Jobs

Contractor Jobs at Propharma Group

(1 - 13 of 13)
  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 ·2 days ago on Broadbean
  2. Key Responsibilities: Completes study-specific requirements for each assigned study which may include GCP training, IATA (dangerous goods) training, and study-specific training. Provides quality DCV services to patients at a location outside of ...
    ProPharma Group ·1 week ago on Broadbean
  3. 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
  4. 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
  5. 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
  6. 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
  7. 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
  8. Key Responsibilities: Completes study-specific requirements for each assigned study which may include GCP training, IATA (dangerous goods) training, and study-specific training. Provides quality DCV services to patients at a location outside of ...
    ProPharma Group ·1 week ago on Broadbean
  9. 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
  10. Key Responsibilities: Completes study-specific requirements for each assigned study which may include GCP training, IATA (dangerous goods) training, and study-specific training. Provides quality DCV services to patients at a location outside of ...
    ProPharma Group ·2 weeks ago on Broadbean
  11. Key Responsibilities: Completes study-specific requirements for each assigned study which may include GCP training, IATA (dangerous goods) training, and study-specific training. Provides quality DCV services to patients at a location outside of ...
    ProPharma Group ·2 weeks ago on Broadbean
  12. Key Responsibilities: Completes study-specific requirements for each assigned study which may include GCP training, IATA (dangerous goods) training, and study-specific training. Provides quality DCV services to patients at a location outside of ...
    ProPharma Group ·2 weeks ago on Broadbean
  13. Key Responsibilities: Completes study-specific requirements for each assigned study which may include GCP training, IATA (dangerous goods) training, and study-specific training. Provides quality DCV services to patients at a location outside of ...
    ProPharma Group ·2 weeks ago on Broadbean
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