Cencora PharmaLex is looking for an experienced Senior Trial Master File Study Owner to work within our Professional Services team on a full-time, 6 month fixed-term contract.
Are you a Trial Master File expert looking for your next role?
Then, Cencora Pharmalex is your career opportunity!
Health Research & Outcomes ManagerLocation: This role can be based in either our Nottingham or London Support OfficeVacancy closing date: 6th June 2024Recruitment Partner: Emily Smith-KennyAs a Health Research & Outcomes Manager, you will be part of the Healthcare Business Unit, and will report into the Head of Health Research & Outcomes within the Healthcare Development & Public Affairs team.About the roleThe Health Research & Outcomes Manager will support the delivery of the pharmacy practice research, health outcomes and clinical trials agenda for Boots UK, demonstrating health economic and outcome as well as provide evidence for the UK pharmacy contracts agenda.
The role will engage with varied stakeholders internally and externally across the healthcare sector.In role you will: Contribute towards strategies that lower the cost of care, improve health outcomes and address health inequalities Lead the research governance process at Boots UK that supports both community pharmacy practice-based research and big data projects that can have either short, medium- or long-term impact Contribute to academic health outcomes research that demonstrates value to internal & external stakeholders.
Collect and capture relevant and appropriate outputs to perform analysis Utilise pharmacy practice and / or clinical expertise to develop and deliver relevant healthcare business initiatives that improve health outcomes and / or lower the cost of care Provide insight and expertise to both internal and external stakeholders, including the right interpretation of data/outputs making sure to select them appropriately Contribute towards future pharmacy contract model design through defining the value that the community pharmacy sector brings to health and social care systems Perform timely and relevant analysis and recommendations to inform business prioritiesWhat you'll need to have Be a pharmacist or have a Bachelor's degree or higher in a health-related field with experience of the pharmacy sector Post graduate experience in research involving healthcare Deep understanding of the UK pharmacy and healthcare environment, especially within the community pharmacy sector Excellent organisational, analytical and presentation skills Collaborative and agile ways of working with multiple stakeholders that supports the delivery of healthcare and business outcomesIt would be great if you also have Graduate/Post graduate level qualifications in Health Economics Contributed towards published academic papers or reports Active engagement in professional committees, professional advisory groups, and / or NHS working groupsOur benefits Boots Retirement Savings Plan Discretionary annual bonus Generous employee discounts Flexible benefits scheme including holiday buying, discounted gym membership, life assurance, activity passes and more.We have a great range of benefits in addition to the above that offer flexibility to suit you - find out more at rewards.
This is an excellent opportunity for an experienced Clincial Trial Regulatory Specialist to join a global pharmaceutical company for an initial 12 months with the potential for this to be extended.
This role has come about due to expansion and an increase in the production of pharmaceutical.
This is an excellent opportunity for an experienced Clinical Trial Submissions Manager to join a global pharmaceutical company for an initial 12 months with the potential for this to be extended.
This role has come about due to expansion and an increase in the production of pharmaceutical.
Ensure the submission strategy for clinical trials planned globally are in accordance with the overarching global regulatory strategy and any risks and issues are highlighted to the Global Regulatory Project Team and study teams.
Deliver CTA regulatory strategies and operations for a designated portfolio of development compounds in specified geographic region.
General
SRG are currently looking for a Regulatory Affairs Manager for a Global Pharmaceutical Company who have opened a new vacancy within their Regulatory Affairs team on an initial 12 Month basis to be based at their office in Maidenhead.