Future Tech Jobs
Future Tech Jobs
This role involves leading the clinical development and strategic oversight of a medicine for cardiovascular and renal conditions. Responsibilities include managing the Clinical Development Team, ensuring high clinical and scientific standards, and authoring key study documents and regulatory submissions.
This role involves leading and developing scientific communication strategies for biopharmaceutical and biotechnology clients. Responsibilities include building strong client relationships, producing high-quality scientific content, and driving business growth through strategic insights and effective team leadership.
This role involves placing photo biomodulation devices into retail locations across Central London. Responsibilities include researching target locations, booking meetings, and providing initial training to staff. The role is about building face-to-face relationships and ensuring successful free trial placements.
Senior Biomedical Scientist Training Lead | Pathology | Full Time | Permanent | ManchesterJob PurposeTo assist in the organisation, management and development of services within a specialised area of the pathology service, or across a range of services provided by...
Clinical Application Specialist – EndoscopyWales & West MidlandsWe’re partnering with a leading global healthcare organisation to recruit a Clinical Application Specialist supporting advanced endoscopy solutions across Wales and the West Midlands.This is a field-based, hands-on role where you’ll work closely...
This role involves developing and implementing biomarker strategies to support the clinical development of late-stage oncology assets. Responsibilities include collaborating with cross-functional teams, validating biomarker strategies, and integrating them into clinical plans to optimize decision-making and identify patient populations. The role also involves managing relationships with various stakeholders and contributing to scientific credibility through publications and presentations.
This role involves developing and implementing biomarker strategies for late-stage oncology clinical trials, collaborating with cross-functional teams to identify patient populations and optimize clinical decision-making. The Director will leverage cutting-edge technologies and methodologies to validate biomarkers and support clinical success.
This role involves leading the clinical safety strategy for drug projects and products, evaluating safety data, and managing risk to patients. You will work closely with regulatory agencies, contribute to global submissions, and ensure the safety and efficacy of AstraZeneca's products throughout their lifecycle.
This position will lead the transformation of project leadership capabilities across the R&D enterprise. On a systemic level, this role will prepare critical GPL roles (Exec Directors) to be CEO of the project via a bespoke leadership/drug development/executive training and...
CSL's R&D organization is accelerating innovation to deliver greater impact for patients. With a project-led structure and a focus on collaboration, we’re building a future-ready team that thrives in dynamic biotech ecosystems. Joining CSL now means being part of an...
This role involves leading the clinical safety strategy for drug projects and products, ensuring the safety and risk management of AstraZeneca's pharmaceuticals. You will work on evaluating adverse events, communicating safety data, and contributing to regulatory submissions, all while collaborating with a global team of experts.
The role involves working in Cell Process Development, supporting projects related to the development and characterization of CAR T-cell manufacturing processes. Responsibilities include laboratory support, flow cytometry, aseptic cell handling, and data analysis. The candidate will gain hands-on experience with various analytical techniques and equipment, and work cross-functionally with R&D and PD departments.
The QC Technician will perform quality control inspections, test materials and finished products, maintain accurate records, and support the Quality Assurance team to ensure compliance with GMP standards. The role involves working in a busy manufacturing environment, maintaining high levels of accuracy, and collaborating with production and QA teams.
This role involves designing and delivering bespoke pharmaceutical process equipment and systems, ensuring compliance with strict regulatory standards. Responsibilities include conducting site surveys, producing detailed drawings, and collaborating with multidisciplinary teams to ensure integrated system functionality.
POSITION SUMMARYYou will provide clinical and scientific support for global Phase 1–4 vaccine clinical studies within the Vaccines portfolio. Working in close partnership with clinical colleagues, this role contributes to study design, clinical data review, safety oversight, and scientific integrity...
ROLE SUMMARYAs a leading biopharmaceutical company, Pfizer is dedicated to the discovery and delivery of high value therapies across a variety of disease areas. It is our mission to bring innovative medicines to patients that significantly improve their lives, and...
