33 Medical Research jobs in London
Research Manager (Healthcare/Pharmaceutical)
Posted today
Job Viewed
Job Description
Are you Research Manager looking to work on in the healthcare and pharmaceutical sectors? Then you could be the perfect fit for this market research agency in this flexible Research Manager role!
JOB TITLE: Research Manager (Healthcare/Pharmaceutical)
SALARY: 40k - 50k
LOCATION: London (Hybrid)
THE COMPANY
An international organisation that fosters a vibrant and friendly environment that deliver bespoke research for a vast range of clients. They have seen a huge amount of growth working throughout the pharmaceutical and healthcare sectors, delivering the best insight for clients in both workstreams.
They are currently looking to bring on Research Manager level candidate, who has experience in or is looking to work projects within the healthcare and pharmaceutical sectors.
KEY DUTIES
- Leading day-to-day project logistics and liaise with suppliers
- Responsible for end-to-end projects within the healthcare and pharmaceutical sectors
- Getting involved in the day to day, from helping shape questionnaires, structuring analysis and delivering debriefs
SKILLS & EXPERIENCE
- Previous experience writing winning proposals, and designing bespoke solutions to answer client's business questions
- Previous experience working with both quantitative and qualitative methodologies
- Previous experience developing and pushing more junior members of the team, helping drive progression
Interested in this Research Manager role? Apply now and let's have a chat!
We Are Aspire Ltd are a Disability Confident Commited employer
Associate Director, Clinical Research
Posted today
Job Viewed
Job Description
- 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.
Associate Director, Clinical Research
Posted 3 days ago
Job Viewed
Job Description
- 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.
Clinical Research Associate (CRA
Posted today
Job Viewed
Job Description
We're currently partnering with a leading international pharmaceutical company to recruit a Junior CRA.
Location: West London
Hybrid: Twice a week in office
DESCRIPTION OF THE ROLE
* Site evaluation and setup for commercial distribution including training of dosing in collaboration with the Clinical Project Manager or designee
* Maintenance of contacts with sites for commercial distribution and sites which may be involved in clinical trials
* Collection of essential documents according to ICH-GCP E6 (R2) and applicable regulations
* Monitoring of data collection and pharmacovigilance/ safety reporting at the sites where a post authorisation study is conducted
* Site setup, initiation, close-out and management (including monitoring) of sites participating in clinical and post-authorisation studies on an as needs basis
* Site management including site supplies, site payment process, etc.
* Study/clinical trial status tracking and progress update to team
* EC/IRB and regulatory submissions
* Participation in investigator meetings and other meetings as necessary
* Attendance of conferences as applicable
* Contribution to other tasks such as creation of newsletters as directed by the Clinical Project Manager or designee
* Assist with audits as required
* Contribute to initiatives and process improvements as required
* Contribute to Literature Reviews.
KEY RESULT AREAS
* Feasibility assessments/visit evaluations for clinical and post-authorisation studies
* Site setup for commercial distribution according to post-authorisation requirements
* Site setup for clinical trials (as needs basis)
* Site management: investigating, following up and escalating site issues as needed.
* Delivery of data accuracy through CRF review through on-site and remote monitoring according to the risk-based monitoring plan to ensure patient safety, compliance and decreased risks.
* Assistance with pharmacovigilance, safety reporting management and investigations of quality complaints
* In-house/ on-site document quality management (including, but not limited to, trial master file, investigator site file).
QUALIFICATIONS/EXPERIENCE
* Graduate qualifications in Biological Sciences, Nursing, Pharmacy or related discipline
* Post-graduate qualifications desirable
* At least 2 years proven experience as a CRA
* Working knowledge of ICH GCP guidelines
* On-site experience
* Proven experience in managing clinical trials/projects
WHAT'S ON OFFER
* A competitive salary with benefits.
* The chance to contribute and be part of team whose work directly benefits healthcare and strives to improve people's lives.
* A real hands-on opportunity to gain a high degree of commercial exposure.
* The chance to work alongside world-leading scientific experts.
* Working with highly-talented and dedicated colleagues in a fast-growing company that combines a focus on cutting-edge science with commercial delivery.
Interested in making a difference?
Apply now or reach out to learn more about this exciting opportunity!
Associate Director Clinical Research
Posted 7 days ago
Job Viewed
Job Description
- 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
Clinical Research Physician - South London
Posted 5 days ago
Job Viewed
Job Description
ICON plc is a world-leading healthcare intelligence and clinical research organization. We're proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development.
**Clinical Research Physician**
**South London - Clinic Based**
Are you looking for an outstanding opportunity to develop your career with a fast growing leading edge Clinical research company and to be involved in the future of medicine across the globe? **_This role is with Accellacare ( , part of ICON's clinical research network, where you'll play a key role in transforming the clinical trial experience for patients and sponsors alike. Our global site network is designed with one goal in mind: to deliver better access, greater efficiency, and improved outcomes in clinical research._**
We are growing our international footprint across the globe and invite you to join us and become part of our success story.
**Main duties and responsibilities of the job**
+ Working as a Sub Investigator on Accellacare clinical trials ( for Research Physician 1 )
+ Comply with ICH/GCP standards and UK clinical trials regulation
+ Interview, screen, enroll and monitor the clinical trial participants
+ Provide medical care for the clinical trial participants
+ Perform study specific tasks ( clinical examination and evaluations, review of blood test results, X rays results, etc )
+ Ensure that the clinical trials participants safety and wellbeing are protected at all times
+ Ensure excellent standards of patient safety and quality of the service
+ Record Adverse events/Serious Adverse events
+ Ensure that Good documentation Practice is followed at all time
+ Develop positive relations with sponsors, clients and monitors as required.
+ Participate in GMC appraisals/Revalidation scheme.
**Skills/qualifications and experience required for the job**
**Research Physician 1**
Fully qualified, GMC registered Physician with a license to practice
Previous research experience ( preferred but not essential )
**Package Description**
Accellacare is a vibrant company with a great team of professionals . We focus on continued professional development and offer a competitive salary package combined with a target bonus scheme. If you would like to find out more about the company, please visit our website at: ICON can offer you:**
Our success depends on the quality of our people. That's why we've made it a priority to build a diverse culture that rewards high performance and nurtures talent.
In addition to your competitive salary, ICON offers a range of additional benefits. Our benefits are designed to be competitive within each country and are focused on well-being and work life balance opportunities for you and your family.
Our benefits examples include:
+ Various annual leave entitlements
+ A range of health insurance offerings to suit you and your family's needs.
+ Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead.
+ Global Employee Assistance Programme, LifeWorks, offering 24-hour access to a global network of over 80,000 independent specialized professionals who are there to support you and your family's well-being.
+ Life assurance
+ Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidized travel passes, health assessments, among others.
Visit our careers site ( to read more about the benefits ICON offers.
At ICON, inclusion & belonging are fundamental to our culture and values. We're dedicated to providing an inclusive and accessible environment for all candidates. ICON is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.
If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know or submit a request here ( in the role, but unsure if you meet all of the requirements? We would encourage you to apply regardless - there's every chance you're exactly what we're looking for here at ICON whether it is for this or other roles.
Are you a current ICON Employee? Please click here ( to apply
Senior Clinical Research Associate (Senior CRA)
Posted today
Job Viewed
Job Description
We're currently partnering with a leading international pharmaceutical company to recruit a Senior Clinica Reasearch Assocaite.
Location: West London
Hybrid: twice a week in office
Job Summary
* Feasibility assessments/ visit evaluations for clinical trials.
* Site setup for commercial distribution and for clinical trials
* Study management
* Site management investigating, following up and escalating site issues as needed.
* Conduct remote and on-site visits in accordance with the protocols, GxP guidelines, applicable local and international regulations and company SOPs to ensure subjects rights, well-being and data reliability, ensuring audit readiness.
* Relationship management with site staff
* Assistance with pharmacovigilance, safety reporting management
* In house/ onsite document quality management
Responsabilties
Include, but are not limited to:
* Management of studies
* Site evaluation and setup for commercial distribution including site training
* Maintenance of contacts with sites for commercial distribution and sites which may be involved in clinical trials
* Collection of essential documents according to ICH-GCP, GVP and applicable regulations.
* Monitoring of data collection and pharmacovigilance/ safety reporting at the sites where a study is conducted
* Site setup, training, initiation, close-out and management (including monitoring) of studies
* Site management including site payment process and reconciliation
* Study/clinical trial status tracking, QC and progress update to team
* Prepare or Review of site visit reports
* Participation in investigator meetings and other meetings as necessary
* Attendance of, and representation at, conferences as applicable
* Contribution to other tasks such as creation of newsletters as directed
* Assist with inspections/audits as required
* Contribute to the preparation of the CSR/publications, informed consents, protocols, and guidelines, sharing ideas with study members
* Prepare documents such as informed consent, monitoring plans and study operating manual for studies.
* Assist in creating project specific training for more junior members and sites
* Takes initiative to identify areas for potential process improvements, bringing these to the attention of the Clinical Operations Manager
* Preparation of Literature Reviews and searches Senior Clinical Specialist
* Contribution to scientific discussions regarding therapeutic areas, treatments, study endpoints and investigational medicinal products.
QUALIFICATIONS/EXPERIENCE
* Graduate qualifications in Biological Sciences, Nursing, Pharmacy or related discipline
* Post-graduate qualifications desirable
* At least 4 years proven experience as a CRA
* On-site experience
* Working knowledge of ICH GCP guidelines
* Proven experience in managing clinical trials/projects
WHAT'S ON OFFER
* A competitive salary with benefits.
* The chance to contribute and be part of team whose work directly benefits healthcare and strives to improve people's lives.
* A real hands-on opportunity to gain a high degree of commercial exposure.
* The chance to work alongside world-leading scientific experts.
* Working with highly-talented and dedicated colleagues in a fast-growing company that combines a focus on cutting-edge science with commercial delivery.
Interested in making a difference?
Apply now or reach out to learn more about this exciting opportunity!
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Senior Clinical Research Manager - Digital Technologies
Posted 9 days ago
Job Viewed
Job Description
**A Day in the Life**
The Digital Technologies Business Unit (DTBU) at Medtronic is implementing cutting-edge AI technology, computer vision, and augmented reality in the operating room (OR) to augment surgical coaching, and eventually, performance. Our goal is to deliver safer surgery around the world. Our Touch SurgeryTM Video solution is an innovative video management and data analytics platform for hospitals that includes the DS1 Computer, our first OR device, allowing surgeons, OR team members, and trainees to securely access videos of their procedures shortly after surgery.
The Senior Clinical Research Manager at Digital Technologies (DT) will report to the Vice President, Clinical Research & Medical Science, Surgical Operating Unit. This leadership role is accountable for developing and executing the global clinical evidence strategy for the Digital Technologies Business Unit (DT BU), with a focus on innovation, quality, and alignment with DT business strategies.
This role partners closely with Medical Affairs, R&D, Marketing, Regulatory Affairs, Health Economics and Outcomes Research (HEOR), and physician investigators to ensure evidence generation drives product adoption, regulatory approvals, and external scientific engagement.
The leader will also mentor and develop talent, foster a culture of collaboration and accountability, and build strategic partnerships to advance clinical and business priorities globally.
**Responsibilities may include the following and other duties may be assigned:**
+ Lead a small team of Clinical Research Specialists, developing talent and building capabilities across clinical strategies and execution.
+ Drive global clinical strategy for digital and AI technologies, including evidence generation for regulatory, market access, and differentiation.
+ Oversee global clinical studies (pre- and post-market), ensuring scientific rigor, compliance, and alignment with business goals.
+ Align with stakeholders (regulators, payers, HCPs, patients, internal teams) to integrate their needs into clinical strategies.
+ Manage clinical budgets and ensure appropriate resource allocation.
+ Build and maintain global KOL networks to support strategy and evidence dissemination.
+ Collaborate cross-functionally (R&D, Regulatory, HEOR, Commercial, etc.) to align resources and accelerate innovation.
+ Lead development and execution of clinical content and publication plans.
+ Represent DT Clinical in global forums, internal reviews, and external industry events.
+ Work with regional teams to tailor global strategies for local execution and insight collection.
+ Identify and escalate clinical business risks and drive mitigation efforts.
+ Partner with Regulatory to develop and implement global product approval strategies.
+ Represent DT Clinical across regions, collecting local insights and building relationships with internal and external stakeholders.
+ Lead both global and local clinical studies across all DT products and therapies.
+ Attend in-person meetings at Medtronic offices, HCOs, or events, as required.
**Required Knowledge and Experience:**
+ Bachelor's degree (Bachelor of Science or Engineering).
+ 7+ years of experience in clinical research in the medical device industry with pre-market and post-market research experience focused on Digital health technologies.
+ 5+ years of managerial experience in clinical research.
+ Strong understanding of AI/ML-enabled medical technologies and associated clinical/regulatory considerations.
+ Proven track record of building and mentoring high-performing clinical teams.
+ Experience engaging with global regulatory bodies (e.g., FDA, Notified Bodies, PMDA).
+ Excellent written and verbal communication skills, including executive presence and influencing skills.
+ Demonstrated success working cross-functionally to deliver business impact through clinical evidence.
Preferred skills include an advanced degree such as an MS, PhD, MD, or MPH, demonstrating a strong academic foundation relevant to the role. Candidates should possess solid financial acumen, with experience in managing complex budgets and adhering to project timelines. Additionally, a history of successful cross-functional collaboration to generate clinical evidence that drives measurable business impact is highly valued.
**Physical Job Requirements**
The above statements are intended to describe the general nature and level of work being performed by employees assigned to this position, but they are not an exhaustive list of all the required responsibilities and skills of this position?
**Benefits & Compensation**
**Medtronic offers a competitive Salary and flexible Benefits Package**
A commitment to our employees lives at the core of our values. We recognize their contributions. They share in the success they help to create. We offer a wide range of benefits, resources, and competitive compensation plans designed to support you at every career and life stage.
This position is eligible for a short-term incentive called the Medtronic Incentive Plan (MIP).
**About Medtronic**
We lead global healthcare technology and boldly attack the most challenging health problems facing humanity by searching out and finding solutions.
Our Mission - to alleviate pain, restore health, and extend life - unites a global team of 95,000+ passionate people.
We are engineers at heart- putting ambitious ideas to work to generate real solutions for real people. From the R&D lab, to the factory floor, to the conference room, every one of us experiments, creates, builds, improves and solves. We have the talent, diverse perspectives, and guts to engineer the extraordinary.
Learn more about our business, mission, and our commitment to diversity here ( lead global healthcare technology and boldly attack the most challenging health problems facing humanity by searching out and finding solutions.
Our Mission - to alleviate pain, restore health, and extend life - unites a global team of 95,000+ passionate people.
We are engineers at heart- putting ambitious ideas to work to generate real solutions for real people. From the R&D lab, to the factory floor, to the conference room, every one of us experiments, creates, builds, improves and solves. We have the talent, diverse perspectives, and guts to engineer the extraordinary.
**We change lives** . Each team member, each day, helps to improve and redefine how the world treats the most pressing health conditions, from heart disease to diabetes. Our industry leadership comes from the passion and ingenuity of our people. That's who we are. Working alongside one another, we use science, medicine, and a profound understanding of the human body to build extraordinary technologies that can transform lives.
**We build extraordinary solutions as one team** . With one Medtronic Mindset defining how we work. Speed and decisiveness run through our DNA. Diverse perspectives inspire our bold answers to any challenge that comes our way. And we deliver results the right way, breakthrough after patient breakthrough.
**This life-changing career is yours to engineer** . By bringing your ambitious ideas, unique perspective and contributions, you will.
+ **Build** a better future, amplifying your impact on the causes that matter to you and the world
+ **Grow** a career reflective of your passion and abilities
+ **Connect** to a dynamic and inclusive culture that welcomes the challenge of life-long learning
These commitments set our team apart from the rest:
**Experiences that put people first** . Respect for people is the hallmark of our humanity. It fuels our team to positively impact even a single life. And it means we put our people first at Medtronic as well, creating a culture of belonging and always pushing to get you the career-building resources you need.
**Life-transforming technologies** . No matter your role, you contribute to technologies that transform lives. What we build empowers patients to live life on their terms.
**Better outcomes for our world** . Here, it's about more than the bottom line. Our Mission to improve human welfare drives us. We advance healthcare, society, and equity with every design, inside and outside our walls.
**Insight-driven care** . Fresh viewpoints. Cutting-edge AI, data, and automation. You're shaping the future of healthcare technology and defining the next generation of breakthroughs in care
It is the policy of Medtronic to provide equal employment opportunity (EEO) to all persons regardless of age, color, national origin, citizenship status, physical or mental disability, race, religion, creed, gender, sex, sexual orientation, gender identity and/or expression, genetic information, marital status, status with regard to public assistance, veteran status, or any other characteristic protected by federal, state or local law. In addition, Medtronic will provide reasonable accommodations for qualified individuals with disabilities.
For sales reps and other patient facing field employees, going into a healthcare setting?is considered an essential function of the job and we expect our employees to comply with all credentialing requirements at the hospitals or clinics they support.
This employer participates in the federal E-Verify program to confirm the identity and employment authorization of all newly hired employees. For further information about the E-Verify program, please click here ( .
For updates on job applications, please go to the candidate login page and sign in to check your application status.
If you need assistance completing your application please email
To request removal of your personal information from our systems please email
In House Clinical Research Associate (CRA)
Posted 9 days ago
Job Viewed
Job Description
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
Senior Primary Care Clinical Research Pharmacist
Posted 360 days ago
Job Viewed
Job Description
ROLE PURPOSE
The role will be working within the Clinical Pharmacy team structure as part of the clinical research team. The role will include delivering research clinics, dispensing medication and Clinical Trial Investigational Medicinal Product (CTIMP) and ensuring appropriate disposal. Additionally, the post holder will actively assist the research team to conduct and design clinical trials. Direct patient contact will be essential to the role and will include delivery of clinics e.g. research clinics and vaccinations. The post holder will also work on Expressions of Interest, Sponsor Site visits and engage proactively with other teams to ensure delivery of an excellent clinical service.
KEY TASKS AND RESPONSIBILITIES
Research
1. Provide operational clinical input into the design and delivery of clinical trial opportunities previously approved by the organisational Research Committee
2. Deliver research clinics – including patient facing functions as determined by agreed specifications
3. Assist assurance of compliance with regulatory or commercial third parties criteria by having clear systems to ensure data integrity, quality control and evidence of protocol compliance
4. Ensure all documentation is completed and records are retained for the correct duration
5. Ensure medicines are stored, supplied and disposed of in line with legislative and best practice guidance and recommendations
6. Work with HCL Clinical Pharmacy Technicians in the oversight of any stored medicines
7. Work with HCL Clinical Pharmacy team to raise profile of research within the organisation
8. Liaise proactively with practice teams where appropriate to engage broader clinical research participation
9. Report any adverse events via national (e.g. MHRA Yellow Card), regional and local systems in a timely fashion
10. Produce reports in line with the requirements of the various clinical trials
11. Remain up to date on best practice with regards to delivering Clinical Trials including completing necessary training as recommended by the Head of Pharmacy or Head of Business Intelligence
12. Assist in the development of Pharmacy policies and procedures to support the delivery of clinical trials involving medication and related substances. Oversee the production, implementation and review of detailed written pharmacy guidance and SOP’s and liaise with pharmacy teams across the HCL/CLH to ensure effective implementation of these SOP’s and initiate change if necessary
13. Train medical, nursing and pharmacy staff in all aspects of handling drugs in clinical trials
14. Report any incidents via HCL Incident Reporting systems to ensure organisational oversight. Incidents should also be reported to external agencies as per the Clinical Trial Protocol and other relevant best practice
15. Work with the Head of Business Intelligence to generate data to evidence impact of trials and role. This may include data gathering and analysis, report writing and presentations.
Support to individual Clinical Trials
a) Set up the trial specific study file with all necessary essential documentation, in preparation for pharmacy sign off by the Trial Chief Investigator
b) Arrange for, and receive investigational medicinal product (IMP) in line with Clinical Trial SOP’s and ensure compliance with GMP legislation
c) Maintain the professional expertise to be able to prescribe – and to employ this during as part of a clinical trial if required and within own scope of competence
d) Support the multidisciplinary team meetings with investigators to initiate, manage and close down trials hence ensuring pharmacy participation
e) Adhere to the appropriate disposal procedure of unwanted trial materials
f) Liaise with the Head of Pharmacy and HCL Research Lead when assessing, approving or initiating new projects, and update all necessary stakeholders
g) Act as a source of Research expertise to advise on complex issues such as trial design, procurement, randomisation, blinding, and documentation for in-house clinical trials and to defend/justify the opinions or decisions if the advice is challenged
Primary Care Clinical Pharmacy service
- Undertake clinical medication reviews with patients with multi-morbidity and polypharmacy and implement prescribing changes (as an independent prescriber) and order relevant monitoring tests
- Manage own case load and run longer term conditions where responsible for prescribing as an independent prescriber for conditions where medicines have a large component whilst remaining within scope of practice and limits of competence
- Work in partnership with healthcare colleagues and implement improvements to patient’s medications – including de-prescribing
- Support practice staff and patients to manage medicines queries
- Identify national and local policy and guidance that affects patient safety through the use of medicines and devices including MHRA alerts, product withdrawals, medicines shortages etc.
- Ensure medication safety processes are implemented for patients in the practice – this could include routine high risk drug monitoring, clinical audits etc.
Professional Role
a) To ensure confidentiality is maintained at all times
b) To be professionally accountable for actions and advice.
c) To be aware of training and competency assessment of pharmacist trainees, diploma pharmacists and student pharmacy technicians and to participate in their training and competency assessment as required
d) Participate in Continuous Professional Development
e) Conduct Clinical Trial medication screening and dispensing checks
f) To attend Clinical Trial specific training course(s) to maintain and update knowledge including web based learning
g) Any other reasonable duties as requested by the Head of Pharmacy
Other services
1. Support the establishment of additional clinical services that may need to be mobilised e.g. Travel clinics
2. Ensure active engagement with Head of Pharmacy and Head of Business Intelligence to ensure joined up working across the services
3. From time to time, it may be necessary to support the HCL Pharmacy team with delivery of clinical tasks as relevant to training, experience and competence
4. Provide clinical and medicines optimisation advice to staff and patients for the service as relevant to role
5. Signpost any queries to the appropriate teams to support patient care
6. Support the site preparedness for CQC inspections – and attend inspections to provide clinical and pharmaceutical assurance to the inspecting team
7. Recognise personal limitations and refer to more appropriate colleagues where necessary
8. Work collaboratively with multi-disciplinary team on site, HCL colleagues as well as other health and social care professionals across the system
Requirements
GPhC registration
Benefits
NHS Pension
Modern office
Hybrid working
Free tea/coffee etc.
Cycle to work scheme
Life Assurance scheme
EAP
Specsavers scheme