Synairgen is a respiratory company developing SNG001, a broad-spectrum antiviral offering potential against a range of respiratory viruses, including common cold, flu and coronaviruses, which can lead to critical illness. By delivering SNG001 directly into the lungs as an aerosol we aim to boost and/or restore the lungs' antiviral responses to clear the virus and improve patients’ outcomes.
We will be running a large Phase 2 trial in patients requiring mechanical ventilation due to respiratory viral infections. These seriously ill patients face mortality rates of between 25% and 45%, and with SNG001, we are looking to demonstrate a significant reduction in mortality.
We are looking forward to conducting this clinical trial and are seeking to recruit a Senior Project Manager to join our Clinical Operations Team.
The role
This is a key role in our trial team, so we’re looking for someone who is willing to get involved in tasks as well as being comfortable with delegating and coordinating them. This is a hands-on role at the heart of the trial team. Recent experience with Project Managing Phase II, global trials. A minimum 5 years’ experience with project managing IMP clinical trials. Flexible to the trial workload and fast-paced environment. Able to work as part of a team and independently on tasks. Ability to identify potential problems before they arise and to make decisions/suggest resolutions as required. Lead and drive tasks delegated by the Lead PM. Good understanding of ICH GCP and UK, EU, and US regulations and requirements. Supportive of the wider clinical trial team. Good communication skills and able to think broadly as well as focus on detail when required. Experience with vendor/contractor selection and contract negotiation from start to finish. Experience project managing clinical trials in infectious diseases and/or respiratory specialties (the intensive care setting and/or viral infections especially). Previous line management of staff. Experience in writing of SOPs. Microsoft Project capability. Ability to travel to sites/vendors and to Southampton as required. Experience with writing/coordinating clinical study reports. To apply, please send your current C.V. and a covering letter to hr@synairgen.com
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This is a key role in our trial team, so we’re looking for someone who is willing to get involved in tasks as well as being comfortable with delegating and coordinating them. This is a hands-on role at the heart of the trial team. Recent experience with Project Managing Phase II, global trials. A minimum 5 years’ experience with project managing IMP clinical trials. Flexible to the trial workload and fast-paced environment. Able to work as part of a team and independently on tasks. Ability to identify potential problems before they arise and to make decisions/suggest resolutions as required. Lead and drive tasks delegated by the Lead PM. Good understanding of ICH GCP and UK, EU, and US regulations and requirements. Supportive of the wider clinical trial team. Good communication skills and able to think broadly as well as focus on detail when required. Experience with vendor/contractor selection and contract negotiation from start to finish. Experience project managing clinical trials in infectious diseases and/or respiratory specialties (the intensive care setting and/or viral infections especially). Previous line management of staff. Experience in writing of SOPs. Microsoft Project capability. Ability to travel to sites/vendors and to Southampton as required. Experience with writing/coordinating clinical study reports. To apply, please send your current C.V. and a covering letter to hr@synairgen.com
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