Adaptimmune is a leader in the research and development
of T cell-based therapies for the treatment of cancer. The business is rapidly
growing with clinical trials ongoing in oncology centres across both the US and
Based near Oxford, UK, Adaptimmune offers the
opportunity to be part of pioneering the commercial development of T cell
therapy. As the company expands an opportunity
exists for a motivated individual to join the clinical team.
Clinical Research Associate :
and management of preferred Contract Research Organization for EU monitoring
and site-level activities
Contribute to site
evaluation, start up, initiation, monitoring, and tracking of clinical trial
activities including source document verification, data review
review of monitoring reports
visits to assess CRO CRAs competency and assist with training of CRAs and sites
Contribute to the
selection of potential investigators
University degree in
Life Sciences, Pharmacy, RN or equivalent
Previous CRA experience
(preferred 5+ years) monitoring industry sponsored oncology trials. Experience with biologics or cell and gene
CRO monitoring for outsourced studies
Able to work
independently as well as team oriented with strong communication skills
A valid driver’s
license and ability to travel
are competitive; benefits include a pension scheme, life insurance, private
health insurance and dental plan, subsidised gym membership. To be involved in
cutting-edge therapeutic research, within a friendly, dynamic environment,
please visit our Careers Page for more details and to apply online: www.adaptimmune.com/careers-uk
Office Based Clinical Research Associate
Medpace is a global, full-service Clinical Research
Organisation (CRO), currently seeking a full-time, office/home-based Clinical
Research Associate. If you want an exciting career in a friendly team, where
you use your previous expertise, develop and grow further, this is the opportunity for you.
As a CRA, you will work within innovative therapeutic fields
and with challenging studies ranging from phase I-IV. We are looking for
proactive, positive and self-motivated individuals to join our supportive and
- Conduct pre-study, initiation, monitoring, and closeout
visits for clinical research sites following applicable SOPs and ICH GCP;
- Oversee and interact with the sites including follow up
between the visits
- University bioscience degree;
- Minimum 2 years of experience as an independent on site CRA;
- Excellent verbal and written communication skills in
- Stable employment history
Travel: up to 80% all over UK
Join Medpace, a mid-size global CRO that is rapidly growing
and offers limitless opportunities in career growth and where you will be
rewarded for strong performance. At
Medpace, you will find work that is both challenging and rewarding,
enthusiastic, friendly team and you will be given the tools and training to
Salary £38,896 - £41,255 (with progression to £46,414)
Closing date 19th May 2016
We have an exciting opportunity for a Senior Trial Manager within our
successful and expanding UK CRC registered Clinical Trials Unit.
The post holder will be part of the leadership team of the Newcastle Clinical Trials Unit
(NCTU) within the Faculty of Medical Sciences.
They will lead a team of trial managers to deliver a wide portfolio of
early and late phase trials. The post
requires an enthusiastic and motivated individual, with excellent negotiating,
communication and interpersonal skills.
Applicants will have a first degree in a relevant discipline, significant
experience in the management of clinical trials and an in-depth knowledge of
the provisions of the EU Clinical Trials Directive and the Research Governance
Framework for Health & Social Care.
Informal enquiries may be made to Prof Elaine McColl, Director of NCTU
via e-mail to email@example.com
about the NCTU can be found on our website
. Applications must be made via the Newcastle
University website (http://www.ncl.ac.uk/vacancies/jobs/
FRONTIERES / DOCTORS WITHOUT BORDERS (MSF)
is offering and exciting and challenging
position for a Clinical Trial Co-Principal Investigator with
knowledge of MDR TB to function as the Clinical Trial Site Lead for the TB PRACTECAL clinical trials to be
conducted in Karakalpakstan, Uzbekistan
MSF is setting up a PRAgmatic Clinical Trial for
a more Effective, Concise And Less toxic MDR-TB treatment regimen
(TB-PRACTECAL). It is a randomised, controlled, open label phase II-III trial to
evaluate the safety and efficacy of regimens containing bedaquiline and
pretomanid for the treatment of adult patients with pulmonary multidrug
TB-PRACTECAL is a ground breaking MDR-TB
clinical trial implemented in collaboration with the London School of Hygiene
and Tropical Medicine (LSHTM), WHO Special Programme for Research and training
in Tropical Diseases (WHO TDR), University College London (UCL), Swiss Tropical
and Public Health Institute (Swiss TPH), Drugs for Neglected Diseases
initiative (DNDi), the Global Alliance for TB drug development and the Ministry
of Health of Uzbekistan. MSF is the sponsor and also takes investigator
responsibilities for this trial.
Clinical Trial Site Lead (Co-PI), Karakalpakstan
The MSF Clinical Trial Site Lead (Co-PI) will
take responsibility for the good and timely conduct of the TB-PRACTECAL
Clinical Trial in close collaboration with the Ministry of Health Principal
Investigator and with MSF and Ministry of Health Project teams on site.
MSF is looking for an individual with a strong
motivation to ensure good conduct of a Clinical Trial in a remote and
challenging setting; someone who possesses the essential medical and research
skills but is also well versed in team building, leadership, project management
This is an excellent opportunity for a Medical
Doctor with Clinical Trial / Medical Research and MDR TB treatment experience
to be involved in ground-breaking work towards a more Effective, Concise And
Less toxic MDR-TB treatment regimen.
For more information and to apply please visit
our website: http://www.msf.org.uk/specific-roles
Faculty of Medicine and Health
School of Medicine
Leeds Institute of Clinical
Senior Trial Manager
Full time or Part time basis -
Open Ended Fixed Funding for 3 years
Want to be part of a leading team that has a national and
international reputation for excellence in conducting complex, multi-centre
The Clinical Trials Research Unit (CTRU) at the University of
Leeds has a national reputation for excellence and conducts national and
international phase II/III, multi-centre trials in the areas of cancer, health
sciences and comprehensive health research.
We require a focused candidate to join our team and take
responsibility for coordinating specific clinical trials from set-up and
recruitment through to trial closure and analysis.
You will directly co-ordinate large multi-centre trials and/or
lead a CTRU portfolio trial management team, ensuring international quality
standards in trial management for the projects/portfolio by supervising complex
trials and associated trial co-ordination staff across the therapeutic area. An
up-to-date knowledge of regulatory frameworks and legislation is essential.
Applicants should have a science degree or equivalent relevant
qualification/experience and experience of trial coordination/trial management
in multi-centre trials involving medicinal products. Effective communication
and organisational skills and knowledge of the regulatory and governance
environment relating to clinical trials are essential.
To apply and for further
information, please visit http://jobs.leeds.ac.uk and search
Closing Date: 17th January 2016
Faculty of Medicine
School of Medicine
Leeds Institute of
Clinical Trials Research
Are you a graduate
with a degree in a Science, Social Science or a health related subject; or do
you have equivalent experience? Do you
have experience of trial coordination or data management in multi-centre
We need focused, hardworking, motivated candidates like you
to fill our Senior Trial Coordinator positions in the Leeds Institute of
Clinical Trials Research which is leading clinical trials research and
impacting on clinical practice by answering important research questions.
You will join an Institute with an international reputation
for conducting multi-centre clinical trials in areas of high importance to the
NHS; such as cancer, mental health, stroke, obesity, older people,
cardiovascular disease, musculoskeletal disease, oral health and skin.
You will join an experienced, multi-disciplinary team where
you will take responsibility for coordinating specific clinical trials from
set-up and recruitment through to trial closure and analysis.
We welcome applications from candidates with a science /
social science / health related degree or equivalent relevant
qualification/experience; and experience of trial coordination or data
management in multi-centre trials or experience of collaborative working across
several organisations in a research capacity. Effective communication and
organisational skills and the ability to develop and maintain good working
relationships are essential; as is an up-to-date working knowledge of Good
Clinical Practice standards and the NHS Research Governance Framework.
To apply and for
further information, please visit http://jobs.leeds.ac.uk and search for MHCTR1040
Co. Ltd is a leading global research and development-based pharmaceutical
company, headquartered in Japan. At Eisai, our human health care (hhc) mission is to give first thought to
patients and their families, and to increasing the benefits that health care
recruiting for a highly experienced, organised and motivated Manager, Clinical
Operations, Oncology to join our established team at
Eisai’s European Knowledge Centre, Hatfield, Herts. The position will report to
an Associate Director, Clinical Operations, Oncology.
Manages one or more clinical studies within the Oncology
Product Creation Unit to ensure that study milestones and deliverables are
achieved according to agreed quality standards, timelines and budget. Ensures
that quality of data are acceptable and suitable for regulatory submission.
Ensures that studies are executed according to ICH/GCP guidelines, applicable
regulatory requirements and Eisai’s standard operating procedures.
Manager may lead the Eisai cross-functional team for
designated study(ies) and/or may coordinate designated regional aspects of
assigned global study(ies) under supervision of study Global Clinical
Proven track record of coordinating international study teams, leading
CRO/vendor management activities and ensuring internal cross-functional
collaboration to deliver high quality Oncology studies.
Full understanding of current ICH/GCP guidelines.
Previous experience of working on studies measuring the
anti-tumour efficacy of investigational oncology agents, including awareness of
current anti-tumour therapies, and be at ease with tools such as RECIST
criteria for tumour assessment, NCI Common Toxicity Criteria.
Must have excellent interpersonal skills and be at ease
working in virtual teams with internal and external collaborators in multiple
to degree level in a relevant field
in Clinical Operations methods and processes in an industry setting
Date: 31 January 2016
Click here to apply
in Oxfordshire/Kidlington or home-based UK wide
Following the stable
and successful growth in the UK, we are expanding the PSI Clinical Operations department
and looking for a Clinical Research Associate II to join our highly
professional and vibrant team.
are keen to work with full-scale complex trials within multiple therapeutic
areas, provide us with your expertise and guidance in the region and be
involved in something new, outstanding and challenging, this job opportunity is
perfect for you!
recognized by a unique combination of team collaboration and independent work,
global dimensions and individual approach. We provide a stable and secure
workplace, while giving opportunities for innovative ways of doing things.
provide high-quality employment, competitive salary, excellent working
conditions and a personable supportive environment. It is a great chance to
join the company that really cares for its people, and invests in their professional
development and success.
value high quality standards, transparent communication lines, excellent
opportunities for professional development, well-established infrastructure and
energetic environment, join PSI and start your career with us!
have a hands-on, go-an-extra-mile approach, enjoy every aspect of clinical
projects, from feasibility and project setup to effective day-today site
management and monitoring – you may be just the person we are looking for!
of responsibilities will include:
Preparation, conduct, and reporting of
selection, initiation, routine and closeout monitoring visits.
Site management, general administration of
clinical research studies in the UK
Contact for clinical investigators, vendors
and support services in regard to study progress
Monitoring trial progress and ensuring that
the project timelines are met
Effective and open communication within the
Delivering onsite training of investigators
Preparation and delivering of presentations
at Investigator’s Meetings
Preparation for and attendance at company’s
Support to Regulatory Affairs in procurement
of site regulatory documents
Maintenance of appropriate documentation
regarding clinical site management
Participation in feasibility research
Participation in query resolution.
Maintenance of study-specific automated tracking systems
University degree in Life
Sciences, Pharmacy, MD or RN or an equivalent combination of education,
training and experience
Significant hands-on industry
experience at a similar position, with full scope of monitoring
experience in the UK and knowledge of the local clinical research environment
Experience in regulatory
submissions, contract negotiations, site management and feasibility assessment
Experience with oncology
Team oriented with excellent
communication and interpersonal skills including a positive and professional
attitude to tasks and projects
Attention to detail, organizational
and time-management skills
Valid driver’s license and
ability to travel
Demonstrated computer skills
Check out our vacancies at www.psi-cro.com,
and start your career with a stable, reputable and successful company where individuals
do make a difference!
To apply for this position please send your CV