Project Manager
| Posting date: | 26 November 2025 |
|---|---|
| Salary: | £58,000 to £68,000 per year |
| Hours: | Full time |
| Closing date: | 26 December 2025 |
| Location: | Sale, Greater Manchester |
| Remote working: | On-site only |
| Company: | CHANDRAWAR IT TECHNOLOGIES PVT LTD |
| Job type: | Permanent |
| Job reference: |
Summary
Summary :
-> 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).
Responsibilities
• Autonomously leads one or more complex / pivotal clinical studies, providing leadership, operational strategy and direction to cross-functional clinical study team members (in-house and outsourced) from concept to closeout
• Works closely with the Clinical Programme Lead (CPL) and Principal CPM to implement operational strategies for optimal study delivery
• May provide mentorship to junior CPMs and Clinical Project Associates (CPAs)
• Contributes to optimisation of Clinical Operations processes and continuous improvement activities
• Manages study timelines, budgets, and quality targets, ensuring effective tracking and forecasting
• Collaborates with Site Management and Engagement on country/site selection and recruitment strategies
Required Experience
• 10 years+ clinical research experience, including 5 years+ in clinical project management (or equivalent) roles
• Experience in managing full-service out-sourced projects
• Experience in Hematology/oncology and/or autoimmune phase I/II studies
• Experience with ATIMPs, site-level management and managing pivotal trials an advantage.
Skills/Specialist Knowledge
• Adept at working in a global setting and matrix environment
• Broad experience in a Clinical Trial Execution discipline (e.g. senior study management expertise, data management experience, clinical leadership expertise)
• Demonstrated project management/leadership experience
• Experience in understanding of key drivers impacting budgets and managing project to budget
• Ability to establish and maintain effective working relationships with co-workers, managers, investigator site personnel and service providers
• Ability to manage in complex and challenging environments
• Thorough knowledge of ICH-GCP guidelines and FDA regulations
• Knowledge of medical terminology and clinical patient management
-> 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).
Responsibilities
• Autonomously leads one or more complex / pivotal clinical studies, providing leadership, operational strategy and direction to cross-functional clinical study team members (in-house and outsourced) from concept to closeout
• Works closely with the Clinical Programme Lead (CPL) and Principal CPM to implement operational strategies for optimal study delivery
• May provide mentorship to junior CPMs and Clinical Project Associates (CPAs)
• Contributes to optimisation of Clinical Operations processes and continuous improvement activities
• Manages study timelines, budgets, and quality targets, ensuring effective tracking and forecasting
• Collaborates with Site Management and Engagement on country/site selection and recruitment strategies
Required Experience
• 10 years+ clinical research experience, including 5 years+ in clinical project management (or equivalent) roles
• Experience in managing full-service out-sourced projects
• Experience in Hematology/oncology and/or autoimmune phase I/II studies
• Experience with ATIMPs, site-level management and managing pivotal trials an advantage.
Skills/Specialist Knowledge
• Adept at working in a global setting and matrix environment
• Broad experience in a Clinical Trial Execution discipline (e.g. senior study management expertise, data management experience, clinical leadership expertise)
• Demonstrated project management/leadership experience
• Experience in understanding of key drivers impacting budgets and managing project to budget
• Ability to establish and maintain effective working relationships with co-workers, managers, investigator site personnel and service providers
• Ability to manage in complex and challenging environments
• Thorough knowledge of ICH-GCP guidelines and FDA regulations
• Knowledge of medical terminology and clinical patient management