This global Medical Device Company is looking for a Data Migration specialist to come in and Project Manage the development of customised interfacing software for medical devices into NHS sites. Unique opportunity to assume full Project Management responsibilities within a Global company.  

Contact Nick@peoplewithchemistry.com for more details 07880230889

Suitable for: Data Migration Specialist, IT Project Manager, IT Services Project Manager, Medical Device Data Manager, NHS Data Manager,

ROLE RESPONSIBILITIES:

·         Develop customised interfacing software for medical devices from initial concept into the NHS services.

·         Dealing with PCT commissioning boards, gaining CAP approval to enable software integration

·         Supporting Business Development teams looking to source new contracts

SKILLS DESIRED:

·         New Service Development experience

·         Project Management of Device and software integration into the NHS spine

·         Database Migration specialist

Commutable locations: UK, South East, Northampton

Salary: £££

***APPLY NOW***

Full job description and company details are available upon application, apply below. This position is being dealt with by Nick Antonelli at Meet, call on + 44 788 023 0889 or email directly at nick@peoplewithchemistry.com to discuss in confidence.

Find out more about us at www.peoplewithchemistry.com

Associated keywords: Data Migration specialist, Data Migration, IT, Project Manager, Medical Device, Medical Devices, NHS, Service Development, Software, Software specialist, PCT, CAP, IT Project Manager, Data Project Manager, Care Commissioning Groups

Clinical Project Manager /Clinical Project Manager – data manager – clinical technologies –

Suitable for; Clinical Project Manager, Clinical Study Manager, Clinical Trial Manager,  Clinical Study Leader, Clinical Project Leader, Clinical Operations Leader, European Study Manager , Global Study Manager, Global LCRA, Lead Clinical Research Associate, data management project manager, data project manager,

We are looking for a talented Clinical Project Manager/  Data project Manager  to join our niche CRO and work within our project management team. We pride ourselves on offering the best service to our clients, these role is highly client facing and for a project manager that likes to work both autonomously and within a team.

Please contact Zoe Benningfield on +44 (0)7896 693960 or email zoe@peoplewithchemistry.com if you would like to know more about this opportunity. This will be 100% confidential.

We are a Niche CRO globally recognised and respected, with a strong focus on data management and clinical technologies. We focus on providing a full service to our Clients that include Pharmaceutical , biotechnology and medical device organisations

ROLE RESPONSIBILITIES

·         Client liaison/ facing

·         Managing full project lifecycle from initiation through to close-out

·         Data management

·         Budge control

·         People management

Please contact Zoe Benningfield on +44 (0)7896 693960 or email zoe@peoplewithchemistry.com if you would like to know more about this opportunity. This will be 100% confidential.

SKILLS DESIRED

4+ years’ experience in Project management

Global or European experience

CRO experience desirable

Excellent ICH-GCP knowledge

Strong communication skills

Full job description and company details are available upon application, apply below. This position is being dealt with by Zoe Benningfield at Meet, call on + 44 203 178 7488 or +44 7896 693960.

e-mail directly at zoe@peoplewithchemistry.com to discuss in confidence.

Find out more about us at www.peoplewithchemistry.com

Meet is a European wide recruitment agency who specialise purely in the pharmaceutical sector. We work in a number of regions across Europe placing both permanent and freelance candidates into Clinical, Regulatory and Data management teams within CRO’s, Pharmaceutical, Generic and Biotech companies.

 If you are interested in finding a new opportunity however the one shown in this advert is not suitable for you please do not hesitate to contact us! Our number is 0203 178 7488 or visit our website - www.peoplewithchemistry.com to upload your CV.

KEY WORDS

CPM, Director, Clinical, Programme, Program, Suite, Study, Studies, Trials, Manage, Matrix, International, Team, CRO, Pharma, Pharmaceutical, Clinical Research Organisation,  data management, clinical technologies, Organization, Clients, Clinical Operations manager, Sponsor, clinical project manager, project manager, global clinical project manager, global project manager, pharma, project manager, Clinical Operations manager, project manager , data manager, clinical technologies Clinical operations  manager, global clinical project manager, global project manager, global project leader, clinical project manager, global clinical project manager, PM, CPM, operations manager, study operations manager, global study operations manager, study manager, clinical study manager, global study manager, Clinical Operations manager, clinical project manager, project manager, study manager, clinical study manager, global study operations manager, Clinical technologies, PM, CPM, proj manager, clin proj manager, project manager, global project manager, data management

Opening for a Junior Account Executive to join a busy Medical Education agency to work on global accounts.

COMPANY BACKGROUND:

Based in Central London, this unique agency hase produced award winning campaigns. Set up nearly a decade ago, the agency has a fantastic reputation in the industry and talent at all levels of the business, with the work force known for being hard working, bright and enthusiastic individuals.

ROLE RESPONSIBILITIES:

·         Completes/performs all professional administrative responsibilities on time and to company standards

·         Produces account ream status reports accurately and on time

·         Produces contact reports from client meetings/calls and ensures they are signed off by a senior member of the team and dispatched to the client within 24 hours

·         Support the Account Manager in tracking client budgets

• Undertakes media monitoring as required by their account teams
• Ensures account team electronic and hard copy files are maintained to ensure rapid access to information
• Demonstrates the ability to prioritize workload of multiple clients/projects at the same time, whilst ensuring high standards of work are delivered to deadlines
• Develops knowledge and demonstrates understanding of different communications disciplines through on the job experience and training
• Identifies training and coaching activities which will help to improve their own performance/personal development
• Responsible for undertaking office reception/operational tasks as assigned

SKILLS REQUIRED: must possess excellent written and verbal communication skills, ability to lead a team, excellent attention to detail, faultless time management skills, ability to work under pressure.

Commutable locations: London, Greater London, Kent

To discuss this role in more detail in confidence please call Laith Al-Hashimi on 0203 178 7488 or out of office hours on 07854045304 E-mail - laith@peoplewithchemistry.com

An exciting new opportunity has arisen for a Junior CRA / Senior CTA to join an award winning Pharmaceutical company. My client is looking for an experienced CTA to take control of site initiation, interim and close out monitoring responsibilities combined with study start up and admin tasks. The role is based in Copenhagen, Denmark and is ideally suited to experienced CTA’s looking to move into their first CRA role.

COMPANY BACKGROUND:

A global Pharma company and highly respected within the industry, my client has experienced excellent growth over their 60+ year history. This is an excellent opportunity to join an established business that can provide structured career progression with realistic opportunities to move into more senior roles in the future.

ROLE RESPONSIBILITIES:

As a Junior CRA working for this growing pharma, you would be expected to work across a variety of trials undertaking such responsibilities as:

·         Perform pre-study, study site initiation, interim monitoring and study site closure visits.

·         Assist with site selection and feasibility

·         Ethics & Regulatory submissions

·         General CTA administrator tasks

SKILLS DESIRED:

·         Previous experience in clinical research (CTA, Coordinator or CRA)

·         Experience with Ethical / Regulatory submissions

·          Life Sciences degree

·         Pharma experience desirable

Commutable locations: Copenhagen, Denmark

Salary: 245,00DKK – 300,000DKK + benefits

Full job description and company details are available upon application, apply below. This position is being dealt with by Jack Doyle at meet, call on +44 203 178 7488 or email directly at jack@peoplewithchemistry.com to discuss in confidence.

Find out more about us at www.peoplewithchemistry.com

Associated keywords:  Associated keywords: Site Monitor, Senior CRA, Clinical Research Associate, CRA II, CRA, Denmark, Copenhagen, Site Monitor, Senior CRA, Clinical Research Associate, CRA II, CRA, Denmark, Copenhagen

Junior Medical Writer – Medical Education Agency – Central London –Competitive salary plus benefits

Our client has an opening for a Junior Medical Writer to join the Medical Education Division of their Healthcare Communications agency. The Junior Medical Writer will be responsible for developing scientifically accurate written material, working closely with their Pharmaceutical clients.  

The agency is based in a central London location and boasts an impressive client roster with the chance to work across some interesting & varied therapeutic areas.

Role responsibilities:

·         Working closely with the editorial and account teams

·         Responsible for the timely delivery and scientific and editorial quality of all work undertaken for designated accounts.

·         Write, re-write, edit and proof-read content to a high editorial standard

·         Liaise with external stakeholders

·         Conduct verification and compilation of reference packs ensuring the scientific accuracy and validity of all content

·         Obtain copyright approvals and permissions as required

·         Conduct internet and telephone research into products, therapeutic areas, congresses and key opinion leaders in support of editorial and account teams

Skills required:

·         Good editorial skills demonstrated in a medical communications/publishing environment

·         Strong writing skills and the ability to tailor writing style to suit different audiences

·         Meticulous attention to detail and tenacity in achieving a high-quality end result

·         Capable proof-reading with awareness of standard proof-reading symbols and common printing and typesetting errors

·         Good research skills including telephone and online strategies

·         Highly organised with good time management and prioritisation skills

·         Able to work in a matrix management structure

·         BSc degree in life sciences – Masters or PhD preferred but not a necessity

Fantastic opportunity for a Junior Writer to join this highly skilled Medical Education team, offering the chance for training and development as well as a highly competitive salary.   

Specializes in the therapeutic area of addiction/drug addiction

To discuss this role in more detail in confidence please call Rebekah Hill 07880291757

E-mail – rebekah@peoplewithchemistry.com

Contact via LinkedIn: http://uk.linkedin.com/in/meetrebekahhill

Follow me on Twitter: http://twitter.com/meet_rebekah

Key Words: Medical writer, associate medical writer, Healthcare Communications, Medical Communications, Medical Education.

Senior Clinical Project Manager /Senior Clinical Study Manager LATE PHASE – Homebased – up to 80,000 Euros

Suitable for; Clinical Project Manager, Clinical Study Manager, Clinical Trial Manager,  Clinical Study Leader, Clinical Project Leader, Clinical Operations Leader, European Study Manager , Global Study Manager, Global LCRA, Lead Clinical Research Associate.

We are looking for a talented Senior Clinical Project Manager/ Senior Clinical Study Manager at all levels, with LATE PHASE experience. You will be working on international studies, this is a global role therefore experience covering Europe, Asia Pac and the Americas is desired.

EXCELLENT opportunity to progress into Director positions

Homebased – Germany

Please contact Zoe Benningfield on +44 (0)7896 693960 or email zoe@peoplewithchemistry.com if you would like to know more about this opportunity. This will be 100% confidential.

COMPANY BACKGROUND:

We are a Top 5 CRO, globally recognised and respected, having won numerous international industry awards . We focus on providing a full service to our Clients that include Pharmaceutical , biotechnology and medical device organisations.

EXCELLENT opportunity to progress into Director positions

Homebased – Germany

ROLE RESPONSIBILITIES

·         Client liaison

·         Managing full project lifecycle from initiation through to close-out.

·         Budge control

·         People management

·         LATE PHASE project management

Please contact Zoe Benningfield on +44 (0)7896 693960 or email zoe@peoplewithchemistry.com if you would like to know more about this opportunity. This will be 100% confidential.

SKILLS DESIRED

4+ years experience in Project management

Global or European experience

CRO experience desirable

Excellent ICH-GCP knowledge

Strong communication skills

Homebased – Germany

Full job description and company details are available upon application, apply below. This position is being dealt with by Zoe Benningfield at Meet, call on + 44 203 178 7488 or +44 7896 693960.

e-mail directly at zoe@peoplewithchemistry.com to discuss in confidence.

Find out more about us at www.peoplewithchemistry.com

KEY WORDS

CPM, Director, Clinical, Programme, Program, Suite, Study, Studies, Trials, Manage, Matrix, International, Team, CRO, Pharma, Pharmaceutical, Clinical Research Organisation, Germany, BERLIN,  Organization, Clients, Clinical Operations manager, Sponsor, clinical project manager, project manager, global clinical project manager, global project manager, pharma, project manager, Clinical Operations manager, project manager, Germany, BERLIN, Clinical operations  manager, global clinical project manager, global project manager, global project leader, clinical project manager, global clinical project manager, PM, CPM, operations manager, study operations manager, global study operations manager, study manager, clinical study manager, Germany, BERLIN, global study manager, Clinical Operations manager, clinical project manager, project manager, study manager, clinical study manager, global study operations manager, PM, CPM, proj manager, clin proj manager, project manager, global project manager, Germany, BERLIN

Late Phase Clinical research associate, Late Phase CRA II/Senior CRA: This internationally recognised CRO is currently looking for an experienced CRA to join their Late Phase CRA division in the Thames Valley. This is an exciting and constantly growing organisation with plenty of scope for making progress with your career whilst cutting down on your travel! Unusual opportunity to work on drugs going to market.

COMPANY BACKGROUND

The client is one of the top CROs in the world and they are continuing their expansion in Europe. As they are a long-established organisation they offer a lot of stability and support for their staff. Working across all of the major therapeutic areas in phases IIIb and IV you will have plenty of variation and exposure to a range of clinical trials. This is a great place to build a career and become part of a talented international team.

ROLE RESPONSIBILITIES

As a Late Phase CRA II/Senior CRA your responsibilities will include:

·         Working full clinical lifecycle – site initiation through to closeout responsibilities

·         Remote and observational monitoring

·         Potential start-up responsibilities when required

·         Phase IIIb-IV studies

·         Multi-therapeutic alignment

SKILLS DESIRED

In order to apply for this job you require:

·         CRA background required – around 18+ months experience as CRA

·         Life sciences degree

·         UK based monitoring responsibilities

·         CRO or Pharma employment history

Commutable locations: Thames Valley (home based option)

Salary: £30k - £39k+ strong benefits

Full job description and company details are available upon application, apply below. This position is being dealt with by Yasmin Dyer at meet, call on + 44 203 178 7488 or email directly at yasmin@peoplewithchemistry.com to discuss in confidence.

Find out more about us at www.peoplewithchemistry.com

Associated keywords: Clinical research associate, CRA, Senior CRA, CRA II, CRO, pharmaceutical, London, Thames Valley, UK, CRA, pharma, clinical research, CRA II, CRA, Senior CRA, Clinical Research Associate, late phase CRA, phase IIIb, phase IV, marketing, post-marketing

LCRA/ Lead Clinical Research Associate  - HOMEBASED

We are currently recruiting for an experienced SCRA/ LCRA( Lead Clinical Research Associate) to join our successful organisation. This is an excellent opportunity to join a  mid-size CRO

You will have both LCRA (lead clinical research associate) and team leadership responsibilities.

Please contact Zoe Benningfield on 07896 693960 or email zoe@peoplewithchemistry.com if you would like to know more about this opportunity. This will be 100% confidential.

ROLE RESPONSIBILITIES

Oversight on project timelines, quality and deliverables Contribution to and review of study documents

Handling of contract negotiations with trial sites/ pharmacies

Preparation and conduct of project trainings

 Organisation and conduct of team meetings

Organisation and participation in investigator meetings

Please contact Zoe Benningfield on +44 (0)7896 693960 or email zoe@peoplewithchemistry.com if you would like to know more about this opportunity. This will be 100% confidential.

This is an office based role

SKILLS DESIRED

2 years plus SCRA/LCRA

Good knowledge of FDA guidelines and GCP

Excellent communication skills

Strong attention to detail

Cardiology and Diabetes

Full job description and company details are available upon application, apply below. This position is being dealt with by Zoe Benningfield at Meet, call on 0203 178 7488 or 07896 693960.

e-mail directly at zoe@peoplewithchemistry.com to discuss in confidence.

Find out more about us at www.peoplewithchemistry.com

Meet is a European wide recruitment agency who specialise purely in the pharmaceutical sector. We work in a number of regions across Europe placing both permanent and freelance candidates into Clinical, Regulatory and Data management teams within CRO’s, Pharmaceutical, Generic and Biotech companies.

 If you are interested in finding a new opportunity however the one shown in this advert is not suitable for you please do not hesitate to contact us! Our number is 0203 178 7488 or visit our website - www.peoplewithchemistry.com to upload your CV.

Associated keywords:

CRA, Clinical Research Associate, Clinical Monitoring Associate, This is a home  based position  - wide Clinical Monitor, CRO, SCRA, Senior clinical research associate, LCRA, This is a home  based position) lead clinical research associate, early phase, late phase, study start-up, study initiation, routine monitoring, study close out, clinical site management, ICH-GCP, co-monitoring, oncology, cardiology, LCRA This is a home  based position  -