Project Manager
| Dyddiad hysbysebu: | 26 Tachwedd 2025 |
|---|---|
| Cyflog: | £58,000 i £68,000 bob blwyddyn |
| Oriau: | Llawn Amser |
| Dyddiad cau: | 26 Rhagfyr 2025 |
| Lleoliad: | Sale, Greater Manchester |
| Gweithio o bell: | Ar y safle yn unig |
| Cwmni: | CHANDRAWAR IT TECHNOLOGIES PVT LTD |
| Math o swydd: | Parhaol |
| Cyfeirnod swydd: |
Crynodeb
-> Project planning and execution
Develop and manage project timelines and budgets.
Create and refine study documents, including the protocol and other plans.
Support the selection of investigational sites and manage vendor selection and relationships.
Plan and conduct investigator meetings.
-> Team and stakeholder management
Serve as the primary point of contact for clients, sponsors, and internal teams.
Lead and motivate cross-functional project teams, including Clinical Research Associates (CRAs), data managers, and others.
Communicate project status, risks, and issues to senior management and stakeholders.
-> Risk and compliance management
Identify and mitigate potential risks and challenges to keep the trial on track.
Resolve issues, such as protocol deviations, and manage quality and compliance with regulatory standards (like GCP).
Oversee the implementation of any protocol amendments.
Ensure all trial communication and documentation is filed correctly, such as in the Trial Master File.
-> Data and quality assurance
Oversee data collection and management processes to ensure accuracy and integrity.
Lead the ongoing review of study data for quality and consistency.
Participate in the preparation of Clinical Study Reports (CSRs).
Develop and manage project timelines and budgets.
Create and refine study documents, including the protocol and other plans.
Support the selection of investigational sites and manage vendor selection and relationships.
Plan and conduct investigator meetings.
-> Team and stakeholder management
Serve as the primary point of contact for clients, sponsors, and internal teams.
Lead and motivate cross-functional project teams, including Clinical Research Associates (CRAs), data managers, and others.
Communicate project status, risks, and issues to senior management and stakeholders.
-> Risk and compliance management
Identify and mitigate potential risks and challenges to keep the trial on track.
Resolve issues, such as protocol deviations, and manage quality and compliance with regulatory standards (like GCP).
Oversee the implementation of any protocol amendments.
Ensure all trial communication and documentation is filed correctly, such as in the Trial Master File.
-> Data and quality assurance
Oversee data collection and management processes to ensure accuracy and integrity.
Lead the ongoing review of study data for quality and consistency.
Participate in the preparation of Clinical Study Reports (CSRs).