Top Biotech Jobs in Charlotte, NC

As a Security Engineer, lead and develop security tools, manage security infrastructure, mentor team members, and support security initiatives at Benchling.

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 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 Senior Product Manager, Retention will enhance customer engagement and retention by leveraging data and cross-functional collaboration to optimize user experiences and lifecycle messaging.

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 Process Safety Engineer provides technical leadership in process safety management, supporting project delivery, training staff, and ensuring compliance in manufacturing operations.

The Sr. Director of Clinical Development will lead the execution of clinical programs, collaborating cross-functionally and managing resources to meet clinical study goals and timelines.

The Senior Director for Quality Risk Management oversees global quality systems, drives standardization, ensures compliance, leads initiatives, and manages cross-functional collaboration.

The Pharmaceutical Sales Rep will promote and sell products, manage territory plans, maintain relationships with healthcare providers, and participate in sales meetings.

The Senior Business Development Manager will drive growth in the lithium, hydrogen, and nuclear sectors, manage customer acquisition, and collaborate with cross-functional teams to meet market needs.

As a Learning & Development Specialist, you will support protocol specific training processes, manage training materials, ensure version control, and contribute to continuous improvement in clinical development.

Lead Clinical Research Associate will oversee and manage clinical trial sites, ensuring adherence to protocols and regulations while mentoring junior staff and ensuring data integrity.

As a Clinical Research Associate, you'll oversee clinical trial activities, ensuring compliance with protocols and regulatory requirements, managing sites, and supporting data integrity and participant safety.

Manage statistical programming for clinical trials, ensuring quality outputs, mentoring programmers, and meeting regulatory standards while collaborating with study teams.

Lead the implementation of data governance strategies for clinical trials and real-world evidence data, ensuring compliance with regulations and operational excellence.