616 Biopharmaceutical Leadership jobs in Remote - United States.

United States

• Skills: Medical Science Liaison, Oncology, Clinical trials, Scientific relationships, Medical affairs, Presentation skills, Pharmaceutical industry, Biotech, Regulatory requirements, Healthcare providers
• Experience: 3+ years in an MSL role in the pharmaceutical or biotech industry; 10+ years relevant clinical or pharmaceutical/biotech experience; Oncology therapeutic experience required; Drug launch experience preferred.
• Type: Full-time

United States

• Skills: patient recruitment, campaign management, medical terminology, federal regulations, GCP, project management, communication skills, team collaboration, digital marketing, strategic planning
• Experience: 3+ years in campaign management
• Type: Full-time

United States

• Skills: cancer care, Virtual Cancer Clinic, oncologist, physician-led, multidisciplinary, patient outcomes, evidence-based, remote healthcare, cross-functional teams, healthcare innovation
• Experience: Experience as an oncologist and physician-leader
• Type: Full-time

United States

• Skills: regulatory affairs, quality systems, marketing authorization, in vitro diagnostics, CDx, regulatory submissions, global clearance, business development, clinical protocols, FDA PMA
• Experience: Minimum 5+ years of experience in a medical device, pharmaceutical management, clinical trial, and/or pharmaceutical services consulting environment, or in vitro diagnostics, preferably with CDx.
• Type: Full-time
• Salary: $110,000 — $160,000 USD

United States

• Skills: clinical trials, oncology, data management, EDC systems, data quality, clinical operations, patient data, UAT, GCP/ICH compliance, study-specific training
• Experience: At least two (2) years in clinical operations and/or, data management or related discipline in either the CRO or pharmaceutical industry
• Type: Full-time

United States

• Skills: regulatory submissions, regulatory strategy, cardiac electrophysiology, regulatory bodies, project management, mentoring, clinical research, healthcare compliance, quality assurance, medical device
• Experience: Experience in regulatory affairs, specifically in cardiac electrophysiology, as well as management experience.

United States

• Skills: regulatory affairs, healthcare consulting, clinical trials, in vitro diagnostics, CDx, regulatory submissions, business development, FDA PMA, quality systems, market authorization
• Experience: Minimum 2+ years of applicable consulting experience with a focus in regulatory affairs; Minimum of 5+ years of experience working in a medical device, pharmaceutical management, clinical trial and/or pharmaceutical services consulting environment.
• Type: Full-time
• Salary: $110,000 — $160,000 USD

United States

• Skills: Clinical Scientist, Oncology standards, Data quality, Clinical trials, EDC systems, Data management, CRAs, FDA & ICH/GCP, Oncology therapeutic, Remote work
• Experience: At least two (2) years in clinical operations and/or data management or related discipline in either the CRO or pharmaceutical industry and/or experience conducting oncology clinical research as a Study Coordinator, Research Nurse or related discipline.
• Type: Remote

United States

• Skills: health economics, outcomes research, systematic literature reviews, quantitative evidence synthesis, pharmaceutical industry, technical reports, project management, client-ready deliverables, methodological expertise, health technology assessment
• Experience: 4 to 6 years’ experience in health economics and outcomes research
• Type: Full-time

United States

• Skills: Medical Science Liaison, oncology, breast cancer, clinical trials, patient recruitment, scientific education, KOL engagement, biomarker testing, presentation skills, compliance
• Experience: 2+ years in an MSL or similar field-based role, ideally in solid tumor oncology with a strong focus on breast cancer

United States

• Skills: biotechnology, regulatory affairs, promotional materials, cell therapies, cross-functional, regulatory strategies, submissions, graft vs. host disease, matrixed environment, commercial planning
• Type: Full-time

United States

• Skills: Medical Science Liaison, Oncology, liquid biopsy, Key Opinion Leaders (KOLs), Health Care Providers (HCPs), scientific exchange, clinical and scientific information, regulatory and compliance requirements, diagnostic tests, patient educational products
• Experience: 2+ years as a Medical Science Liaison or similar position in oncology, diagnostic experience preferred
• Type: Remote
• Salary: $220,000 total compensation package; base pay range of $180,000-$200,000

United States

• Skills: medical communications, account manager, project management, client relations, medical affairs, budgeting skills, team management, Veeva, scientific knowledge, business development
• Experience: 3+ years experience working in a medical communications agency or ad agency on medical affairs projects
• Salary: $70,000 — $94,000 USD

United States

• Skills: clinical management, study design, execution, analysis, reporting, vendor management, investigator selection, cross-functional team, clinical trials, process improvement

United States

• Skills: Safety Statistician, biostatistical, safety data analysis, clinical trials, aggregate safety data, statistical analysis, cross-functional teams, Bayesian methodology, data visualization, regulatory guidelines
• Experience: Doctorate degree and 2 years of statistical clinical trial experience, or a Master's degree and 4 years, or a Bachelor's degree and 6 years, etc.
• Type: Full time
• Salary: 153,319.00 USD - 181,444.00 USD

United States

• Skills: communication, relationship management, attention to detail, critical thinking, time management, stress management, clinical trials, monitoring, patient outcomes, regulatory adherence

United States

• Skills: Research, Development, Healthcare, Engineering, Innovation, Medical Devices, Quality, Clinical, Manufacturing, Technology
• Type: Full time

United States

• Skills: clinical trials, evidence generation, obesity, endocrinology, biopharmaceutical, safety, regulatory interactions, clinical development, medical monitor, cross-functional collaboration
• Experience: 2 years of clinical research experience and/or basic science research
• Type: Full-time
• Salary: 261,969.00 USD - 329,723.00 USD

United States

• Skills: Clinical Trials, CRA, Functional Service Provider, Site Monitor, Remote, Clinical Research Associate, FSP, Site Care Partner, Clinical Operations, Biostatistics

United States

• Skills: clinical research, monitoring, study management, Good Clinical Practice, site management, data integrity, regulatory submissions, recruitment, documentation, communication
• Experience: Some organizations require completion of CRA training program or prior monitoring experience.
• Type: Full time
• Salary: $71,900.00 - $189,000.00

United States

• Skills: Clinical Research, Statistical Programming, Data Management, Regulatory Consulting, Clinical Trials, Sponsor Collaboration, Therapeutic Areas, Career Development, Flexible Work Arrangement, Health Economics

United States

• Skills: clinical development plans, phase 1 clinical trials, first-in-human, clinical research, IND filings, clinical trial protocols, biomarkers, medical monitor, cross-functional team, collaborative environment
• Experience: 5+ years of hands-on experience in industry clinical trials
• Type: Remote Only
• Salary: $220,000 to $330,000 per year

United States

• Skills: Clinical Research, Trial Master File, administrative activities, regulatory compliance, clinical documents, clinical data, Microsoft Office, Good Clinical Practice, time management, communication
• Experience: 3 years administrative support experience
• Type: Full time

United States

• Skills: CMC Regulatory Affairs, project management, healthcare products, medical devices, cosmetics, regulatory strategies, product development, quality management, technical documentation, compliance
• Experience: Minimum of 7 years of relevant work experience, preferably in CMC Regulatory Affairs or R&D.

United States

• Skills: Regulatory Affairs, Regulatory Strategy, Global Regulation, Product Development, Regulatory Approval, Biotech, Leadership, Team Building, Communication Skills, Risk Management
• Experience: Doctorate degree and 4 years of regulatory experience in biotech or science OR Master’s degree and 7 years OR Bachelor’s degree and 9 years
• Type: Full time
• Salary: 197,095.00 USD - 236,022.00 USD

United States

• Skills: biostatistics, clinical development, statisticians, methodological expert, regulatory submissions, development strategies, Bayesian approaches, FDA meetings, leadership, team collaboration

United States

• Skills: Business Consulting, Life Sciences, Regulatory Affairs, Clinical Strategy, Operations, Quality and Safety, R&D, Project Management, Client Relations, Digital Technology
• Experience: 2+ years of consulting experience
• Type: Full-time
• Salary: $70,000 - $140,000

United States

• Skills: Veterinary, Clinical Pathology, Drug Development, Biopharmaceutical, Safety Assessment, Toxicologic Pathology, Therapeutic Targets, Consultation, Biologics, Laboratory Animal Medicine
• Experience: 4 years of toxicologic pathology experience in a biopharmaceutical setting
• Type: Full time
• Salary: 239060.00 - 272341.00 USD

United States

• Skills: R&D, consulting, clinical development, regulatory affairs, pharmacovigilance, project management, business development, leadership, SaaS, thought leadership
• Experience: 8+ years of consulting experience
• Type: Full-time
• Salary: $85,000 - $210,000

United States

• Skills: Quality Assurance, Medical Writing, Healthcare, Clinical Research, Compliance, Regulatory Affairs, Patient Care, Innovation, Manufacturing, Diversity
• Type: Full-time

United States

• Skills: consulting, R&D, pharmaceutical, Regulatory Affairs, Clinical Strategy, Operations, Quality, Safety, business development, project management
• Experience: 5+ years consulting experience
• Type: Full-time
• Salary: $80,000 - $200,000