Top Pharmaceutical Jobs in Raleigh-Durham, NC

The Director will lead U.S. commercialization efforts for neuroscience assets, focusing on market assessment, competitive analysis, brand strategy, and portfolio planning to ensure successful product launches and investments.

Lead a team of 10 sales representatives to achieve sales targets, coach team members, and develop sales plans in the psychiatry field.

The PV Project Manager will oversee project activities, manage client expectations, prepare project scope, and report progress to stakeholders while ensuring quality in pharmacovigilance services.

The People Partner provides HR case management support, advises management on HR policies, and collaborates with various HR teams to implement business changes and improve HR services.

Lead design, development, and verification of mixed-signal electronic hardware and embedded firmware for medical devices. Develop system/subsystem requirements, prototype and debug PCBA and FPGA/microcontroller designs, author test plans, perform root-cause analysis, ensure IEC 60601/EMC and IEC 62304 compliance, and support product lifecycle, manufacturing, and design control activities.

Manage a sales territory promoting pharmaceutical products to physicians and healthcare providers. Build relationships, create territory plans, gain formulary acceptance, use consultative selling and clinical knowledge, leverage data, and meet sales goals while following regulations and ethical standards.

The Clinical Research Physician in Ophthalmology at Lilly will oversee clinical trials, develop strategies, and act as a medical expert in ophthalmology, ensuring safe and effective product development.

The Territory Leader is responsible for sales execution in the eye care industry, focusing on account management, business growth, and relationship building with key stakeholders to drive product success.

Provide technical support for pharmaceutical manufacturing by overseeing commissioning and qualification activities, ensuring compliance with regulatory standards, and managing documentation related to equipment and systems.

The Senior Clinical Research Associate is responsible for site management and monitoring of clinical trials, ensuring compliance with regulations and quality standards, and enhancing investigator site relationships.