701 Clinical Trials jobs in the United Kingdom

Clinical Trial Assistant

Reading, South East IQVIA

Posted 4 days ago

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Job Description

IQVIA is a leading global provider of contract research services, advanced analytics and technology solutions to the life sciences industry formed through the merger of IMS Health and Quintiles.
Take your therapeutic expertise to the next level and help drive the evolution of clinical development for a variety of sponsors.
As a Clinical Trial Assistant within our full-service model, you'll have the opportunity to embrace your passion for a specific therapeutic area and work with cutting-edge technology developed specifically for CTAs.
With access to world-class training and professional development, we'll give you the tools you need to create the career you want.
Do you want to know more about IQVIA? then see what Forbes said about us!
Functions of a Clinical Trial Assistant (CTA)**
+ Assist Clinical Research Associates (CRAs)/In-house Clinical Research Associate (iCRA) and Regulatory and Start-Up (RSU) with accurately updating and maintaining clinical systems that track site compliance and performance within project timelines.
+ Assist the clinical team in the preparation, handling, distribution, filing, and archiving of clinical documentation and reports according to the scope of work and standard operating procedures. Assist with periodic review of study files for completeness.
+ Assist CRAs/iCRAs and RSU with preparation, handling and distribution of Clinical Trial Supplies and maintenance of tracking information.
+ Assist with the tracking and management of Case Report Forms (CRFs), queries and clinical data flow.
+ Act as a central contact for the clinical team for designated project communications, correspondence and associated documentation.
+ May accompany CRAs on site visits to assist with clinical monitoring duties upon completion of required training and with required approval.
+ May perform assigned administrative tasks to support team members with clinical trial execution.
**Required Knowledge and Skills**
+ Awareness of applicable clinical research regulatory requirements; i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines
+ Knowledge of applicable protocol requirements as provided in company training
+ Computer skills including working knowledge of Microsoft Word, Excel and PowerPoint
+ Good written and verbal communication skills including excellent command of English
+ Effective time management and organizational skills
+ Ability to establish and maintain effective working relationships with coworkers, managers and clients
*Please note - this role is not eligible for UK visa sponsorship*
_IQVIA is a strong advocate of diversity and inclusion in the workplace. We believe that a work environment that embraces diversity will give us a competitive advantage in the global marketplace and enhance our success. We believe that an inclusive and respectful workplace culture fosters a sense of belonging among our employees, builds a stronger team, and allows individual employees the opportunity to maximize their personal potential._
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 Trials Prosthetist

Basingstoke, South East Blatchford

Posted today

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Do you want to put your clinical expertise to work in a whole new way? Help shape the future of Blatchford products by using your clinical insight to help bring amazing ideas to reality that truly make a difference. Blatchford is a multi-award winning, global manufacturer of some of the world’s most advanced prosthetic technology, bespoke seating solutions and orthotic devices. Our evidence-based approach and commitment to continuously challenge possibilities ensures our mobility solutions prioritise the wellbeing and long-term health of our users. Through science, technology, and maintaining a clear focus on people, we make mobility possible. We are driven by a clear purpose: to deliver superior clinical outcomes. We have a brand new, exciting opportunity for a Clinical Trials Prosthetist to strengthen our global clinical research team and ensure our pioneering technologies are validated with the highest standards of safety, ethics, and scientific rigor. The role As Clinical Trials Prosthetist , you will focus on prosthetic products, along with supporting other product/clinical areas. This is a flexible opportunity to share your expertise, influence product development, and help bring innovative mobility solutions to life. Key duties: Providing clinical oversight for all participants in Blatchford-sponsored clinical trials across our varied products. Providing direct clinical input to our prosthetic R&D and Marketing advocates to maintain your clinical registration. Ensuring compliance with clinical trial protocols, Good Clinical Practice and regulatory requirements. Supporting trial design by contributing clinical expertise to protocol development, feasibility assessments, and outcome measures. Liaising with our clinical teams based in the UK and Norway and our global educators to ensure their ‘on the ground’ feedback is heard and incorporated when appropriate. Presenting our clinical findings at national and international conferences Serving as the clinical point of contact for investigators, study coordinators, regulatory authorities, and internal teams. Overseeing accurate clinical documentation and supporting the interpretation of trial data. Contributing to Blatchford’s mission of advancing mobility by ensuring our innovations are validated with robust clinical evidence. What can we offer you? As Clinical Trials Prosthetist, you will receive the following: Benefits Highly competitive salary Flexible, hybrid working. 25 days holiday (rising with service) Option to purchase additional annual leave. Pension Death in service Discounted shopping and leisure activities Health cash plan Cycle to work scheme. A meaningful role where your work directly improves patients’ mobility and independence. A collaborative, international research environment at the forefront of medical technology. Opportunities for professional growth and development within a global innovation leader. What are we looking for? Key skills Qualified Prosthetist experience. Good level of clinical experience. Strong product knowledge in lower-limb prosthetics, including familiarity with microprocessor and mechanical prosthetic systems. Have experience of clinical trials or research. Good knowledge of ethics, and regulatory standards. Excellent communication and collaboration skills, with the ability to work across multidisciplinary and international teams. Passionate about advancing patient outcomes and bringing life-changing technologies to market. If you feel like you meet the above criteria for this exciting Clinical Trials Prosthetist opportunity, then please apply now!
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Clinical Trials Prosthetist

Basingstoke, South East Blatchford

Posted 7 days ago

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Do you want to put your clinical expertise to work in a whole new way?


Help shape the future of Blatchford products by using your clinical insight to help bring amazing ideas to reality that truly make a difference.


Blatchford is a multi-award winning, global manufacturer of some of the world’s most advanced prosthetic technology, bespoke seating solutions and orthotic devices. Our evidence-based approach and commitment to continuously challenge possibilities ensures our mobility solutions prioritise the wellbeing and long-term health of our users.


Through science, technology, and maintaining a clear focus on people, we make mobility possible.


We are driven by a clear purpose: to deliver superior clinical outcomes. We have a brand new, exciting opportunity for a Clinical Trials Prosthetist to strengthen our global clinical research team and ensure our pioneering technologies are validated with the highest standards of safety, ethics, and scientific rigor.


The role


As Clinical Trials Prosthetist , you will focus on prosthetic products, along with supporting other product/clinical areas. This is a flexible opportunity to share your expertise, influence product development, and help bring innovative mobility solutions to life.


Key duties:


  • Providing clinical oversight for all participants in Blatchford-sponsored clinical trials across our varied products.
  • Providing direct clinical input to our prosthetic R&D and Marketing advocates to maintain your clinical registration.
  • Ensuring compliance with clinical trial protocols, Good Clinical Practice and regulatory requirements.
  • Supporting trial design by contributing clinical expertise to protocol development, feasibility assessments, and outcome measures.
  • Liaising with our clinical teams based in the UK and Norway and our global educators to ensure their ‘on the ground’ feedback is heard and incorporated when appropriate.
  • Presenting our clinical findings at national and international conferences
  • Serving as the clinical point of contact for investigators, study coordinators, regulatory authorities, and internal teams.
  • Overseeing accurate clinical documentation and supporting the interpretation of trial data.
  • Contributing to Blatchford’s mission of advancing mobility by ensuring our innovations are validated with robust clinical evidence.


What can we offer you?


As Clinical Trials Prosthetist, you will receive the following:


Benefits


  • Highly competitive salary
  • Flexible, hybrid working.
  • 25 days holiday (rising with service)
  • Option to purchase additional annual leave.
  • Pension
  • Death in service
  • Discounted shopping and leisure activities
  • Health cash plan
  • Cycle to work scheme.
  • A meaningful role where your work directly improves patients’ mobility and independence.
  • A collaborative, international research environment at the forefront of medical technology.
  • Opportunities for professional growth and development within a global innovation leader.



What are we looking for?

Key skills


  • Qualified Prosthetist experience.
  • Good level of clinical experience.
  • Strong product knowledge in lower-limb prosthetics, including familiarity with microprocessor and mechanical prosthetic systems.
  • Have experience of clinical trials or research.
  • Good knowledge of ethics, and regulatory standards.
  • Excellent communication and collaboration skills, with the ability to work across multidisciplinary and international teams.
  • Passionate about advancing patient outcomes and bringing life-changing technologies to market.


If you feel like you meet the above criteria for this exciting Clinical Trials Prosthetist opportunity, then please apply now!

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Clinical Trials Pharmacist

Chelsea, London NHS

Posted today

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The trials team is expanding, and we have a fantastic opportunity for a passionate, motivated, and dynamic pharmacist to join the Pharmacy Clinical Trials team at The Royal Marsden (RMH) NHS Foundation Trust.

An exciting time to join our service, focussing on delivering high-quality care to patients and staff. The RMH is a world-leading cancer centre with sites in Chelsea and Sutton, plus a Medical Day Care Unit at Kingston Hospital.

Prior clinical trials experience; oncology or haemato-oncology knowledge is an advantage. Working alongside pharmacists, technicians, and assistants as part of a Multi-Disciplinary Team committed to delivering outstanding patient care.

Our team supports the research strategy of "taking personalized cancer treatment to the next level," with approximately 380 active IMP studies and increasingly complex new clinical trials across all specialties, including gene therapies and cellular therapies studies.

The RMH, in association with its partner, The ICR, has an unparalleled global reputation for patient care, research, and education. Through our partnership, we pioneer new cancer therapies through complex transitional studies and Phase I-III clinical trials, making us one of

Europe's largest comprehensive cancer centres.

The hospital has recently introduced the EPIC digital health record system, and we are looking to use the full capabilities of this system to support the pharmacy teams and become a more efficient and truly paperless.

  • To contribute to the provision of the pharmacy clinical trials service to the Dispensaries (Chelsea & Sutton), Medical day Unit, West Wing Clinical Research Centre (WWCRC), Oak ward and day case areas of the Drug Development Unit and the Clinical Trial Dispensary across both sites.
  • To assist the Clinical Trials Team with any day-to day clinical, dispensing, ward and research day units' queries.
  • To provide clinical trials advice while covering the research clinics and attending MDT.
  • To support research clinic prescribing
  • Provide clinical trial support and advice to other areas within pharmacy e.g. aseptic service, clinical services and to the research teams.
  • To support the clinical trial team with clinical trial set-up of new studies, revision of amendments for ongoing studies already open at the trust, to provide continued support for the running and maintenance of current trial activity.
  • To contribute to the provision of the pharmacy clinical trials service to the individual clinical units, R&D and the Trust.

The RMH NHS Foundation Trust is a world-leading cancer centre, offering patients the best cancer care available anywhere in the world, and to continue to make a global contribution to finding better ways of diagnosing and treating cancer. We have two hospitals – one in Chelsea, London, and one in Sutton, Surrey – as well as a Medical Day-care Unit in Kingston Hospital

At RMH, we deal with cancer every day, so we understand how valuable life is. When people entrust their lives to us, they have the right to demand the very best. That's why the pursuit of excellence lies at the heart of everything we do.

At the heart of the hospital is our dedicated team. We offer a stimulating and dynamic working environment, a wide range of staff benefits and learning and development opportunities.

We are looking for employees who aspire to excellence, share our values and can play a crucial role in our on-going achievements. A variety of other staff benefits including employee assistance programme, discounted gym membership, onsite fitness classes, car schemes.

For further information on this role, please see the attached detailed Job Description and Person Specification:

Ensure that clinical trial services policies and procedures are adhered to and accreditation records and training documents are completed appropriately.

Promote optimal and appropriate drug use and high quality prescribing practice within the Trust.

To respond appropriately to requests from medical and nursing staff for information and advice about selection and use of drug therapy.

Support the Lead Pharmacist, Clinical R&D and the Chief Technician, Clinical Trials in work towards maintaining quality standards required by Medicines and Health products Regulatory Agency and ensuring principles of Good Clinical Practice are applied at all times.

To support the Lead Pharmacist, Clinical R&D with the Clinical Governance and Risk Management Strategy within the department and throughout the Trust.

Take part in clinical trials audit or any other project work relevant to this post.

Participate in any pharmacy initiatives or working groups as appropriate.

To support the Trial Team in maintaining up to date of Key Performance Indicators for all trail activities.

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Clinical Trials Manager

SO15 0AA Southampton, South East £50000 Annually WhatJobs

Posted 8 days ago

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full-time
Our client is seeking an experienced and diligent Clinical Trials Manager to oversee the planning, execution, and monitoring of clinical studies within their pharmaceutical division. This critical role, based in our Southampton, Hampshire, UK facility, requires a strong understanding of clinical trial processes, regulatory requirements, and project management principles. You will be responsible for ensuring that all trials are conducted in accordance with protocol, GCP guidelines, and ethical standards, while maintaining the highest quality and integrity of data. Responsibilities will include:
  • Developing comprehensive clinical trial protocols and study plans.
  • Identifying, selecting, and managing investigative sites and study personnel.
  • Overseeing the day-to-day operations of clinical trials, including patient recruitment, data collection, and monitoring.
  • Ensuring compliance with all applicable regulatory requirements (e.g., FDA, EMA, MHRA) and Good Clinical Practice (GCP).
  • Managing clinical trial budgets and timelines effectively.
  • Developing and maintaining strong relationships with investigators, study coordinators, and other stakeholders.
  • Preparing and submitting study-related documents, including Investigator Brochures and Essential Documents.
  • Risk assessment and mitigation planning for clinical trials.
  • Managing vendors and external service providers involved in clinical trials.
  • Contributing to the development and implementation of Standard Operating Procedures (SOPs) related to clinical trial management.
  • Ensuring accurate and timely data management and reporting.
  • Leading and motivating clinical research associates (CRAs) and other study team members.
Qualifications:
  • Bachelor's or Master's degree in Life Sciences, Nursing, Pharmacy, or a related field.
  • Minimum of 5 years of experience in clinical trial management within the pharmaceutical or biotechnology industry.
  • In-depth knowledge of GCP, ICH guidelines, and regulatory submission processes.
  • Proven experience in managing multiple clinical trials simultaneously.
  • Strong project management skills with a demonstrated ability to manage complex projects.
  • Excellent leadership, communication, and interpersonal skills.
  • Proficiency in clinical trial management software and electronic data capture (EDC) systems.
  • Ability to travel as required to investigative sites and meetings.
  • Strong problem-solving abilities and attention to detail.
  • Experience in (specific therapeutic area, e.g., oncology, cardiology) is a significant advantage.
This is an exceptional opportunity for a dedicated professional to play a pivotal role in bringing life-changing medicines to patients by ensuring the successful execution of clinical trials.
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Clinical Trials Prosthetist

Basingstoke, South East Blatchford

Posted today

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Job Description

Job Description

Do you want to put your clinical expertise to work in a whole new way?


Help shape the future of Blatchford products by using your clinical insight to help bring amazing ideas to reality that truly make a difference.


Blatchford is a multi-award winning, global manufacturer of some of the world’s most advanced prosthetic technology, bespoke seating solutions and orthotic devices. Our evidence-based approach and commitment to continuously challenge possibilities ensures our mobility solutions prioritise the wellbeing and long-term health of our users.


Through science, technology, and maintaining a clear focus on people, we make mobility possible.


We are driven by a clear purpose: to deliver superior clinical outcomes. We have a brand new, exciting opportunity for a Clinical Trials Prosthetist to strengthen our global clinical research team and ensure our pioneering technologies are validated with the highest standards of safety, ethics, and scientific rigor.


The role


As Clinical Trials Prosthetist , you will focus on prosthetic products, along with supporting other product/clinical areas. This is a flexible opportunity to share your expertise, influence product development, and help bring innovative mobility solutions to life.


Key duties:


  • Providing clinical oversight for all participants in Blatchford-sponsored clinical trials across our varied products.
  • Providing direct clinical input to our prosthetic R&D and Marketing advocates to maintain your clinical registration.
  • Ensuring compliance with clinical trial protocols, Good Clinical Practice and regulatory requirements.
  • Supporting trial design by contributing clinical expertise to protocol development, feasibility assessments, and outcome measures.
  • Liaising with our clinical teams based in the UK and Norway and our global educators to ensure their ‘on the ground’ feedback is heard and incorporated when appropriate.
  • Presenting our clinical findings at national and international conferences
  • Serving as the clinical point of contact for investigators, study coordinators, regulatory authorities, and internal teams.
  • Overseeing accurate clinical documentation and supporting the interpretation of trial data.
  • Contributing to Blatchford’s mission of advancing mobility by ensuring our innovations are validated with robust clinical evidence.


What can we offer you?


As Clinical Trials Prosthetist, you will receive the following:


Benefits


  • Highly competitive salary
  • Flexible, hybrid working.
  • 25 days holiday (rising with service)
  • Option to purchase additional annual leave.
  • Pension
  • Death in service
  • Discounted shopping and leisure activities
  • Health cash plan
  • Cycle to work scheme.
  • A meaningful role where your work directly improves patients’ mobility and independence.
  • A collaborative, international research environment at the forefront of medical technology.
  • Opportunities for professional growth and development within a global innovation leader.



What are we looking for?

Key skills


  • Qualified Prosthetist experience.
  • Good level of clinical experience.
  • Strong product knowledge in lower-limb prosthetics, including familiarity with microprocessor and mechanical prosthetic systems.
  • Have experience of clinical trials or research.
  • Good knowledge of ethics, and regulatory standards.
  • Excellent communication and collaboration skills, with the ability to work across multidisciplinary and international teams.
  • Passionate about advancing patient outcomes and bringing life-changing technologies to market.


If you feel like you meet the above criteria for this exciting Clinical Trials Prosthetist opportunity, then please apply now!

This advertiser has chosen not to accept applicants from your region.

Clinical Trials - Sales Lead

Vet-AI

Posted today

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Who we are: We are Vet-AI, and we are delivering the future of pet care and clinical research. While our flagship app, Joii Pet Care, makes pet care affordable and accessible for all pet owners, we are also at the forefront of digital veterinary trials. Our platform enables efficient and effective clinical research for veterinary medicine, leveraging the insights gained from Joii's extensive user base. Our mission: To make pet care affordable and accessible for everyone. To improve the lives and wellbeing of everyone working within the veterinary industry. To advance veterinary medicine through digitally led trials, using Joii Pet Care to connect research sponsors with pet owner databases Quite simply, we want vet care to be available to everyone, to ensure the people who are delivering it with us are as happy as they can be, and to drive innovation in animal health through our trials platform, all while keeping the spirit of Joii alive. Role Summary: As Clinical Trials - Sales Lead, you will take full ownership of the sales function for our Clinical Trials business line. You’ll be responsible for developing strategy, building a high-quality pipeline, and converting opportunities into long-term partnerships with pet food companies and other pet care businesses. Working closely with leadership, you will design client solutions and ensure a seamless journey from first contact through to proposal and closure. This is a unique opportunity to shape and grow a key revenue stream in a scaling business. Job Responsibilities: Define and implement a sales strategy for the Clinical Trials division. Own the end-to-end sales cycle: prospecting, lead generation, consultative solution design, proposal development, negotiation, and closing. Build strong relationships with decision-makers in the pet food and pet care industries. Maintain a healthy, well-documented sales pipeline with accurate forecasting and reporting. Collaborate with internal teams to design solutions that deliver real value for clients. Represent the company at industry events, conferences, and networking forums. Essential: We are looking for someone ambitious, commercially minded, and excited about scaling a business in a dynamic sector. Proven track record in clinical trials sales, pet care, healthcare, or life sciences. Experience selling into pet food companies and the wider pet care sector. Demonstrated success in building and managing a sales pipeline. Strong consultative sales skills, with the ability to design and present compelling solutions. Experience working in a startup or scale-up environment, comfortable building processes and taking ownership. Excellent communication, influencing, and relationship management skills. Desirable: Established a network within the pet food or pet care industries. Knowledge of clinical trial operations, regulatory frameworks, or R&D partnerships in pet health. Our brand values: Brave; We are not afraid to disrupt the status quo. Championing what’s right for pets and standing confidently behind our purpose. Even when it’s challenged. We have the courage and confidence to tackle things that nobody has done before. We may face hurdles, adversity, and the fear of failure but we have the conviction to keep going. Boundless; We do not constrain ourselves to the expectations of traditional pet care; we’re young, bright and full of fresh ideas. We bring energy and pro-activity to everything we do. We’re problem solvers, with a ‘can do’ outlook. Our boundless attitude brings the joy. Togetherness; We share an ‘in-it-together’ mindset. We’re one team; we don’t leave anyone to face problems alone when we can help. We champion empathy and compassion; caring about what our customers and our colleagues are going through. Going above and beyond when they need us. We strive for constant collaboration, no matter where we are in the world What you’ll get: We are a startup transitioning to a scale-up, so if you like a slow pace, we’re not the company for you. However, if you do like a supportive team, a fun culture, and the feeling of creating incredible work - you’ll fit right in! Some of the perks you’ll get with us are: Fully remote (UK Access to a co-working space budget Private Medical Insurance & Group Life Assurance Headspace Membership Employee Assistance Programme Enhanced Family Leave and fertility support Enhanced company sick pay Contribution to professional development and professional membership budget ️33 days of paid holiday including the usual UK public bank holidays (pro rata’d) Frequent remote and in-person social ⌚Flexible start and finish times Free use of the platform New starter home office setup contribution Twice yearly Continuous Performance Management Reviews Diversity and Inclusion We’re building an inclusive and diverse team. We truly believe that surrounding ourselves with different opinions means that we’ll challenge our own assumptions instead of thinking we know the correct answer. We welcome applications from everyone and will foster an encouraging and caring workplace. If you aren’t sure if you qualify, send us your CV anyway. We’ll take the time to look over your application and give you feedback. Interview Process We want candidates to feel supported and informed throughout. Our typical process is: Initial screening call (15–30 mins) with our People Team to understand your background and motivations. Competency interview (60 mins) with the Sales Director to explore your sales experience, clinical trials/petcare knowledge and to align our business values and team dynamics. Final interview with leadership (2), focusing on values, team fit, and role vision. We aim to complete the process in 2–3 weeks and will provide feedback at every stage. Earn a competitive salary with exciting OTE potential - your performance drives your reward!
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Remote Clinical Trials Coordinator

SO14 0AA Southampton, South East £40000 annum (pro- WhatJobs

Posted 9 days ago

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contractor
Our client is seeking a highly organized and experienced Remote Clinical Trials Coordinator to support the execution of complex clinical research studies. This position is fully remote, allowing you to contribute to vital medical advancements from the comfort of your home office. You will be instrumental in ensuring that clinical trials are conducted ethically, efficiently, and in compliance with all regulatory standards. Your role will involve meticulous record-keeping, patient coordination, and data management, working closely with investigators, study participants, and regulatory bodies.

Key Responsibilities:
  • Coordinate all aspects of assigned clinical trials remotely, adhering to study protocols and Good Clinical Practice (GCP) guidelines.
  • Assist in the preparation and submission of study-related documents, including Investigational New Drug (IND) applications and Institutional Review Board (IRB) submissions.
  • Recruit, screen, and enroll eligible participants for clinical trials, conducting initial remote assessments and consultations.
  • Schedule and manage participant appointments, ensuring adherence to the trial schedule and protocol requirements.
  • Collect, manage, and maintain accurate study data in electronic data capture (EDC) systems.
  • Monitor study progress, identify potential issues or deviations, and implement corrective actions as needed.
  • Communicate effectively with investigators, study coordinators, and other site personnel to ensure smooth trial operations.
  • Prepare and submit regulatory and progress reports as required.
  • Ensure the proper storage and handling of investigational products and biological samples.
  • Maintain all study-related documentation and files in a compliant and organized manner.
  • Conduct remote monitoring visits to ensure protocol adherence and data integrity.
  • Provide support and education to study participants regarding trial procedures and requirements.
Qualifications and Skills:
  • Bachelor's degree in a life science, nursing, or a related field; Master's degree preferred.
  • Minimum of 3-5 years of experience in clinical research coordination or a similar role.
  • In-depth knowledge of GCP, ICH guidelines, and regulatory requirements for clinical trials.
  • Proficiency with electronic data capture (EDC) systems and other clinical trial management software.
  • Excellent organizational, time management, and multitasking abilities.
  • Strong written and verbal communication skills, with the ability to communicate effectively with diverse stakeholders.
  • Demonstrated ability to work independently and proactively in a remote setting.
  • Detail-oriented with a commitment to data accuracy and integrity.
  • Experience in specific therapeutic areas (e.g., oncology, cardiology) is a plus.
  • Certification as a Clinical Research Professional (e.g., ACRP, SoCRA) is highly desirable.
This is a critical role within our research division, demanding a high level of professionalism and expertise. If you are passionate about advancing medical research and thrive in a remote work environment, we invite you to apply.
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Clinical Trial Assistant - Student Placement

High Wycombe, South East J&J Family of Companies

Posted 5 days ago

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At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at Function:**
Career Programs
**Job Sub** **Function:**
Non-LDP Intern/Co-Op
**Job Category:**
Career Program
**All Job Posting Locations:**
High Wycombe, Buckinghamshire, United Kingdom
**Job Description:**
The Clinical Trial Assistant supports the Local Trial Manager (LTM) and/or Site Manager (SM) to
ensure optimal management of all documents with logistical and administrative tasks related to
trial start-up, execution and closing of clinical trials. Ensures trial related activities are
compliant with GCO SOPs, policies and local regulatory requirements. May contribute to
process improvement.
**Role Title:** Clinical Trial Assistant
**Duration** : 12 months
**Intake:** June 2026
**Position summary:**
You will join our team in the role of a Clinical Trial Assistant and will be given exposure to many aspects of the Clinical Trials process. This is primarily an office-based role.
Working within a study team, you will provide clinical trial operational support across many different disease areas. These tasks are associated with trial start-up, execution and close out, mainly in phases II-III of clinical trial development. Activities are assigned by the Clinical Operations Clinical Research Managers, Local Trial Managers and Clinical Research Associates (Site Managers).
Throughout the course of the placement, we seek to provide extensive experience in multiple disease areas and across different aspects of conducting a clinical trial. You will be encouraged to become familiar with the regulatory and ethical frameworks, including the principles of International Committee of Harmonisation Good Clinical Practice (ICH GCP).
This is a **one-year** industrial placement, for a **Clinical Trial Assistant** in the **UK Clinical Operations Team** at **J&J Innovative Medicine** . Experience is not required for this role, however a good understanding of life sciences and a desire to be involved in the development of new medicines is essential.
**Main duties and responsibilities:**
+ Contribute to UK study management team meetings (face-to-face or virtual).
+ Update the clinical trial management system
+ Perform quality review checks of the filing system to ensure inspection readiness at all times.
+ Ensure current versions of the required trial documents, trial-related materials and supplies are distributed to the hospital site within required timeframes.
+ Support the UK study team perform as assessment of hospital site feasibility (the ability to conduct a clinical trial).
+ Support to collect/prepare documents required for study start-up/submission to Health Research Authority and Ethics Committees.
+ Collect, file and archive study documents.
+ Collaborate with the student cohort on fundraising and charity events.
+ Support the onboarding activities of placement student successors.
**Education & Key Skills/Competencies Requirement:**
+ **2 years** of undergraduate degree level study completed at the start of the placement year **(June 2026)** in a **Life Sciences** degree ( **e.g. Biology, Chemistry, Biochemistry, Nursing, Pharmacy** ).
+ The industrial placement year is part of your overall undergraduate degree course.
+ A minimum of **2:1** achieved in first year of study.
+ Good Microsoft Office (Word, PowerPoint, and Excel) skills.
+ Passionate and enthusiastic for working in the pharmaceutical industry.
+ Motivated to develop and learn.
+ Excellent communication skills, both written and oral forms.
+ Analytical, with good problem-solving skills.
+ Flexible and adaptable team player, who actively contributes to the team.
+ Actively seeks feedback, appreciates and uses to learn.
+ Bounces back quickly from mistakes; learns and moves on quickly.
+ High level of accuracy and attention to detail.
+ Seeks opportunities to learn and grow professionally.
+ Takes initiative, can prioritise and manage own workload autonomously.
+ Proficient digital literacy, good interpersonal skills and the ability to collaborate and balance multiple priorities.
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Pharmaceutical Clinical Trials Project Manager

BN1 1AA East Sussex, South East £70000 Annually WhatJobs

Posted 3 days ago

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full-time
Our client, a cutting-edge pharmaceutical company, is seeking a dynamic and experienced Pharmaceutical Clinical Trials Project Manager to join their expanding research and development division. This role offers a hybrid working model, combining the flexibility of remote work with essential in-office collaboration. You will be responsible for the planning, execution, and oversight of complex clinical trials, ensuring they are conducted in accordance with ethical standards, scientific rigor, and regulatory requirements. Your duties will encompass managing trial budgets, timelines, and resources, selecting and managing clinical investigator sites, and ensuring the quality and integrity of data collected. This includes developing study protocols, case report forms (CRFs), and other essential trial documents. You will liaise closely with internal departments, including regulatory affairs, data management, and biostatistics, as well as external vendors and collaborators. Strong leadership, excellent communication, and problem-solving skills are essential for navigating the challenges of clinical trial management. The ideal candidate will possess a deep understanding of clinical trial processes, Good Clinical Practice (GCP) guidelines, and regulatory submissions. A scientific or medical background, such as a degree in life sciences, pharmacy, or nursing, is required, along with substantial experience managing Phase I-IV clinical trials. Proficiency in clinical trial management software and a proven ability to manage multiple projects simultaneously are critical. This is an excellent opportunity to contribute to the development of life-saving therapies and advance your career within a supportive and innovative environment located in **Brighton, East Sussex, UK**.
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