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If you are a current Jazz employee please apply via the Internal Career site. Jazz Pharmaceuticals is a global biopharma company whose purpose is to innovate to transform the lives of patients and their families. We are dedicated to developing life-changing medicines for people with serious diseases — often with limited or no therapeutic options. We have a diverse portfolio of marketed medicines, including leading therapies for sleep disorders and epilepsy, and a growing portfolio of cancer treatments. Our patient-focused and science-driven approach powers pioneering research and development advancements across our robust pipeline of innovative therapeutics in oncology and neuroscience. Jazz is headquartered in Dublin, Ireland with research and development laboratories, manufacturing facilities and employees in multiple countries committed to serving patients worldwide. Please visit ___ for more information. Location: This role can be based either in Cambridge or Kent Science Park, Sittingbourne Job Role: We are looking for dynamic, creative, and talented computational chemist to join our expanding Discovery & Medicinal Chemistry Department. Reporting to the Director of Medicinal Chemistry, you will apply your expertise, leadership and guidance to discover and develop novel small-molecule therapeutic agents. You will be working within a patient-focused, science-driven, and multi-disciplinary biopharmaceutical environment, covering all stages of the drug discovery process. You will collaborate with scientists from other disciplines within Jazz Pharmaceuticals and with external collaborators to build an innovative portfolio of therapeutics across our exciting and growing oncology and neuroscience pipelines. Working at the forefront of drug discovery you will advance projects from target selection to preclinical drug candidates and FiH trials, and contribute to the growth of the medicinal chemistry team. Key Responsibilities: • Utilize modern molecular modelling methods to support different stages of R&D programs., • Collaborate effectively with other departments and functions to advance research discovery projects expeditiously from hit identification to high quality preclinical candidates., • Design, lead and drive computational studies on projects throughout the several discovery phases and ensure execution on agreed deliverables., • Opportunities to lead or co-lead projects in addition to drive discipline-specific endeavours., • Set the vision and strategy for computational chemistry., • Foster innovative thinking in all areas of departmental activities, with a particular focus on computational and medicinal chemistry., • Manage CRO compchem activities, providing expertise and guidance., • Present plans and results internally, including at board level, and externally at conferences., • Contribute to the writing of patent applications, scientific publications, and internal reports., • Develop and mentor less experienced staff., • Keep up to date with the latest scientific advances and trends in drug discovery to deliver the next-generation therapies., • MSc/PhD in a relevant scientific discipline (Pharmaceutical Sciences, Chemistry, Computational Chemistry) with a solid foundation in molecular modelling built in a pharma/biotech/CRO setting., • Expert knowledge in CADD software packages and modern molecular modelling techniques., • Sound knowledge in cutting-edge cheminformatic tools, AI/ML-enabled technologies, and in silico drug design, including both structure- and ligand-based methodologies., • Passion for drug discovery with a deep entrepreneurial and problem-solving attitude., • Mastery of all the theoretical and practical principles of medicinal chemistry and drug design., • Broad knowledge of biophysical, biochemical, and cell-based assays used in the early stages of the drug discovery process., • In depth understanding of multi-parameter optimization and ability to integrate disease biology, ADME/DMPK and toxicology data to solve complex drug discovery problems., • Excellent leadership, management, organizational and team-working skills, and a talent to deliver project milestones within the expected time frame., • Demonstrated track record of scientific publications., • Exceptional oral, written, and interpersonal communication skills, and ability to develop and grow strong cross-functional collaborations. #LI-onsite #LI-SM1 Jazz Pharmaceuticals is an equal opportunity/affirmative action employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability status, protected veteran status, or any characteristic protected by law. The successful candidate will also be eligible to participate in various benefits offerings, including, but not limited to, medical, dental and vision insurance, retirement savings plan, and flexible paid vacation. For more information on our Benefits offerings please click here: ___.

Electrician Cambridge £32,000-£34,000 + salary increase once fully trained + Training + Development + Pension + 40 days holiday Excellent opportunity for an electrician to join a leading research facility offering an incredible working environment and outstanding training to help you develop your electrical and engineering skills. This organisation is part of a renowned scientific research group, oper... ZIPC1_UKTJ

£37,364 to £44,614 per annum (depending on post-PhD experience) The Babraham Institute is a charity which is world renowned for its research in life sciences to enhance lives and improve wellbeing. We are seeking an enthusiastic and talented Postdoctoral Research Scientist to join the David group at the Babraham Institute in Cambridge. Our overarching goal is to discover mechanisms that promote healthy ageing and alleviate age-related diseases such as Alzheimer's disease. Our group has uncovered mechanisms that prevent age-related protein aggregation, a major contributor to functional decline. Notably, we discovered a proteostasis network that safeguards proteins from aggregation in the extracellular space in C. elegans (PMID: ). Our group is embedded within the Signalling Programme, which offers a vibrant, collaborative environment and access to world-class facilities. In this role, you will have the opportunity to develop an independent research project investigating mechanisms of protein quality control in the extracellular space. Your work will combine in vitro assays to characterize protein aggregation and in vivo studies in C. elegans using imaging, proteomics, and functional assays to explore how extracellular proteostasis influences organismal health. This position is ideal for a curiosity-driven scientist who thrives on tackling challenging questions and pushing the boundaries of knowledge. Applicants should hold a PhD in biochemistry, cellular or molecular biology, or a related discipline, and demonstrate a strong track record in academic research. Prior experience in molecular cloning and biochemical techniques, including protein purification and western blotting, is essential. Additional expertise in microscopy, cell culture and proteomics is highly desirable, and familiarity with C. elegans research would be advantageous, although not required. For more information on the work of the group, please visit: Informal enquiries can be made to Dr Della David at . Postdocs have access to excellent career development courses in the Postdoc Academy (University of Cambridge) and high-quality scientific training is offered by the different core facilities at the Babraham Institute. Funding for this position is initially available for three years. A full job specification can be found attached to this vacancy. Closing date for applications is Monday, 5th January 2026. We reserve the right to close the vacancy early depending on the volume of applications received. For further details about this position or to apply online visit Further information about the Institute can also be found on our website (). The Babraham Institute welcomes applications from all sections of society. NO AGENCIES PLEASE The Babraham Institute holds a silver Athena SWAN award and is committed to promoting and developing a culture of excellence, diversity and mutual respect that supports the Institute's ambitions and attracts highly motivated and talented people. The Babraham Institute abides by the principles of the government's Disability Confident Scheme and has a positive approach to employing disabled people. The Babraham Institute receives strategic funding from the Biotechnology and Biological Sciences Research Council and is an Equal Opportunities Employer.

If you are a current Jazz employee please apply via the Internal Career site. Jazz Pharmaceuticals is a global biopharma company whose purpose is to innovate to transform the lives of patients and their families. We are dedicated to developing life-changing medicines for people with serious diseases — often with limited or no therapeutic options. We have a diverse portfolio of marketed medicines, including leading therapies for sleep disorders and epilepsy, and a growing portfolio of cancer treatments. Our patient-focused and science-driven approach powers pioneering research and development advancements across our robust pipeline of innovative therapeutics in oncology and neuroscience. Jazz is headquartered in Dublin, Ireland with research and development laboratories, manufacturing facilities and employees in multiple countries committed to serving patients worldwide. Please visit for more information. Brief Description: The Associate Director, Medical Writing, is responsible for the efficient preparation of high-quality, strategically aligned medical writing deliverables within one or more program. S/he will work directly with cross functional teams to author regulatory documents (eg, protocols, clinical study reports, briefing books, submission documents, investigator brochures). For programs with multiple deliverables, s/he may be responsible for managing writers. The incumbent will ensure that strategically aligned communication points are conveyed in medical writing deliverables and that the communication points are consistent across program documentation. S/He will mitigate risk associated with medical writing and disclosure processes by contributing to Best Practices and SOPs. This role has global responsibilities, including participation in global teams and interaction with regulatory agencies in multiple regions. This role may have line management responsibilities. Essential Functions/Responsibilities Works with the cross functional team to ensure effective communication of data in the respective documents. Works with the cross functional team to ensure that communication needs for the clinical data are considered early in the development program to enable consistency of data presentation and messaging throughout the clinical program lifecycle. Analyzes study level documents for their ability to deliver the information required by the target audience (eg, health authorities). Communicates proactively and efficiently within the MW team and across R&D. Ensures quality of medical writing deliverables and that work on assigned projects adheres to departmental procedures / practices, and industry / international standards. Possible oversight of contract medical writers to ensure efficient preparation of medical writing deliverables for assigned clinical program(s) according to budget and timelines. Collaboration and strategic partnership with cross functional team members to ensure understanding of program strategy and the nature of medical writing services required to deliver on company objectives. Required Knowledge, Skills, and Abilities Exceptional English language skills and ability to write and edit complex material to ensure accuracy, clarity, and effectiveness. Clear understanding of lean authoring for clinical regulatory documents. A solid understanding of the clinical development process, including the documents that are required at each stage. For early development: knowledge of pre-clinical and nonclinical regulatory requirements and reporting is required. Prior contribution to, and an understanding of, global submissions. Expert MS Office skills with a special focus on word processing, tables, spreadsheets, presentations, graphics and templates. Excellent written and oral communication skills and demonstrated coaching and problem-solving abilities. Knowledge of ICH and CTD guidelines for clinical and regulatory submission documents Ability to think strategically; demonstrated negotiating skills and resourcefulness. Demonstrated ability to manage several projects simultaneously. Ability to critically analyze and synthesize complex scientific information. High degree of influencing skills in shaping and developing content and wording. Demonstrated ability to work collaboratively; multicultural sensitivity, builds positive and productive relationships, seeks input and demonstrates an appreciation for diverse views by incorporating them into decisions / proposals. Successful track record of leading complex clinical / regulatory writing projects. Demonstrated ability to make decisions even in the absence of complete information. An excellent understanding of all aspect of ICH-GCP; keen insight on external clinical publication practices and standards (ICMJE, AMA, GPP). Excellent organizational and time management skills and attention to detail. Required/Preferred Education and Licenses BA/BS with at least 8 years (or advanced degree with at least 5 years) writing experience in the pharmaceutical industry across therapeutic areas required. Advanced degree preferred. LI-DM1 Jazz Pharmaceuticals is an equal opportunity/affirmative action employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability status, protected veteran status, or any characteristic protected by law. FOR US BASED CANDIDATES ONLY Jazz Pharmaceuticals, Inc. is committed to fair and equitable compensation practices and we strive to provide employees with total compensation packages that are market competitive. For this role, the full and complete base pay range is: $154,400.00 - $231,600.00 Individual compensation paid within this range will depend on many factors, including qualifications, skills, relevant experience, job knowledge, and other pertinent factors. The goal is to ensure fair and competitive compensation aligned with the candidate's expertise and contributions, within the established pay framework and our Total Compensation philosophy. Internal equity considerations will also influence individual base pay decisions. This range will be reviewed on a regular basis. At Jazz, your base pay is only one part of your total compensation package. The successful candidate may also be eligible for a discretionary annual cash bonus or incentive compensation (depending on the role), in accordance with the terms of the Company's Global Cash Bonus Plan or Incentive Compensation Plan, as well as discretionary equity grants in accordance with Jazz's Long Term Equity Incentive Plan. The successful candidate will also be eligible to participate in various benefits offerings, including, but not limited to, medical, dental and vision insurance, 401k retirement savings plan, and flexible paid vacation. For more information on our Benefits offerings please click here: .

If you are a current Jazz employee please apply via the Internal Career site. \n Jazz Pharmaceuticals is a global biopharma company whose purpose is to innovate to \ntransform the lives of patients and their families. We are dedicated to developing \nlife-changing medicines for people with serious diseases — often with limited or no \ntherapeutic options. We have a diverse portfolio of marketed medicines, including leading \ntherapies for sleep disorders and epilepsy, and a growing portfolio of cancer treatments. \nOur patient-focused and science-driven approach powers pioneering research and development \nadvancements across our robust pipeline of innovative therapeutics in oncology and \nneuroscience. Jazz is headquartered in Dublin, Ireland with research and development \nlaboratories, manufacturing facilities and employees in multiple countries committed to \nserving patients worldwide. Please visit\n more information. \n Brief Description The Business & Technology Capabilities (B&TC) Sr. Analyst works closely with B&TC and GCDO colleagues, in collaboration with Information Services (IS) to support cross functional clinical study teams regarding the implementation and management of digital systems/technology used by GCDO including but not limited to Veeva Clinical Vault. The B&TC Sr. Analyst demonstrates a good understanding of Veeva Clinical Vault functionality. The B&TC Sr. Analyst works with the ‘Performance and Training’ function to facilitate the collation, visualization, analysis & storage of relevant metrics for GCDO to ensure optimal trial performance and aid continuous improvement Essential Functions/Responsibilities • Establishes and maintains, digital systems on behalf of GCDO primarily the Veeva Clinical Vault applications eTMF, CTMS, SSU and Site Connect, plus other Clinical Systems as required, • Carry out required activities in JV eTMF for all Clinical Vault/eTMF user access requests in accordance with the documented process, • Carry out required system maintenance in JV eTMF to ensure end users can perform their role in accordance with the documented process, • Works closely with Business owners and system owners of digital system including but not limited to Veeva Clinical Vault, to ensure GCDO teams are trained appropriately in the functionality of relevant digital systems, • Collaborates with other functional areas/departments and key stakeholders to maximize the utilization of the digital systems (e.g. creating dashboards, reports, ensuring best use of all Clinical Vault functionality, • Collaborates with partner vendors, as needed, in relation to system knowledge sharing and utilization, • Collaborates with subject matter experts on development of relevant digital system training materials, QMS documentation, and Validation activities and documentation, • Maintains a sound familiarity with Jazz’s systems and related processes, • Establishes and maintains, digital systems on behalf of GCDO primarily the Veeva Clinical Vault applications eTMF, CTMS, SSU and Site Connect, plus other Clinical Systems as required, • Carry out required activities in JV eTMF for all Clinical Vault/eTMF user access requests in accordance with the documented process, • Carry out required system maintenance in JV eTMF to ensure end users can perform their role in accordance with the documented process, • Works closely with Business owners and system owners of digital system including but not limited to Veeva Clinical Vault, to ensure GCDO teams are trained appropriately in the functionality of relevant digital systems, • Collaborates with other functional areas/departments and key stakeholders to maximize the utilization of the digital systems (e.g. creating dashboards, reports, ensuring best use of all Clinical Vault functionality, • Collaborates with partner vendors, as needed, in relation to system knowledge sharing and utilization, • Collaborates with subject matter experts on development of relevant digital system training materials, QMS documentation, and Validation activities and documentation, • Maintains a sound familiarity with Jazz’s systems and related processes, • Identifies improvement opportunities related to digital systems, and assists with developing enhancement plans and roadmaps, • Organizes and delivers relevant specialist training sessions and workshops with a key focus on digital systems Required Knowledge, Skills, and Abilities • IT-literate and passionate/experienced towards new technology and digital systems including, but not limited to Microsoft-based applications and Veeva Clinical Vault applications CTMS, eTMF, SSU and Site Connect, • An experienced clinical trials professional who is well versed in the field of clinical study management activities, combined with excellent project management, training & mentoring capabilities, • Previous experience working in Veeva Clinical Vault as an end user, business, or system administrator, • Ability to effectively interface with CROs and software vendor, • Previous experience working in clinical trials, with emphasis on GxP and compliance, • Has a sound working knowledge of clinical operations, clinical processes, Trial Master File regulations medical terminology, global CROs and vendor management, • Excellent interpersonal and communication skills, both written and verbal, • Good time management and organizational skills, • Quality driven with a focus on attention to detail, • Ability to work independently and take initiative, • Flexible approach with respect to work assignments and new learning, • Ability to prioritize workload and manage multiple and varied tasks with enthusiasm, • Ability to work effectively in a matrix environment and to demonstrate, and foster, teamwork within the group, as well as across the organization Required/Preferred Education and Licenses • A minimum of a BA/BS, preferably in the scientific/healthcare and/or technology field, • A minimum of 5 years of experience in clinical related technology for the pharmaceutical/biotechnology industry, • Knowledge of FDA/ICH guidelines and industry standard practices regarding the management of clinical trial data and studies., • Working knowledge of FDA Guidance Documents: Computerized Systems Used in Clinical Trials, General Principles of Software Validation. FOR US BASED CANDIDATES ONLY Jazz Pharmaceuticals, Inc. is committed to fair and equitable compensation practices and we strive to provide employees with total compensation packages that are market competitive. For this role, the full and complete base pay range is: $100,000.00 - $150,000.00 Individual compensation paid within this range will depend on many factors, including qualifications, skills, relevant experience, job knowledge, and other pertinent factors. The goal is to ensure fair and competitive compensation aligned with the candidate's expertise and contributions, within the established pay framework and our Total Compensation philosophy. Internal equity considerations will also influence individual base pay decisions. This range will be reviewed on a regular basis. At Jazz, your base pay is only one part of your total compensation package. The successful candidate may also be eligible for a discretionary annual cash bonus or incentive compensation (depending on the role), in accordance with the terms of the Company's Global Cash Bonus Plan or Incentive Compensation Plan, as well as discretionary equity grants in accordance with Jazz's Long Term Equity Incentive Plan. The successful candidate will also be eligible to participate in various benefits offerings, including, but not limited to, medical, dental and vision insurance, 401k retirement savings plan, and flexible paid vacation. For more information on our Benefits offerings please click here: .

Senior Software Developer (Full Stack) .UK or Canada, Hybrid / Remote .Full time, Monday to Friday .Who are Cambridge Cognition and what do we do?.We are a talented global team based in the UK, Canada and USA.Backed by over 30 years of scientific discovery and validation, Cambridge Co

Starting Salary £33,419 - £37,582 per annum (plus opportunities for paid overtime).MRC Laboratory of Molecular Biology, Cambridge Biomedcal Campus, UK.The MRC Laboratory of Molecular Biology, Cambridge (LMB) is an internationally recognised scientific research institution.We are looking to recruit

The job will provide full training so if you are from an Engineering background with some experience of mechanical or electrical maintenance then this could be the role for you. STEM Recruitment is a Scientific, Engineering and Manufacturing Recruitment business supplying talented staff to permanent

Scientific Operations Assistant Location: 20 Cambridge Science Hub, Bar Hill, CB23 8SQ Salary: Competitive, DOE + Excellent Benefits! Contract: Full time, Permanent, Monday – Friday, 8am – 5pm Benefits: 21 days holiday + 8 bank holidays and an additional day off for your birthday, compre

What You'll Need HNC (or higher) in Engineering or a Scientific discipline Experience in a lab, technical, mechanical or electrical environment A self-starter mindset with strong.

Develop strong working relationships with internal and external customers consulting with them to solve problems from a technical perspective. Working closely with the field sales team you will provide application, product knowledge and sale support during customer visits.

Electronics Engineer - Cancer Instrumentation - Cambridge A growing Medical Devices Division is currently seeking an Electronics Engineer to contribute to the development of new Cancer Instrumentation devices, based in South Cambridge. However, experience in other Medical Devices or Scientific Inst

Our client has a permanent opportunity for a Scientific Product Specialist – Sales Support.

Project Manager Location – Cambridge Sector – Biotechnology Salary – £45-55K (depending on interview performance & experience) Full time, permanent role Hybrid – 1-2 days a week onsite We are currently offering the opportunity for an experienced scientific Project

Leads cross-functional proposal processes, stakeholders, and timelines to ensure contract proposals and/or modifications are completed accurately throughout the project lifecycle.Essential Functions and Other Job Information:.Leads the proposal bid and budget negotiation process, synthesizing detail

General Manager/MD – Cambridge (Onsite - 5 days a week) Turnaround Leadership | Sales Acceleration | Cultural Reset My client is a specialist manufacturer of scientific instrumentation, backed by an expanding group of specialist scientific and R&D business’s, they are entrepreneurial a

As a member of the Colleague Services Fleet Operations Team, the Car Fleet Coordinator will be responsible for our leased company vehicles and assist colleagues with company car inquiries via our case management system. Our goal is to ensure a superior Colleague Experience by resolving cases promptl

Are you a Field Service Engineer looking to upgrade your career into a regional role which includes the Midlands, South, with some European travel? Due to our rapid expansion, an opportunity has arisen for a Technical Service Engineer / Scientific Support Engineer, to manage our state-of-the-art rob

Robert Half are delighted to be partnering with a rapidly growing, next-generation start-up based in Cambridge, as they look to hire an Assistant Management Accountant to join their expanding finance team. This is a newly created role due to growth, reporting directly into the Financial Controller, and will play a key part in strengthening their financial foundations as they scale their R&D, manufacturing, and operational capabilities. If you're looking for a role that offers true variety, exposure across the business, and the opportunity to develop your management accounting skills in a complex, high-growth environment - this provides exactly that. Key Responsibilities: Month-End & Management Accounts Support preparation of monthly management accounts to review stage. Prepare accruals, prepayments and journals with clear audit trails. Reconcile key balance sheet accounts, ensuring accuracy and control. Assist with monthly reporting packs and variance analysis across scientific and operational departments. Financial Controls & Processes Contribute to an efficient month-end close timetable. Process monthly payroll to review stage for UK employees. Complete bank reconciliations, purchasing card reconciliations and project spend analysis. Support cashflow forecasting by maintaining robust cash schedules. Project & Operational Support Assist with project-level budget tracking across R&D and operational teams. Partner with scientific and non-financial stakeholders to improve cost visibility and strengthen financial understanding. Ensure accuracy of financial information relating to grants and external reporting requirements. Compliance & Other Duties Support VAT returns, payroll reconciliations and external audit requests. Assist with process improvements, system developments and automation initiatives. Handle ad hoc finance tasks as required within a fast-moving environment. Skills & Qualifications: Actively studying ACCA / CIMA / ACA. Strong grounding in accounting principles and exposure to month-end processes. Confident user of Excel (lookups, PivotTables, data analysis). Comfortable working with both scientific and non-financial teams. High attention to detail, strong organisational skills and a proactive mindset. Desirable Experience: Experience within biotech, pharma, life sciences or other regulated industries. Understanding of project accounting, CAPEX, or R&D cost categories. Exposure to process improvements, finance system rollouts or automation. Salary & Benefits: The role of Assistant Management Accountant is offered with a competitive salary (dependent on experience) plus a strong benefits package. This company operates a hybrid model , with around two days a week in their Cambridge office . Robert Half Ltd acts as an employment business for temporary positions and an employment agency for permanent positions. Robert Half is committed to diversity, equity and inclusion. Suitable candidates with equivalent qualifications and more or less experience can apply. Rates of pay and salary ranges are dependent upon your experience, qualifications and training. If you wish to apply, please read our Privacy Notice describing how we may process, disclose and store your personal data: roberthalf.com/gb/en/privacy-notice. TPBN1_UKTJ

Job Description Company Summary: Quotient Therapeutics, Inc.Flagship Pioneering, an innovation enterprise that conceives, creates, resources, and grows first-in-category life sciences companies.Flagship Pioneering has created over 100 groundbreaking companies over the past twenty years, all of whi

A specialist scientific manufacturer based in Cambridge is seeking a General Manager/MD to lead a transformative journey in sales performance and internal culture.

TetraScience is the Scientific Data and AI company.We are catalyzing the Scientific AI revolution by designing and industrializing AI-native scientific data sets, which we bring to life in a growing suite of next gen lab data management solutions, scientific use cases, and AI-enabled outcomes.TetraS

Science Group plc is an international science and technology consultancy and systems organisation operating at the cutting edge of science and technology innovation.The core business is an international science and technology consultancy providing technical/scientific advisory, product development a

This is an excellent opportunity for someone with a strong interest in laboratory work, scientific processes, and practical lesson support to play a key role in a department that prides itself on high-quality teaching, exciting practical demonstrations, and outstanding student engagement across Biol

Oversee and be accountable for the quality of scientific communications tactics and deliverables developed by in-house scientific writers; review deliverables to ensure strategic alignment and scientific accuracy. As a growing scientific communications agency, we are seeking a self-motivated, strate

A health communications agency in Greater London seeks a Senior Scientific Director to lead a writing team for significant accounts. The role involves fostering team performance, managing client relationships, and developing scientific strategies.

A leading health communications agency in Greater London is looking for a Scientific Director to lead their medical strategy and education team.

A leading healthcare consultancy group in Manchester is looking for a Scientific Director to manage client business and relationships while driving business development and strategic direction. The role requires a strong background in medical communications and a proven ability to lead scientific in

A health communications agency in Greater London is seeking a Scientific Director to lead a medical writing team, ensuring excellence in content development for high-profile accounts.

Scientific/Medical Knowledge PV Expertise. Provides in-depth medical/scientific expertise in the safety evaluation and risk management of key GSK assets or in clinical development and/or the post-marketing setting. Ensures scientifically sound review and interpretation of data and management of safe

As the Senior Inspector Scientific Officer, you will form part of a dynamic team responsible for carrying out complex and sensitive regulatory and technical activities, while both working in and leading teams of inspectors. SC Level 3 $129,211 - $142,460 pa (PSCSAA 2024) Permanent - Full Time Cannin

FINDS deliver scientific services ensuring the integrity of records held on the National DNA Database (NDNAD), the National Fingerprint Unified Collection (IDENT1), the National Footwear System (NFS), and the Police National Computer (PNC), on behalf of policing and the wider Criminal Justice System

A global healthcare company is seeking a SERM Scientific Director to provide expertise in safety evaluation and risk management.

A leading medical communication agency is seeking a Vice President, Scientific Services to guide strategic leadership and operational excellence. The role involves ensuring scientific rigor across client accounts and promoting innovative solutions including AI integration. Candidates must possess an

LIST is now seeking an outstanding and forward-thinking Scientific Director to join its Executive Committee and drive the organisation's next phase of scientific excellence. Reporting directly to the Chief Executive Officer, the Scientific Director will play a pivotal role in further strengthening L

A global communications company is seeking a Scientific Director in Greater London to lead a medical writing team. You will be responsible for overseeing scientific content for large accounts, inspiring team performance, and building strong client relationships.

A leading scientific communications agency is looking for a Scientific Director to lead strategic medical communication initiatives.

In this director-level role, you will lead a high-performing writing team, being accountable for scientific knowledge and content development on large, high-profile accounts for the business. Lead scientific pitch research and presentation. Be seen as a content and scientific expert across multiple

We are seeking a Vice President, Scientific Services who will play a pivotal leadership role in guiding the strategic direction and operational excellence of our scientific teams, ensuring the highest standards of scientific rigour and innovation across client accounts. Proven scientific leadership

Provides in-depth medical/scientific expertise in the safety evaluation and risk management of key GSK assets or in clinical development and/or the post‑marketing setting. Ensures scientifically sound review and interpretation of data and management of safety issues and escalates safety issues ide

Act as scientific lead on assigned accounts, providing strategic direction and scientific leadership. Establish, maintain and lead scientific relationships/communications with clients, medical experts and third parties, supporting junior team members to ensure they develop this skill. Demonstrate a

In this director‑level role, you will lead a high‑performing writing team, being accountable for scientific knowledge and content development on large, high‑profile accounts for the business. Lead scientific pitch research and presentation. Be seen as a content and scientific expert across mul

In this director-level role, you will lead a high performing writing team, being accountable for scientific knowledge and content development on large, high-profile accounts for the business. Lead scientific pitch research and presentation. Be seen as a content and scientific expert across multiple

A leading health communications agency in Greater London is seeking a Scientific Director to lead a high-performing medical writing team.

In this director‑level role, you will lead a high‑performing writing team, being accountable for scientific knowledge and content development on large, high‑profile accounts for the business. Lead scientific pitch research and presentation. Be seen as a content and scientific expert across mul

Lead the development of therapy area and/or brand scientific strategy. Experience in scientific and content leadership for multiple accounts. In this director‑level role, you will lead a high‑performing writing team, being accountable for scientific knowledge and content development on large, hi

A leading multidisciplinary research organisation in Greater London is seeking an outstanding Scientific Director to drive scientific excellence.

Coaches and mentors SERM colleagues in the scientific / medical aspects of signal evaluation methodology and risk management and preparation of regulatory safety reports and other documents. Provides excellent medical / scientific judgment, strong analytical skills, proactive approach in drug safety