Top Biotech Jobs in Charlotte, NC

The Senior Oncology Account Specialist promotes Pfizer's products to healthcare providers, educating them on appropriate use, while managing accounts to improve patient experience and care quality.

The Software Engineer will enhance developer experience by creating efficient tools for production releases and streamline workflows while collaborating with various teams.

The Medical Science Liaison will support Tempus by educating healthcare professionals on oncology products and gathering insights for future developments, focusing on molecular oncology and genomic profiling.

The Chief Operating Officer will lead operational execution and manage delivery teams, drive company-wide operating rhythms, and partner closely with the CEO and leadership team to scale the organization and enhance operational effectiveness.

The Sales Representative will sell Vocera products in the K-12 education sector, build customer relationships, manage sales cycles, and drive revenue growth through effective sales strategies.

Manage demand planning for the Applied Water segment, coordinating processes, improving forecast accuracy, and supervising demand planning team. Lead strategic reviews and supply chain projects while ensuring operational consistency.

Lead continuous improvement initiatives across multiple sites, delivering training, coaching, and mentoring while analyzing performance trends and promoting lean methodologies.

Lead business analysis for customer-facing digital platforms, collaborating with teams to enhance user experience and drive engagement through data analysis and process mapping.

The role involves leading a team in design and human factors engineering for delivery devices, ensuring compliance with regulations and enhancing product innovation.

The Sr. Director HSE will lead health, safety, and environmental functions, ensuring compliance, developing systems, and promoting safety at the Concord site.

The Clinical Research Physician will progress clinical assets, contribute to trial designs, compliance, and collaboration with research teams in early drug development.

The Senior CTA will support clinical trial management by handling documentation, coordinating meetings, and ensuring compliance with regulatory requirements while collaborating with teams and maintaining stakeholder relationships.

The Principal Manager, CQM leads document development and management, oversees compliance with procedures, and supports audits in clinical trials.

The Clinical Research Associate will design and analyze clinical trials, ensure protocol compliance, and maintain data integrity during studies.

The Director, Regional Community Oncology Expert will co-develop and implement Community Oncology strategies, support education and research initiatives, and represent Gilead in interactions with stakeholders in the US healthcare system. Responsibilities include presenting scientific data, leading real-world evidence studies, providing training, and collaborating with cross-functional teams.

Oversee clinical research site operations, ensure compliance with regulations, drive patient enrollment, manage teams, and develop performance strategies.