- Regulatory Program Manager
Our client is a pioneer in Drug Discovery and Development. As a leading Pharmaceutical company, they work in a vast number of drug & therapeutic areas and are highly recognized internationally. They are currently looking for a Regulatory Program Manager
- Regulatory Program Manager
Responsible for regional (EU, ROW) regulatory strategic and operational management of a project, or part of a complex project, or a portfolio of projects
Primary Responsibilities and Accountabilities:
Represents and/or supports the Regulatory Leader in representing the regional function on cross-functional teams (e.g. ...
- Regulatory Affairs Project Manager
You will be preparing and delivering regulatory operational plans for assigned projects/products. Project manage regulatory submissions to agreed deadlines. Be provide regulatory and intelligence and guidance in cross-functional teams. Be able to work flexibly within and across Therapeutic Areas to ensure the delivery of product team and business objectives.
- PW 6524 Clinical Science Director / Clinical Development Director
As Clinical Science Director for this small, global Pharma Company based in London, you’ll have responsibility for all scientific aspects and strategic planning of EU & US clinical projects across a broad range of therapeutic areas. You’ll hold responsibility for implementing Clinical Development Plans, whilst managing effective communication with internal and external stakeholders regarding issues and actions related to the successful completion of projects.
- Regulatory Submissions Manager
As a Regulatory Submissions Manager you will be working for a niche bio-pharmaceutical company, which develops medicines for unmet medical needs. The company is at the forefront of developing therapeutic and diagnostic solutions to address patient needs in metabolic and inflammatory diseases currently recruiting for a Regulatory Submissions Manager.
- UBC- Regulatory Manager, Research & Clinical Services (London)
Responsible for the supervision, training and mentoring of the EU regulatory affairs team.Responsible for process implementation and ensure process compliance within the EU regulatory affairs team.Create high quality reports and other outputs according to the defined specifications to ensure timely reporting of team metrics to senior management.To ensure that new studies are registered correctly and in a timely fashion.
- Senior Regulatory Affairs Manager (Associate Director Level) North Carolina - USA
An Excellent opportunity have arisen to work in one of the most exciting areas of modern medicine within this innovative pharmaceutical company within the US - North Carolina - OFFICE based in the RTP - PERMANENT postion.
- Clinical Programme Manager (Oncology)
Key People are recruiting for an office based Clinical Programme Mananger for a global pharmaceutical company in France
- Quality Assurance Manager - Surrey
Quality Assurance Manager - Surrey
Our client is a globally recognised company specialising in IVD's and medical devices operating in over 50 countries worldwide.
- **Senior Pharmacovigilance Quality Manager - Belgium**
A large and well known Global Pharmaceutical company is looking to make additions to the Pharmacovigilance Quality team in Europe. This role of Manager/Senior Manager will be based from their Brussels office. The chosen candidate will have experience conducting and leading PV Audits on a Global level, and will also be adept in working with the PV Quality System. In this role you will be implementing a strategy, including delivery of a risk based audit program.