Open Positions
Project Manager I
Regulatory And Compliance Consultant I
Regulatory And Compliance Consultant I
USA/Canada | Permanent Position
The Project Manager will manage activities regarding GXP audits and monitor investigational sites, laboratories, and other entities for research studies to ensure compliance to the study protocol, Standard Operating Procedures (SOPs) , applicable FDA regulations, the guidelines of ICH-GXP and/or ISO standards.
The candidate will also be charged with ensuring the quality and integrity of data, and assessing the overall risk of the entities.
Regulatory And Compliance Consultant I
Regulatory And Compliance Consultant I
Regulatory And Compliance Consultant I
USA/Canada | Permanent Position
The Regulatory and Compliance Consultant will audit and monitor investigational sites, laboratories, and other entities for research studies to ensure compliance to the study protocol, Standard Operating Procedures (SOPs), applicable FDA regulations, the guidelines of ICH-GXP and/or ISO standards.
The candidate will also be charged with ensuring the quality and integrity of data, and assessing the overall risk of the entities.
Clinical Research Consultant I
Clinical Research Consultant I
Clinical Research Consultant I
USA/Canada | Permanent Position
The Clinical Research Consultant (CRC) will audit and monitor investigational sites, laboratories, and other entities for research studies to ensure compliance to the study protocol, Standard Operating Procedures (SOPs) , applicable regulations, and the principles of ICH-GCP and/or ISO standards.
The CRC will also be charged with ensuring the quality and integrity of data, and assessing the overall risk of the entities.
IT Consultant I
Clinical Research Consultant I
Clinical Research Consultant I
USA/Canada | Permanent Position
The IT Consultant will implement state of the art GxP compliant information technologies to help clients ensure compliance to the study protocol, Standard Operating Procedures (SOPs), applicable regulations, and the principles of ICH-GCP and/or ISO standards.
The IT Consultant will design and implement state of the art GxP compliant information technologies to help clients ensure compliance to the applicable regulations, GAMP5 and the principles of applicable GxPs. These technologies can include areas such as:
- Quality Management
- Document Management
- e Signatures
- Learning Management Systems
- Clinical Trial Management Systems
- Distributed Control Systems
- electronic Case Report Forms
The IT Consultant will also be charged with ensuring the quality and integrity of data, and assessing the overall risk of the entities supporting our clients.