9 Research And Development jobs in Bracknell

Founded in 2003 Wasabi's vision is to lovingly create and serve delicious Asian food for a busy nation.

Wasabi now has 40 thriving restaurants across London and major UK cities and 4 in New York and in 2019, we introduced Wasabi Home Bento, launched exclusively in Sainsbury’s. Building on that success, the grocery business broadened its reach to Tesco in September 2022, followed by exciting launches in Co-op and Morrisons in 2024. Today, Wasabi proudly stands as the No. 2 chilled ready-meal brand, setting new standards for quality and innovation.

Wasabi’s menu is celebrated for its unique character, exceptional freshness, and bold flavours. Our diverse range is designed to delight a wide audience, delivering both comfort and excitement with every bite.

We have an ambitious 5-year growth strategy, focusing on new restaurants, franchise partnerships, and international expansion.

As we prepare for our next phase of growth and innovation, we have an incredibly exciting opportunity for a P roduct Development Technologist to join our Food Team based in Park Royal.

The Role:

Play a key role in technical food development, driving launch-ready projects and converting kitchen recipes into scalable, operational products.

Key Responsibilities (but not limited to):

• Lead the hands-on development of new and existing food products, ensuring alignment with briefs and technical standards.

• Collaborate with chefs, procurement, and technical teams to create and refine commercially viable recipes suitable for production.

• Adapt recipes to CPU and factory capabilities, solving challenges to deliver optimal results.

• Accurately document recipes, preparation methods, yields, nutritional information, and costing according to company standards

• Write cooking and reheating instructions and complete product attribute documentation for gate approvals.

• Conduct organoleptic and shelf-life testing during development to validate product performance and feasibility.

• Manage new product development (NPD) and existing product development (EPD) from concept through to launch, including critical path ownership.

• Present products at key stages of development and lead handovers to process and production teams.

• Source and validate new raw materials with procurement, ensuring suitability for culinary and operational requirements.

• Attend CPU upscale trials and support process development to maintain quality and consistency at scale.

• Drive food quality improvement initiatives, including resolving quality issues and customer complaints.

• Facilitate and participate in taste panels, benchmarking sessions, and regular product quality reviews.

• Prepare and provide samples for presentations, photography, and marketing, including food styling support.

• Maintain a clean and organised development kitchen, managing stock and ordering raw materials as needed

 

Our Requirements:

• Previous experience working as a Process or Food Technologist within the food manufacturing industry.
• Qualified degree in a food related discipline – food science, technology, home economics.
• Demonstrates an above standard knowledge of food, ingredients, and culinary practices.
• Highly creative and passionate about food with knowledge of South Asian, Japanese and Korean food trends and good industry awareness.
• Certificate in Food Hygiene
• A proactive personality, with the ability to communicate effectively at all levels.
• A methodical approach, be organised with good prioritisation skills, the ability to work to short deadlines and attention to detail.
• Excellent planning and organisational skills.
• Can work on multiple projects simultaneously with ease and thriving in a busy fast-paced environment.

In return we provide:

• A great working environment
• Pension scheme
• Target Bonus
• Refer A Friend Scheme
• Free Sushi or hot food (vegan options available)
• 50% discount in our Branches
• Employee Assistant Programme
• Hybrid working model
• Long Service Awards
• Wagestream - a financial wellbeing benefit that lets you access your pay as you earn it in real time and manage savings
• Life Assurance
• Cycle To Work
• Free on-site parking
• A variety of discounts (shopping, food & drink, entertainment and health & fitness) through Perkbox and
• The opportunity to develop your skills within a growing company.

 
Our people make us who we are. If you're looking for an exciting challenge and this sounds like the job for you please apply today as we can't wait to hear from you. 

COME ROLL WITH US!

Research Scientist / Associate – Upstream Process Development

Roles: Full-time, permanent

Location: Harrow, London

Salary: Competitive + bonus + benefits

The Role:

we’re seeking a proactive and methodical Research Scientist / Research Associate to join our growing Upstream Process Development team. You will support our cell culture operations (revival, subculture, cryopreservation, cell culture media preparation), optimising mammalian cell culture parameters through our Ambr250 bioreactors and other advanced process development equipment. Working across the clone lifecycle in the bioreactors, you’ll perform inoculation till harvest including daily monitoring activities and associated data analysis in-line with all quality and safety requirements.

To ensure the best results, you’ll undertake regular data analysis (such as cell density, viability parameters, metabolite analysis, etc.) from advanced process development equipment and troubleshoot technical activities. To support the smooth running of the department, you will complete COSHH, risk assessment and peer review lab documentation and maintain equipment-specific SOPs. Design of Experiments will be routinely performed for process development activities, producing data summary and progress reports, along with participating in safety inspections, stock checks and maintaining our ‘state of the art’ machines. In this exciting role, you’ll get the opportunity to learn and work collaboratively with the different workstream teams (in the UK and with our colleagues abroad from our established Biopharma unit at Intas Pharmaceuticals) and to grow with the team to support our ambitious growth plans.

The Person:

• Experience in a similar Research Scientist / Research Associate role within the biopharma / biotech / contract research labs sector, with good technical experience in automated bioreactors for mammalian cell culture (e.g. ambr250/small scale bioreactors & 5-10 L Bioreactors).
• Experienced in Biosimilar development upstream process development activities
• Experience in daily monitoring and primary recovery of bioreactors.
• Good knowledge of GLP and understanding of GMP requirements.
• Good understanding of therapeutic antibody / protein quality attributes.
• Good IT and data analysis skills, including use of Microsoft Office (i.e. Excel, Word, PowerPoint) and biopharma analysis software (e.g. Biopat process insights, MFCS, DoE software etc.)
• Excellent communication skills (written and spoken English), confident working with colleagues of all seniority levels and able to navigate cultural differences with ease.
• Proactive and agile team player, but equally comfortable working on own initiative.
• Strong organisation skills, able to manage conflicting tasks to meet deadlines and to solve problems on your feet, even in a busy and changeable work environment.
• Degree / Masters / PhD level qualification in a Biological Science or technical scientific discipline.

The Rewards:

In return, we offer a competitive salary package (with bonus, holiday and pension scheme), and a range of other benefits to support our team. Not to mention the opportunity to be part of a new department within a progressive and expanding business with increasing global reach, and the support of ongoing training and development.

How to Apply:

If you possess the experience, passion and ability to make this role a success then we would like to hear from you. Please complete your Candidate Profile on our careers site to apply for this role. The closing date is 03/08/2025 . For more information, you can contact us on:

A Bit About Us:

Accord Healthcare Europe is one of the fastest growing pharmaceutical companies in Europe and has one of the largest market footprints of any European generic and biosimilars companies, selling generic medicines in over 80 countries around the world. This global footprint enables us to deliver vital, affordable medicines to national health systems, supporting healthcare professionals to transform patient lives worldwide. The approach of Accord is agile and inventive, always seeking to improve products and patients' access to them. Accord is driven to think differently and deliver more for the benefit of patients worldwide.

To continue our growth, we’re looking for the best and brightest technical minds and forward-thinking business professionals. Keeping our people at the heart of all we do, we offer rewarding opportunities for those looking for continued personal and professional growth, investing in training and development tailored to each individual’s focus. So, if you’re looking for an inclusive company to take your career to the next level, you’re certainly in the right place; come and join us to make it better.

Our team is growing, join us on our mission to drive healthcare forward!
What We Offer / USPs
+ The chance to work on cutting edge medicines at the forefront of new medicines development
+ IQVIA has access to significant data pools allowing better site selection and recruitment. This helps drive performance of sites making the CRA role more efficient and discussions at site more productive. Next generation clinical development!
+ We offer genuine career development opportunities for those who want to grow as part of the organization
+ We invest in keeping our teams stable, so workload is consistent
+ As a CRA you will receive an iPad and use of key developments such as site visit app's, site visit report app's that allow CRA's to do their day job more efficiently
Responsibilities
+ Perform site monitoring visits (selection, initiation, monitoring and close-out visits) in accordance with contracted scope of work and regulatory requirements, i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines
+ Work with sites to adapt, drive, and track subject recruitment plan in line with project needs to enhance predictability
+ Administer protocol and related study training to assigned sites and establish regular lines of communication with sites to manage ongoing project expectations and issues
+ Evaluate the quality and integrity of study site practices related to the proper conduct of the protocol and adherence to applicable regulations. Escalate quality issues as appropriate
+ Manage the progress of assigned studies by tracking regulatory submissions and approvals, recruitment and enrollment, case report form (CRF) completion and submission, and data query generation and resolution. May support start-up phase
+ Ensure copies/originals (as required) site documents are available for filing in the Trial Master File (TMF) and verify that the Investigator's Site File (ISF) is maintained in accordance with GCP and local regulatory requirements
+ Create and maintain appropriate documentation regarding site management, monitoring visit findings and action plans by submitting regular visit reports, generating follow-up letters and other required study documentation
+ Collaborate and liaise with study team members for project execution support as appropriate
+ If applicable, may be accountable for supporting development of project subject recruitment plan on a per site basis
+ If applicable, may be accountable for site financial management according to executed clinical trial agreement and retrieve invoices according to local requirement
Requirements
+ You should be life science degree educated
+ You have experience of independent on-site monitoring experience
+ You've handled multiple protocols and sites across a variety of drug indications
+ Flexibility and ability to travel
+ Strong communication, written and presentation skills
*** 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

Join Us on Our Mission to Drive Healthcare Forward
IQVIA cFSP (sponsor-dedicated) are seeking experienced Clinical Research Associates in the UK.
Why IQVIA?
+ IQVIA is recognized as #1 in its category on the 2025 Fortune® World's Most Admired Companies list for the FOURTH consecutive year!
+ We offer genuine career development opportunities for those who want to grow as part of the organization.
+ The chance to work on cutting edge medicines at the forefront of new medicines development.
+ IQVIA has access to significant data pools allowing better site selection and recruitment. This helps drive performance of sites making the CRA role more efficient and discussions at site more productive. Next generation clinical development!
Responsibilities
+ Perform site monitoring visits (selection, initiation, monitoring and close-out visits) in accordance with contracted scope of work and regulatory requirements, i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines
+ Work with sites to adapt, drive, and track subject recruitment plan in line with project needs to enhance predictability
+ Administer protocol and related study training to assigned sites and establish regular lines of communication with sites to manage ongoing project expectations and issues
+ Evaluate the quality and integrity of study site practices related to the proper conduct of the protocol and adherence to applicable regulations. Escalate quality issues as appropriate
+ Manage the progress of assigned studies by tracking regulatory submissions and approvals, recruitment and enrollment, case report form (CRF) completion and submission, and data query generation and resolution. May support start-up phase
+ Ensure copies/originals (as required) site documents are available for filing in the Trial Master File (TMF) and verify that the Investigator's Site File (ISF) is maintained in accordance with GCP and local regulatory requirements
+ Create and maintain appropriate documentation regarding site management, monitoring visit findings and action plans by submitting regular visit reports, generating follow-up letters and other required study documentation
+ Collaborate and liaise with study team members for project execution support as appropriate
Requirements
+ Experience of independent on-site monitoring
+ You have successfully managed multiple clinical trial protocols across diverse investigative sites.
+ In depth knowledge of Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines
+ Life science degree educated or equivalent industry experience
+ Flexibility to travel to sites
Apply today and forge a career with greater purpose, make an impact, and never stop learning!
#LI-ADAMTHOMPSON
*Please note - 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

**Job Description Summary**
This role is to provide in house (limited travel) support relating to study set-up, monitoring and close-out activities to ensure the compliant and efficient conduct of GE HealthCare clinical studies.
GE HealthCare is a leading global medical technology and digital solutions innovator. Our mission is to improve lives in the moments that matter. Unlock your ambition, turn ideas into world-changing realities, and join an organization where every voice makes a difference, and every difference builds a healthier world.
**Job Description**
**Responsibilities**
+ Perform initial contact and participate in the assessment and selection of qualified investigators for inclusion in clinical programs.
+ Serve as the primary in-house contact for sites and investigators participating in studies.
+ Work with on-site monitors, to ensure compliant and efficient study conduct at site.
+ Support the conduct of Pre-Selection (feasibility), Initiation, Monitoring, and Closeout site visits. Attending (co-monitoring) as required (minimal travel expected for this in house role).
+ Support with reviews of monitoring visit reports as required.
+ Provide input to the preparation of study documentation such as protocols, amendments, Case Report Forms, and study reports.
+ Facilitate and support the preparation of regulatory and IEC/IRB submissions
+ Facilitate the collection and processing (upload to eTMF) of essential documents and correspondence.
+ Ensure that the files for the site (TMF and working files) for which the job holder is responsible are up to date, accurate and include all essential documents as detailed in ICH-GCP.
+ Assist in the conduct of internal and external Trial Master File Audits, in accordance with applicable SOPs and regulations/guidelines.
+ Negotiate and track site/trial budget according to financial agreement with each site and facilitation of site contract execution.
+ Develop and/or review Patient information and Informed Consent Forms and other patient facing materials as required.
+ Assist with the tracking of subject enrollment at each trial site, and provide management with detailed reports of clinical activities, as requested.
+ Ensure that clinical sites have adequate supplies (IMP and Non-IMP) to perform the study.
+ Actively attend study team meetings, including follow-up on assigned action items.
+ Develop a thorough knowledge of the diagnostic/therapeutic field and clinical programme(s) for the studie(s) to which the job holder is assigned.
+ Support oversight of vendor(s), e.g. Central Laboratory, as needed.
+ Participate in the development and review of Standard Operating Procedures, guidelines, forms and checklists.
+ Assist in the coordination of investigator meetings.
+ Perform training to site personnel, vendor and internal study personnel, as required.
+ Actively identify and communicate areas for improvement within the global clinical research infrastructure at GE HealthCare
**Qualifications**
+ PhD, MSc or BSc in a scientific / medical discipline with at least 3 years Clinical Research (preferably monitoring) or equivalent experience
+ Thorough understanding of the processes that are part of the day-to-day work of Clinical Research
+ Demonstrable team-work, communication, interpersonal, and problem-solving skills
+ A good understanding of the relevant Regulatory Authority regulations, guidance and the drug development process
+ The ability to manage multiple priorities and work well under pressure and time constraints
+ Strong process improvement mindset, passion for quality.
+ Technical aptitude (i.e. able to read and comprehend technical documentation, ability to comprehend and execute procedures, demonstrated understanding of system documentation).
+ Strong organizational skills with high attention to detail.
+ Familiarity with industry standard computerised system applications (e.g. eTMF, EDC, CTMS)
+ Experience with Veeva or other document/information management systems desired
+ Ability to work independently
**Inclusion and Diversity**
GE HealthCare is an Equal Opportunity Employer where inclusion matters. Employment decisions are made without regard to race, color, religion, national or ethnic origin, sex, sexual orientation, gender identity or expression, age, disability, protected veteran status or other characteristics protected by law.
**Behaviours**
We expect all employees to live and breathe our behaviors: to act with humility and build trust; lead with transparency; deliver with focus, and drive ownership - always with unyielding integrity.
**Total Rewards**
Our total rewards are designed to unlock your ambition by giving you the boost and flexibility you need to turn your ideas into world-changing realities. Our salary and benefits are everything you'd expect from an organization with global strength and scale, and you'll be surrounded by career opportunities in a culture that fosters care, collaboration, and support.
#LI-MG1
#LI-HYBRID
**Additional Information**
**Relocation Assistance Provided:** No

• Title: Associate Director, Clinical Research
• Contract: ASAP until 29-May-2026
• Location: Weybridge Hybrid - approx. 2 days on site

SRG are working with a world-leading consumer company who are seeking an Associate Director, Clinical Research to join the team.

Job Overview

Responsible for leading clinical research activities with a focus on clinical efficacy, effectiveness (through prospective Real World Evidence studies) and other clinical evidence generation activities by ensuring that high quality clinical research expertise is provided to meet state-of-the-art scientific, industry and regulatory standards (as needed).

Lead clinical development evidence generation activities in line with specific category/ sub-category project strategies.

Responsible for the development, this role will provide support to cross-functional category/ sub-category / Business Unit teams on clinical research, new opportunities/business development and R&D strategies. The role will require significant interaction with several internal teams including but not limited to Category and Business Unit Medical Affairs, Clinical Operations, Biostatistics & Data Management as well as external groups/ individuals such as investigators/ academic researchers, Clinical Research Organizations and Health Care Practitioners to help achieve company objectives and to build company reputation.

Key Responsibilities

• Provide appropriate scientific/technical contribution or author the clinical development plan for the studies/projects assigned.
• With support from the Clinical Research Director, design fit-for-purpose clinical strategies and other clinical evidence generation strategies to support the business for innovation product/therapy area including medical devices, in line with ICH GCP and other regulatory requirements (as needed).
• Support peer review publications/input to clinical section of regulatory dossiers to ensure that they are scientifically robust from a medical and scientific standpoint.
• Responsible for the design, implementation, reporting, interpretation, disclosure and publication of company sponsored clinical studies to ensure these follow external e.g. GCP, internal Medical Governance and other internal policy requirements.
• Responsible for contributing clinical content to regulatory submissions and other regulatory engagements for clinical research activities.
• Responsible for supporting clinical/medical due diligence for external opportunities from a clinical research point of view.

Knowledge/ Education / Previous Experience Required

• Advanced Scientific degree e.g. M.S. or MSc in Clinical Science or Medical/Dental or related discipline
• Minimum 8 years' experience in clinical research/drug development in the Pharmaceutical/CRO or Healthcare industry, preferably in a Consumer Healthcare / FMCH / Pharmaceutical business Consumer Health care experience is greatly preferred.
• Previous experience within Oral Health, Wellness, Pain relief or Respiratory is an advantage.
• Proven ability to effectively liaise and influence internally and externally
• Ability to work in a multi-functional team
• Excellent verbal and written communication skills
• Excellent scientific writing skills
• Demonstrated experience and proven track record of delivering clinical development programs/clinical studies/clinical evidence gathering activities
• Demonstrated experience representing an organization with external stakeholders
• Demonstrated competent business acumen
• Excellent verbal and written communication skills in English
• Strong computer literacy including competency in Microsoft Office software

Carbon60, Lorien & SRG - The Impellam Group STEM Portfolio are acting as an Employment Business in relation to this vacancy.

• Title: Associate Director, Clinical Research
• Contract: ASAP until 29-May-2026
• Location: Weybridge Hybrid - approx. 2 days on site

SRG are working with a world-leading consumer company who are seeking an Associate Director, Clinical Research to join the team.

Job Overview

Responsible for leading clinical research activities with a focus on clinical efficacy, effectiveness (through prospective Real World Evidence studies) and other clinical evidence generation activities by ensuring that high quality clinical research expertise is provided to meet state-of-the-art scientific, industry and regulatory standards (as needed).

Lead clinical development evidence generation activities in line with specific category/ sub-category project strategies.

Responsible for the development, this role will provide support to cross-functional category/ sub-category / Business Unit teams on clinical research, new opportunities/business development and R&D strategies. The role will require significant interaction with several internal teams including but not limited to Category and Business Unit Medical Affairs, Clinical Operations, Biostatistics & Data Management as well as external groups/ individuals such as investigators/ academic researchers, Clinical Research Organizations and Health Care Practitioners to help achieve company objectives and to build company reputation.

Key Responsibilities

• Provide appropriate scientific/technical contribution or author the clinical development plan for the studies/projects assigned.
• With support from the Clinical Research Director, design fit-for-purpose clinical strategies and other clinical evidence generation strategies to support the business for innovation product/therapy area including medical devices, in line with ICH GCP and other regulatory requirements (as needed).
• Support peer review publications/input to clinical section of regulatory dossiers to ensure that they are scientifically robust from a medical and scientific standpoint.
• Responsible for the design, implementation, reporting, interpretation, disclosure and publication of company sponsored clinical studies to ensure these follow external e.g. GCP, internal Medical Governance and other internal policy requirements.
• Responsible for contributing clinical content to regulatory submissions and other regulatory engagements for clinical research activities.
• Responsible for supporting clinical/medical due diligence for external opportunities from a clinical research point of view.

Knowledge/ Education / Previous Experience Required

• Advanced Scientific degree e.g. M.S. or MSc in Clinical Science or Medical/Dental or related discipline
• Minimum 8 years' experience in clinical research/drug development in the Pharmaceutical/CRO or Healthcare industry, preferably in a Consumer Healthcare / FMCH / Pharmaceutical business Consumer Health care experience is greatly preferred.
• Previous experience within Oral Health, Wellness, Pain relief or Respiratory is an advantage.
• Proven ability to effectively liaise and influence internally and externally
• Ability to work in a multi-functional team
• Excellent verbal and written communication skills
• Excellent scientific writing skills
• Demonstrated experience and proven track record of delivering clinical development programs/clinical studies/clinical evidence gathering activities
• Demonstrated experience representing an organization with external stakeholders
• Demonstrated competent business acumen
• Excellent verbal and written communication skills in English
• Strong computer literacy including competency in Microsoft Office software

Carbon60, Lorien & SRG - The Impellam Group STEM Portfolio are acting as an Employment Business in relation to this vacancy.

• Title: Associate Director, Clinical Research
• Contract: ASAP until 29-May-2026
• Location: Weybridge Hybrid – approx. 2 days on site

SRG are working with a world-leading consumer company who are seeking an Associate Director, Clinical Research to join the team.

Job Overview

Responsible for leading clinical research activities with a focus on clinical efficacy, effectiveness (through prospective Real World Evidence studies) and other clinical evidence generation activities by ensuring that high quality clinical research expertise is provided to meet state-of-the-art scientific, industry and regulatory standards (as needed).

Lead clinical development evidence generation activities in line with specific category/ sub-category project strategies.

Responsible for the development, this role will provide support to cross-functional category/ sub-category / Business Unit teams on clinical research, new opportunities/business development and R&D strategies. The role will require significant interaction with several internal teams including but not limited to Category and Business Unit Medical Affairs, Clinical Operations, Biostatistics & Data Management as well as external groups/ individuals such as investigators/ academic researchers, Clinical Research Organizations and Health Care Practitioners to help achieve company objectives and to build company reputation.

Key Responsibilities

• Provide appropriate scientific/technical contribution or author the clinical development plan for the studies/projects assigned.
• With support from the Clinical Research Director, design fit-for-purpose clinical strategies and other clinical evidence generation strategies to support the business for innovation product/therapy area including medical devices, in line with ICH GCP and other regulatory requirements (as needed).
• Support peer review publications/input to clinical section of regulatory dossiers to ensure that they are scientifically robust from a medical and scientific standpoint.
• Responsible for the design, implementation, reporting, interpretation, disclosure and publication of company sponsored clinical studies to ensure these follow external e.g. GCP, internal Medical Governance and other internal policy requirements.
• Responsible for contributing clinical content to regulatory submissions and other regulatory engagements for clinical research activities.
• Responsible for supporting clinical/medical due diligence for external opportunities from a clinical research point of view.

Knowledge/ Education / Previous Experience Required

• Advanced Scientific degree e.g. M.S. or MSc in Clinical Science or Medical/Dental or related discipline
• Minimum 8 years’ experience in clinical research/drug development in the Pharmaceutical/CRO or Healthcare industry, preferably in a Consumer Healthcare / FMCH / Pharmaceutical business Consumer Health care experience is greatly preferred.
• Previous experience within Oral Health, Wellness, Pain relief or Respiratory is an advantage.
• Proven ability to effectively liaise and influence internally and externally
• Ability to work in a multi-functional team
• Excellent verbal and written communication skills
• Excellent scientific writing skills
• Demonstrated experience and proven track record of delivering clinical development programs/clinical studies/clinical evidence gathering activities
• Demonstrated experience representing an organization with external stakeholders
• Demonstrated competent business acumen
• Excellent verbal and written communication skills in English
• Strong computer literacy including competency in Microsoft Office software