Healthcare & Pharma Careers

This role will communicate with patients and performs clinical services to ensure high quality patient care in a fast-paced environment. We do this in pursuit of our mission to improve the health and happiness of the communities we serve by providing quality care to all, regardless of situation or c

Medical Billing Specialist with demonstrated. Medicaid MCO billing experience. Medical Billing Specialist (Revenue Cycle Management) – Bilingual Spanish Preferred.

Responsible for the regulatory CMC leadership of one or more commercial and development projects, including responsibility for regulatory strategy, IND/CTA preparation, maintenance and update activities, interaction with and preparation for key milestone meetings with regulatory agencies with focus

Deep clinical domain knowledge including understanding of clinical workflows, medical terminology, and healthcare delivery processes. Clinical Concept Mapping: Translate complex clinical concepts and workflows into explicit data element mappings across diverse source systems, ensuring semantic accur

Partners closely with Clinical Development, Safety, Commercial, CMC, Quality, and Legal to ensure aligned and value-generating regulatory strategies. The Executive Director, Regulatory Strategy – Endocrinology is a senior regulatory leader responsible for shaping and driving global regulatory stra

The Associate Director, Regulatory Affairs Project Planning & Coordination is responsible for developing, implementing, and monitoring project plans and best practices that facilitate how the Global Regulatory Affairs department executes its strategic and functional goals. Coordinate governance

Associate Director, Regulatory Affairs Project Planning & Coordination to lead project planning and ensure regulatory strategy efficiency. This role involves developing regulatory project plans for submissions and coordinating with the Global Regulatory Affairs team. The ideal candidate has a Ba

A biopharmaceutical company in San Diego seeks an Associate Director, Regulatory Affairs CMC. The ideal candidate has 10 years of experience in Regulatory Affairs within the biopharmaceutical industry, including supervisory roles. This role focuses on regulatory strategy execution for drug developme

Supervisor will oversee and manage the clean-up project for quality assurance. Supervises staff in Patient Financial Services overseeing daily team operations to ensure timely billing for Homecare and Pharmacy billing team. Ensures all billing & collection activities are compliant with federal, stat

Qualified candidates should have a medical degree and 3+ years of experience in clinical research. The University of Southern California's Keck School of Medicine seeks a Clinical Monitor for Alzheimer's research. This role involves overseeing clinical trial progress, ensuring adherence to protocols

Reporting to the Senior Vice President of Quality, the Director of Clinical Quality Assurance will lead the Clinical QA function and provide strategic leadership and operational oversight across global early to late-stage clinical programs. Ensure reporting of potential or confirmed violations to re

Responsible for the regulatory CMC leadership of one or more commercial and development projects, including responsibility for regulatory strategy, IND/CTA preparation, maintenance and update activities, interaction with and preparation for key milestone meetings with regulatory agencies with focus

Project Manager, Regulatory Affairs (Clinical and CMC). Join our team as a Project Manager in Regulatory Affairs, focusing on Clinical and CMC. This remote contract role involves leading cross-functional regulatory activities, enhancing project management standards, and mentoring junior project mana

The ideal candidate will advise on company clinical quality strategy, ensure compliance to regulations, oversee quality management systems and interact directly with cross functional clinical, regulatory and quality teams. The ideal candidate will have at least 10 years of experience in clinical qua

Partners closely with Clinical Development, Safety, Commercial, CMC, Quality, and Legal to ensure aligned and value-generating regulatory strategies. The Executive Director, Regulatory Strategy Endocrinology is a senior regulatory leader responsible for shaping and driving global regulatory strateg

The Senior Manager, Quality Assurance GCP will support the Good Clinical Practice (GCP) Quality Assurance (QA) function, and performance of GCP QA operations. Provide GCP guidance and feedback for research and development activities; participate in clinical study team meetings and discuss clinical s

Regulatory Affairs, Licensing and Accreditation Supports multi?hospital regulatory readiness and ongoing compliance with Joint Commission, CDPH, CMS, and other applicable regulatory and accreditation agencies. The Senior Specialist works collaboratively with operational leaders, quality, patient saf