Top Biotech Jobs in Charlotte, NC

The role involves improving population health through data analytics and pharmacoeconomic evaluations, educating customers on Pfizer products, and developing strategic medical partnerships.

The Product Manager will define and execute the product strategy and roadmap for Benchling's small molecule R&D solution, collaborating with teams to deliver solutions for scientific research.

As a Product Solutions Associate, you will support clinicians by resolving software issues, documenting solutions in Salesforce, and collaborating with cross-functional teams in a remote environment.

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 Foot & Ankle Sales Representative sells Stryker products, maintains relationships with surgeons, organizes inventory, and ensures product knowledge in healthcare environments.

The Manager, Technical Accounting will provide expertise on complex accounting topics, monitor new standards, support M&A integrations, and manage cross-functional collaborations, while training teams and promoting process efficiencies.

The role involves supporting endpoint devices, managing incidents, working with enterprise tools, and documentation to enhance technology solutions.

The Contract Administrator oversees contract governance, reviews and coordinates contract processes, ensures compliance, and supports internal stakeholders in maintaining accurate documentation.

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

Manage and oversee GMP processes and analytical methods for radiopharmaceutical manufacturing, ensuring compliance and timely regulatory filings while leading vendor relationships and project strategies.

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.

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.

The Lead Clinical Research Associate oversees clinical trial sites, ensuring compliance with regulations and protocols while mentoring CRAs and collaborating with teams to execute trials effectively.

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.

The role involves developing and executing Community Oncology strategies, leading initiatives, collaborating across teams, and representing Gilead in Community Oncology practices.

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.

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