in robotic-assisted surgery and minimally invasive care, developing technologies like the da Vinci surgical system and Ion. It is a team of engineers, clinicians, and innovators united by one purpose: to make surgery smarter, safer, and more human.

$85,000–$115,000/yr

  • Support Clinical Trial Managers with study start-up, protocol development, and Trial Master File preparation.
  • Coordinate with clinical sites on documentation, training, and compliance with FDA and GCP requirements.
  • Assist with tracking study payments and providing operational support across the full study lifecycle.

The company is a partner organization specializing in clinical research and development, operating through Jobgether. It offers a structured clinical operations environment with cross-functional teams and professional growth opportunities.

$200,000–$240,000/yr
Global Unlimited PTO

  • Develop and maintain peer-to-peer relationships with key opinion leaders and healthcare providers in metabolic and oncology therapeutic areas.
  • Provide scientific support through virtual or on-site presentations, advisory boards, and medical congress staffing.
  • Critically evaluate emerging scientific literature to inform internal strategy and external engagement.

Rezolute is a late-stage rare disease biopharmaceutical company focused on developing transformative therapies for severe metabolic and endocrine disorders. The company is mission-driven to bring hope to patients and families affected by rare diseases through scientific innovation and collaboration.

  • Lead clinical pharmacology and pharmacometrics strategy for rare disease and oncology programs.
  • Design clinical studies and author regulatory documents for IND, NDA, and other submissions.
  • Collaborate with cross-functional teams including discovery, translational, and clinical development.

Recursion is a clinical-stage TechBio company decoding biology to improve lives, advancing a portfolio of investigational medicines in oncology and rare disease. With a team of bilingual scientists and AI experts, the company operates automated labs in Salt Lake City and Oxfordshire, and offices in global hubs.

$330,000–$370,000/yr
Unlimited PTO

  • Build the clinical development plan and first-in-human strategy from the ground up.
  • Design the Phase 1 protocol: dose, endpoints, population, pharmacodynamic readouts, and design nuance across two therapeutic areas.
  • Shape the translational and biomarker strategy to turn a preclinical mechanism into a credible human proof-of-mechanism readout.

Enveda is a clinical-stage, AI-enabled biotech discovering medicines four times faster than the industry standard. They recently raised $311M in a Series E, are recognized as one of America's Best Startup Employers by Forbes, and a Top 100 Most Loved Workplace by Newsweek, building a rare company with a collaborative and direct culture.

  • Lead and grow a multidisciplinary team focused on applied scientific research, biomedical data stewardship, and community engagement around Sage’s data assets.
  • Oversee data management, curation, and governance to ensure FAIR and GA4GH-aligned sharing, and champion data quality and harmonization for cross-study reuse.
  • Represent Sage externally with data generators, researchers, and funders, while mentoring team members and contributing to grant proposals and funding strategies.

Sage Bionetworks uses open science and collaboration to improve human health, bringing together scientific, technical, and operational expertise to advance biomedical research. A Seattle-founded nonprofit since 2009, they value curiosity, diverse perspectives, and radical collaboration with a mission-driven, interdisciplinary team.