Exciting opportunity to join our Life Sciences Team who have had a extremely succesful year and won a numbe of large client projects.

As a Research Associate/Scientist in the newly-formed biopharma team you will be supporting analytical development for analysis of biopharma/biosimilars. You will support with a range of techniques such as HPLC/UPLC, Mass Spec, UV/Vis plates and more.

As a Research Scientist in the bioanalytical department you will be responsible for supporting mammalian cell culture passaging, design & optimisation of a range of bioassays, and supporting process development and validation.

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

As a Senior Engineer supporting the R&D Team you will be responsible for leading a range of projects relating to product and process maintenance/improvements, developing and executing a range of tests whilst complying with regulatory standards.

• 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.

This role is responsible for managing a portfolio of clinical trials and research studies, providing oversight and direction to project delivery team for the full project life cycle. The projects span a variety of indications and trial phases including those in start-up or complex delivery stages.

The Senior Project Manager role will oversee and provide direction for full project life cycle support to all assigned projects. The role will be responsible for a wide portfolio of projects ranging from start-up, delivery phase and those to be handed over once established. This pivotal role ensures project delivery, achieving targets and continuous improvement by collaborating with other departments, external partners, sponsors and customers.

The GCP QA Manager is responsible for implementing and maintaining Good Clinical Practice (GCP) compliance programs to support clinical trial activities

The post holder will work with and support the Clinical and Quality teams to ensure operational excellence and to exercise overall responsibility for compliance of clinical development with GCP.

I'm currently recruiting for a Quality Manager to join a well established Medical Device company in Cambridge. You will be required to manage the Quality Team, Compliance, QMS and you will also have some exposure to the HSE of the company as well.

As a QC Stability Analyst based in Liverpool you will be responsible for assisting with stability studies, supporting with protocol generation, setting up studies and subsequent data analysis.

This role entails adapting and reviewing a variety of documents to ensure that the clients needs are met. You would be part of a global business but a small writing team, meaning the training you receive will be personal.

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.

You will engage with C-suite pharma and biotech executives and through focused lead-generation help build research-driven industry-leading agendas to support the growth targets of the Pharma events portfolio

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

You will be responsible for oversight of user-initiated clinical activities, data gathering, generating clinical materials including medical science and evidence generation activities. You will support the research activities and work with the clinical, regulatory and marketing teams towards the organisations goals in expanding US and global indications for the device.

Developing and further detailing out Integration Workplan together with Single Point Of Contacts (SPOC) of affected business functions.
Frequent follow-up on status of the various integration actions of the Integration Workplan and corresponding reporting.
Support SPOC / Function in resolving upcoming challenges when implementing integration workplan.

This role is a hybrid role with the business based in Cambridge. You would be responsible for operations, projects and external events alongside pushing engagement activity in collaboration with other teams within the organisation.

An exciting opportunity to a join growing Medical team, looking at candidates with Medical Communications experience.

Under the supervision of the Clinical Trials Manager we are looking for an energetic, focused individual to set up, monitor and close-out clinical trials involving the Swift medical device. This position is a key role and is ideal for a candidate who has experience in clinical research trials.

As a Lead Scientist you will be responsible for conducting manufacturing operations of pharmaceutical early-phase product, ensuring adherence to GMP at all times. You will support and co-ordinate daily activities of the wider team.

An exciting opportunity to a join growing Medical team, looking at candidates with Medical Advisor experience looking to further develop their career.

An exciting opportunity to a join growing Medical team, looking at candidates with Medical Advisor experience looking to further develop their career.

As a Technical Advisor you will support the Environmental Health sector of group with focus on the area of insecticides for both Custom Solutions and Branded Products. This includes support of ongoing product development projects.

The role consists of developing and growing our clients global access solutions working closely with members of senior management team and consulting colleagues. This will include project management/delivery and business development.

• CDISC data standard experience.
• Based in the UK.

• CDISC data standard experience.
• Based in the UK.

• CDISC data standard experience.
• Based in the UK.

• Bachelors in Computer Science.
• Based in the UK.