231 Research Study jobs in the United Kingdom

Our client, a pioneering biotechnology company based in **Newcastle upon Tyne, Tyne and Wear, UK**, is seeking an experienced Senior Scientific Research Associate to contribute to their groundbreaking work in drug discovery and development. This role is crucial for advancing our client's pipeline by conducting rigorous scientific research, developing innovative assays, and troubleshooting complex experimental challenges. The ideal candidate will possess a strong background in molecular biology, biochemistry, or a related field, with hands-on experience in a research and development laboratory setting. You will be responsible for designing, executing, and analyzing experiments, meticulously documenting findings, and contributing to the interpretation of data within a broader research program. The Senior Scientific Research Associate will play a key role in optimizing existing protocols and developing novel methodologies to accelerate research timelines. This position demands excellent problem-solving skills, a keen eye for detail, and the ability to work independently while also collaborating effectively with a multidisciplinary team of scientists. Maintaining a safe and organized laboratory environment, adhering to GLP/GMP standards, and staying current with scientific literature are also integral aspects of this role. This is an exceptional opportunity to join a dynamic team at the forefront of scientific innovation and make a tangible contribution to developing life-changing therapeutics.

Responsibilities:

• Design, perform, and optimize complex experiments in molecular biology and biochemistry.
• Develop and validate new assays and experimental protocols.
• Analyze experimental data using appropriate statistical methods and software.
• Troubleshoot experimental issues and identify solutions.
• Accurately record and meticulously document all experimental procedures and results in electronic lab notebooks.
• Collaborate with project teams, present findings, and contribute to research strategy discussions.
• Maintain laboratory equipment and ensure compliance with safety regulations.
• Stay updated on relevant scientific literature and emerging technologies.
• Contribute to manuscript preparation and patent applications as needed.

Qualifications:

• MSc or PhD in Molecular Biology, Biochemistry, Biotechnology, or a related life science discipline.
• Minimum of 5 years of post-graduate research experience in an industrial or academic R&D setting.
• Proven expertise in cell-based assays, molecular cloning, protein expression and purification, or similar relevant techniques.
• Strong understanding of drug discovery and development processes.
• Proficiency in data analysis software (e.g., GraphPad Prism, R).
• Excellent laboratory technique, attention to detail, and record-keeping skills.
• Strong written and verbal communication abilities.
• Ability to work independently and as part of a collaborative team.
• Experience with high-throughput screening (HTS) is a plus.

Join our client's dedicated team and contribute to significant advancements in biotechnology.

We are seeking an experienced operations professional to manage critical data acquisition infrastructure supporting advanced AI model development. This contract role requires exceptional operational acumen, demonstrated ability to scale complex workflows, and meticulous attention to quality standards across high-volume data collection initiatives.

Primary Responsibilities

Strategic Operations Management

• Oversee end-to-end execution of multiple concurrent data acquisition programs encompassing speech, visual, textual, and audio content streams

• Develop and implement scalable operational frameworks ensuring consistent achievement of volumetric targets while maintaining stringent quality thresholds

• Drive continuous process improvement through systematic identification and elimination of operational inefficiencies

Stakeholder & Contributor Management

• Design comprehensive contributor engagement strategies optimizing recruitment, onboarding, retention, and successful task completion

• Establish robust support infrastructure delivering timely resolution of technical and procedural inquiries

• Cultivate productive relationships with internal stakeholders through transparent communication and data-driven insights

Quality Assurance & Compliance

• Implement rigorous quality control methodologies maintaining data acceptance rates exceeding 95%

• Ensure strict adherence to data governance protocols, consent management, and regulatory requirements

• Develop predictive quality indicators enabling proactive intervention and remediation

Performance Analytics & Reporting

• Generate comprehensive operational intelligence providing actionable insights for strategic decision-making

• Establish KPI frameworks measuring throughput, quality, efficiency, and contributor satisfaction

• Deliver regular executive summaries highlighting achievements, challenges, and optimization opportunities

Working Arrangements

This position offers complete location flexibility within European time zones. Candidates must maintain reliable high-speed internet connectivity and professional home office environment conducive to managing distributed operations.

Application Requirements

Qualified candidates should demonstrate clear alignment with outlined competencies and provide specific examples of operational excellence in similar environments. We value diverse perspectives and encourage applications from candidates with non-traditional backgrounds who possess relevant transferable skills.

Required Qualifications

Professional Experience

• Minimum 1-3 years operational management experience within data-intensive environments (crowdsourcing platforms, research operations, content moderation, or similar domains)

• Demonstrated success managing distributed contributor networks (100+ simultaneous participants)

• Proven ability to meet aggressive performance targets while maintaining exceptional quality standards

Technical & Analytical Competencies

• Proficiency in operational tools and platforms for workflow management, data tracking, and process automation

• Strong analytical capabilities with experience translating complex data into actionable operational strategies

• Familiarity with quality assurance methodologies and statistical sampling techniques

Communication & Leadership

• Exceptional written and verbal communication skills in English (additional languages highly valued)

• Experience delivering technical support through multiple channels (email, chat, ticketing systems)

• Ability to influence without authority and drive results through collaborative partnerships

Overview

Scientific Computing Apprentice (Research Software Engineering) – The Institute of Cancer ResearchnJoin to apply for the

Scientific Computing Apprentice (Research Software Engineering)

role at

The Institute of Cancer Research .nSalary: £25,275nDuration of Contract: Fixed Term for 24 monthsnHours per week: Full Time (28 hours per week with 7 hours dedicated to learning/studying time, Monday to Friday)nLocation: Sutton/Chelsea. This role is eligible for hybrid working.nClosing Date: 14th September 2025nThis Master’s degree level apprenticeship will see you developing, maintaining, and optimising the software and computational tools that support and advance scientific research. The role is ideal for a proactive and motivated individual with a passion for scientific computing and an interest in research software engineering, wishing to work and learn in a diverse research community. This opportunity provides a great way to build your career.nResponsibilities

Develop, maintain, and optimise software and computational tools used in scientific research.nWork within the Digital Services Directorate alongside researchers to support HPC, data storage, data management, and research software engineering needs.nEngage with a structured Master’s curriculum while gaining hands-on, real-world training.nQualifications and Requirements

Apprenticeship at Master’s degree level (Master’s degree funded as part of the program).nInterest in scientific computing and research software engineering.nProactive, motivated, and able to work in a diverse research community.nBenefits

Fully-Funded Master’s Degree: We’ll cover 100% of your master’s degree, allowing you to earn a postgraduate qualification without the financial burden.nReal-World Impact: Work at the forefront of cancer research, directly supporting scientists and clinicians.nComprehensive Training: Structured Master’s curriculum combined with hands-on, real-world training.nAbout The Institute Of Cancer Research

The Digital Services Directorate provides technology access and IT support to the ICR’s research community. Scientific Computing is a unit within Digital Services offering HPC, Research Data Storage (RDS), Research Data Management (RDM), and Research Software Engineering (RSE).nFor more information, please access the attached job pack and associated MSc Applied Data Science (Degree Apprenticeship) details. For informal discussion, contact Rachel Alcraft at or via email.nEqual Opportunity

We champion diversity and are committed to equal opportunity for all applicants regardless of ethnicity, gender, age, sexual orientation, disability, or any other dimension of diversity. The Institute encourages overseas applicants where applicable.

#J-18808-Ljbffrn

Overview

Our global technology client is looking for an experienced

Software Engineer

to join their pioneering Reality Labs research team, working on the next generation of immersive devices such as smart glasses and VR headsets. This role focuses on building and optimising systems for

audio, video, and sensor data collection , ensuring efficient, reliable, and accurate capture from cutting-edge prototype devices.nWhat You’ll Do

Develop Python-based software for integrating and managing prototype wearable devices.noptimise the distributed data collection platform to enhance accuracy and efficiency.nWork with

audio, video, and inertial measurement

recording equipment.nDeploy, test, and monitor system upgrades.nDebug and perform root cause analysis on hardware/software issues onsite.nCollaborate with engineers and researchers to scope tasks, design solutions, and implement best practices.nWhat You’ll Bring

Required:n8+ years in software engineering.nLinux and shell scripting proficiency.nStrong knowledge of RESTful APIs and distributed systems.nExperience with FastAPI or similar frameworks.nSolid problem-solving skills and ability to work in cross-functional teams.nExperience with hardware multimedia sensors.nKnowledge of audio, video, and image formats.nDatabase experience (SQL, NoSQL, or graph).nFamiliarity with frontend frameworks (React, JS).nWhy Join

Work on innovative AR/VR projects shaping the future of connected experiences.nCollaborate with world-class researchers and engineers.nGain hands-on experience with state-of-the-art devices and data systems.nApply now

and please send your CV, daily rate, and availability to:

#J-18808-Ljbffrn

The Clinical Data Standards Architect (CDSA)- Data Collection and Delivery implements and maintains efficient standard content in the data collection tools and delivery tools and defines and maintains the standard metadata supporting the data flow from data collection to data delivery.
The CDSA configures standards to the specific needs and requirements of a Therapeutic Area, compound Disease Area, generating the expected efficiencies through optimal adoption and reuse of standards. The CDSA also supports the functions adopting the standards in the clinical trials, in close collaboration with the clinical data collection team. 
The CDSA is responsible for implementing efficient standards in the Rave EDC system (Medidata Solutions). 
Responsibilities:
+ Implements the standard content in the data collections and delivery tools with the goal of creating efficiencies within the trials, consistency across the trials and automating the CRF build and the data flow from collection to SDTM.
+ Examples of standard content for the _data collection focus_
+ Standard Case Report Form Mockups 
+ Standard Questionnaires, Rating Scales and Clinical Outcome Assessments 
+ Standard Validation Rule Specifications 
+ Standard Integrations (e.g. with IWRS) 
+ Examples of standard content for the _data delivery focus_
+ Study Data Tabulation Model (SDTM)
+ Annotated Case Report Forms (CRFs)
+ Support the data transfer agreement (DTA) standards with SDTM
+ Data Review Model (DRM: internal SDTM like model)
+ Mapping metadata from data collection (CRF and DTA) to DRM
+ Mapping metadata from DRM to SDTM
+ Implements standard content in the collection and delivery tools compliant to the industry standards and health authority regulations, meeting best computer system validation practices where applicable.
+ Responsible for the correct testing and QC of the collection tools and mapping metadata and therefore collaborates with the respective functions in Integrated Data Analysis and Reporting.  
+ Defines and maintains the standard clinical data collection and the clinical data delivery standards for use in clinical trials. 
+ Maintains the data collection and delivery and metadata standards at a master level to meet additional scientific or operational requirement supporting the R&D portfolio. To that end the CDSA will guarantee formal change management control and versioning of the standards is applied and adhered to.
+ Governs formally all the changes to standards and manages multiple versions in line with adoption needs of the clinical trials and drug development programs. 
+ Pre-configures the standards in line with the specifications of the data lifecycle plans, while maintaining the traceability and lineage of the data. Documents and manages correctly the lineage between master standards and the many pre-configured standards.   
+ Provides the necessary support to the clinical data standards team and the clinical analysis team who facilitate the consistent adoption of standards in the studies (internally or outsourced to a CRO).  
+ _Data delivery focus only:_ Annotates the CRF with SDTM metadata and collaborates with his/her team members on the correctness of the annotated case report form meeting submission, scientific and operational requirements and guidelines.
Education and Experience:
+ Deep expertise in Rave EDC (Medidata Solutions) 
+ Experience with running SAS programs, coding experience preferred.
+ Experience with coding and running SAS programs
+ Knowledge of Rave EDC (Medidata Solutions)
+ Expertise with CDISC standards: SDTM, CDASH, Controlled terminology and define.xml. 
+ Experience with SAS LSAF and Pinnacle 21
+ BS/BA degree in life sciences or computer science or equivalent by work experience 
+ 2 years of relevant operational experience in clinical data management or standards
+ Relevant operational experience in clinical data standards is preferred 
+ Experience in prioritizing and managing multiple tasks simultaneously 
+ Outstanding written and verbal communication skills in English 
**This role is not eligible for UK visa sponsorship**
IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create connections that accelerate the development and commercialization of innovative medical treatments. Everything we do is part of a journey to improve patient outcomes and population health worldwide.
To get there, we seek out diverse talent with curious minds and a relentless commitment to innovation and impact. No matter your role, everyone at IQVIA contributes to our shared goal of helping customers improve the lives of patients everywhere. Thank you for your interest in growing your career with us.
EEO Minorities/Females/Protected Veterans/Disabled

Location: Remote (Video Call)
Type: One-time Research Session
Duration: 30-45 minutes
Positions Available: Multiple

Join us in advancing AI technology that protects against deepfake videos! Your Personal AI is conducting important research to improve systems that detect manipulated video content. Your participation directly contributes to making digital media more trustworthy and secure.

This is a one-time, fully guided video session where you'll help train AI systems to distinguish between authentic and altered faces. No technical expertise required - our moderator provides complete support throughout the session.

What You'll Do

During your 30-45 minute session, you will:

• Join a video call with our professional moderator

• Answer 8-10 simple interview questions (e.g., "What's your favorite food?" or "Tell us about a happy memory")

• Test different video filters while answering questions

• Receive step-by-step guidance for all technical aspects

The Process:

1. Schedule your session at a convenient time

2. Join a Microsoft Teams call with your moderator

3. Get help setting up Amazon DCV (secure remote system)

4. Complete 4 short interview rounds with different filters

5. Receive payment upon completion

Ideal Participants

We welcome participants from all backgrounds! We're looking for:

• Reliable individuals who can commit to their scheduled session

• People comfortable with video calls

• Those interested in contributing to AI research

• Participants with diverse faces and backgrounds to ensure robust AI training

Important Notes

• Privacy: Your data is used solely for research purposes and handled with strict confidentiality

• Technical Support: Our moderator assists with all technical setup - no prior experience needed

• Time Commitment: Please ensure you can dedicate the full 30-45 minutes without interruption

• Equipment: Sessions work best on computers less than 4 years old

Essential:

• Computer or laptop (manufactured 2020 or later for optimal performance)

• Stable internet connection

• Working webcam

• Ability to commit 30-45 minutes without interruption

• Comfortable being on camera

• English language proficiency

**Job Description**
**Are You Ready to Make It Happen at Mondelēz International?**
**Join our Mission to Lead the Future of Snacking. Make It Matter.**
As an organization we are committed to developing the next generation of Makers and Bakers. Joining us at an early career stage in our fast paced and ever changing environment will enable you to do more, learn more and grow more. You will be encouraged to step outside your comfort zone- you may even surprise yourself! We will ensure you are given the support you need to be at your best and enable you to be yourself and bring passion and personality. Here you can lean in and speak up and bring your own flavor.
**Big enough to reach the top. Small enough to help you get off the ground.**
Are you studying towards a Degree in Food Science, Engineering, or other scientific discipline (e.g., Chemistry, Biology, Biochemistry, Food & Nutrition, Physical Sciences, Materials Science, Physics)? Do you want a taste of the career you could have with Mondelez? Sink your teeth into one of our sweet internships. 
Our Internships are 12 months long (although some roles have the flexibility to be shorter) and during your placement, we'll make you an integral part of our team and give you a real job - with real responsibilities - from day one. We hope to help you expand your horizons and encourage your personal and professional development. 
We want to make sure you get the most from your time with us. That's why once you join we'll work out ambitious but achievable goals for you. Then through the support of a mentor and regular reviews with your manager, we'll help you achieve them.
**Life in Research Development Quality:**
As an intern in R&D at Mondelēz International, you'll take ownership of projects. You will contribute to the future of snacking by keeping the consumer at the heart of our innovation. Deliverables may include producing technical reports and presentations, sharing insights with stakeholders and fostering transparency and collaboration. You will have the opportunity to work with the broader RDQ community, business functions, and external suppliers, building your network and confidence. Beyond your primary project, you may support ongoing activities, gaining diverse experiences and contributing to a sustainable future. For some roles, occasional international travel may be required.
**About the role** :
**Scientific and Regulatory Affairs (SARA):**
This internship offers a unique opportunity to gain hands-on experience in the exciting world of food innovation. As an R&D-Scientific and Regulatory Intern, you'll work alongside experienced food scientists, chemists, chemical engineers, contributing to the creation and improvement of some of the world's most beloved snack brands. This is a chance to learn about the entire product development lifecycle and work with global and regional stakeholders to drive innovation, product quality, productivity and sustainability.
**Key Responsibilities:**
+ Ensures that finished products for EU and UK markets are compliant with European legislations, local legislations, company policies, and are marketed in responsible, fair and honest matter.
+ Helps in review & approval of commercial advertising, consumer and trade press releases, websites, and social media to ensure they comply with Food Labelling Regulation.
+ Helps to devise legal names and to validate claims on new product development.
+ Prepares and coordinates finished product labelling (Product Label Reports) for low complexity projects by working closely with Regulatory Affairs team, R&D, PCM and Marketing.
+ Reviews product labelling (Artwork) and submits comments into Artwork Approval System to ensure all mandatory elements are present and are compliant with all relevant regulations (legal name, ingredient list, allergens, nutritional information, product claims, storage, net weight.).
+ Takes part in specification system Data Excellence, Digitalization initiatives.
+ Supports the Scientific Affairs team with horizon scanning, monitoring of EU and UK emerging regulations, assesses their impact and builds communication materials. Supports development and implementation of our external advocacy positions.
+ Creates and updates our Global, EU and UK trackers on food labelling, health and nutrition policies.
**What we're looking for:**
**Education** : Currently pursuing a Bachelor's Degree in Food Science, Engineering, or other scientific discipline (e.g., Chemistry, Biology, Biochemistry, Food & Nutrition, Physical Sciences, Materials Science, Physics) with a predicted end grade of a 2:1 - (or equivalent).
+ **Communication skills** : Demonstrates strong analytical, communication and presentation abilities.
+ **Technical Rigour:** Able to apply scientific approach to new situations whilst maintaining a well thought out approach. Has strong attention to detail.
+ **Initiative** : A pro-active and highly motivated team player who thrives on new challenges, building relationships, and working autonomously.
+ **Agility:** Able to manage multiple tasks, adapt quickly, and respond to feedback constructively.
+ **Collaborative Mindset:** Comfortable working in diverse teams with project managers, marketers, scientists, engineers, and suppliers.
+ **Creativity & Curiosity** : You love to explore, ideate, and challenge the norm. You're not afraid to ask, "what if?". You show eagerness to grow and learn and bring fresh ideas.
**This position does not meet the minimum salary requirements for Skilled Worker visa sponsorship. Therefore, we are unable to consider applicants who require sponsorship. Applicants must already have the right to work in the UK.**
**Additional desirable skills:**
Passion/inquisitiveness about food, food labelling and regulations, nutrition, wellbeing and food production.
**What you'll gain:**
It's the people that makes Mondelez a great place to work and there is a comprehensive onboarding and training plan with buddies on hand to fully support your time with us.
+ Hands-on experience of the regulatory compliance process in the diverse, multilingual team in a leading global snacking company's R&D team.
+ Technical skills in product recipe assessment, labelling preparation and food legislations.
+ The opportunity to network with experienced scientists and engineers in the food industry in a diverse and multicultural environment.
+ Contribute to the regulatory compliance of innovative and exciting new products.
+ Additional benefits: Access to discounted staff shop, discounted on-site gym membership and online GP services.
**Starting salary: £23,000**
Closing date for applications is midday **Tuesday 21st October 2025** .
We will be holding our final stage assessment center for this role in-person at our Bournville offices on **Tuesday 25th & Wednesday 26th of November 2025** . Reasonable travel expenses will be covered.
**A word from one of our 23-24 interns:**
_"Join our team and play a vital role in ensuring our products are safe, compliant, and clearly communicated to consumers. This internship offers a unique blend of regulatory and scientific exposure. You'll collaborate with Regulatory Affairs, Marketing, and R&D, reviewing labels, artwork, and claims to meet EU and UK food legislation._
_Beyond approvals, you'll support horizon scanning projects and develop communication materials, gaining insight into how food policies shape innovation. You'll be encouraged to share your questions and ideas, taking ownership of your projects._
_This experience will strengthen your technical knowledge, cross-functional collaboration, and communication skills. You'll leave with a deeper understanding of regulatory affairs and a real sense of accomplishment. Be prepared to learn a lot and contribute meaningfully!"_
For more details on our Early Careers schemes and advice on our application process, visit our careers site today - Early Careers - UK | Mondelēz International, Inc. (mondelezinternational.com) ( is a diverse and inclusive employer with an objective to ensure a fair and equal hiring process. If you require any reasonable adjustments to apply or throughout our assessment process please contact stating "UK&I Early Careers" as the subject.**
**Our candidate requirements are based on criteria to enable you to succeed in the role. If you have narrowly missed the above requirements and there are extenuating circumstances that you would like us to consider, you can let us know by contacting stating "UK&I Early Careers" as the subject and attaching a letter from your school/university to confirm your extenuating circumstances.**
**Relocation Support Available?**
**Business Unit Summary**
**We value our talented employees, and whenever possible strive to help one of our associates grow professionally before recruiting new talent to our open positions. If you think the open position you see is right for you, we encourage you to apply!**
**_Our people make all the difference in our succes_**
Mondelēz International is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, gender, sexual orientation or preference, gender identity, national origin, disability status, protected veteran status, or any other characteristic protected by law.
**Excited to grow your career?**
We value our talented employees, and whenever possible strive to help one of our associates grow professionally before recruiting new talent to our open positions. If you think the open position you see is right for you, we encourage you to apply!
**IF YOU REQUIRE SUPPORT TO COMPLETE YOUR APPLICATION OR DURING THE INTERVIEW PROCESS, PLEASE CONTACT THE RECRUITER**
**Job Type**
Intern (Fixed Term)
Interns
Early Careers
At Mondelēz International, our purpose is to empower people to snack right through offering the right snack, for the right moment, made the right way. That means delivering a broader range of delicious, high-quality snacks that nourish life's moments, made with sustainable ingredients and packaging that consumers can feel good about.
We have a rich portfolio of strong brands - both global and local. Including many household names such as Oreo, belVita and LU biscuits; Cadbury Dairy Milk, Milka and Toblerone chocolate; Sour Patch Kids candy and Trident gum. We are proud to hold the number 1 position globally in biscuits, chocolate and candy as well as the No. 2 position in gum
Our 80,000 Makers and Bakers are located in our operations in more than 80 countries and are working to sell our products in over 150 countries around the world. They are energized for growth and critical to us living our purpose and values. We are a diverse community that can make things happen, and happen fast.
Join us and Make It An Opportunity!
Mondelez Global LLC is an Equal Opportunity/Affirmative Action employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability, protected Veteran status, sexual orientation, gender identity, gender expression, genetic information, or any other characteristic protected by law. Applicants who require accommodation to participate in the job application process may contact for assistance.

Job Position: Data Architect (6-Month Contract)

Role: Data Architect

Contract Duration: 6 months

IR35 Status: Outside IR35

Location: Hybrid working model based in Leeds, Manchester, or Blackpool (as required).

Start Date: ASAP

Daily Rate: Competitive

Role Summary: We are seeking a highly skilled and experienced Data Architect for a 6-month contract. The successful candidate will be responsible for designing and building data models, ensuring data integrity, and aligning data infrastructure with business requirements. This is a critical role to help shape our data strategy and ensure our systems are optimized for performance and security.

Required Experience:

• Proven experience in a Data Architect role.
• Strong knowledge of data management, modelling, and governance.
• Essential: experience with debt systems.
• Ability to work effectively with both technical and non-technical stakeholders.
• Experience in an agile environment is a plus.

How to Apply

If you are the right person for this role and have the required experience, please apply directly via the job advert.

Job Position: Data Architect (6-Month Contract)

Role: Data Architect

Contract Duration: 6 months

IR35 Status: Outside IR35

Location: Hybrid working model based in Leeds, Manchester, or Blackpool (as required).

Start Date: ASAP

Daily Rate: Competitive

Role Summary: We are seeking a highly skilled and experienced Data Architect for a 6-month contract. The successful candidate will be responsible for designing and building data models, ensuring data integrity, and aligning data infrastructure with business requirements. This is a critical role to help shape our data strategy and ensure our systems are optimized for performance and security.

Required Experience:

• Proven experience in a Data Architect role.
• Strong knowledge of data management, modelling, and governance.
• Essential: experience with debt systems.
• Ability to work effectively with both technical and non-technical stakeholders.
• Experience in an agile environment is a plus.

How to Apply

If you are the right person for this role and have the required experience, please apply directly via the job advert.