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- Responsible for orchestrating and managing clinical aspects of regulatory strategies
- Review of clinical data, oversight of analyses and interpretation of trial data and
- Lead cross-functional asset team(s) to drive project strategy and participate in clinical
- company boards, and externally, including investors, medical and regulatory
- Lead interactions with academic thought leaders, investigators, and other clinical
- Demonstrating leadership through compliance and promotion of all company policies,
- Complete all appropriate GXP/SOP training and adhere to all role specific SOP
- 5 years minimum experience in clinical practice treating patients and pharmaceutical
- Experience in Phase 1-3 clinical research and trial designs as well as the successful
- Must have a thorough knowledge of clinical research concepts, practices, and GCP
- Northreach is an equal opportunity employer and we do not discriminate against any employee or applicant for employment based on race, colour, religion, sex, national origin, disability, or age. We are committed to promoting diversity, equity, and inclusion in the workplace and hiring practices, therefore only partner with businesses that promote DEI.
Clinical Study Manager - Oxfordshire, United Kingdom - Northreach
Description
Northreach is a fast growing and next gen recruitment business set up in 2015, specialising in Biotechnology, IT, Finance and Embedded Talent Acquisition solutions in the UK, USA and Middle East.
We're a growing company that believes in offering outstanding delivery, over and above quality and a consistency which our clients love.
We operate from a modern, fully serviced and spacious office, a stone's throw from Billericay station.As well as a nifty casual dress code, we work with a smart attitude, supporting one another achieve personal goals and targets.
To become the number one, go-to agency in the Biotech and Fintech marketplace. My client, is a growing Biotechnology company at the forefront of groundbreaking Cancer Research.It is an exciting time for the business as they look to take a new indication of their technology to the clinic within the autoimmune disease space.
Reporting to the Chief Medical officer, the Medical Director will drive the strategy andexecution of new clinical development assets across my client. responsible for the strategy, medical oversight, direction and execution of the company's
clinical development plans.
well-financed cutting-edge Biotech companies, employing a truly novel corporate model
transformative medicines.
Development of clinical strategies and planning for small molecules,
including drafting of clinical trial protocols.
Contribute to the maintenance of an external data room as appropriate.
Oncology preferred
development