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The latest Study Manager jobs

Jobs: (Study Manager)

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Regulatory Submissions (Study Start-up) Manager
Germany
Jan 19
Regulatory Submissions (Study Start-up) Manager Our client is a global, full-service Clinical Research Organization (CRO) specializing in a multitude of therapeutic areas. They are active in over 45 countries across the globe. They continue to steadily grow and are looking to add to their team! Their clinical operations activities are growing rapidly, and we are currently seeking a full-time, office-based Regulatory Submissions Manager to join our Clinical Operations team. ...
Freelance: Clinical Study Manager – UK
England
Jan 19
Gabriel Roberts of Umbilical Life is recruiting for a Clinical Study Manager to join a global Biopharma.
Immediately Available - Clinical Study Manager required
England
Jan 18
An award winning Biotech company based in Geneva is looking to expand their clin ops department. 
Senior Non-Clinical Study Manager
London
Jan 18
ProClinical is seeking a Senior Non-Clinical Study Manager to join an innovative UK based biotechnology company. This is a fixed term contract role to be based in London.The Senior Nonclinical Study manager will assess the nonclinical safety profile of candidate company programmes, plan and implement regulatory and other toxicology studies, complete nonclinical gap analyses and represent the comapny and Collaborating Organisations in Competent Authority Scientific and Innovation meetings. ...
Study Start-Up Manager (m/w) Munich
Germany
Jan 16
Regulatory Submissions (Study Start-up) Manager Our client is a global, full-service Clinical Research Organization (CRO) specializing in a multitude of therapeutic areas. They are active in over 45 countries across the globe. They continue to steadily grow and are looking to add to their team! Their clinical operations activities are growing rapidly, and we are currently seeking a full-time, office-based Regulatory Submissions Manager to join our Clinical Operations team. ...
Junior Study Manager - Poland - Small CRO
Warsaw, Poland
Jan 16
This company is a game changer in the CRA world. They are looking to expand their resources for national and international projects. Are you a CRA with field experience looking to be a Project Manager? This client is a small niche company looking to help train and develop an experienced CRA into a Project Manager to help run their studies on an international scale.
Regulatory Submissions (Study Start-up) Manager
London
Jan 15
POSITION SUMMARYMedpace is a global, full-service Clinical Research Organization (CRO) specializing in a multitude of therapeutic areas. Our headquarters are located in Cincinnati, Ohio and we are active in over 40 countries across the globe. We continue to steadily grow and are looking to add to our team! Our clinical operations activities are growing rapidly, and we are currently seeking a full-time, office-based Regulatory Submissions Manager to join our Clinical Operations team. ...
Brussels Scientific Study Manager Oncology
Brussels
Jan 15
Radek Weichert at Skills Alliance is recruiting for a Scientific International Trial Manager / Clinical Project Manager for Oncology studies. This role is to provide end-to-end...
Regulatory Submissions Manager, Study Start-Up
Italy
Jan 15
A top quality provider and global CRO is currently seeking a Regulatory Submissions Specialist to join their team. You will play a key role in the management process for study start up and clinical trials by managing start-up of projects while being provided with training to ensure career progression. This is a full-time permanent position based in Milan, Italy.
Global Study Manager
Switzerland
Jan 15
Provides the operational expertise and leadership to one or more clinical operations teams to ensure the effective and efficient delivery of all operational aspects of one or more studies through all phases of Clinical Study Management (Plan, Initiate, Conduct, Close), in accordance with the appropriate quality standards including ICH/GCP and applicable regulations.
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Global Study Manager
England
Jan 13
The Position: Working in Product Development Operations, within our Immunology, Inflammation, Ophthalmology and Neuroscience (I2ON) Study and Sample Management function we are looking for a Global Studies Manager to provide the operational expertise to enable us to deliver our late phase I2ON clinical trials (Phase II & III). You will provide direction and leadership to one or more clinical operations teams and be a key member of the study management team. ...
Regulatory Submissions (Study Start-up) Manager (m/w)
Germany
Jan 12
Regulatory Submissions (Study Start-up) Manager Our client is a global, full-service Clinical Research Organization (CRO) specializing in a multitude of therapeutic areas. They are active in over 45 countries across the globe. They continue to steadily grow and are looking to add to their team! Their clinical operations activities are growing rapidly, and we are currently seeking a full-time, office-based Regulatory Submissions Manager to join our Clinical Operations team. ...
Global Senior Study Manager - Oncology
Espoo
Jan 11
ProClinical is working on an amazing job opportunity for a Global Senior Study Manager - Oncology at a multinational pharmaceutical company based in Espoo, Finland. With over 5000 products, found in virtually every area of human activity this company is associated with some of the leading brands around the world. ...
Local Study Manager
Belgium
Jan 10
An experienced Local Study Manager is needed ASAP with an established Pharmaceutical company.
Study Start Up Manager (m/w), office-based in Munich
München (81249)
Jan 10
Regulatory Submissions (Study Start-up) Manager Our client is a global, full-service Clinical Research Organization (CRO) specializing in a multitude of therapeutic areas. They are active in over 45 countries across the globe. They continue to steadily grow and are looking to add to their team! Their clinical operations activities are growing rapidly, and we are currently seeking a full-time, office-based Regulatory Submissions Manager to join our Clinical Operations team. ...
Regulatory Submissions (Study Start-up) Manager
Germany
Jan 10
Regulatory Submissions (Study Start-up) Manager Our client is a global, full-service Clinical Research Organization (CRO) specializing in a multitude of therapeutic areas. They are active in over 45 countries across the globe. They continue to steadily grow and are looking to add to their team! Their clinical operations activities are growing rapidly, and we are currently seeking a full-time, office-based Regulatory Submissions Manager to join our Clinical Operations team. ...
Study Start Up Manager
Germany
Jan 9
A specialist medical device firm is looking to expand their German office following very exciting developments. 
Clinical Study Manager – boutique Biopharma - massachusetts
Boston
Jan 8
Clinical Study Manager - boutique Biopharma - Boston, MassachusettsAre you an experienced a Study Manager looking to make the next move in your career? Do you have a passion for Rare Disease trials? Would you like the chance to work with a boutique Biopharma where you can make an impact and help influence the direction of the company? Well i-Pharm has the role for you!
Clinical Operations Manager – Study Start Up focus - Global Pharma - Munich - Up to €70,000 P/A + Bonus and Benefits
Munich - Germany
Jan 8
Clinical Operations Manager – Study Start Up – Global Pharma – Munich – Up to €70,000 P/A + Benefits + Bonus – Zero Travel – Management of Clinical Operations – Coordination of submissions – Oversight of study budgets including contract negotiations and site payments
In-Vitro Metabolism Study Manager
Cambridgeshire
Jan 5
Zest Scientific are looking to identify an experienced In-Vitro Metabolism Study Manager for a key client in Cambridgeshire. We are keen to hear from scientists with proven experience in in-vitro assays and DMPK studies, with particular preference for Cytochrome P450 research.
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Clinical Study manager - Utrecht
Utrecht
Jan 5
Clinical Study Manager/Senior Clinical Project manager - Well known Pharmaceutical Org CRA, Research, Study, Cardiovascular, Valves, Medical Devices, Drug development, Disease, Nutrition, Pumps, Cylinders, Clinical Studies, Research, Trials, Project Manager, Project Leader, Continuous Improvement, Service Orientated, Stakeholder Management, Senior, Dutch, English, Biotech, Pharmaceuticals, CRO, Post market, Registration, Monitoring, Initiation, FDA/Audit, Mentoring My client needs someone ...
Junior Study Manager - Poland - Small CRO
Poland
Jan 4
This company is a game changer in the CRA world. They are looking to expand their resources for national and international projects. Are you a CRA with field experience looking to be a Project Manager? This client is a small niche company looking to help train and develop an experienced CRA into a Project Manager to help run their studies on an international scale.
Clinical Study Manager
Surrey/Hampshire/South East UK
Jan 3
This is a "classic" clinical study manager position (no monitoring) full time OR we may consider someone 4 days/week. Working in a fast paced and dynamic UK clinical operations department. We will consider home based as long as you are happy to come to the office THREE DAYS/WEEK - so being a reasonable commute to junction 4 of the M3 is an advantage. You would be employed by Chiltern and seconded to a Pharmaceutical Company.
Associate Clinical Study Manager - Late Phase
Middlesex
Jan 2
I am currently partnered exclusively with a leading Bio-Pharma who are recruiting for an Associate Study Manager to join their Late Phase team. This is...
Interim Clinical Study Manager, Clinical Trial Manager (CTM) - Infectious disease - Office-Based - Middlesex - Big Pharma - 12 months contract.
United Kingdom
Dec 21
Interim Clinical Study Manager, Clinical Trial Manager (CTM) - Infectious disease - Office-Based - Middlesex - Big Pharma - 12 months contract.
Global Clinical Study Manager, Clinical Trial Manager (CTM) - HIV - Office-Based - Middlesex - Big Pharma - 6 months contract.
United Kingdom
Dec 21
Clinical Trial Manager (CTM) - HIV - Office-Based - Middlesex - Big Pharma - 6 months contract.
Junior Study Manager
London
Dec 21
Great opportunity for an experienced Senior CRA, Lead CRA or Junior Study Manager to join a top 20 Biopharma, this position is permanent and office-based...
Study Start Up Manager
Germany
Dec 20
At Covance, you’ll redefine what’s possible and discover your extraordinary potential. You’ll have the opportunity to personally advance scientific research and make a difference in peoples’ lives with your bold ideas and unique point of view. We are looking for a Clinical Operations Manager (Study Start Up) to be office based in Munich and working for one of our clients.
Clinical Study Manager (Local PM), Poland
Warsaw
Dec 20
Here at Syneos Health we are currently recruiting for a Clinical Study Manager (CSM) to be based in Warsaw and dedicated to Global Pharmaceutical company.
Study Manager/Clinical Research Manager
New York
Dec 19
Study Manager/Clinical Research Manager An innovative life science and health care business providing various patient centric services to Clinical trials is looking for a Study manager or Clinical Research Associate to be based in the New York area.
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STUDY DATA MANAGER - United Kingdom
Swansea, United Kingdom
Dec 18
An outstanding opportunity to join one of the world’s leading contract research organisations and be part of a dynamic and growing international company. Join PRA Health Sciences as a Study Data Manager and help realize your career potential.
Study Manager I
Harrogate
Dec 1
COVANCE is a leading global drug development services company and we provide support to the Pharmaceutical and Biotechnology industries. We are recruiting for our Early Development Unit in Harrogate and are currently seeking to hire a Study Manager (I) role to help support the Immunology & Immunotoxicology team. This is a full time and permanent contract.
Study Manager I - Harrogate, North Yorkshire, UK
Harrogate, North Yorkshire, UK
Nov 26
COVANCE is a leading global drug development services company and we provide support to the Pharmaceutical and Biotechnology industries.
Clinical PM/ Study Manager Role - Innovative Pharma - Hertfordshire
England
Nov 15
New role for a Clinical Project Manager for a growing and innovative pharma company. My client requires someone with experience in clinical research to project manage vendor relationships, manage clinical development objectives and coordinate through multi-disciplinary teams. You would be a vital member of the clinical operations department, supporting the delivery of objectives and KPIs as well as having involvements in CRO relationships and working in the suitable regulatory aspects required.
Study Manager - Pharmacology, Cardiovascular Toxicology
Cambridgeshire
Nov 8
Are you interested in working for a globally renowned CRO that specialises in biopharmaceutical drugs & vaccine development for human & animal health, using your in-depth skill-set & knowledge in project management and cardiovascular toxicology within a small-team.
Global Study Manager
United Kingdom
Oct 18
TalentSource Life Sciences is currently searching for an experienced Global Study Manager to work with one of our partner pharmaceutical companies in the Hertfordshire area.       This is a temporary position with TalentSource for 12 months with the possibility of being extended, on a full time basis. The Study Manager will be fully office based for the first three months, with some flexibility to work from home thereafter.
(Senior) Clinical Study Manager
North London
Oct 17
A very exciting opportunity to join a fast growing Biotech company with an interesting pipeline. Permanent Senior Clinical Study Manager role based North of London...
Junior Study Manager / Clinical Trial Manager
Hertfordshire
Oct 5
A very rare opportunity for an experienced Lead CRA / Junior Study Manager / Clinical Trial Manager to join an exciting start-up Biotech, this position is permanent...
Regulatory Submissions (Study Start-up) Manager
Stirling
Sep 20
Medpace is a global, full-service Clinical Research Organization (CRO) specializing in a multitude of therapeutic areas. Our headquarters are located in Cincinnati, Ohio and we are active in over 40 countries across the globe. We continue to steadily grow and are looking to add to our team! Our clinical operations activities are growing rapidly, and we are currently seeking a full-time, office-based Regulatory Submissions Manager to join our Clinical Operations team. ...
OPERATIONAL STUDY MANAGER - Europe
Europe
Sep 20
An outstanding opportunity to join one of the world’s leading contract research organisations and be part of a dynamic and growing international company. Join PRA Health Sciences as a Operational Study Manager and help realize your career potential.
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Clinical Study Manager/Clinical Project Manager
UK Based
Sep 15
This is a "classic" clinical study manager position (no monitoring) full time OR we may consider someone 4 days/week.
Clinical Operations Manager (FSP) - Study Start Up - Russia, Moscow - Permanent Contract - Sponsor Office based opportunity
Russia
Sep 9
Clintec is actively recruiting for a Clinical Operations Manager (FSP) to join our company in Russia, Moscow – this is a Permanent Office based opportunity. The successful candidate will work fully assigned to one of our sponsors, a top 5 pharmaceutical company. The COM (FSP) will be accountable for the execution and oversight of local operational clinical trial activities in Country. The COM will also be responsible for local regulatory and financial compliance for assigned protocols.
Regulatory Submissions (Study Start-up) Manager
Stockholm
Aug 29
Medpace is a global, full-service Clinical Research Organization (CRO) specializing in a multitude of therapeutic areas. Our headquarters are located in Cincinnati, Ohio and we are active in over 40 countries across the globe. We continue to steadily grow and are looking to add to our team! Our clinical operations activities are growing rapidly, and we are currently seeking a full-time, home-based Regulatory Submissions Manager to join our Clinical Operations team. ...
Regulatory Submissions (Study Start-up) Manager
Vaals
Aug 25
Medpace is a global, full-service Clinical Research Organization (CRO) specializing in a multitude of therapeutic areas. Our headquarters are located in Cincinnati, Ohio and we are active in over 45 countries across the globe. We continue to steadily grow and are looking to add to our team! Our clinical operations activities are growing rapidly, and we are currently seeking a full-time, office-based Regulatory Submissions Manager to join our Clinical Operations team. ...
Clinical Study Manager (CTM) - Pharma Dedicated - Munich-131092
Europe, Middle East and Africa-Germany-Bavaria-Munic
Jun 28
PPD has an exciting opportunity for a Clinical Trial Manager/Clinical Study Manager to join us dedicated at one of our strategic pharmaceutical partners in Munich.  PPD works in collaboration with this partner; you will be dedicated to clinical projects for Germany, working with PPD’s successful study management team who are dedicated and on onsite with this large pharmaceutical company.  You will be working to their systems and processes with the full support and development from PPD. ...
Regulatory Submissions (Study Start-up) Manager
Milano
Jun 22
POSITION SUMMARYMedpace is a global, full-service Clinical Research Organization (CRO) specializing in a multitude of therapeutic areas. Our headquarters are located in Cincinnati, Ohio and we are active in over 40 countries across the globe. We continue to steadily grow and are looking to add to our team!Our clinical operations activities are growing rapidly, and we are currently seeking a full-time, office-based Regulatory Submissions Manager to join our Clinical Operations team. ...
Regulatory Submissions (Study Start-up) Manager
München (81249)
Apr 13
Medpace is a global, full-service Clinical Research Organization (CRO) specializing in a multitude of therapeutic areas. Our headquarters are located in Cincinnati, Ohio and we are active in over 45 countries across the globe. We continue to steadily grow and are looking to add to our team!Our clinical operations activities are growing rapidly, and we are currently seeking a full-time, office-based Regulatory Submissions Manager to join our Clinical Operations team. ...
Clinical Study Manager - Oncology
Frankfurt am Main
Jun 20
Key People are looking for an experienced Clinical Study Manager with Oncology experience to join an exciting team with our pharmaceutical client based in Frankfurt.
study AND manager jobs : 48
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