Jobs at ProPharma Group

The Senior Business Analyst (Proposal Development) is responsible for overseeing the production of accurate proposal budgets and strategy documents while collaborating with various departments. This r...

The Senior Clinical Project Manager is responsible for overseeing and conducting clinical research trials, ensuring compliance with regulations and quality standards. This role involves strategic plan...

The Freelance CSV Auditor will be responsible for planning and conducting CSV audits on behalf of clients, acting as a Subject Matter Expert for CSV auditing and supplier management projects. This rol...

The HPC Engineer will be responsible for deploying new applications and services to cloud environments, overseeing operational support, and managing infrastructure aspects of the platform. This role r...

The Senior Clinical Contract and Budget Specialist is responsible for administering and negotiating site contracts to support global clinical trial setup and execution. This role involves ensuring com...

The Clinical Lead is responsible for managing assigned clinical trials, focusing on investigational site management and monitoring activities. This role ensures compliance with regulations and quality...

The Senior Medical Writer is responsible for authoring high-quality medical writing deliverables with a focus on quality, accuracy, and efficiency. This role involves managing client expectations, men...

The Medical Promotional Review Consultant is responsible for providing compliant, medically accurate, and scientifically sound solutions for promotional and non-promotional materials in the pharmaceut...

GCP/GLP/GCLP Auditor and SOP Technical Writer, QA Compliance Consultant responsible for supporting Clinical CQA projects and providing quality consulting and technical writing services to clients in t...

Consulting opportunities available for a 6 to 12 month technology transfer project in San Diego for IOPQ/Tech Transfer Consultants (CAR T Cell). Various roles available in QC, MFG, and Operations with...

The PV/Regulatory Audit position at ProPharma involves auditing PV - Regulatory Operations, Post-IND support, Medical writing, and commercial PV. Experience in PV audit, BIMO inspection auditing, PV s...

The Medical Promotional Review Consultant is responsible for providing compliant, medically accurate and scientifically sound solutions for promotional materials in the pharmaceutical industry, while...

The Compliance and Quality Assurance Consultant (CQA) position at ProPharma involves supporting Clinical CQA projects, providing quality consulting, technical writing, and contracted services to addre...