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Regulatory Clinical Trials Submission Manager
UNITED KINGDOM, , UNITED KINGDOM
ProPharma Group is the leading global, independent, single-source provider of regulatory, clinical, and compliance services serving pharmaceutical, biotechnology, and medical device companies. Our team of experts brings a comprehensive portfolio of regulatory sciences, clinical research solutions...
Head Of Clinical Data (Healthtech/Clinical Trials)
LONDON, ENGLAND, UNITED KINGDOM
Overview The Clinical Data Lead holds a pivotal role within a Series A healthtech/clinical trials company, requiring a candidate with a medical background. They will spearhead the establishment and management of crucial clinical data contracts with hospitals, both domestically and internationally...
Regulatory Specialist
MAIDENHEAD
p strong SRG /strong are currently looking for Regulatory Specialist for a Global Pharmaceutical Company who have opened new vacancies within their Regulatory team on an initial 12 Month basis to be based at their office in Maidenhead/Remote. /p p br br Learn more about the general tasks...
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CLINICAL NURSE MANAGER II- ONCOLOGY DAY WARD (Relocation - Cork)
£48,944 - £57,863 a year
, GB
CLINICAL NURSE MANAGER II- ONCOLOGY DAY WARD br / br / Full-time Permanent br / br / Are you an Oncology Nurse Manager looking to relocate to Ireland? br / br / Bon Secours Hospital Cork offer a top remuneration package along with a relocation package . Please contact Aine via...
Chief Executive Officer of the Royal Free Hospital
Competetive
LONDON, UNITED KINGDOM
...the development and clinical trials of the vaccines for COVID-19. We are a major teaching and research centre and one of the major partners of UCL university and deliver nationally and internationally renowned specialist clinical services alongside a wide range of local core services. The...
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Regulatory Clinical Trials Submission Manager
UNITED KINGDOM, UNITED KINGDOM
p ProPharma Group is the leading global, independent, single-source provider of regulatory, clinical, and compliance services serving pharmaceutical, biotechnology, and medical device companies. Our team of experts brings a comprehensive portfolio of regulatory sciences, clinical research...
Head of Clinical Data (Healthtech/Clinical Trials)
LONDON, ENGLAND, UNITED KINGDOM
Overview The Clinical Data Lead holds a pivotal role within a Series A healthtech/clinical trials company, requiring a candidate with a medical background. They will spearhead the establishment and management of crucial clinical data contracts with hospitals, both domestically and internationally...
Maternity Sales Specialist
BIRMINGHAM, WEST MIDLANDS (COUNTY)
MATERNITY SALES SPECIALISTNATIONAL/ BIRMINGHAM£55K + CA + 30% BONUSSUMMARYOur global medical devices client is looking for an experienced Maternity Sales Specialist with a clinical or sales background in maternity. This role will work with current Sales, clinical and marketing team in...
Regulatory Specialist
MAIDENHEAD, ENGLAND, UNITED KINGDOM
SRG are currently looking for Regulatory Specialist for a Global Pharmaceutical Company who have opened new vacancies within their Regulatory team on an initial 12 Month basis to be based at their office in Maidenhead/Remote. The Role: The Regulatory Associate is responsible for providing global...
Clinical Psychiatrist
, , UNITED KINGDOM
Clinical Research Psychiatrist London CRO focused in Psychedelic Therapies The Company Carrot have partnered with an innovative and leading Research organisation specialising in the delivery of scientifically grounded Clinical Trials using its collaborative Contract Research Organisation...
Senior Clinical Quality Assurance Specialist
, , UNITED KINGDOM
...Quality Assurance Specialist to join their team. This successful candidate will be reporting to the Senior Clinical Quality Assurance Manager coordinate the implementation of the company quality management system relevant to GCP (including laboratory analysis of clinical samples) including...
Clinical Data Programmer
UNITED KINGDOM, , UNITED KINGDOM
One of our clients is seeking Clinical Data Programmers to the support the clinical data systems programming. Role The Clinical Data Programmer will support the configuring and management of studies in the clinical repository system. This is an exciting opportunity to be involved in end-to-end...
Associate Director/Senior Manager, Clinical QA (remote)
LONDON, ENGLAND, UNITED KINGDOM
Proclinical is seeking an Associate Director, GCP Quality to contribute to the mission of developing better medicines, faster to work remotely. In this role, you will lead the GCP Quality support for interventional clinical trials, serve as a GCP Quality expert to the business, and establish strong...
Quality Assurance Specialist
, , UNITED KINGDOM
...Medicinal Product for clinical trials. Provide input to support of Packaging, Labelling & Distribution of IMP as required. In addition, you will support the delivery of QA activities for their assigned portfolio of projects and provide advice to support the development, implementation and...
Quality Team Lead
LEICESTER, ENGLAND, UNITED KINGDOM
Are you experienced in GMP, with a quality background and people management experience? We have a Quality Team Lead opportunity within the Quality team here at Myonex. This is a role leading a GMP team to label and pack product for clinical trials, as well as work cross-functionally to support...
Associate Director - Quality Assurance
, , UNITED KINGDOM
...high level specialist expertise to both the A team and key stakeholders in relation to this manufacturing site. The role has responsibility for building and managing a small team of A professionals and creating a strong quality culture on the site. The individual will deputise for...
External Data Manager
UNITED KINGDOM, , UNITED KINGDOM
...development strategy / clinical trial / and data management processes. Previous experience in a data management role. Understanding of different types of data sources within clinical trials. Ability to drive decision making and influence study teams. This role will see you work on a global scale...
Director Regulatory Affairs
, , UNITED KINGDOM
...possible approvals of clinical trials and marketing authorization applications. What you will do: As the Regulatory Affairs Director, your duties and responsibilities will include: Managing all aspects of submissions relevant to assigned projects and programs, in accordance with submission and...
GCP QA Manager
OXFORDSHIRE, ENGLAND, UNITED KINGDOM
We are currently working with a pharma organisation who are a growing ecosystem of drug development companies, that provide integrated and specialist operational support for rapidly scaling biotech ventures. They are looking for a GCP QA Manager who will work closely with the Head of Quality and...
Technology & Science (Insurance) Account Executive
GREATER BRISTOL AREA, UNITED KINGDOM, UNITED KINGDOM
Our client are a leading insurance and risk management advisor to the Technology /Life Science sector, offering specialist insurance and best in class service to the sector. Working with ambitious start-ups through to large multi-national businesses and providing a full client service, taking care...
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