Due to growth my client are looking to recruit a Director Of Consultancy Services - Life Sciences CRO in a new remote role.
- Remote Role
- Contract and Perm Opportunity
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
- Competitive Salary
- Flexible Working
- Applying comprehensive understanding of S&N's commercial priorities in setting the clinical strategy for the AWM portfolio
- Flexiblity
- Competitive salary
- Applying comprehensive understanding of S&N's commercial priorities in setting the clinical strategy for the AWM portfolio
- Flexiblity
- Competitive salary
- Providing oversight as delegation to ensure study delivery of both internally - run and outsourced studies.
- Flexiblity
- Competitive salary
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.
- Join a market leader in Med Comms
- Further your career as an Editor
Review clinical trial documents; SAPs, CRFs, CSRs
Program and QC TFLs
- Flexiblity
- Competitive salary
Taking on projects and representing analytical development as a customer contact
- Flexiblity
- Competitive salary
The Principle Regulatory Affairs Specialist will develop Regulatory strategies related to regulatory documents, submissions, investigations, product development planning and regulatory agency interaction
- Global Medical Device Business
- Excellent career progression opportunities
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.
- Fantastic opportunity to be apart of a global Medical Device Business
- Great opportunity to be apart of a dynamic team working on exciting projects
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.
- Competitive Salary
- Flexible Working
This role is part of the MDR project for a global leading Medical Devices manufacturer.
- Excellent opportunity to work for a leading Medical Devices manufacturer
- Excellent opportunity to join a dynamic team, working on exciting MDR projects
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
- Fantastic opportunity to be apart of a global Medical Device Business
- Excellent opportunity to join a dynamic team, working on exciting MDR projects
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
- Fantastic opportunity to be apart of a global Medical Device Business
- Excellent opportunity to be apart of a globally growing business
This role contributes to the success of the Regulatory Affairs department by managing, collecting, storing and maintaining all documentation related to Regulatory Affairs.
- Excellent opportunity to work for a global Med-Tech business
- Great opportunity to be apart of a dynamic team working on exciting projects
Exciting opportunity to join a fast growing and innovative consultancy looking for a Associate Director to join the high performing team.
- Remote Based Role
- Rapidly Expanding Consultancy
