What Jobs are available for Research And Development in Didcot?

Job Location
READING TECH CENTER
Job Description
Ready to fuel the success of globally renowned brands like Gillette? Do you want to be part of the innovation and technological advancement of products used every day by millions of the world's consumers? Want to work for a company consistently recognised as one of the UK's leading graduate employers?
We are offering 12-month placement opportunities at our Reading Innovation Centre which will start in July 2026.
About our Reading Innovation Centre
This role is available in our Reading Innovation Centre which is home to over 200+ scientists and engineers responsible for innovating consumer products in several business areas including Personal Health Care (Vicks) Oral Care (Oral-B), Grooming (Gillette and Venus) and Beauty Care (Olay).
The site is a specialist Healthcare & Grooming Research & Development Hub in Europe and supports our European Beauty Franchise business. The site is friendly, diverse and has a rich history in innovation in multiple business areas.
Our site is located close to the town centre and is served by motorway networks of M4 and M25 as well as the A33. We're within 20 mins of Reading Central and Green Park railway stations and are served by buses that run every 10 minutes.
What To Expect:
Research and Development (R&D) at P&G will help you to discover the essence behind crafting some of the world's most renowned brands. Delve into a realm where science takes centre stage. Some of the best scientists in the world go to work making our products just right for the billions of consumers who use them. We're talking cutting edge technology, "hands-on" labs and pilot plants, 41,000+ active patents and a team full of inventors.
During your 12-month placement, you will get a first-hand experience of what a career in R&D with P&G involves, and if it is right for you. You will be working on live business R&D projects and expected to dive straight in and take the lead.
Each intern receives a customized learning plan to ensure they get the right levels of coaching, mentoring, and training as they deliver their work. If you are looking for an exciting and challenging experience, have a passion for winning, strong leadership credentials and an interest in pursuing a career at P&G - this placement is for you!
Please note that this programme is designed as a 12-month industrial placement for students graduating in 2028 with a placement year as part of their degree. However, we have a limited number of 6-month placements available for students graduating in 2026, 2027 or those who have already graduated starting 1st July 2026.
What You Will Gain:
+ Responsibilities and Real Work from Day 1: You will be given specific projects and responsibilities working on real and live business challenges, just like a true P&Ger.
+ Continuous training & coaching: You will work with passionate people and receive both formal training as well as day-to-day mentoring from your manager.
+ Competitive Compensation & Benefits: The annual salary for this 12-month placement is £31,500. On top of this you'll enjoy the option of a range of benefits including a competitive double-matched pension scheme, private health insurance, participation in a stock ownership scheme, and your very own 'Flex4Me' Fund which enables you to allocate a portion of your benefits package to the areas that matter most to you.
+ Full Time Role Successful interns have the potential to secure a full-time position with P&G after graduation. As a 'build from within' company, our people start at entry level and progress through the organization. When we make a job offer, it's with the expectation that you will grow into one of our future leaders, and to help you get there, you will work closely with skilled P&G veterans for mentoring and coaching at every step.
Job Qualifications
What We Look For:
+ University students pursuing a degree in a scientific or engineering discipline graduating in 2028 with a placement year as part of their degree who will participate in our 12-month industrial placement.
+ We also welcome applications from students graduating in 2026 or 2027, or those who have already graduated who we can accommodate 3/6-month placements.
+ Evidence of passion and achievements in academic and/or non-academic activities. Tell us what you're proud of - be it playing a musical instrument or holding down a job alongside your studies. We want to get to know you during your application!
+ Demonstrated leadership skills and a strong passion for research and innovation.
+ Strong verbal and written English language skills.
Start date:
The 12-month industrial placement is available from 1st July 2026 until 30th June 2027. We expect you to be available for the full duration. We can also consider offering 6-month placements in line with course requirements.
Right to work
For our placement roles, you will need to provide your own right to work in the UK for the full duration of your placement without requiring sponsorship from P&G. Note, this will require your right to work permission to be valid between 1st July 2026 until 30th June 2027 for a minimum of 37.5 hours per week.
P&G is legally required to ensure all candidates have the right to work in the UK from Day 1 of their employment. All applicants will therefore be asked to provide evidence of their right to work at the conclusion of the recruitment process as a condition of employment.
Application Deadline:
1pm (GMT) November 24th, 2025. You must apply by the deadline. We encourage you to apply and complete our online assessments as soon as possible, as we may close early if positions are filled.
Application Process:
+ Complete your Application (Deadline 1pm GMT 24th November 2025)
+ Complete our Online Assessments (Deadline 1pm GMT 5th December 2025)
+ Virtual Interviews (These will run from October until our roles are filled)
At P&G #weseeequal
We are an equal opportunity employer and value diversity at our company. At P&G we strive to build a culture where everyone feels welcome, included, and able to bring their full selves to work.
We champion social mobility and believe socio-economic status should not be a barrier to accessing job opportunities. That's why in addition to this internship being paid, we offer provision of all the necessary technology and electronic equipment, access to a range of benefits, and financial support if you need to relocate for your internship - such as covering the cost of travel to your internship location.
We ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process. Please click here ( if you require an accommodation during the application process. Please make sure to wait to hear back from us regarding your accommodation before proceeding with the online assessment, we thank you in advance for your patience.
Job Schedule
Full time
Job Number
R
Job Segmentation
Internships

Our client, a world-renowned academic and research institution, is seeking ambitious and bright graduates to join their prestigious Graduate Rotational Programme in Oxford, Oxfordshire, UK . This programme offers a unique opportunity for recent graduates to gain exposure to a variety of cutting-edge research and development projects, fostering their career growth within a leading scientific environment. Over a 18-month period, participants will rotate through different departments, contributing to diverse projects in areas such as biotechnology, materials science, computational modelling, and experimental physics. Each rotation will provide hands-on experience, mentorship from senior researchers, and opportunities to develop advanced technical skills. The programme is designed to identify and nurture future leaders in scientific innovation. Participants will be involved in data collection, analysis, experimental design, literature reviews, and contributing to the writing of research papers and reports. Collaboration with research teams, adherence to laboratory safety protocols, and effective communication of findings are essential. This role offers a hybrid work model, blending essential in-lab or office-based work with remote access to data and resources, promoting a balanced and productive working experience. The ideal candidate will possess a strong academic background in a relevant STEM field, a curious and inquisitive mind, and a genuine passion for scientific discovery. Excellent analytical skills, strong problem-solving abilities, and a proactive approach to learning are paramount. Graduates will gain invaluable experience, build a robust professional network, and lay the foundation for a successful career in research and development. This is an exceptional chance to contribute to groundbreaking scientific endeavours and develop essential professional competencies.
Programme Structure:

• 18-month rotational programme across various R&D departments.
• Exposure to diverse scientific disciplines and research methodologies.
• Hands-on experience in experimental design, data analysis, and scientific reporting.
• Mentorship from leading researchers and scientists.
• Opportunities to present findings and contribute to publications.
• Development of technical skills and professional competencies.
• Hybrid work environment to foster collaboration and flexibility.

Eligibility & Qualifications:

• Recent graduate with a Bachelor's or Master's degree in a relevant STEM field (e.g., Biology, Chemistry, Physics, Engineering, Computer Science, Mathematics).
• Achieved or predicted to achieve a 2:1 degree classification or higher.
• Demonstrated passion for research and scientific inquiry.
• Strong analytical and problem-solving skills.
• Excellent communication and interpersonal abilities.
• Ability to work effectively both independently and as part of a team.
• Eligibility to work in the UK.

Job Location
Schwalbach Am Taunus
Job Description
Are you passionate about the science behind everyday products? Do you want to develop innovation for the world's biggest brands? Are you curious about how the daily job of Scientists and Engineers in Research and Development looks like?
Then join us in our PhD Seminar, a 4-day event at P&G, where you will discover how to leverage your academic skills for innovating on favorite consumer products. A technical career at P&G could be exactly what you're looking for!
Be our guest at the German Innovation Center in Schwalbach and Kronberg from Sunday, April 19th through Thursday, April 23rd , 2026. Your travel and stay will be fully covered by P&G.
Why join the PhD Seminar?
+ You visit our German Innovation Center, meet scientists and engineers, and get to ask them all your questions
+ You get a chance to gain insights into how our scientists innovate our superior products
+ You will get to practice the skills needed to be successful when working in the industry by collaborating with other international PhD Students and experienced R&D managers
+ You will gain insights into the typical day of a scientist or engineer in R&D, the daily challenges of the business and the career opportunities in R&D
+ You will discover if a career in a global company such as P&G is the right thing for you.
During the seminar you will be able to practice and up-skill in:
+ Using technical knowledge to address real problems
+ Making difficult and tough decisions
+ Setting priorities
+ Communicating ideas
+ Motivating people and teams
+ Working as part of a team
Job Qualifications
YOUR PROFILE
+ Science and Engineering Ph.D. Students in the last year of their PhD
+ Disciplines considered are Natural, Life or Physical Sciences, Data Science, Electrical, Mechanical, Biotechnological, Chemical and other Engineering disciplines
+ Your graduation should ideally be betwe en January 2026 and May 2027
Are you keen to get more details? Please explore more information about P&G and the seminar by clicking the insightful links below:
+ P&G is driven to make life better, not just within the company, but across the globe. Click here ( to check out how we make a meaningful impact on the world.
+ We are the world's largest consumer goods company. Click here ( to discover our iconic brands.
Our recruiting process consists of three main steps:
+ Application
+ Online assessment
+ Interviews
Click here ( to get all the tips to be fully prepared.
The application deadline is February 1, 2026. After that date, we will start the selection process.
Seminar Attendees and others who pass our initial requirements will afterwards be considered for interviews for full-time positions in one of our European Innovation Centers.
YOUR FUTURE EMPLOYER
From its foundation 186 years ago as a soap and candle start-up, P&G today is a leading consumer goods company. We are home to iconic, trusted brands that touch 5 billion consumers worldwide and make life a little bit easier in small but meaningful ways every day.
We want you to bring your insight, creativity, and passion to join our dedicated teams who have helped us grow into a global company.
Our people are our greatest asset : with our philosophy of promotion from within, we place strong emphasis on employee development and are committed to finding and fostering world-class talent. Learn from our inspiring leaders, shape our supportive and welcoming culture, and place your personal development at the core of your work!
AT P&G #WESEEEQUAL
We are an equal opportunity employer and value diversity at our company. At P&G we strive to build a culture where everyone feels welcome, included, and able to bring their full selves to work.
We ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process. Please click here ( if you require an accommodation during the application process. Please make sure to wait to hear back from us regarding your accommodation before proceeding with the online assessment, we thank you in advance for your patience.
Job Schedule
Full time
Job Number
R
Job Segmentation
Entry Level

Our client is seeking bright and enthusiastic Graduate Trainees to join their esteemed Research and Development department. This is an exceptional opportunity for individuals with a strong academic background and a passion for innovation to gain invaluable practical experience in a leading research environment. You will be involved in various stages of the R&D lifecycle, contributing to groundbreaking projects under the guidance of experienced scientists and engineers.

Key Responsibilities:

• Assist senior researchers and engineers in conducting experiments and gathering data.
• Perform literature reviews and synthesize information on relevant scientific and technological advancements.
• Contribute to the design and execution of research projects.
• Analyze experimental data using statistical and analytical tools.
• Prepare technical reports, presentations, and documentation of research findings.
• Operate and maintain laboratory equipment and ensure adherence to safety protocols.
• Collaborate with team members to troubleshoot technical challenges and propose solutions.
• Stay updated on industry trends and emerging technologies within the R&D field.
• Participate in team meetings and contribute to project planning and discussions.
• Support the development and testing of prototypes or new product features.
• Ensure meticulous record-keeping of all research activities and results.
• Adhere to quality control standards and company R&D procedures.

Qualifications:

• A recent graduate with a Bachelor's or Master's degree in a relevant scientific or engineering discipline (e.g., Physics, Chemistry, Biology, Engineering, Computer Science).
• Strong analytical and problem-solving skills.
• Excellent research and information synthesis abilities.
• Proficiency in data analysis and relevant software (e.g., Excel, MATLAB, R, Python).
• Good written and verbal communication skills.
• Ability to work effectively both independently and as part of a team.
• Strong attention to detail and commitment to accuracy.
• A genuine interest in research and development and a desire to learn.
• Familiarity with laboratory practices and safety procedures is a plus.
• Proximity to Oxford, Oxfordshire, UK is required for this role.

This is an exciting entry-level position for motivated graduates eager to make their mark in the world of research and development.

Our client, a cutting-edge pharmaceutical company, is actively seeking a highly skilled and motivated Senior Research Scientist to contribute to their groundbreaking drug discovery and development programs. This is a fully remote position, enabling you to leverage your scientific expertise from anywhere in the UK. You will play a pivotal role in designing and executing complex research projects, analyzing data, and contributing to the advancement of novel therapeutic agents. The ideal candidate will possess a strong background in medicinal chemistry or a related pharmaceutical science discipline, coupled with a deep understanding of drug development processes.
Key Responsibilities:

• Design, develop, and execute research experiments to identify and validate new drug targets.
• Synthesize and characterize small molecules with potential therapeutic activity.
• Utilize advanced analytical techniques (e.g., HPLC, GC-MS, NMR) for compound analysis and purification.
• Interpret complex experimental data, draw conclusions, and propose future research directions.
• Collaborate effectively with multidisciplinary teams, including biologists, pharmacologists, and clinical researchers.
• Prepare detailed research reports, manuscripts for publication, and presentations for scientific conferences.
• Contribute to the intellectual property portfolio through patent filings.
• Ensure compliance with all safety regulations and laboratory best practices.
• Stay current with the latest scientific literature and emerging technologies in pharmaceutical research.
• Mentor junior scientists and contribute to the overall scientific advancement of the department.

Qualifications:

• PhD in Medicinal Chemistry, Organic Chemistry, Pharmacology, or a closely related field.
• Minimum of 4 years of post-doctoral or industry research experience in drug discovery.
• Proven expertise in synthetic organic chemistry and modern medicinal chemistry techniques.
• Hands-on experience with various spectroscopic and chromatographic analytical methods.
• Strong understanding of drug discovery pipelines and pharmaceutical development stages.
• Excellent data analysis and interpretation skills.
• Exceptional written and verbal communication skills for scientific reporting and collaboration.
• Ability to work independently and manage multiple research projects simultaneously.
• Demonstrated experience in a remote research environment is a plus.
• A passion for scientific innovation and a commitment to advancing human health.

This research opportunity, based conceptually in **Reading, Berkshire, UK**, is ideal for a dedicated scientist seeking to make a significant impact in a remote-first setting. If you possess the scientific acumen and collaborative spirit, we encourage you to apply.

Our client, a pioneering biopharmaceutical company dedicated to advancing human health, is seeking a highly skilled and innovative Senior Research Scientist to join their world-class, fully remote R&D team. This role is crucial for driving forward cutting-edge drug discovery and development programs. The ideal candidate will possess a deep understanding of pharmaceutical sciences and a proven track record in experimental design, data analysis, and project leadership. This remote position offers an unparalleled opportunity to contribute to life-changing therapies from a location of your choice.

Key Responsibilities:

• Design, execute, and interpret complex experiments related to drug discovery and development, focusing on target validation, lead optimization, and preclinical studies.
• Develop and implement novel assays and methodologies to assess drug efficacy, safety, and pharmacokinetic profiles.
• Analyze and critically evaluate experimental data, generating comprehensive reports and presenting findings to internal teams and external collaborators.
• Lead research projects, providing scientific direction, mentoring junior scientists, and managing timelines and resources effectively within a remote setting.
• Collaborate closely with cross-functional teams, including medicinal chemistry, biology, pharmacology, and regulatory affairs, to advance projects through the pipeline.
• Stay abreast of the latest scientific literature, technological advancements, and industry trends in pharmaceutical research.
• Contribute to the preparation of scientific publications, patents, and regulatory submissions.
• Ensure strict adherence to laboratory safety standards and good experimental practices.
• Actively participate in team meetings and scientific discussions, contributing valuable insights and fostering a collaborative research environment.

Qualifications:

• Ph.D. in Pharmacology, Biochemistry, Molecular Biology, or a related life science discipline.
• Minimum of 5 years of post-doctoral or industry experience in pharmaceutical research and development.
• Demonstrated expertise in one or more therapeutic areas and associated research methodologies.
• Strong track record of successful experimental design, execution, and data interpretation.
• Excellent understanding of drug discovery processes and regulatory requirements.
• Proven ability to lead projects and mentor scientific staff.
• Exceptional written and verbal communication skills, with the ability to present complex scientific information clearly and concisely.
• Proficiency in relevant scientific software and data analysis tools.
• Ability to work independently, manage priorities effectively, and thrive in a remote, collaborative environment.
• Experience with in vivo models and preclinical development is highly desirable.

This fully remote role offers a competitive compensation package, comprehensive benefits, and the chance to make a significant impact on global health. Our client is committed to fostering a diverse and inclusive workplace and encourages applications from all qualified individuals, especially those located near **Oxford, Oxfordshire, UK**, but not exclusively.

**Join Us on Our Mission to Drive Healthcare Forward**
As a Clinical Research Associate at IQVIA, you'll play a vital role in advancing clinical research and improving patient outcomes. We're expanding our Site Management team and looking for passionate CRAs who are ready to make a difference. This role offers a mix of on-site and remote monitoring, supporting work-life balance while contributing to cutting-edge clinical trials.
**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
**Profile**
+ 6 months + independent on-site monitoring experience, ensuring compliance with GCP, protocol requirements, and regulatory guidelines.
+ You have successfully managed multiple clinical trial protocols across diverse investigative sites.
+ Hands-on experience in the Oncology therapeutic area.
+ Flexibility and commitment to nationwide travel
** This role is not eligible for UK Visa Sponsorship**
#LI-AdamThompson
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**
As a Clinical Research Associate at IQVIA, you'll play a vital role in advancing clinical research and improving patient outcomes. We're expanding our Site Management team and looking for passionate CRAs who are ready to make a difference. This role offers a mix of on-site and remote monitoring, supporting work-life balance while contributing to cutting-edge clinical trials.
**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
**Profile**
+ Over 2 years of independent on-site monitoring experience, ensuring compliance with GCP, protocol requirements, and regulatory guidelines.
+ You have successfully managed multiple clinical trial protocols across diverse investigative sites.
+ Hands-on experience in the Oncology therapeutic area.
+ Flexibility and commitment to nationwide travel
** This role is not eligible for UK Visa Sponsorship**
#LI-AdamThompson
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