Top Pharmaceutical Jobs in Raleigh-Durham, NC

As a Senior Research Scientist, you'll oversee statistical programming for cancer care research, provide expertise in data analysis, and collaborate with cross-functional teams.

The Senior Manager, GMP Quality Assurance oversees compliance with regulatory standards in GMP activities, conducts audits, and integrates AI technologies for quality assurance improvements.

The Senior Portfolio Lead will oversee data management services for clients, ensuring quality deliverables, strategic oversight, and optimal clinical data flows, while leading cross-functional teams and managing complex client relationships.

The Sales Director will lead the sales process to close partnerships with research sites, managing all sales activities including discovery and negotiation, while collaborating with Customer Success for onboarding.

The Sr. Events Manager will oversee event logistics for B2B marketing across various industry conferences, ensuring effective planning, execution, and cross-functional collaboration to drive commercial value.

The Senior Manager will oversee account alignment and data validation for vaccine contracts, ensuring accurate market share data, and will liaise with representative teams to resolve data issues.

Review and process provider appeals, ensure regulatory compliance, conduct internal audits, draft appeal decision letters, serve as SME on complex cases, mentor peers, train new hires, and meet monthly metrics for attendance, production, and quality.

The Automation Engineer will deliver automation expertise in pharmaceuticals, lead automation projects, ensure compliance, and support process automation systems. Responsibilities include interfacing with multiple departments, providing training in automation technologies, and participating in regulatory inspections.

As a Production Manager, you'll oversee production efficiency, ensure compliance with regulations, lead a team, and manage site validation. Responsibilities include planning, documentation, and maintaining a safe working environment while driving continuous improvement initiatives.

The Senior Clinical Project Manager will lead Phase III oncology and hematology trials, managing projects and cross-functional teams while ensuring timely and quality delivery.

Manage end-to-end customer contract process, negotiate financial and contractual terms, coordinate with Pricing/Proposals and Project Leads, maintain CRM and contract records, meet departmental metrics and turnaround times, and support resolution of contractual and financial issues. Occasional travel (up to 25%).

Lead R&D and scientific strategy in neuroscience, oversee clinical trials, provide medical insight, and engage with clients to ensure project success.

Negotiate, draft, review, and finalize clinical trial agreements, amendments, and ancillary documents with study sites. Maintain stakeholder communication, track contract progress in ICON/client systems, identify risks, support site start-up, file contractual documents, and participate in study team calls while adhering to SOPs and training requirements.

Conduct site qualification, initiation, monitoring, and close-out visits; ensure protocol compliance, data integrity, and patient safety; collaborate with investigators and site staff; perform data review and query resolution; contribute to study documentation and clinical study reports.

Lead clinical data review for studies, ensuring the interpretation of efficacy and safety data, and collaborating with cross-functional teams.