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• Contract Clinical Operations Managers for international Oncology studies
• Project and team oversight of Country Lead Monitors and outsourced monitoring activities
• Key member of study project team in global pharma organisation
• 12 month extendable contracts based in Reading with scope to work from home
• Outside IR35 contract with competitive daily rate and 7 hour working day
• Will suit Senior / Lead CRA, Clinical Operations Manager, Study PM, Lead Monitor etc
Summary
Based in Reading, Berkshire, with scope to work from home once established, we have new contract opportunities overseeing international clinical operations of oncology studies. These opportunities are available due to new study funding. We provide an outside of IR35 contract, long term placements, a competitive daily rate, 7 hour working day and the security of a 2 month notice period. To meet the needs of new studies Clinical Operations Managers (Study Lead Monitors, however no monitoring is involved) are required to take responsibility for site management and monitoring activities overseeing and, interfacing with, locally based Country Lead Monitors. These roles will suit Senior / Lead CRAs looking to progress, Clinical Operations Managers, Clinical Project Managers or Lead Monitors.
The Company
The company is a highly successful pharmaceutical company that exceeded all worldwide targets last year. The organisation boasts a high investment ratio in drug development with a record number of products in clinical studies. Oncology is a strategic therapeutic area where the company is boosting its pipeline in cancer research as it continues to maintain its position as a leading innovator in this field.
The Role
Working within Global Clinical Development Operations in the Oncology TA the Study Lead Monitor (SLM) is a key member of the Study Team responsible for representing and overseeing all aspects of Site Management and Monitoring activities. The SLM works in close collaboration with the Study Manager and the Study Team for trials that are outsourced to CROs. Leading, managing and motivating globally dispersed local Country Lead Monitors and CRAs, the SLM will be responsible for training and quality oversight of site management activities identifying potential operational issues. The role encompasses developing Study Monitor plans, Training plans, Verification initiatives, coordinating Study Investigator Meetings and reviewing Country Study Reports. Acting as the expert advisor to the Study Team the SLM will ensure study processes, procedures and expectations correspond to the practicality of conducting the trial from study feasibility through to close out. While some international travel will be necessary at study launch time ongoing travel requirements will not be extensive and will be at the discretion of the job holder to meet their project needs.
The Contract
The contract will be for an initial 12 months and will be extendable for 12 month periods usually contracted at the start of month 10. This will include a discretionary annual rate review with the expectation to work for the company for the duration of study phase as a minimum. We offer a client approved contract outside of IR35 and a highly “contractor friendly” environment with genuine career progression opportunities through recognition and long-term placements. The contract provides the security of a 2 month notice period with a competitive daily rate and 7 hour working day.
Experience
We are seeking experienced individuals with Oncology study operational monitoring expertise at Senior CRA, Lead CRA, Clinical Project Manager, Clinical Operations Manager, Study Manager, Project Manager, Country Lead Monitor or Study Lead Monitor level. The roles require a comprehensive knowledge of Oncology studies plus GCP, drug development processes, monitoring and site management processes. Candidates will be considered from CRO, pharmaceutical, biotech and not-for-profit company environments.
Keywords: Oncology, Senior Clinical Research Associate, Lead Clinical Research Associate, SCRA, LCRA, Country Study Monitor, Clinical Operations Manager, Study Operations Manager, CSM, Study Lead Monitor, Study Manager, Study Leader, Clinical Project Manager, Clinical Project Leader, SLM, M4 Corridor, Reading, Berkshire
These are contract positions.
Expired
- Salary: £ Competitive
- Job Type:Contract
Posted almost 7 years ago
- Contact: Brian Tappy
- Contact Email: brian.tappy@nextphaserecruitment.com
- Contact Phone: +44 1403 216216
- Duration: 12 months
- Start Date: ASAP
- Job Ref: 15520+BT
• Project and team oversight of Country Lead Monitors and outsourced monitoring activities
• Key member of study project team in global pharma organisation
• 12 month extendable contracts based in Reading with scope to work from home
• Outside IR35 contract with competitive daily rate and 7 hour working day
• Will suit Senior / Lead CRA, Clinical Operations Manager, Study PM, Lead Monitor etc
Summary
Based in Reading, Berkshire, with scope to work from home once established, we have new contract opportunities overseeing international clinical operations of oncology studies. These opportunities are available due to new study funding. We provide an outside of IR35 contract, long term placements, a competitive daily rate, 7 hour working day and the security of a 2 month notice period. To meet the needs of new studies Clinical Operations Managers (Study Lead Monitors, however no monitoring is involved) are required to take responsibility for site management and monitoring activities overseeing and, interfacing with, locally based Country Lead Monitors. These roles will suit Senior / Lead CRAs looking to progress, Clinical Operations Managers, Clinical Project Managers or Lead Monitors.
The Company
The company is a highly successful pharmaceutical company that exceeded all worldwide targets last year. The organisation boasts a high investment ratio in drug development with a record number of products in clinical studies. Oncology is a strategic therapeutic area where the company is boosting its pipeline in cancer research as it continues to maintain its position as a leading innovator in this field.
The Role
Working within Global Clinical Development Operations in the Oncology TA the Study Lead Monitor (SLM) is a key member of the Study Team responsible for representing and overseeing all aspects of Site Management and Monitoring activities. The SLM works in close collaboration with the Study Manager and the Study Team for trials that are outsourced to CROs. Leading, managing and motivating globally dispersed local Country Lead Monitors and CRAs, the SLM will be responsible for training and quality oversight of site management activities identifying potential operational issues. The role encompasses developing Study Monitor plans, Training plans, Verification initiatives, coordinating Study Investigator Meetings and reviewing Country Study Reports. Acting as the expert advisor to the Study Team the SLM will ensure study processes, procedures and expectations correspond to the practicality of conducting the trial from study feasibility through to close out. While some international travel will be necessary at study launch time ongoing travel requirements will not be extensive and will be at the discretion of the job holder to meet their project needs.
The Contract
The contract will be for an initial 12 months and will be extendable for 12 month periods usually contracted at the start of month 10. This will include a discretionary annual rate review with the expectation to work for the company for the duration of study phase as a minimum. We offer a client approved contract outside of IR35 and a highly “contractor friendly” environment with genuine career progression opportunities through recognition and long-term placements. The contract provides the security of a 2 month notice period with a competitive daily rate and 7 hour working day.
Experience
We are seeking experienced individuals with Oncology study operational monitoring expertise at Senior CRA, Lead CRA, Clinical Project Manager, Clinical Operations Manager, Study Manager, Project Manager, Country Lead Monitor or Study Lead Monitor level. The roles require a comprehensive knowledge of Oncology studies plus GCP, drug development processes, monitoring and site management processes. Candidates will be considered from CRO, pharmaceutical, biotech and not-for-profit company environments.
Keywords: Oncology, Senior Clinical Research Associate, Lead Clinical Research Associate, SCRA, LCRA, Country Study Monitor, Clinical Operations Manager, Study Operations Manager, CSM, Study Lead Monitor, Study Manager, Study Leader, Clinical Project Manager, Clinical Project Leader, SLM, M4 Corridor, Reading, Berkshire
These are contract positions.