55 Biopharmaceutical Leadership jobs in Raleigh.

Durham

• Skills: Clinical Research, Stakeholder Engagement, Site Network Expansion, Key Opinion Leaders, Strategic Leadership, Performance Metrics, International Expansion, Commercial Models, Business Development, Staff Management
• Type: Full time
• Salary: 153200 - 284400 USD

Raleigh

• Skills: Clinical Operations, eTMF, CTMS, Site Connect, Study Training, Study Startup, Payments solutions, implementation, customer success, life sciences
• Experience: 8+ years of experience working with or for organizations in Pharmaceutical, Biotechnology, Healthcare, and/or Medical Device and Diagnostics
• Type: Full-time
• Salary: $80,000 - $200,000

Raleigh

• Skills: medical affairs, clinical, regulatory, research, innovation, healthcare, manufacturing, sustainability, patient care, team collaboration
• Type: Full time

Durham

• Skills: data management, clinical data management, project management, negotiations, quality management, financial tracking, process improvements, Good Clinical Practices, regulatory guidelines, compliance
• Experience: 5 years direct Data Management experience, including 3 or more years as a CDM project lead.
• Type: Full time
• Salary: $82,300.00 - $173,900.00

Raleigh

• Skills: Medical Science Liaison, Neuroimmunology, Healthcare, Clinical Experience, Patient Relations, Research Support, Territory Management, KOL Engagement, Immunology, Neurology
• Experience: 2-3 years MSL experience and/or 2-3 years relevant work experience (clinical or research experience)
• Type: Field-based

Durham

• Skills: Clinical Trials, CRA, Functional Service Provider, Statistical Programming, Biostatistics, Data Management, Epidemiology, Oncology, Remote, IT

Raleigh

• Skills: Alliance Management, gene therapy, collaborations, research programs, contract negotiation, operational execution, relationship management, biopharmaceutical, clinical development, strategic evaluation
• Experience: At least 5 years’ experience in contract negotiation and execution, budgeting, timelines, and risk assessment.
• Type: Hybrid
• Salary: $175,000 - $250,000 USD

Morrisville

• Skills: regulatory, compliance, leadership, medical devices, pharmaceutical, submissions, registrations, quality management, customer centric, inspections
• Experience: 7+ years’ experience in a highly regulated environment such as medical device, pharmaceutical, or other highly regulated environments; Minimum of 3 years regulatory affairs/compliance leadership experience

Durham

• Skills: cancer detection, revenue cycle management, billing operations, prior authorization, billing data entry, leadership, strategic planning, eligibility functions, workflow activities, clinical studies
• Type: Hybrid

Cary

• Skills: Medical Affairs, Healthcare, Clinical, Therapies, Products, Innovation, Patient Care, Diversity, Collaboration, Growth
• Type: Full time

Raleigh

• Skills: translational biology, in vivo studies, biomarker discovery, cell therapy, chronic kidney disease, analytical assay, sample management, study coordination, CRO partnerships, multi-omic integration
• Experience: 10+ years of industry experience in translational research, cell therapy, and/or chronic kidney disease.
• Type: Full-time

Durham

• Skills: project leadership, team management, data processes, client relationships, analytical expertise, life sciences, Pharma commercial functions, coding skills, data visualization software, employee engagement
• Experience: 8 to 10 years of professional experience in the life sciences/pharma industry.
• Type: Full-time

Morrisville

• Skills: Project Management, Product Life Cycle, Portfolio Optimization, Anesthesia, Emergency Medicine, Cross-Functional Collaboration, Strategic Planning, Market Evaluation, Technical Assessments, Regulatory Compliance
• Experience: Minimum of 5-7 years of demonstrated experience in project management working multi-year projects in medical device, pharmaceutical, or manufacturing in a regulated environment.

Raleigh

• Skills: Project management, Validation, Engineering, Quality/compliance, Consulting services, Cutting-edge patient treatments, Advanced therapy manufacturing, Cross-functional collaboration, Travel, Patient Focused
• Experience: Bachelor’s degree in Life Science, Engineering, or related discipline and/or comparable military experience.
• Type: Full-time
• Salary: $50,000 - $240,000 USD

Raleigh

• Skills: clinical trials, clinical mentorship, FDA regulations, GCP guidelines, clinical expertise, research protocols, patient assessments, clinical research, safety evaluation, collaboration

Raleigh

• Skills: clinical data management, EDC, programming, SQL, clinical trials, customer-facing, data analysis, data collection, regulatory compliance, SaaS
• Experience: 5+ years of experience working with EDC clinical software solutions in end-to-end data management related activities.
• Type: Full-time
• Salary: $80,000 - $200,000

Morrisville

• Skills: clinical trials, clinical research, clinical evidence, protocol design, regulatory strategies, study management, clinical studies, GCP, CRO management, medical technologies
• Experience: At least ten years in clinical trials or outcomes research in industry
• Type: Full-time
• Salary: $185,000 - $195,000

Chapel Hill

• Skills: procedural support, safety, training, clinical expertise, pulmonary oncology, hospital staff, program development, data capture, stakeholder communication, travel
• Experience: minimum of 1 year sales experience, leadership experience or clinical experience

Raleigh

• Skills: medical science liaison, oncology, KOL development, scientific exchange, clinical research, therapeutic area, scientific expertise, medical education, product support, scientific presentation

Chapel Hill

• Skills: Regulatory, Medical Devices, Global Regulatory Intelligence, EU MDR, clinical evaluation, Product claims, Regulatory submissions, EU Notified Body, Advertising and Promotion, Regulatory Trends
• Experience: 10+ years
• Type: Full-time

Raleigh

• Skills: project management, clinical trials, radiopharmaceuticals, cancer, Duchenne muscular dystrophy, ALS, Stargardt’s, study plans, project meetings, regulatory standards
• Type: Contract

Raleigh

• Skills: RNA formulations, formulation strategies, delivery modalities, analytical characterization, formulation development, agricultural formulations, scaling up, stability studies, product development, biotechnology
• Type: Full-time

Raleigh

• Skills: clinical trial, business development, CRO, pharma, biotech, partnerships, pipeline management, client retention, sales, medical devices
• Experience: 5+ years of business development experience in CRO and pharmaceutical environments

Durham

• Skills: Program Management, Cross-Functional Teams, Regulatory Frameworks, Design Control, Operational Readiness, Clinical Laboratory Operations, Product Development, Risk Management, Strategic Leadership, Biotech
• Experience: 8–12 years of relevant experience; or 5–8 years with a Master’s or 2–5 years with a PhD in diagnostics, medical device, pharmaceutical, or biotech industry
• Type: Full-time
• Salary: $163K-$204K annually

Raleigh

• Skills: Investigational Product handling, clinical trial, patient consultations, research protocol, documentation, regulatory compliance, multidisciplinary team, communication, training, Good Clinical Practice

Durham

• Skills: toxicology, dietary exposure, risk assessment, GLP, OECD Guidelines, genetically modified crops, safety assessment, scientific literature, project management, technical documents
• Type: full_time
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