Scintillant specialises in the recruitment of high quality candidates in the scientific sector. We have an excellent opportunity for an Account Executive to provide day to day project support to the Client Services team. Account Executive’s Main Duties: Supporting logistical delegate management for events; including tracking registrations, organising travel, accommodation, transfers and liaison with hotels/venues to book meeting space, etc Preparing meeting materials (ie, welcome packs, collation of delegate folders, printing, etc) Completing contract templates and tracking/filing of signed contracts as well as collating details and managing payments to delegates/faculty, etc Ensuring awareness and understanding of relevant compliance guidelines and applying these as appropriate to applicable projects and project tasks Assisting with proposal/budget development and financial tracking of a project Coordinating artwork jobs with studio/programmers and cross checking of documents for quality control Coordinating meetings/teleconferences and preparing minutes and updating status reports General team administration (ie, booking couriers, flights, coordination the QC, studio and project support schedules, basic Zinc uploading, updating status reports, etc ). Providing overflow reception cover as needed Requirement for a high level of attention of detail within all documents and communications and adherence to internal processes at all times Account Executive’s Education/Qualifications/ Experience: Some experience in a similar role in the medical education/communications industry or logistics/travel industry Science degree or interest in the area Proficient with Microsoft Office - in particular Outlook, Excel, Word and PowerPoint Excellent customer service skills

Scintillant specialises in the recruitment of high quality candidates in the scientific sector. We have an excellent opportunity for an Applications Scientist, FTIR to join a British & Danish Diagnostics organisation. The primary responsibility of the Applications Scientist is to assist with the commercial development of a diagnostic application for an acute unmet clinical need. The role includes FTIR experimental planning/execution and protocol development. Method optimisation and instrument responsibility will be part of the work, as well the use of quantitative software to develop, monitor and improve the quality of our analyses. Applications Scientist’s Main Duties: Optimising sample preparation and FTIR spectroscopic measurements of human fluid samples Chemometric modelling Supporting multi-phase clinical trials for method validation and commercial medical diagnostics development Liaising with external engineering and laboratory equipment/consumables/software suppliers Project planning and experimental design Guiding and conducting experiments in collaboration with team and external partners Performing all work in accordance with company quality assurance procedures and GLP Developing new and improving existing methods and tools Acting as project lead for (parts of) company project development plan Applications Scientist’s Education/Qualifications: MSc/PhD in Chemistry, Biochemistry, Chemical engineering, or equivalent Six years’ hands-on lab experience and excellent practical laboratory skills High degree of expertise and demonstrated experience in FTIR spectroscopy Awareness of assay development and validation Prior experience of working with commercial method development & prototype optimisation Excellent oral and written English communication skills Applications Scientist’s Preferred Qualifications Supporting clinical trials Experience in Mass Spectrometry Highly numerate, knowledge of Chemometric methods Engineering/ technical hardware and software skills Knowledge of GLP regulations and quality assurance Development and working knowledge of materials science and photonics Additional Details The Company is highly innovative, breaking new ground in diagnostics and clinical care. This is an opportunity to be part of an expert multidisciplinary team and an experienced commercial team. The company is in the advanced stages of clinical development, offering an opportunity to experience the exciting transition from the lab into the clinic.

Scintillant specialises in the recruitment of high quality candidates in the Life Sciences sector. We have an excellent opportunity for a Head of Research & Development person to join a British & Danish Diagnostics organisation. The primary responsibility of the Head of R&D is to coordinate all scientific activities needed to transition a laboratory-developed test (LDT) to a point-of-care diagnostic. The current project addresses an acute unmet clinical need and the know-how gained will be applied to other business opportunities. The role includes the management of scientific method optimisation using both in-house FTIR vibrational spectroscopy experimental protocols and external contract laboratories/consultants over entire product lifecycles. The success of this role is tantamount to a successful commercialisation pathway which encompasses clinical trials, hardware/software development, machine learning, and regulatory compliance. Head of Research & Development’s Main Duties: Building a team of scientists/technicians Managing activities of external contract laboratory and consultants Optimising a laboratory method which includes sample preparation, FTIR measurements, reference data analysis and chemometric data analysis Performing all work in accordance with company quality assurance procedures and GLP Liaising with specialised engineering consultancy and strategic suppliers Supporting multi-phase clinical trials for method refinement and point-of-care medical diagnostics development Project planning, experimental and protocol design Head of Research & Development’s Education/Qualifications: PhD in Chemistry, Biochemistry, Chemical engineering, or equivalent Six years’ scientific management experience in a commercial medical diagnostics or pharmaceutical organisation Proven laboratory management skills Quantitative analysis of laboratory data GLP and/or GMP experience and QC Experience in assay development, validation, and delivery Experience of working with commercial method development and prototype optimisation Excellent oral and written English communication skills Head of Research & Development’s Preferred Qualifications Scientific support of clinical trials Experience in FTIR and Mass Spectrometry analysis Highly numerate, knowledge of Chemometric methods Engineering/technical hardware and software skills Understanding of data science algorithms Additional Details The Company is highly innovative, breaking new ground in diagnostics and clinical care. This is an opportunity to be part of an expert multidisciplinary team and an experienced commercial team. The company is in the advanced stages of clinical development, offering an opportunity to experience the exciting transition from the lab into the clinic.

Scintillant specialises in the recruitment of high quality candidates in the life sciences sector. We have an excellent opportunity for a Technical Support Specialist to join a successful team based in Kent. Salary- Basic £24,000 + Bonuses (also part time would be considered) Job Summary: Main Duties: Respond to product and technical enquiries in a timely and efficient manner. Diligently manage and resolve issues raised by customers regarding product performance. Follow through commercial leads to a satisfactory completion. Regularly interact with customers by email and/or telephone in the provision of information on product enhancements and new technologies. Support and regularly communicate with Distributors ensuring knowledge on company products and technologies is valid and up-to-date. Provide information which will support and improve e-marketing and sales campaigns. Integrate with technical staff to maximise their input to supporting the sales process. Regularly and extensively evaluate competitor products and technologies. Develop marketing support materials to assist sales staff in the placement of product. Interact with customers in the co-development of application notes and technology tips. Key Skills and Requirements: A Life Science Degree or equivalent. Minimum of 12 months experience working in a Life Science laboratory. Sound practical skills in the management of Molecular Biology, DNA and Biochemistry technologies. IT proficient and skilled in the use of Excel, Word, Photoshop and possibly a CRM. Strong administration skills. An outward personality with excellent communication and interactive skills.

Main Duties: To provide general and clinical trial contractual advice and expertise to colleagues in both the Enterprise Unit and the joint Clinical Research & Development Office at the Royal Marsden NHS Foundation Trust (RM). To draft, review, negotiate and conclude agreements that relate to clinical trials run by or at The ICR and/or RM. To identify and meet the expectations of stakeholders in performing the clinical trials contract function. To represent the ICR and/or RM in negotiations with prospective partners and sponsors and at trade shows and conferences To be a member of the Enterprise Unit team and contribute actively to team meetings Under the direction of the Head of Clinical Trials Contracts and working closely with scientific colleagues at all levels in ICR and RM and with external legal advisors and insurers where necessary: Draft, review, negotiate and conclude (through to approval for signature) clinical trials-related contracts on behalf of the RM and The ICR and the Mount Vernon Cancer Centre (MVCC) including contracts with commercial and non-commercial sponsors and associated supplier and laboratory research contracts. Analyse the levels of risks posed in contracts and manage appropriately ensuring contracts are fair, equitable and enforceable. Manage and track all contracts using the contract record system including handling incoming requests from both external and internal parties and contract amendments. Work closely with study teams in RM and ICR to ensure that arrangements within clinical trials contracts meet all protocol and regulatory requirements and that key contractual obligations are identified. Where required, work with RM and ICR staff to ensure appropriate costing of research activities and pharmacy provision and governance of the clinical trial process in final contracts. Contribute as needed to the development of RM clinical research and development management systems. Advise senior management on rights, obligations and constraints in agreements and authorise them for signature. Build upon the existing relationships with the clinical study teams to develop an understanding of the nature of contracts management needed, including intellectual property protection. Maintain an up-to-date working knowledge of relevant legislation, codes of practice and guidelines governing clinical research managed and run at RM and The ICR through external training where appropriateand assess the impact of any changes. Provide advice and guidance to colleagues in the Enterprise Team, elsewhere in the ICR, the joint Clinical Research & Development Directorate and study teams with regard to contractual issues in the context of clinical research. Where appropriate contribute to training and development. Review and develop new template agreements as required to ensure compliance with regulatory and governance requirements. Work closely with colleagues in The Enterprise Unit to ensure that provisions in RMH clinical trial agreements do not conflict with undertakings in ICR collaborative research agreements. Negotiate and agree routine agreements such as material transfer agreement and confidentiality agreements relating to clinical trials. Reply promptly to queries from scientists, clinicians and study teams and keep them apprised of progress. Attend trial related meetings where needed. Depending on the skills of the post holder, develop areas of expertise in intellectual property management and commercialisation. Other duties: Communicate verbally and in writing with internal (clinicians and researchers) and external parties (pharmaceutical companies, governmental entities, etc.) in a cordial, articulate and timely manner to build and develop an understanding of their needs and maintain fruitful relationships. Identify potential conflicts of interest between the objectives of the various stakeholders, and all other risks and liabilities and mitigate against their impact. Contribute to the review of the policies and procedures relating to clinical trials and related activities including insurance, IP management, governance and potential conflicts of interest. Contribute to regulatory and funder inspections as required. Attend and actively participate in Clinical R&D and Enterprise Unit meetings and contribute to discussions on strategic and general issues. Maintain sector awareness relevant to clinical trials at the ICR and RM Maintain and continue to expand established external networks, develop strategic relationships and promote partnering with the ICR and RM. Represent the ICR independently at trade exhibitions and conferences. Undertake occasional formal presentations within ICR or externally. Contribute to the development and maintenance of management information systems for contracts and other Enterprise Unit information; the preparation of management reports, metrics and other management information. Any other duties as may be required which are consistent with the nature and grade of the post. This post will hold an honorary contract with the RM. Essential Specifications: Life Science degree. Extensive and recent practical experience of successfully drafting, negotiating and concluding contracts and closing deals with external partners. Comprehensive knowledge of contract law. Strong IT skills, with the ability to use computerised and web-based administrative systems and data sources effectively. Desirable Specifications: Working knowledge of clinical trials, particularly related to applicable regulatory and ICH guidance regarding clinical research and GCP. Legal qualification. Experience of working with and applying the EU Clinical Trial Directive and other regulations appropriate to clinical trials run in the UK. Experience of working in the NHS or the higher education sector. Experience in the pharmaceutical or biotechnology sectors.