Top Tech Jobs & Startup Jobs in Charlotte, NC

The Associate Director of Project Management will lead oncology program execution, drive cross-functional collaboration, manage timelines, and provide strategic support to ensure successful project outcomes.

The Manager of Quality Control and Stability oversees testing and stability programs for pharmaceutical products, ensuring compliance and data management, while collaborating with other teams and managing external partnerships.

The IT Compliance Manager oversees compliance activities, ensuring adherence to regulations like SOX and GDPR, conducting audits, and developing compliance policies.

Oversee pharmacovigilance operations, vendor management, process improvements, compliance, and cross-department collaboration while ensuring quality and safety reporting.

Lead mechanistic modeling (PBPK/QSP) to support IND-enabling decisions and FIH dose selection; integrate preclinical, biomarker, and early clinical data; oversee population PK/PKPD and exposure-response analyses; contribute to regulatory submissions; mentor staff and build internal pharmacometrics capabilities while partnering cross-functionally.

Lead commercial FP&A for forecasting, gross-to-net, expense planning, and performance analysis. Partner with Commercial, Accounting, NPP, and S&OP to drive forecast accuracy, ROI analysis, purchase order controls, and strategic financial recommendations for senior leadership.

Lead mechanistic and quantitative modeling (PBPK/QSP) to inform IND-enabling decisions, FIH dose selection, and early clinical strategy. Integrate preclinical, biomarker, and clinical data, review population PK/PK-PD analyses, support regulatory submissions, and collaborate across DMPK, biology, toxicology, and clinical teams while mentoring junior staff.

As a Therapeutic Specialist, you will engage healthcare professionals to enhance patient care, manage territory relationships, and exceed sales goals while collaborating with internal teams.

The Associate Director, Quality Assurance oversees GCP QA operations, conducts audits, supports clinical study activities, and ensures compliance with GCP regulations.

The Associate Manager oversees centralized monitoring for clinical trials, focusing on risk management, data surveillance, and regulatory compliance while ensuring quality and participant safety.