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The latest Study Manager jobs

Jobs: (Study Manager)

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What we searched for: job/title:study AND manager
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Global Clinical Study Manager
England
Dec 15
Office-based in Hertfordshire Contract for 12 months with possibility of extension or renewal A successful pharmaceutical company with an extensive and innovative pipeline and product portfolio across many therapeutic areas is seeking a Global Clinical Project Manager to provide operational expertise and lead clinical operations team to ensure the effective and efficient delivery of all operational aspects of studies through all phases of clinical study management. ...
Clinical Study Manager | Global Bio-pharma | In-House NY/NJ area
West New York
Dec 14
Senior Clinical Study Manager Role | Global Bio-pharma | In-House NEW YORK/NEW JERSEY area Currently there is a contract position available at an internationally renowned biopharma. Relatively...
Clinical Project (Study) Manager
Brussels
Dec 5
Clinical Project (Study) ManagerClinical Project ManagerClinical project manager, late phase, senior clinical researcher, Monitoring, coordination, documentation, quality, auditing, senior research associate, CPM, CSM, Study Manager, Interim, FreelanceAre you looking for an exciting new challenging at a pharmaceutical company? Do you have the necessary skills and experience to hit the ground running? This could be a great opportunity for you. ...
Study Start-Up Manager (m/w) Munich
Germany
Dec 4
Study Start-Up Manager (m/w) MunichWe are currently looking for an experienced Study Start Up Manager for the Start-Up department at our client’s office, an international CRO in Munich. Next to an attractive salary package, the company offers a great working atmosphere and very attractive work-life balance. ...
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.
Junior Study Manager (Pharma/Biotech)
Rotterdam
Nov 27
Junior Study Manager (Pharma/Biotech)Clinical Study Manager (Junior)CPM, CSM, Study Manager, Junior, CRA, Medical device, Clinical Research, Clinical Research Associate, Pharmaceutical, Biotech, freelance, Netherlands, Clinical research, Senior CRA, ConsultancyMy client is a leading CRO committed to improving access to healthcare and supporting the people they serve throughout the continuum of care. ...
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 Study Manager - Stevenage
Stevenage
Nov 24
Lucy Stendall is recruiting for a Clinical Study Manager to join a world leading pharmaceutical company at their site based in Stevenage on a contract...
Contract Clinical Study Manager
Boston, Massachusetts
Nov 23
We are looking to appoint a contract clinical study manager to the team on what will initially be a 12 month contract working on a Phase I study within the Fetal/Maternal space. We are looking for somebody with a strong background within study management, able to understand protocols in detail and support sites in operationalizing protocols in collaboration with CRO CRA’s.
Freelance: Clinical Study Manager - Switzerland
Switzerland
Nov 21
Gabriel Roberts of Umbilical Life is recruiting a Clinical Study Manager to work with a big player in the Pharmaceutical industry, assigned to key projects.
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Associate Study Manager - Bio-Pharma - Exclusive
Middlesex
Nov 21
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...
Freelance Clinical Study Manager
French Speaking part of Switzerland
Nov 21
A leading Medical Device company in Switzerland is urgently looking to recruit a freelance Clinical Study Manager who has a strong international clinical operations management background and vendor management experience. 
Regulatory Submissions Manager - Study Start Up - CRO
England/Scotland
Nov 17
Regulatory Submissions Manager - Study Start Up - CRO - Home based flexibility
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.
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.
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.
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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. ...
Clinical Study Manager (Clinical Project Manager)
Surrey Hampshire Berkshire
May 19
Home or Office Based (Camberley - junction 4 off the M3) - Full Time or 4 days/week - Pure Project Management - No Monitoring!
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. ...
Study Start Up (SSU) Manager (Europe) - Novella Clinical
Homebased
Jan 30
A new and pivotal position within the European operation as we look to streamline the start up process and introduce the Study Start-Up department. This will be a first time hire for this department and we are looking for people based across the EU, primarily interested in professionals in Italy, UK, Spain, Germany, France or Belgium. Experience in Study-Up for local/EU Clinical trials including Quality Assurance, Regulatory Submissions related to Study Start Up.
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 : 29
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