Top Biotech Jobs in Charlotte, NC

Responsible for scientific oversight and quality of clinical trials in Late-Stage Oncology, collaborating with teams and presenting data, while ensuring compliance and optimizing procedures.

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

The role involves creating and managing marketing materials for the commercial team, focusing on storytelling and presentation quality while developing systems for efficiency.

Support the implementation of OncoEMR in oncology clinics, providing training, ensuring customer satisfaction, and driving practice workflow changes. Collaborate with teams and stakeholders to customize applications and manage training delivery both online and in-person.

Lead cybersecurity requirements for the Digital Health Application (DiGA), including regulatory compliance and vulnerability management tasks.

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 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.

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

The Enterprise Data Architect will design and guide the evolution of data architecture across cloud and legacy platforms, ensuring data management aligns with organizational strategy through advanced analytics.

The Clinical Sales Manager oversees account development, product training, and customer relations while executing strategic sales initiatives for a medical device company.

As a Senior Lead Data Manager at ICON, you will lead data science projects, design strategies for clinical trial analysis, and mentor team members while collaborating with stakeholders to provide actionable insights.

Oversee site contracts for clinical studies, manage contract development, collaborate with teams, ensure financial management, and mentor others.

Oversee clinical trials, ensuring compliance with protocols and regulatory requirements while managing and mentoring clinical study teams.

The Operations Associate will support the commissioning and qualification of parenteral areas and ensure operational readiness, collaborating across functions to meet performance metrics. Responsibilities also include training personnel and leading safety and quality initiatives.