Due to growth my client are looking to recruit a Director Of Consultancy Services - Life Sciences CRO in a new remote role.

The Clinical Supplies Manager is instrumental in timely planning, accurate forecasting and managing investigational supplies for all phases of clinical trials. The position requires flexibility, teamwork, attention to detail and rapid response to issues as they arise

You will be the technical lead for Viral Vector Analytics, developing analytical assay procedures, providing analytical services to support commercial and major R&D projects, and contributing to the development of new analytical assays.

This is an exciting opportunity to join a well established Research and Development company in the cell and gene area, my client is looking for someone passionate about Quality to join their team and grow their expertise. This is a permanent position and is based in Oxford.

As Head of Policy & Science you will develop the policy function and lead the UK-based science team to better align key research projects with upcoming policy needs, ensuring the science agenda contributes to and influences policy change.

• Applying comprehensive understanding of S&N's commercial priorities in setting the clinical strategy for the AWM portfolio

• Applying comprehensive understanding of S&N's commercial priorities in setting the clinical strategy for the AWM portfolio

• Providing oversight as delegation to ensure study delivery of both internally - run and outsourced studies.

The Senior Editor is a remote role for a large Med Comms agency. They are looking for you to act as a role model to junior team members and lead the team.

Review clinical trial documents; SAPs, CRFs, CSRs
Program and QC TFLs

In this role you will be writing regulatory and clinical documents such as clinical study reports and DSURs. You will be providing expertise in Medical Writing, leading the in house Medical Writing function.

Taking on projects and representing analytical development as a customer contact

The role will be part of a small team of regulatory data specialists and will focus on providing support for the Product and Lifecycle Registration (PLcR) capability based on the InSight for Registrations software platform. This is a global role focussed on supporting the data needs in EU, US and Rest of the World.

Exciting opportunity to join a growing pharamceutical business to a newly formed role as Regulatory Affairs And Pharmacovigilance Specialist.

The Principle Regulatory Affairs Specialist will develop Regulatory strategies related to regulatory documents, submissions, investigations, product development planning and regulatory agency interaction

Leads Regulatory Affairs MDR projects with small to medium complexity to develop and commercialize new products for the company

To combine knowledge of scientific, regulatory and business issues to enable product development, manufacture and life cycle maintenance to meet applicable regulatory requirements and applicable technical standards.

Responsible for overseeing processes for Design Examination; Technical Documentation reviews and Vigilance for medical devices, with particular emphasis on Pre-Clinical and Clinical issues. Ensure the effective interaction between Product Assessors, In house Clinicians and Medical Device Technical team to provide an efficient and compliant service to the approved body and global delivering affiliates.

This role is part of the MDR project for a global leading Medical Devices manufacturer.

The Regulatory Affairs Specialist will be responsible for determining and supporting the regulatory activities which lead to, and maintain regulatory compliance and approval for the company products globally

The Regulatory Affairs Specialist is responsible for determining and supporting the regulatory activities which lead to, and maintain regulatory compliance and approval for products globally

Exciting opportunity to join a fast growing globably pharamaceutical in the UK and IRE team.

Exciting opportunity to join a marketing leading pharmaceutical provider.

This role contributes to the success of the Regulatory Affairs department by managing, collecting, storing and maintaining all documentation related to Regulatory Affairs.

Exciting opportunity to join a fast growing and innovative consultancy looking for a Associate Director to join the high performing team.