714 Science jobs

South West Water now have an exciting opportunity as a Water Quality Technician based in Plymouth. South West Water provide reliable, efficient and high quality drinking water and waste water services throughout Cornwall, Devon, and parts of Somerset and Dorset. We believe that by investing in the future of our region, we are not only improving the quality of life for today's residents and visitors but are also taking responsibility for future generations. Our aim is to continually drive up standards, particularly in the areas that matter most to our customers and be amongst the best in the water industry. We now have an exciting opportunity to join one of the South West's leading employers as a Water Quality Technician based at Crownhill Depot, Plymouth. The Role The Water Quality Technician will provide sampling activities and on site analysis to meet the requirements of the Company and the Regulators. You'll assist the Scientists in the investigation of breaches of regulatory standards, and in the resolution of customer enquiries relating to water quality. You'll be responsible for the effective planning and delivery of sampling, monitoring and customer support activities and undertake service reservoir security checks and booster chlorination activities as required. The Ideal Water Quality Technician: Ability to follow procedures to the exacting standards demanded by the Regulator and business A good geographical knowledge of the South West Excellent attention to detail with the ability to keep accurate records Logical approach to tasks and the confidence to use initiative Ability to work alone whilst keeping team members informed Excellent customer service skills with the ability to act with tact and diplomacy Full UK Driving License Rewards & Benefits: In return for your hard work as our Water Quality Technician, we can offer a starting salary of £17,364 - £21,585 per annum dependent on skills and experience + a weekend working supplement . We also offer a progression scheme and a range of benefits. If you have the skills and experience to join our team as a Water Quality Technician, click apply today. No terminology in this advert is intended to be deemed discriminatory. We are happy to accept applications from all suitably qualified persons regardless of their age, gender, race, religion, disability, sexual orientation or marital status.

Bulk Analyst - Manchester - P401 £22,000 - £26,000 + Benefits 'Do you want to have career progression?' An excellent opportunity to join a well-respected and leading Asbestos and Engineering consultancy. My client is looking for a Bulk Analyst who will work on samples from both the private and public sector. My client is looking for a Bulk Analyst who is BOHS P401 qualified and has a years' experience in this role. Duties of a Bulk Analyst include: Testing bulk samples that are potentially Asbestos Ensuring all samples are stored away safely and are in a secure location Ensuring the laboratory is in a clean state Keeping a record of your daily work Experience Required: BOHS P401 qualified Previous experience in this role Excellent writing skills Excellent communication skills Hardworking attitudeWith a competitive basic salary and great added benefits this is a great opportunity to progress with your career. For more information please contact Jack Wadelin at Penguin Recruitment on (phone number removed), or email your CV to Similar Job Titles: Asbestos Consultant, Asbestos Analyst, Asbestos Lab Analyst Commutable Locations: Warrington, Manchester, Liverpool, Stockport, Wigan, Macclesfield, Blackburn, Bury, Bolton, Oldham, Rochdale, Altrincham, Sale, Stretford, Stockport, Northwich, Preston, Huddersfield, North West

A unique opportunity for an experienced and ambitious R&D Scientist to join a highly collaborative project, focussing on the delivery a novel point of care diagnostic device! Calling upon your expertise in Lateral Flow assay development, you will work alongside key industry partners to design and deliver a Rapid Diagnostic capable of detecting the presence of COVID-19 antibodies in the field. Successful candidates will possess: - Extensive experience developing Lateral Flow assays, Immunoassays and/ or medical devices - Thorough knowledge of antibody conjugation & nanoparticles - Proven experience meeting deadlines/ commercially aware - Excellent communication skills Apply now to VRS to be considered for this highly rewarding opportunity! Please note: This role is initial offered a 12-month contract with potential to extend. Key Words: research, development, ELISA, antibody, conjugation, purification, chromatography, life science, ISO9001, GMP, GLP, manufacturing, fragmentation, enzymes, proteins, particles, lateral flow, nanoparticles, Manchester, Chester, Cheshire, North West, VRS6645CR

Editorial Team Leader Publications £60,000 - £70,000 + Bonus Oxford/Manchester/London/Bollington ** PLEASE BE AWARE HIRING IS ONGOING VIA VIDEO DURING THE COVID-19 PANDEMIC. ** Albion Rye Associates are proud to have been assigned as the exclusive recruitment partner to a well-established, highly regarded and market leading Medical Education agency. This is an amazing opportunity for an experienced Editorial Team Leader who has a passion for working in a high science environment, covering a wide range of publications and non-publication materials on behalf of clients across the globe. Knowledge and Responsibilities: Develop positive relationships with clients and clinical experts Offer scientific input and insight to clients and internal account teams Contribute to the company's strategy and business development activities Provide training and mentorship to medical writers within the team Skills and Experience: 100% Publications, so preferably a publications specialist Oncology experience preferred but not essential CMPP or ISMPP friendly Excellent written and oral communications skills Able to take ownership of assigned projects Detail-focused and organised Able to work as part of a highly motivated and experienced team Enthusiastic towards continuing professional development and training In return you can expect and excellent salary, flexible working and a host of benefits including pension, healthcare, dedicated training budget, regular bonuses, 28 days holidays and more. If this sounds like you - I'd love to discuss this role in more detail. For further information, contact us. Alternatively, email me with your CV. ** ON BEHALF OF ALBION RYE ASSOCIATES, PLEASE STAY HOME, STAY SAFE & WASH YOUR HANDS **

Editorial Team Leader Rare Diseases £33,000 - £38,000 + Bonus Oxford Office - Home based flexibility ** PLEASE BE AWARE HIRING IS ONGOING VIA VIDEO DURING THE COVID-19 PANDEMIC. ** Albion Rye Associates are proud to have been assigned as the exclusive recruitment partner to a well-established, highly regarded and market leading Medical Education agency. This is an amazing opportunity for an experienced Editorial Team Leader who has a passion for working in a high science environment, covering a wide range of promotional and non-promotional materials on behalf of clients across the globe. Knowledge and Responsibilities: The supervision of the delivery of high-quality content across the agency, within agreed timelines and budgets. Develop positive relationships with clients and clinical experts Offer scientific input and insight to clients and internal account teams Contribute to the company's strategy and business development activities Provide training and mentorship to medical writers within the team Skills and Experience: Established/experienced medical writing team leader Rare disease experience preferred but not essential Senior or principal writer (mentoring/training available, progression to step up) Able to take ownership of assigned projects Able to work as part of a highly motivated and experienced team Excellent written and oral communications skills Detail-focused and organised Enthusiastic towards continuing professional development and training In return you can expect and excellent salary, flexible working and a host of benefits including pension, healthcare, dedicated training budget, regular bonuses, 28 days holidays and more. If this sounds like you - I'd love to discuss this role in more detail. For further information, contact us. Alternatively, email me with your CV. ** ON BEHALF OF ALBION RYE ASSOCIATES, PLEASE STAY HOME, STAY SAFE & WASH YOUR HANDS **

Graduate Laboratory Technician Norwich Permanent £17,000 to £19,000 DOE My client, based in Norfolk, are currently looking for an entry level Molecular Biology Technician ideally with experience working with life or plant tissue cultures, to join their growing team on a permanent contract. With fantastic training opportunities and further growth this is a great opportunity to gain valuable industry experience. To be eligible to apply for the role you must meet the following criteria: Be educated to BSc level within the Life Sciences or Plant Sciences Have experience working in a laboratory environment (academia or industry) Be able to work with great attention to detail Any experience working with tissue cultures would be highly desirable for this position If this sounds like the role for you and you possess the required skills and experience, then please apply below.

Asbestos Laboratory Analyst £24,000 - £28,000 + Benefits Harlow, Essex Our client is an award-winning and UKAS accredited analytical testing company that specializes in Environmental Testing, Microbiology, Waste and Asbestos. Due to a recent company expansion, they now have an opening available for an experienced Asbestos Laboratory Analyst to their state-of-the-art laboratory in Essex. To be considered for this role, it is essential that applicants possess the BOHS P401/RSPH3 certification with a minimum of 6 months experience working within a UKAS accredited laboratory. A high level of IT and numeracy skills is essential along with strong communication skills and a key eye for detail. As an Asbestos Laboratory Analyst, you will be required to carry out the analysis of bulk samples for traces of asbestos, maintain records for all laboratory procedures, participate in QC schemes and assist in maintenance programmes for analytical instrumentation. On offer is a very competitive basic salary along with a full benefits package which includes a fantastic company pension scheme, 25 days holiday + bank holidays, life assurance, private medical insurance and a wide range of additional flexible benefits! Intersted? Contact Recruitment on (phone number removed), or send an updated CV direct to for immediate consideration! Commutable locations: Chelmsford, Chesunt, Welwyn Garden City, Romford, Brentford, Bishops Stortford, St Albans, Hatfield, Hertfordshire, Essex

TFS Healthcare are looking to recruit a suitably qualified Band 6 BMS. Our client is looking for someone to work full time, Monday - Friday, 08.00 - 16.00. This role requires the successful candidates to have at least 1 years' UK experience in Microbiology and must be HCPC registered. This role is due to start ASAP and is ongoing. Key details Must be a qualified Biomedical Scientist Must have HCPC registration Proven experience working within Microbiology Pay rates of Band 6 between £23 - £30TFS Healthcare is one of the UK's premier specialist recruitment agencies, covering all disciplines of AHP & HSS staffing. TFS are a CPP & HTE approved supplier, recruiting into the NHS & private organisations offering both locum and permanent recruitment services. TFS Healthcare have access to a vast number of roles across the UK and we are confident of finding you the right job, in the right place at the right rate. We also offer: Dedicated, specialist recruitment consultants Fast track compliance process with free DBS processing & mandatory training Market leading pay rates Daily payroll Access to CPD fund and annual incentivesIf you are not available for this role, why not recommend a friend or colleague and earn £250 bonus for each successful placement - there is no limit to the number of people you can refer! (T&Cs apply) TFS Healthcare is an equal opportunity employer and do not discriminate based on race, religion, gender, age, sexuality, gender identification, or physical ability. TFS Healthcare will make reasonable adjustments and provide support for anyone who needs it either to apply or to succeed in the role. We will also support people to access our clients' organisations with sensitivity, respect and care

Organic Chemist We are currently looking for PhD Organic Chemist to join a leading Pharmaceutical company in the South East. The role: As an Organic Chemist you will conduct complex organic synthesis for the development of API's. Duties include: Carry out organic synthesis to develop target molecules. Conduct multi-step synthesis and laboratory scale up though to pilot plant and GMP manufacturing. Manage and oversee custom synthesis projects keeping the client up date at all stages of the project. Prepare and review client reports and other technical documentation. Maintain an up-to-date knowledge of synthetic chemistry. Ideal candidates will have a PhD in Organic Chemistry and have excellent working knowledge and practical skills in Organic Synthetic Chemistry. Candidates who have recently gained their PhD are encouraged to apply. Key words: Organic Chemistry, Synthesis, GMP, Pharmaceutical, Synthetic, Chemist, APIs, Research and development.

HRS are currently looking for a Quality Control Analytical Scientist to join a leading biologics manufacturing company based in the Staffordshire area. As the Quality Control Analytical Scientist you will report to the QC Team Leader and be responsible for performing raw material release testing. KEY DUTIES AND RESPONSIBILITIES: Your duties as the Quality Control Analytical Scientist will be varied however the key duties and responsibilities are as follows: 1. As the QC Analyst you will analyse incoming raw materials for use in manufacturing. 2. You will perform routine testing and laboratory procedures in compliance with GMP. 3. You will be responsible for maintaining and verifying equipment as was as performing general laboratory housekeeping. 4. The Quality Control Analyst will also assist with the execution of analytical method validation. ROLE REQUIREMENTS: To be successful in your application to this exciting opportunity as the Quality Control Analytical Scientist we are looking to identify the following on your profile and past history: 1. Relevant degree in a Life Sciences related discipline plus industry experience. 2. Proven industry experience of raw material testing. 3. A working knowledge and practical experience working in a GMP environment. Key Words: QC, Quality Control, Analyst, Raw Materials, Analytical, Laboratory, Life Sciences, Biologics, Biopharmaceutical, Manufacturing, GMP, cGMP. Hyper Recruitment Solutions Ltd (HRS) is an Equal Opportunities employer who are certified by Investors in People for talent development. We therefore welcome applications for any interested parties who fulfil the role requirements for this position. HRS is a company exclusively supporting the science and technology sectors, and is made up of a collaboration of recruitment professionals and scientists. We look forward to helping you with your next career moves.

Job Title: Real World Evidence Manager Salary: 55k 75k with benefits Location: Wokingham An exciting position has opened at a leading Global Pharmaceutical company for a Real-World Evidence/Data Specialist to lead the production of key studies to ensure HTA submissions have flawless epidemiological evidence. Your role includes: Designing and leading production of successful Real-World Data studies in order to raise awareness of product specific outcomes and sharing results and clear interpretation throughout the Franchise and Sales teams. Produce Real-World Data to ensure that Health Technology Assessment submissions contain rigorous epidemiological evidence. Providing epidemiological and statistical expertise to Health Economists to support economic modelling and data analysis for HTA submissions Taking a prominent role in cross-functional Franchise teams and being a recognised authority to ensure that Market Access is integral to brand strategy and tactics Experience and Qualifications required: Relevant post-graduate qualification, e.g., MSc/PhD in Epidemiology or related discipline In-depth knowledge of epidemiological methods, and medical statistics applied to epidemiology Proven knowledge in the management of epidemiological data and methods used to organise and analyse large sets of data Knowledge and experience of running epidemiological studies, from proposal writing to publication of results Desirable: Good Understanding of both CPRD (Or equivalent anonymised patient-level database) and the UK Health system Please email your CV to , or alternatively call and ask for Rob for more information.

Clinical Program Manager - Late Phase An exciting opportunity has arisen to join our leading Bio-tech client in their Clinical Operations Late Phase team based in West London as a Clinical Program Manager to be responsible for the management of post-authorisation studies, investigator sponsored research and compassionate use programs across different therapeutic areas. Job Requirements Successfully manages all aspects of assigned post-authorisation studies within designated program budgets and timelines with primary focus on studies detailed in the product Risk Management Plan. Maintain current knowledge of both local & regional legislation regarding execution of post-authorisation studies. Responsible for development and monitoring of study budgets and timelines and managing adjustments as necessary. Actively lead Study Management Teams for assigned studies and provide strategic and operational advice as required. Actively participate in CRO study calls as appropriate. Conduct study feasibility in conjunction with internal Medical Affairs and Clinical Operations staff and/or external collaborators or CROs. Develops RFPs, select CROs/vendors, and manages external resources. Communicates project status and issues and ensure project team goals are met. Anticipates moderately complex obstacles and client difficulties and implements solutions to achieve project goals. Contributes to development of abstracts, presentations, and manuscripts. Co-monitoring may be required. Provide support to Investigator Sponsored Trials including Fair Market Value and feasibility assessment, contract milestone advice, tracking and publication follow-up as required Identify any "best practice" opportunities to share across Therapeutics Areas and sites. Ensure local consistency & alignment with GSI global process & procedure, whilst providing regional perspective & expertise. Participate in the development of SOPs, Clinical Study Reports, INDs, NDAs, and other clinical, regulatory and safety documents as required. With limited supervision may participate in or lead departmental strategic initiatives. Develop good working relationships with the Global Late Phase operational team and cross-functional staff internationally as required. Participate as an active member of the Global Clinical Operations Late Phase extended Leadership team and other team meetings. Serve as an ambassador for Clinical Operations internally and externally. Provide training to colleagues on process changes/improvements as necessary. Recruit, hire, mentor, and manage direct reports as required and support their professional development. Occasional travel is required. Knowledge, Experience And Skills BSc Life Sciences. A MSc or PhD would be advantageous (or international equivalent). Relevant clinical experience in the pharmaceutical industry. Experience in managing staff as well as mentoring and developing junior staff. Experience in clinical study management including the delivery of Phase IV and non-interventional studies is essential. Experience in the review and oversight of Investigator Sponsored Research. Knowledge of post-marketing requirements and different types of Drug Utilisation Studies and Post Authorisation Safety and Efficacy Studies. Experience in the provision of compassionate use would be beneficial. Knowledge of regulatory affairs and drug safety. Experience in developing RFPs and selection and management of CROs/vendors. Ability to write study protocols, plans, study reports and regulatory documents (e.g. IND, DNA, etc.) with little supervision. Excellent interpersonal skills, and demonstrated ability to lead is required. Strong communication and influence skills and ability to create a clear sense of direction is necessary. Must be able to resolve problems using national and international regulations, guidelines, and investigator interaction. Extensive knowledge of ICH GCP, FDA, EMEA regulations & guidelines. Knowledge of drug development & commercialisation processes. Functional expertise to initiate, author, or contribute to SOP development, implementation, and training. Ability to participate in and/or lead departmental or interdepartmental strategic initiatives under limited supervision. Parkside Recruitment Ltd is acting as an Employment Agency in relation to this vacancy. Parkside Recruitment is an Equal Opportunities Employer.

CK Clinical are recruiting for a Senior Scientific Information Coordinator for a global pharmaceutical company to work at the UK office in Buckinghamshire. Location: Office Based - Full Time. The Role: This position will take the lead in being responsible for operational activities within the Medical Department, including, medical information, pharmacovigilance, compliance and the Management of Procedural Documentation within the UK. Experience & Qualifications: - Life science graduate, ideally with a relevant PhD, pharmacy or medical qualification. - Experience in the pharmaceutical industry working in a PV or Medical Information Role. - Proven track history of effective project management. - Expert knowledge of ABPI, EFPIA and IFPMA codes of practice. For more information or to apply for this Senior Scientific Information Coordinator, please contact CK Group, quoting job ref 47882. It is essential that applicants hold entitlement to work in the UK.

Senior Clinical Research Associate / CRA II job, Pharmaceutical, CRO, Rare Disease, Gene Therapy Your new company This globally based CRO are looking for the right dynamic and organized person to fit in as a Senior Clinical Research Associate. This is a unique opportunity to work at a multi award-winning CRO that provides services for biotechnology, pharmaceutical, medical device and government and public health industries. Their focus, finding cures for debilitating diseases for the chronically and critically ill, requires only the best and brightest - putting you in good company. Your new role You will be working for a continually growing company with an average 95% annual retention rate, based in their office in Kings Cross. You will be working to identify, select, initiate, monitor and close-out investigational sites for clinical studies (Phases I-IV) and averaging around 6 on site visits a month. A bachelor's degree in science, an allied health field or equivalent is essential, and you should have over 18 months experience of direct site monitoring in a Bio, Pharma or CRO. Furthermore, previous experience in Rare Disease or Gene Therapy is preferred (although not essential). This is an office-based position, candidates must be able to come into the office. What you'll need to succeed Main Responsibilities Conduct site visits (including validation, initiation, monitoring, close-out, etc.) Perform clinical study site management/monitoring activities in compliance with ICH-GCP, sponsor SOPs, Local laws & Regulations, Protocol and Site Monitoring Plan Assist with regulatory and study start-up activities including contract and budget negotiations What you'll get in return This is a unique opportunity to work for a CRO that is responsible for the global development of drugs and devices that save lives and improve the quality of life of the chronically and critically ill. You will not only be working for an awarded Top Work Place but have continuous opportunities for progression. This company retains 95% of its staff, 25% of which are promoted every year and they have never had a layoff in their 20 years. What you need to do now If you're interested in this role, click 'apply now' to forward an up-to-date copy of your CV, or call us now. If this job isn't quite right for you but you are looking for a new position, please contact us for a confidential discussion on your career.

HRS are currently looking for a QC Analytical Scientist to join a leading biotechnology company based in the North Wales area. As the QC Analytical Scientist you will be responsible for aiding in the analytical testing of Biological Pharmaceutical products in accordance with GMP. KEY DUTIES AND RESPONSIBILITIES: Your duties as the QC Analytical Scientist will be varied however the key duties and responsibilities are as follows: 1. You will be responsible for the development and validation of electrophoresis-based assays. 2. As the QC Analytical Scientist you will perform analytical testing using techniques such as HPLC, ELISA and MS . 3. You will be responsible for laboratory maintenance and ensuring that activities are in compliance with Health & Safety Guidelines, including COSHH. 4. As the Quality Control Analytical Scientist you will partake in the documentation of laboratory results in accordance with cGMP. ROLE REQUIREMENTS: To be successful in your application to this exciting opportunity as the QC Analytical Scientist we are looking to identify the following on your profile and past history: 1. Relevant degree in a Life Sciences related discipline plus industry experience. 2. Proven industry experience working in an analytical testing laboratory, performing techniques such as electrophoresis, HPLC, ELISA and MS. 3. A working knowledge and practical experience working in a GMP environment. Key Words: QC, Quality Control, Analytical, Scientist, Laboratory, HPLC, UV, MS, LC, ELISA, Immunoassay, Cell Culture, FTIR, Electrophoresis, Life Sciences, Biotechnology, Laboratory, Biopharmaceutical, Biologics, cGMP, GMP, GXP. Hyper Recruitment Solutions Ltd (HRS) is an Equal Opportunities employer who are certified by Investors in People for talent development. We therefore welcome applications for any interested parties who fulfil the role requirements for this position. HRS is a company exclusively supporting the science and technology sectors, and is made up of a collaboration of recruitment professionals and scientists. We look forward to helping you with your next career moves.

You have an interest in nutrition and food and are looking to further build your career in this sector. This progressive business who services all the major retailers across the UK is the company to do this at. You can join a growing specifications team who ensure products are launched to market at pace and on time. You will be responsible for collecting, updating, inputting and maintaining technical information across a number of product ranges, predominately within baked goods. Location: Blackpool. Salary:c£26,000 Hours: Permanent role, Monday - Friday Benefits: 25 days holiday, free onsite parking, generous pension and subsidised canteen If you're a specification technologist already who wants to take the next step in your career or currently in a hybrid role where you want to focus more on specifications we would love to hear from you. We are open to your experience, so even if you're a recent graduate who has completed a placement year and want to take your first steps into a role like this apply today.

An excellent opportunity for an experienced French Speaking Regulatory Affairs Advisor to join this highly successful company who provide major retailers and brands with accurate labelling, consumer information and regulatory advice. THE ROLE The primary function is to provide input on food packaging artwork from pack copy to approval, adhering to regulatory requirements and corporate policies. You will also be providing food regulatory advice on French or Spanish markets to clients, translators and internal teams. Responsible for providing high quality food regulatory advice on specific countries/regions to clients, translators and internal teams, you will answer clients' queries, participate and contribute in leading projects to ensure a high level of customer service. The role also involves input on artwork from pack copy to approval, adhering not only to regulatory requirements, but also corporate policies. The International Regulatory Advisor carries out research on regulatory developments in the countries/regions they cover and other markets which may be of interest to the business to ensure that they are up to date to perform their day-to-day duties. Also to provide input on company products/services and contributes to the development of new products/services of interest to clients. You may be required to do presentations on food regulatory topics to clients and industry stakeholders in training courses and may need to attend meetings with clients and other stakeholders. THE IDEAL CANDIDATE Food Science or similar degree, or a Food Law/Trading Standards/Environmental Health (Food Standard) qualification Excellent knowledge of EU and UK food legislation. Experience of a regulatory role within the food industry. Ability to interpret complex food legislation. Understanding of the food retail and food manufacturing environment. Conversant with specification completion and able to review specifications and artwork. If this job is of interest and you would like to investigate further, apply TODAY! "Kandhu Recruitment will consider all applications based on each candidate's suitability to the role or similar roles within the Food Sector and if we feel you are a relevant candidate we will process your application by adding you to our secure recruitment database and then contacting you to progress job opportunities further. We do not contact unsuitable applicants." Kandhu GDPR & Privacy Policy Statement Kandhu has fully implemented GDPR & Privacy Policies across its business and a copy of our Privacy Policy can be found by visiting our website. By applying for this role Kandhu will add your details to our database - assuming you have the right level of experience for the roles you apply for, after which we will be in touch.

Clinical Trial Manager - Late Phase job, IV, Post-Authorisation, Non-Interventional, Investigator Sponsored Your new company This world renowned and globally based Biotech are looking for the right proactive and organized person to fit in as a Clinical Trial Manager - Late Phase in their office in Uxbridge. This is a unique opportunity to work for an immensely reputable company and play a part in changing the world and help millions of people live healthier and better lives. Your new role You will be working in a large scale, fast paced environment, responsible for the management of the European component of Global post-authorisation studies and Investigator Sponsored Research. The role will include providing support and oversight for these trials including Fair Market Value and feasibility assessment, contract milestone advice, tracking and publication follow-up as required. Previous experience in the management of Late-Phase/Phase IV and Non-Interventional studies is essential. Any previous experience with Investigator Sponsored Research is desirable. What you'll need to succeed Main Responsibilities Managing the conduct of Post-Authorisation studies on a European level from study design to close out within designated budgets and timelines. Manage and help select CROs/vendors for studies, as primary point of contact. Contribute to development of RFPs along with the writing and reviewing of relevant documents (protocols, informed consents, CRFs, monitoring plans and clinical study plans) What you'll get in return This is not only a chance to work for a globally revered company with thousands of staff around the world, but also have your voice heard, tangibly seeing your contributions take effect. You will be working with some of the sharpest minds in the industry and also have internal growth opportunities amongst them, along with chances to enhance your skills and career through ongoing development. What you need to do now If you're interested in this role, click 'apply now' to forward an up-to-date copy of your CV, or call us now. If this job isn't quite right for you but you are looking for a new position, please contact us for a confidential discussion on your career.