Jobs

Science Jobs at Propharma Group

(1 - 15 of 19)
  1. The Clinical Research Associate position is responsible for clinical monitoring for assigned protocols and investigational sites as well as ensuring that studies are conducted and documented in accordance with the study protocol, standard opera...
    ProPharma Group ·16 hours ago on Broadbean
  2. The Clinical Research Associate position is responsible for clinical monitoring for assigned protocols and investigational sites as well as ensuring that studies are conducted and documented in accordance with the study protocol, standard opera...
    ProPharma Group ·16 hours ago on Broadbean
  3. The Commissioning Qualification Validation Consultant position is responsible for performing and completing validation assignments. *This is a fulltime, exempt role* ESSENTIAL FUNCTIONS * Develop Installation, Operational and Performance qua...
    ProPharma Group ·2 days ago on Broadbean
  4. The Clinical Lead position is responsible for the management of assigned clinical trials with a focus on investigational site management and monitoring activities. The Clinical Lead will ensure that site management and monitoring aspects of cli...
    ProPharma Group ·2 days ago on Broadbean
  5. Essential Functions: * Represent the company in assigned areas of quality assurance and regulatory / GxP. * Provide consultation and support the management of projects within the CQA business practice. * Keep pace with the regulatory and techn...
    ProPharma Group ·5 days ago on Broadbean
  6. The Billing Specialist is a key part of ProPharma Group's Accounting team and is responsible for supporting all F&A related facets of TPG's project and consulting businesses client billings, month-end project accounting and assisting the project t...
    ProPharma Group ·5 days ago on Broadbean
  7. The QA Val CSV Engineer II position is responsible for performing Computer System Validation (CSV) projects and providing consulting and contract services to clients under the guidance of more experienced CSV professionals. Essential Functions ...
    ProPharma Group ·1 week ago on Broadbean
  8. Document controllers follow established document process flows to ensure the integrity and control of documents per site and company standards. This includes understanding the cross linking of documents and the affect of changes within the documen...
    ProPharma Group ·1 week ago on Broadbean
  9. Coordinators utilize process flows to clear roadblocks, schedule events and provide status updates per site and company standards. This includes understanding the organization structure, roles and responsibilities as well as infrastructure support...
    ProPharma Group ·1 week ago on Broadbean
  10. The Computer Systems Validation Engineer I position is responsible for performing Computer System Validation (CSV) projects for clients under the guidance of more experienced CSV professionals. Essential Functions * Participate on teams of inte...
    ProPharma Group ·1 week ago on Broadbean
  11. CSV Data Integrity Quality Assurance is responsible for CSV / Data Integrity Quality Management, Review of Weekly and Monthly KPI's Deviation / CAPA Management & trending, partner site QA Supervisor for End Line Trending, and document management i...
    ProPharma Group ·1 week ago on Broadbean
  12. The Principal Computer Systems Validation & Data Integrity Consultant position is responsible for independently managing Computer System Validation (CSV) and Data Integrity (DI) related projects and providing consulting and contract services to cl...
    ProPharma Group ·1 week ago on Broadbean
  13. Job Summary: The Business Analyst II, Proposals position is responsible for development and analysis of competitive proposal text, budget, client bid grids (if applicable) while working closely with the internal proposal key stakeholders. Essent...
    ProPharma Group ·2 weeks ago on Broadbean
  14. For the past 20 years, Pro Pharma has improved the health and wellness of patients by providing advice and expertise that empowers biotech, med device, and medical organizations of all sizes to confidently advance scientific breakthroughs and intr...
    2 weeks ago on ListedBuy
  15. The Vice President, Nonclinical Emerging Therapies is responsible for the conduct of regulatory activities associated with the nonclinical development of therapeutic drug, biologic, and device products. This role will serve as the point person int...
    ProPharma Group ·4 weeks ago on Broadbean
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