102 Medical Research jobs in the United Kingdom
Clinical Research Physician
Posted today
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Clinical Research Nurse
Posted 12 days ago
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Job Description
We are looking for full-time Clinical Research Nurse on a fixed term contract until December 2026
Working Monday – Friday with no requirement to work nights.
We are looking for Registered nurses who are based in Winchester and are able to travel to the following regions: Southampton and Portsmouth up through Reading, Basingstoke, Slough, and High Wycombe.
Requirements
You will be responsible for managing clinics on the BEST 4 mobile unit and will be trained to administer the capsule sponge test. You will work alongside established clinical teams, researchers, research nurses and administrators to facilitate recruitment, sample collection, data entry and providing clinical support as required. You will therefore be required to travel to various sites and undertake clinics in a mobile unit.
You will also need to liaise closely with the clinic coordinator regarding appointments and cover on the unit. You will work closely with the Clinical Coordinator, Clinical Research Team and Project managers at KCL, Cambridge and EMS to ensure we meet the study objectives. You will be responsible for ensuring clinical and regulatory compliance, and that each participant journey and their individual experience is to the highest standard, which is a vital part of this role.
Essential requirements
- NMC Registration with continued CPD
- Previous research experience or Upper GI experience
- knowledge of research methodology
- Significant post- registration clinical experience
- Experience in performing nurse-led clinics.
- You must have full UK residency and hold a full and clean valid driving licence.
Desirable
- Degree in related subject area
- ICH GCP Training
- Knowledge of research regulations at national level
- Prior experience in cancer research and endoscopy
- Prior experience of working with capsule sponge test.
The salary we are offering for this role is £38,000 -£42,000 dependent on experience.
Benefits
You work hard for us; we work hard for you. It is that simple. And we know, it sounds too good to be true (we hear that a lot). But trust us, this could be the best decision you make.
- Bank holidays, plus 25 days annual leave, increasing to 28 after 5 years
- 1 Occasion Day each year; this could be your child’s first day of school, their nativity play, or your own birthday – the choice is yours!
- Healthshield
- Subsidised company events and gatherings
- A gift for your birthday
- Well being support from our qualified Mental Health First Aiders, as well as via our health scheme
If you want to join us as our Clinical Research Nurse - click apply now!
Senior Clinical Research Associate
Posted 8 days ago
Job Viewed
Job Description
- Job Title: Senior CRA / Senior CRA II
- Location: Remote in UK
- Salary: £50,000 - £58,000
- Additional Benefits: Car allowance (or company car) and bonus
- Company: Global CRO
RBW Consulting is thrilled to present an exciting opportunity on behalf of one of our esteemed clients. As one of the few rapidly growing Contract Research Organizations (CROs) for UK studies, our client is expanding their site management team with multiple hires this year. They are involved in a diverse range of studies, including cutting-edge research in advanced therapies such as CAR-T.
Join a highly experienced team dedicated to excellence in clinical research. We are seeking skilled monitors with a minimum of 3 years of CRA experience. In this role, you will benefit from a supportive management team committed to your professional growth. They provide clear guidance on the skills needed for advancement and offer fluid career development opportunities across various departments.
This company prioritizes quality over metrics and is currently generating significant excitement within their UK team.
Key accountabilities
- Autonomy of investigator sites with full responsibility for the successful management of sites through study life cycle (start-up to close-out);
- Conduct feasibility, pre-study, initiation, monitoring, and closeout visits for research sites, mainly phase 1 to 3 and within all available therapeutic areas;
- Prepare accordingly and attend investigator meetings, coordinating timely delivery and subsequent proper storage and accountability of clinical supplies and following-up of drug safety issues;
- Perform source document verification and case report form review;
- Perform regulatory document review;
- Conduct study drug inventory;
- Perform adverse event and serious adverse event reporting and follow-up; and
- Assess patient recruitment and retention.
Qualifications
- Bachelor of Science in health-related field (or equivalent)
- Proven CRA experience; 3 years minimum
Why Join?
- Supportive Environment : Build strong relationships with a transparent management team focused on your development.
- Innovative Approach : Work with a company that embraces a 360 monitoring approach and leverages AI to enhance efficiency and save time.
- Results-Driven KPIs : Our client's key performance indicators are centered around tangible study outcomes, such as patient recruitment, visit reports, and resolving site issues.
To apply
Please click ‘apply’ or contact Joe Pearce for any further information
About RBW Consulting
RBW Consulting is a life sciences talent & strategic consultancy with purpose, delivered through what we call Human Intelligence. We help life sciences businesses change the world by giving them the people, insight & networks to innovate and scale. We are proud of our role in helping companies deliver better health and wellbeing outcomes for patients We give back by playing an active role in funding initiatives that change lives We’ve created a culture rooted in support, transparency and mutual commitment. We lead with our values from the inside; empowering and investing in our people is more important than short-term commercial gain.
We are an equal opportunities Recruitment Business and Agency
RBW Consulting is an equal opportunity workplace. We prioritize talent (both current and potential) over resumes, challenge the status quo, and value people as our most important asset. We do not discriminate on the basis of race, ethnicity, colour, sex, gender identity or expression, sexual orientation, religion, age, marital status, visible or invisible disability, medical condition, national origin, veteran status, or any other protected status. We strive to be a diverse workforce that is representative at all levels and are committed to building a team that represents a variety of backgrounds, perspectives, and skills.
Lead Clinical Research Associate
Posted 8 days ago
Job Viewed
Job Description
- Job Title: Lead Clinical Research Associate
- Location: Remote in UK
- Salary: £56,000 - £62,000
- Additional Benefits: Car allowance (or company car) and bonus
- Company: Global CRO
RBW Consulting is thrilled to present an exciting opportunity on behalf of one of our esteemed clients. As one of the few rapidly growing Contract Research Organizations (CROs) for UK studies, our client is expanding their site management team with multiple hires this year. They are involved in a diverse range of studies, including cutting-edge research in advanced therapies such as CAR-T.
Join a highly experienced team dedicated to excellence in clinical research. In this role, you will benefit from a supportive management team committed to your professional growth. They provide clear guidance on the skills needed for advancement and offer fluid career development opportunities across various departments.
This company prioritizes quality over metrics and is currently generating significant excitement within their UK team.
Key accountabilities
- Autonomy of investigator sites with full responsibility for the successful management of sites through study life cycle (start-up to close-out);
- Conduct feasibility, pre-study, initiation, monitoring, and closeout visits for research sites, mainly phase 1 to 3 and within all available therapeutic areas;
- Prepare accordingly and attend investigator meetings, coordinating timely delivery and subsequent proper storage and accountability of clinical supplies and following-up of drug safety issues;
- Perform source document verification and case report form review;
- Perform regulatory document review;
- Conduct study drug inventory;
- Perform adverse event and serious adverse event reporting and follow-up; and
- Assess patient recruitment and retention.
Qualifications
- Bachelor of Science in health-related field (or equivalent)
- Proven CRA experience; 3 years minimum
Why Join?
- Supportive Environment : Build strong relationships with a transparent management team focused on your development.
- Innovative Approach : Work with a company that embraces a 360 monitoring approach and leverages AI to enhance efficiency and save time.
- Results-Driven KPIs : Our client's key performance indicators are centered around tangible study outcomes, such as patient recruitment, visit reports, and resolving site issues.
To apply
Please click ‘apply’ or contact Joe Pearce for any further information
About RBW Consulting
RBW Consulting is a life sciences talent & strategic consultancy with purpose, delivered through what we call Human Intelligence. We help life sciences businesses change the world by giving them the people, insight & networks to innovate and scale. We are proud of our role in helping companies deliver better health and wellbeing outcomes for patients We give back by playing an active role in funding initiatives that change lives We’ve created a culture rooted in support, transparency and mutual commitment. We lead with our values from the inside; empowering and investing in our people is more important than short-term commercial gain.
We are an equal opportunities Recruitment Business and Agency
RBW Consulting is an equal opportunity workplace. We prioritize talent (both current and potential) over resumes, challenge the status quo, and value people as our most important asset. We do not discriminate on the basis of race, ethnicity, colour, sex, gender identity or expression, sexual orientation, religion, age, marital status, visible or invisible disability, medical condition, national origin, veteran status, or any other protected status. We strive to be a diverse workforce that is representative at all levels and are committed to building a team that represents a variety of backgrounds, perspectives, and skills.
Clinical Research Nurse II
Posted 5 days ago
Job Viewed
Job Description
Standard (Mon-Fri)
**Environmental Conditions**
Office
**Job Description**
At Thermo Fisher Scientific, you'll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life - To enable our customers to make the world healthier, cleaner and safer. We provide our teams with the resources needed to achieve individual career goals while taking science a step beyond through research, development and delivery of life-changing therapies.
Alongside clinical research through our PPD® clinical research portfolio, our work in Accelerated Enrollment Solutions optimizes each step of the patient journey in clinical trials, such as securing sites and recruiting patients, allowing for more patients to participate in clinical research. Your determination to put patients at the heart of every decision will improve health outcomes that people and communities depend on - now and in the future.
**Are you passionate about improving patient's lives for the better?**
We are currently looking to recruit a Clinical Research Nurse for our Synexus Clinical Research site in Birmingham, United Kingdom
Working days, Monday to Friday, 37 hours a week, the main priority will always be patient safety. The Clinical Research Nurse conducts multiple ongoing clinical trials involving patients or healthy volunteers/subjects. Completes all paperwork required to capture all data as specified by a study protocol, and for ensuring subject safety, understanding, and cooperation during the study process. Interacts with the research site team and other interdepartmental staff. Engages in the entire site operations process, which includes recruitment, enrollment, and retention of study participants.
**Key responsibilities for a Clinical Research Nurse are as follows:**
+ Conducts clinical studies according to FDA/GCP and ICH regulations and guidelines.
+ Provides medical care to patients, always ensuring patient safety comes first.
+ Schedules subject visits within protocol windows, ensuring scheduling capacity is maximized.
+ Performs all defined study activities (i.e., informed consent, screening, and protocol procedures which include but not limited to vital signs, pregnancy tests, height, weight, ECG's, etc.).
+ Records all patient information and results from tests as per protocol on required forms.
+ Where required, may complete IP accountability logs and associated information.
+ Reports suspected non-compliance to relevant site staff.
+ Ensures that IRB approval is obtained prior to study initiation and IRB requirements are met throughout the study.
+ Promotes the company and builds a positive relationship with patients to ensure retention.
+ Attends site initiation meetings and all other relevant meetings to receive training on protocol.
+ May be required to call patients, do patient bookings and follow-up calls to confirm bookings or provide information or results.
+ Logs/completes information on sponsor systems and ensures all information provided is accurate (i.e., case report forms, EDC, etc.) and ensures it is completed within timeframe.
+ Gathers and maintains source documents, updates patient files and notes, always ensuring relevant and most up to date information is recorded.
+ Adheres to company COP/SCOP.
+ May be required to dispose of waste according to standards and assist in keeping a general neat appearance of the facility.
**To be considered for this exciting opportunity you will require the following skills and experience:**
+ Solid understanding of the clinical research process (i.e., GCP, SOPs, informed consent, safety monitoring, etc.)
+ Capable of working independently, analyzing and working with attention to detail, processing and prioritizing sensitive complex information and problem solving
+ Demonstrated ability to exercise discretion and sound judgement
+ Good decision-making, negotiation and influencing skills - Good communication skills and English fluency will be an advantage
+ Good organizational skills
+ Good proficiency in basic computer applications
+ Good interpersonal skills to work in a team environment
Our Mission is to enable our customers to make the world healthier, cleaner and safer. Watch as our colleagues explain 5 reasons to work with us. As one team of 100,000+ colleagues, we share a common set of values - Integrity, Intensity, Innovation and Involvement - working together to accelerate research, solve complex scientific challenges, drive technological innovation and support patients in need. #StartYourStory with PPD, part of Thermo Fisher Scientific, where diverse experiences, backgrounds and perspectives are valued.
Thermo Fisher Scientific is an EEO/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other legally protected status.
Thermo Fisher Scientific is an EEO/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other legally protected status.
Clinical Research Nurse II
Posted 5 days ago
Job Viewed
Job Description
**Environmental Conditions**
**Job Description**
At Thermo Fisher Scientific, you'll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life - To enable our customers to make the world healthier, cleaner and safer. We provide our teams with the resources needed to achieve individual career goals while taking science a step beyond through research, development and delivery of life-changing therapies.
Alongside clinical research through our PPD® clinical research portfolio, our work in Accelerated Enrollment Solutions optimizes each step of the patient journey in clinical trials, such as securing sites and recruiting patients, allowing for more patients to participate in clinical research. Your determination to put patients at the heart of every decision will improve health outcomes that people and communities depend on - now and in the future.
**Are you passionate about improving patient's lives for the better?**
We are currently looking to recruit a Clinical Research Nurse for our Synexus Clinical Research site in Cardiff, United Kingdom
Working days, Monday to Friday, 37 hours a week, the main priority will always be patient safety. The Clinical Research Nurse conducts multiple ongoing clinical trials involving patients or healthy volunteers/subjects. Completes all paperwork required to capture all data as specified by a study protocol, and for ensuring subject safety, understanding, and cooperation during the study process. Interacts with the research site team and other interdepartmental staff. Engages in the entire site operations process, which includes recruitment, enrollment, and retention of study participants.
**Key responsibilities for a Clinical Research Nurse are as follows:**
+ Conducts clinical studies according to FDA/GCP and ICH regulations and guidelines.
+ Provides medical care to patients, always ensuring patient safety comes first.
+ Schedules subject visits within protocol windows, ensuring scheduling capacity is maximized.
+ Performs all defined study activities (i.e., informed consent, screening, and protocol procedures which include but not limited to vital signs, pregnancy tests, height, weight, ECG's, etc.).
+ Records all patient information and results from tests as per protocol on required forms.
+ Where required, may complete IP accountability logs and associated information.
+ Reports suspected non-compliance to relevant site staff.
+ Ensures that IRB approval is obtained prior to study initiation and IRB requirements are met throughout the study.
+ Promotes the company and builds a positive relationship with patients to ensure retention.
+ Attends site initiation meetings and all other relevant meetings to receive training on protocol.
+ May be required to call patients, do patient bookings and follow-up calls to confirm bookings or provide information or results.
+ Logs/completes information on sponsor systems and ensures all information provided is accurate (i.e., case report forms, EDC, etc.) and ensures it is completed within timeframe.
+ Gathers and maintains source documents, updates patient files and notes, always ensuring relevant and most up to date information is recorded.
+ Adheres to company COP/SCOP.
+ May be required to dispose of waste according to standards and assist in keeping a general neat appearance of the facility.
**To be considered for this exciting opportunity you will require the following skills and experience:**
+ Solid understanding of the clinical research process (i.e., GCP, SOPs, informed consent, safety monitoring, etc.)
+ Capable of working independently, analyzing and working with attention to detail, processing and prioritizing sensitive complex information and problem solving
+ Demonstrated ability to exercise discretion and sound judgement
+ Good decision-making, negotiation and influencing skills - Good communication skills and English fluency will be an advantage
+ Good organizational skills
+ Good proficiency in basic computer applications
+ Good interpersonal skills to work in a team environment
Our Mission is to enable our customers to make the world healthier, cleaner and safer. Watch as our colleagues explain 5 reasons to work with us. As one team of 100,000+ colleagues, we share a common set of values - Integrity, Intensity, Innovation and Involvement - working together to accelerate research, solve complex scientific challenges, drive technological innovation and support patients in need. #StartYourStory with PPD, part of Thermo Fisher Scientific, where diverse experiences, backgrounds and perspectives are valued.
Thermo Fisher Scientific is an EEO/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other legally protected status.
Thermo Fisher Scientific is an EEO/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other legally protected status.
Clinical Research Associate I
Posted 5 days ago
Job Viewed
Job Description
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 sponsor-dedicated team and looking for passionate CRAs who are ready to make a difference.
**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 12 months 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.
+ 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
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Clinical Research Associate I
Posted 5 days ago
Job Viewed
Job Description
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 sponsor-dedicated team and looking for passionate CRAs who are ready to make a difference.
**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 12 months 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.
+ 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
Clinical Research Associate I
Posted 5 days ago
Job Viewed
Job Description
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 sponsor-dedicated team and looking for passionate CRAs who are ready to make a difference.
**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 12 months 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.
+ 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