Remote Biotech research and development Jobs · US

Job listings

  • Lead analytical strategy and method lifecycle management for small molecule drug substance and drug product development.
  • Oversee external analytical partners, CDMOs, and testing laboratories to ensure cGMP compliance and quality.
  • Support regulatory submissions, specifications, stability programs, and commercialization readiness.

Mineralys Therapeutics is a clinical-stage biopharmaceutical company focused on developing medicines to target hypertension and related comorbidities such as chronic kidney disease and obstructive sleep apnea. The company is headquartered in Radnor, Pennsylvania and operates as a fully remote company.

$144,000–$180,000/yr
US 3w PTO

  • Serve as study statistician for Phase 1-3 vaccine clinical trials, leading statistical design, analysis, and reporting.
  • Oversee statistical CROs, develop analysis plans, and ensure regulatory and scientific rigor.
  • Provide statistical consultation across CVIA programs and represent PATH at scientific meetings.

PATH is a global nonprofit dedicated to achieving health equity, developing and scaling innovative solutions to pressing health challenges. With more than 40 years of experience, PATH fosters a culture of collaboration and partnership across diverse teams.

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.

  • 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.

  • Provide statistical expertise and hands-on support for Phase III oncology clinical trials, including study design and analysis.
  • Author and review TFL and ADaM specifications, collaborating closely with Statistical Programming.
  • Manage deliverables across multiple concurrent clinical studies, ensuring timelines and quality expectations are met.

ClinChoice is a global full-service CRO supporting pharmaceutical, biotechnology, medical device, and consumer health companies in clinical development. With over 4,000 professionals in more than 20 countries, they emphasize a quality-driven 'one-team' culture and below-industry-average turnover.

  • Build and lead the full operating model for clinical research execution at network practices, including staffing, capacity planning, and performance metrics.
  • Develop scalable training infrastructure, playbooks, and SOPs for a distributed clinical research staff and operations team.
  • Partner with cross-functional leaders to align operational priorities with broader network strategy and serve as an escalation point for site-level risks.

N-Power Medicine aims to revolutionize drug development by integrating clinical trials with clinical practice, enhancing physician and patient participation. It is a mission-driven, well-funded, rapidly growing company with a balanced and flexible work environment, offering competitive benefits and a 401K plan.

  • Provide medical direction and scientific leadership for the pancreatic and colorectal cancer programs.
  • Lead clinical study subteams, design efficient clinical trials, and monitor safety and efficacy data.
  • Contribute to global regulatory filings, author clinical documents, and present at scientific meetings.

Erasca is a clinical-stage precision oncology company focused on discovering, developing and commercializing medicines for patients with cancer. The company's programs target the RAS/MAPK pathway, and it is driven by an audacious mission to erase cancer.

$100,000–$130,000/yr

  • Lead preclinical research programs in hair biology to discover new biological targets and ingredients.
  • Manage external research collaborations, including lab identification, experiment design, and data analysis.
  • Communicate scientific findings through presentations, publications, and internal reports.

Nutrafol is a pioneer in hair wellness, creating clinically tested products for hair growth using a patented blend of natural ingredients. It is a growing company with a culture that embraces individuality and continuous growth, recommended by over 7,500 physicians.