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 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

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.

In this role you will be writing regulatory and clinical documents such as clinical study reports and DSURs. You will be providing expertise in Medical Writing, leading the in house Medical Writing function.

• Support and collaborate with the study management team.
• Contribute to the functional and leadership aspects of the business process cycle.

In this role you will be working within the clinical strategy operations function in late phase for R&D.

You would be joining a growing team as a Senior Regulatory Writer in an expanding Med Comms business. You would have experience in CTD Modules, ISS, ISE, Scientific advice/briefing documents.

• Provide statistical consultancy to the clients and colleagues understanding the research questions
• Develop and deploy novel and computationally challenging statistical analysis for ongoing studies

Taking on projects and representing analytical development as a customer contact

The Technician will work within the Process Development team to provide key support in the development of Gamma Delta T cell therapy products. The role will consist of a mixture of routine lab maintenance (stock control, cell line maintenance, record-keeping) as well as lab activities to support process development projects

Business development with a global remit.

Looking for a successful candidate to become a Senior Manager, Bioinformatics to create new methods of interpretation and analysis of next generation sequencing in generated data using TPS.

We are currently hiring a Facility Manager to oversee the daily operations and compliance of a pharmaceutical animal testing facility.

This role is to provide pre clinical expertise to support Medical Writing activities for product lifecycle management and regulatory submissions.

To identify & evaluate clinical and pre-clinical stage opportunities to expand pipeline in oncology, CNS, woman health, paediatrics and other new Therapeutic areas through innovative partnerships & licensing in activity.

Overseeing data management and direct line reports to meet project objectives.

Fully remote role that offers project autonomy and the opportunity to develop junior members of staff.

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.

Overseeing support functions to cross functional teams both internally and Clint focused

As a Statistics manager you will be overseeing various projects and managing a team to ensure project deadlines are met within client and regulatory specification.

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.

As a Regulatory Affairs Associate / Senior Associate you will be responsible to provide technical and regulatory input to new development projects at Cycle and support the planning of ongoing product registrations at Cycle. You will be working across different therapeutic areas.

Co-ordinates, prepares, submits and follows up registration applications to the UK and/or Irish regulatory authorities, expeditiously and to high standards, to ensure that marketing authorisations are obtained and maintained in line with the company's plans and goals. Provide support in the preparation, distribution and follow up of registration documentation required for UK and Ireland.

The local role is essential for Scientific Affairs to stay close to its most important stakeholders: the customers, patients, consumers and HCPs.

The Senior Regulatory Affairs Specialist will develop Regulatory strategies related to regulatory documents, submissions, investigations, product development planning and regulatory agency interaction

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.

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.

This role is part of the MDR project for a global leading Medical Devices manufacturer.

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