Life Sciences recruitment consultant working with organisations that need help to find top talent that can help them succeed in their endeavour to save patients lives across the globe.

A hugely varied and autonomous paralegal role in a rapidly expanding business.

Leading the Risk and outsourced Internal Audit function of a fast-paced life sciences non-profit in London.

Senior Policy Associate (life sciences)

- Fast-growing global Medcoms business (circa 400 people)

- Permanent TA Manager role - Salary £45,000-55,000 based on experience - Central London based with flex working

My client is a top 10 CRO who are at the forefront of scientific discoveries into new treatments. Offering a wide range of bio-pharmaceutical services to a diverse portfolio of clients. They are looking for a Senior Clinical Research Associate who is an innovative, tech-savvy problem solver that is confident and resourceful. The successful candidate will be joining a business that is dedicated to both the personal and professional growth of their team.

Execute Qualified Person (QP) responsibilities, duties, batch certification and disposition as defined in 2001/83/EC, 2001/82/EC, 2011/62/EU and Eudralex Volume 4, Annex 16.

If the product is to be released to the US market, all appropriate cGMP's requirements as defined is US. "CFRs" and other relevant regulations should be complied with.

Reporting to the Innovation Adoption Director, the Head of Digital and AI is responsible for the leading, delivering and measuring the impact of programmes and projects, to facilitate the development and adoption of digital, artificial intelligence (AI) and robotic innovation in the health and social care sectors, including development and maintenance of the Digital Health Ecosystem Wales (DHEW) programme.

This role is responsible for ensuring that all Lintbells products comply with the regulations of the regions that Lintbells want to distribute in to enable the business to achieve it's desired goals.

Exciting opportunity to join a global well known pharmaceutical business who have ambitious growth plans and due to expansion are looking for a Regulatory Affairs Manager to join the team.

You will be joining an industry-leading bio-pharmaceutical company as a QC Incoming & Components Analyst compliantly performing component testing, data review and data interpretation in accordance with approved SOPs.

You will join a faced-paced environment as a QC Analyst performing QC laboratory testing, data review and data interpretation in accordance with approved SOPs.

To ensure continued compliance with all relevant regulatory requirements

QC Validation Specialist (Initial 6 month contract)

To co-ordinate the validation activities within the production facilities at Liverpool to ensure that the appropriate site and regulatory standards are applied and work is completed in a timely manner.

Supporting the implementation of specialist test isolators.

Site based with some working from home.

This is an exciting opportunity to join an industry leading company working on cutting-edge vaccinations. They are looking for an exceptional candidate to join as a QC Validation Specialist, responsible for co-ordinating validation activities within the production facilities at Liverpool, and to ensure the appropriate site and regulatory standards are applied with work being completed in a timely manner.

To ensure regulatory compliance of products globally, drive regulatory processes and activities such as change control and continue to develop strong working relationships with internal and external customers.

Job Summary

Manage end-to-end delivery of data management services for all projects with minimal guidance, ensuring quality deliverables on time and within budget, to customer satisfaction. Provide comprehensive data management expertise to Clinical Data Management (CDM) team to provide high-quality data management products that meet customer needs. with the option to join the FSP team, Generalist team and/or the RWE team.

To operate as Statistics Manager, leading on technical tasks as project manager, managing career progression within the team and supporting the business operations management team. You can choose to be allocated to FSP team, generalist team, and/or real World evidence team depending on your preference and where your skills best suit you so you will be able to maximise your impact on the business, using your expertise.

Purpose of the role

You will be reporting to the Global Head of the Antibody Discovery.

Purpose of the role

You will be reporting to the Head of Research carrying out work related to antibody discovery.

Purpose of the role

As a Senior Statistician, you will function independently as a project lead or lead statistician. You will be overseeing all statistical aspects in the design and analysis of clinical trials, including project management, statistical analysis, report preparation, and advising other less senior statisticians.

Purpose of the role

As a Principal Statistician, you will lead in statistical, process and regulatory knowledge to the department. Act as the most senior reviewer on projects, and with additional oversight as needed on more complex studies. You will be involved throughout the full clinical trial process, from study design and protocol writing, over defining the statistical analyses (SAP) to reviewing all study outputs and the CSR.

Permanent Quality Assurance analyst for a start-up Biotechnology company based in London. Role includes ownership of documentation within companies eQMS systems, assisting and creating SOPs, developing clear plans and communicating them to the team ad management.

Great chance to be a part of a established CRO and a Global start up at the same time.

The company are searching for an exceptional Quality Control Executive to work within their in-house Technical and Quality Department based in London. The role will entail monitoring quality requirements and trends against the product, and raising / querying quality issues.

You will project manage the overall development, verification and validation of the Company's products to regulatory compliance and market requirements.

• You will lead a project team to develop and deliver diagnostic assays to meet the product requirements for launch in line with the company's goals and timelines.
• You will be responsible for the technical leadership of the project as well as the continuous growth and development of the projects scientific team.

The purpose of this role is to educate the healthcare community

Medical Monitoring with a Medical Strategic input

SAS Programming opportunity for someone with a minimum of 2 years experience working with SAS. You will have the opportunity to work with patient data in an industry leading Real World Evidence organisation.