Clinical Project Manager / Clinical Study Manager – HOMEBASED

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 talented Clinical Project Managers at all levels. This role is open to candidates with all therapeutic  backgrounds and is mainly focussed on Phases 2-3, you will be working on international studies, however we feel we have a strong internal employee development programme, meaning we can consider candidates with European project management experience only.

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.

ROLE RESPONSIBILITIES

·         Client liaison

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

·         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

2+ years’ experience in Project management

Global or European experience

CRO experience desirable

Excellent ICH-GCP knowledge

Strong communication skills

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.

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

KEY WORDS

CPM, Director, Clinical, Programme, Program, Suite, Study, Studies, Trials, Manage, Matrix, International, Team, CRO, Pharma, Pharmaceutical, Clinical Research Organisation, 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, 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, PM, CPM, proj manager, clin proj manager, project manager, global project manager

Clinical Project Manager / Clinical Study Manager – HOMEBASED - UROLOGY

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 talented Clinical Project Managers at all levels. This role is open to candidates with all therapeutic backgrounds, though it would be ideal to have experience in Urology and is mainly focussed on Phases 2-3, you will be working on international studies, however we feel we have a strong internal employee development programme, meaning we can consider candidates with European project management experience only.

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.

ROLE RESPONSIBILITIES

·         Client liaison

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

·         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

2+ years’ experience in Project management

Global or European experience

CRO experience desirable

Excellent ICH-GCP knowledge

Strong communication skills

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.

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

KEY WORDS

CPM, Director, Clinical, Programme, Program, Suite, Study, Studies, Trials, Manage, Matrix, International, Team, CRO, Pharma, Pharmaceutical, Clinical Research Organisation, 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, 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, PM, CPM, proj manager, clin proj manager, project manager, global project manager

Clinical Project Manager / Clinical Study Manager– HOME/ Office based UK – Up to £45K– medical devices

We are currently recruiting for an experienced  Clinical Project Manager to join our successful organisation medical device CRO. This is an excellent opportunity to lead and manage both national and international (Europe) Medical Device trials, with strong career development in the future.

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.

ROLE RESPONSIBILITIES

Manage study across the UK and Europe

Coordinate and perform some  aspects of the clinical monitoring and site management

Conducts site visits - assessing protocol and regulatory compliance, managing required documentation

Develops and maintaining collaborative relationships with investigational sites and client company personnel.

Leading on assigned clinical studies

Mentor and manager CRA team

SPONSOR based –BIOTECH

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

2 years plus monitoring experience

Medical Device experience

Good knowledge of FDA guidelines and GCP

Excellent communication skills

Strong attention to detail

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.

Associated keywords:

CRA, Clinical Research Associate, Clinical Monitoring Associate, Clinical Monitor, CRO, SCRA, Senior clinical research associate, LCRA, 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, Germany

Clinical Project Manager / Clinical Study Manager – FRANKFURT

Passend für; “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”.

Wir suchen ein “Clinical Project Manager”. Diese Rolle ist Kandidaten mit allen therapeutischen Hintergrunden offen, aber Onkologie und kardiovaskulären Medizin wäre auch ein großen Vorteil. Wir behandeln von vorklinisch- auf Nachvermarktung, aber für diese Stelle konzentrieren Sie sich auf Phase 2-3 Studien.

Ort:

FRANKFURT

Bitte Zoe Benningfield anrufen - +44 789 669 3960 oder per Email zoe@peoplewithchemistry.com kontaktieren, wenn Sie mehr über die Gelegenheit wissen möchten. Es ist 100% vertraulich.

Hintergrund der Firma:

Wir sind eine pharmazeutische Firma mit viel Erfahrung und Fachkenntnissen. Wir haben eine ausgezeichnete “Product Pipeline”, um eine ausgezeichnete Stabilität der Firma und berufliche Aufsteigsmöglichkeiten für die hochleistungsfähige Angestellte zu sichern. Ort: Berlin

Ihre Aufgaben:

- CRO Management

- Die Haushaltssteuerung

- Personalmanagement

- für eine komplette Arbeitsbeschreibung:

Bitte Zoe Benningfield anrufen - +44 789 669 3960, oder per Email zoe@peoplewithchemistry.com kontaktieren, wenn Sie mehr über die Gelegenheit wissen möchten. Es ist 100% vertraulich.

Ihre Qualifikationen:

- 2+ Jahre Projekt Management Erfahrung

- Global oder europäische Erfahrung

- CRO/ Pharma Erfahrung

- Monitoring Erfahrung

- Ausgezeichnete ICH-GCP Erfahrung

- Gute Kommunikationsfähigkeiten

Ort: FRANKFURT

Kontakt:

Man kann eine komplette Arbeitsbeschreibung und Details über die Firma nach ihrer Bewerbung bekommen, bewerben Sie sich herunter. Bitte Zoe Benningfield anrufen - +44 789 669 3960 oder

Mann kann Ihr CV zoe@peoplewithchemistry.com im Vertrauen schicken

Bitte unsere Website besuchen – www.peoplewithchemistry.com

Stichworte:

CPM, Director, Clinical, Programme, Program, Suite, Study, Studies, Trials, Manage, Matrix, International, Team, CRO, Pharma, Pharmaceutical, Berlin , Germany, Clinical Research Organisation, 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, Berlin , Germany ,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, Berlin, Germany, global study manager, Clinical Operations manager, clinical project manager, project manager, study manager, clinical study manager, global study operations manager, PM, CPM, Berlin, proj manager, clin proj manager, project manager, global project manager, Germany, Berlin , Klinischer Projekt Manager

An exciting new role has become available with a growing, small / medium sized CRO in Poland. As a Regulatory Submissions Manager you be responsible for all start-up aspects of a study on an international basis. You will work closely with sponsors to achieve project goals, interact with international regulatory / ethical bodies and have an active role in bid defences. Office based in UK, Germany, Italy, Poland and Belgium.

COMPANY BACKGROUND:

A growing CRO with offices in 40 countries across the globe. This is fantastic opportunity to join a highly regarded small/medium sized CRO that are looking to expand operations across Europe due to recent success. A great chance to join an expanding CRO that have over 19 years within the industry and can provide a clear pathway to more senior positions. 

ROLE RESPONSIBILITIES

·         Responsible for TMF documentation at study start up

·         Responsible for organising Start-up regulatory documentation

·         Advice other clinical teams relating to regulatory compliance

·         Liaise with CRA/Site/Clinical Teams

Great opportunity to join a growing business that can offer sound knowledge in regulatory documentation, vital for progressing to more senior positions

SKILLS DESIRED

·         3 years experience in start up /regulatory

·         EU / International submissions experience

·         Life science degree 

Commutable locations: Poland

Salary: €35,000-€55,000 + Benefits

Full job description and company details are available upon application. 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.

Top 5 CRO looking for a CRA in Switzerland to be homebased. This CRA will be Directly outsourced to the Sponsor. 

This position is being dealt with by Vishal Sharma at Meet, call on 00447794411452 or email directly at Vishal@peoplewithchemistry.com to discuss in confidence.

Find out more about us at www.peoplewithchemistry.com

ROLE RESPONSIBILITIES                         

As Senior CRA, you will collaborate with study coordinators, investigators and Clinical Trial Managers, key responsibilities will include:

-Scheduling monitoring visits

-Site selection and feasibility

-Conducting pre-site visits, study initiation, monitoring and close-out visits

-Completion of study reports and continuous site correspondence

-Ethic submissions

SKILLS REQUIRED               

-Life Science degree

-Min 4 years’ monitoring experience

-Fluent in German, good knowledge of English

-MUST be eligible to work in the EU

-Ability to travel 60% and happy to do overnight stays

Commutable locations: Switzerland

Salary: €55k - €60k + benefits

Full job description and company details are available upon application, apply below. This position is being dealt with by Vishal Sharma at Meet, call on 0203 178 7488 or email directly at Vishal@peoplewithchemistry.com to discuss in confidence.

Find out more about us at www.peoplewithchemistry.com

Associated keywords: Senior Clinical Research Associate, Senior CRA, Clinical Research Associate II, CRA II, clinical trials, Phase I-IV, study coordinator, home-based, office-based, home/office-based flex, CRO, Munich, Germany, Senior Clinical Research Associate, Senior CRA, Clinical Research Associate II, CRA II, clinical trials, Phase I-IV, study coordinator, home-based, office-based, home/office-based flex, CRO, Lausanne, Berne, Geneva, Basel, Baden,Baar, Zurich

Associated keywords: Clinical Research Associate, CRA, Senior CRA, Clinical Research Associate II, CRA II, clinical trials, Phase I-IV, study coordinator, office based, Warsaw, Poland.

Clinical Research Associate (CRA) Manager – Friendly small to mid-sized CRO – Poland

Clinical Research Associate Manager, CRA Manager: An emerging international CRO is currently looking for a CRA Manager to join their CRA division in in the UK. This is a fantastic opportunity to join a slightly smaller CRO with a global presence and take responsibility for a CRA team based out of their offices in the south east, giving the company valued input and ideas. This position requires a CRA background and proven people management skills so it will be a great challenge!

COMPANY BACKGROUND

The client is a small to mid-size global CRO which prides itself on the relationships that it has built worldwide. Following a strong 2011 they are looking to continue their expansion, with a particular emphasis on their European offices. They offer a stimulating and supportive work environment where CRAs can cover a range of Phases from I to IV in cardiovascular, endocrine/metabolic, and oncology.

ROLE RESPONSIBILITIES

As a CRA Manager, your responsibilities will include:

•Ensuring excellent communication between CRA’s and line management
•Evaluating CRA performance by carrying out appraisals and writing reports
•Accompanying CRAs on site visits
•Monitoring and evaluating CRA workload by liaising with the Project Manager(s)
•Identifying and designing necessary training

SKILLS DESIRED

·         Life sciences degree

·         Solid Lead CRA/CRA Manager experience

·         Excellent monitoring exposure – Full lifecycle, Phase I-IV

·         Line management experience

·         Full driving licence

Commutable locations:  Warsaw

Salary: Circa + car/allowance + bonus + benefits

Full job description and company details are available upon application, apply below. This position is being dealt with by Paul Crawford at meet, call on + 44 777 233 8996 or email directly at paulc@peoplewithchemistry.com to discuss in confidence.

Find out more about us at www.peoplewithchemistry.com

Associated keywords: London, CRA, Manager, Clinical Research Associate, Clinical research, CRO, UK, Clinical trials, CRA Manager, South East, England, CRA, leadership, mentoring, development, Kent, Surrey, London, CRA Manager, Lead CRA, Manager, Clinical Operations Manager, Clinical Operations Lead, Monitoring Manager