Remote Biotech research and development Jobs · Project Management

Job listings

  • Act as primary representative for eClinical Solutions and sponsor data management interaction, ensuring quality and timelines within scope.
  • Define specifications and collaborate with technical teams on configuration of elluminate for data cleaning strategy and oversight.
  • Perform quality oversight and data trending via elluminate reporting to identify risks and develop mitigation strategies.

eClinical Solutions helps life sciences organizations accelerate clinical development initiatives with expert data services and the elluminate Clinical Data Cloud. The company is a people-first organization with an inclusive culture, recognized as a 2025 Top Workplaces USA Award winner for Remote Work.

  • Lead a 6-person MSL team in Plastics & Regenerative Medicine while maintaining a personal field territory.
  • Ensure scientific engagement plans align with brand strategy and medical objectives.
  • Provide coaching, training, and performance management to the MSL team.

AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. The company operates globally in immunology, oncology, neuroscience, and aesthetics.

$78,000–$97,000/yr

  • Lead participatory research and co-design projects with partner organizations to develop AI Civics toolkits and training resources.
  • Steward relationships with national partners in K-12 education, labor, faith, or advocacy sectors.
  • Produce case studies, reports, and academic publications to advance public understanding of AI governance.

Data & Society is an independent nonprofit research organization studying the social implications of data-centric technologies and automation. It is a small to medium-sized organization that values empirical evidence and respect for human dignity, with a collaborative culture focused on inclusive engagement and anti-racist practices.

UK 5w PTO

  • Lead complex toxicology and regulatory projects for UK and international clients.
  • Provide strategic scientific and regulatory advice across chemicals, consumer products, food/feed, and biocides.
  • Drive business development and client engagement to expand toxicology services.

Ramboll is a global architecture, engineering, and consultancy company focused on sustainable change. With over 18,000 employees across 35 countries, it fosters an inclusive culture rooted in openness and curiosity.

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.

$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.

  • Own the scientific basis of the Battery Index, designing and standardizing methodology for assessing recycler safety globally.
  • Lead field execution of air, soil, and blood lead level sampling across multiple low-resource countries.
  • Collaborate with the research community to build evidence and ensure data-driven classification of recyclers.

The Partnership for Battery Action aims to eliminate over 80% of unsafe used lead-acid battery recycling globally by consolidating the industry toward safer facilities. Incubated by the Global Development Incubator, it is a small, results-oriented team with an ambitious 15-year goal.