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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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Clinical Study Manager - Hungary + Serbia + Croatia - Global Pharma
Budapest
Apr 24
Radek Weichert at Skills Alliance is recruiting for a Local Study Manager / Clinical Trial Lead for a global pharmaceutical company. This role is to provide...
Clinical Study Manager - Poland - Global Pharma
Warszawa
Apr 24
Radek Weichert at Skills Alliance is recruiting for a Local Study Manager / Clinical Trial Lead for a global pharmaceutical company. This role is to provide...
Clinical Study Manager - Hungary - Global Pharma
Warszawa
Apr 23
Radek Weichert at Skills Alliance is recruiting for a Local Study Manager / Clinical Trial Lead for a global pharmaceutical comany. This role is to provide...
Clinical Study Manager - Poland - Global Pharma
Warszawa
Apr 23
Radek Weichert at Skills Alliance is recruiting for a Local Study Manager / Clinical Trial Lead for a global pharmaceutical comany. This role is to provide...
Junior Clinical Study Manager - Global Biotech
Cambridge
Apr 20
We are partnered exclusively with a leading global biotechnology company who are urgently seeking a Clinical Study Manager or Junior Study Manager to join the...
Global Clinical Study Manager
Cambridge
Apr 20
We are partnered exclusively with a leading global biotechnology company who are urgently seeking a Clinical Study Manager or Junior Study Manager to join the...
Clinical Study Manager - Oncology Biotech
Hertfordshire
Apr 18
An exclusive Clinical Study Manager role with an excitng and growing advanced therapy Biotech. This is a permanent and office-based role working in Oncology. This...
Senior Clinical Study Manager
Hertfordshire
Apr 17
OverviewRole Title: Senior Clinical Project/Study ManagerEmployment Type: PermanentLocation: HertforshireSalary/Rate: £55,000 to £65,000 + bonus, pension, package Role SummaryA small and quality-driven CRO is looking to add a Senior CPM to its team to lead Clinical Project/Study Management activities for global Oncology trials Role ResponsibilitiesTo be responsible for the delivery and day-to-day management of complex Oncology projects within the clinical operations department. ...
Clinical Study Manager (m/f)
Neuss,Germany
Apr 17
DOCS has partnered with a highly prestigious organization with one of the most robust pipelines within the industry. This is a great chance for candidates with two or more years of trial management experience to become part of this company and participate in its ongoing successes in the future. Our client offers an exciting and challenging work environment for clinical research professionals looking for an opportunity to contribute to the success of a company dedicated to...
Early Phase, Senior Clinical Study Manager - United Kingdom
England
Apr 16
Senior Clinical Study Manager
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International Clinical Study Manager
Greater Stockholm,Sweden
Apr 16
Why Apply This position is with an innovative Biopharmaceutical company, who is known for their innovative and market leading products, a stable workforce and a positive company culture. To express your interest and to find out more about the role, please send your CV today to Claudia.JorgensenRankine@docsglobal.com. *Applicants who have not had a response within two weeks should assume their application has been unsuccessful.
Global Clinical Development Manager / Global Study Leader - Warsaw,Poland (office-based)
Warszawa,Poland
Apr 14
DOCS has partnered with a highly prestigious biotech organisation with one of the most robust pipeline within the industry. We have a great job opportunity for candidates with clinical project management experience who are ready to further develop their career.
Contract Clinical Study Manager
London
Apr 13
ProClinical is working with a world leading company and is seeking a Contract Clinical Study Manager. This role is a critical role at this company, holding key responsibilities for the execution of the clinical trial and driving day-to-day activities in support of clinical trial milestones. A CTS takes on a primary role as a Regional or overall Study Lead for the company’s Clinical Operations. ...
Study Manager
United States
Apr 13
Study Manager Location: US   CROMSOURCE is looking for a Study Manager to join one of our partner Medical Device companies, who specialize in Cardiology and Neurology devices.   You will initially oversee the start-up of 2 registry studies running in Canada and the US and manage the IRB and Ethics submissions, site contract negotiation and study start-up and will be responsible for assuring the co-ordination of the operational aspects and proper conduct of a clinical...
Global Manager of Study Start Up – International Organisation – Munich – Up to €90,0000
Munich
Apr 12
Global Study Start Manager - International Organisation – Munich - Up to €90,000 P/A
Global Study Manager
London
Apr 10
An exciting job vacancy has emerged for a Global Study Manager to join one of the world's largest global CROs. This contract research organisation provides support services to many of the biggest names in pharmaceuticals, biotech, medical devices and health care, and has helped to commercialise many leading therapies. This position will be based at their UK site in Reading. ...
Clinical Research Study Manager
Switzerland
Apr 10
Fantastic 12 month contract with one of the worlds leading pharmaceutical companies based in Basel, Switzerland.
Registries Data Entry Coordinator/Data manager/Research Nurse/Study Site coordinator/CTA
London. Cambridge or Manchester
Apr 10
This is a permanent PAYE employed position with CHILTERN, a Covance company. You would be outsourced to our Client - a pharma company specialising in very RARE diseases - on a rolling 12 months contract - but 100% home based. There is SIGNIFICANT travel in this role to three sites in Manchester , London and Cambridge. Staying away from home regularly is part and parcel of this job.
Clinical Project Manager / Clinical Study Management - Early Phase, global studies - 14 months - global Pharma - Hertfordshire, UK
Hertfordshire
Apr 9
Clinical Management role which combines end-to-end design, execution, and reporting of early-phase (phase I & IIa) clinical pharmacology, patient, and Proof Concept / Proof Mechanism studies with leadership in project teams and across matrix teams. This role will contribute to individual studies in addition to project level activities. This includes responsibility and accountability for the set-up, coordination, execution and delivery of multi-studies across a variety of therapeutic areas.
Clinical Study Manager - Stevenage
Stevenage
Apr 6
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...
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Clinical Study Manager
South East
Apr 4
A very exciting opportunity to join a fast growing Gene Therapy Biotech. Permanent Clinical Study Manager role based in Hertfordshire offering an excellent salary and...
Clinical Study Manager – Small Pharma – Central London
London
Mar 27
Clinical Study Manager is required by global Pharma that is looking to expand due to their most recent success. This is an office based position with some flexibility to work from home and would suit an existing Study Manager with sound Pharma experience and a CRA background. This role will involve working across Phase II and III studies within Rare Disease. ...
GLOBAL STUDY MANAGER – SOUTH EAST – £67,000 + CAR ALLOWANCE
England
Mar 26
Looking for experienced clinical project managers with strong communication skills and excellent attention to detail. This role offers working from home flexibility, along with excellent salary package and bonus.
Senior Clinical Study Manager – Top Pharma – UK Office based up to £75k + Benefits
England
Mar 26
We are working with a global pharma looking to expand their team in the UK and therefore in search for an experience study manager to help them lead their clinical team.
Global Study Start Up Manager
flexible location in Europe
Feb 22
As Study Start Up Manager, you will manage a global team of Study Start Up Associates within our Centralized Patient Consent Team.   The core purpose of this role is to coordinate, manage and facilitate the activities related to preparation, review and approval of Study Master, country related and site level Informed Consent documents in accordance with internal / external SOPs.
Clinical Trial Manager/Study Manager-144543
Europe, Middle East and Africa-Germany-Hamburg-Hambu
Feb 15
PPD has an exciting opportunity for a Clinical Team Manager (CTM) join us onsite exclusively for one of our strategic pharmaceutical partners in Hamburg OR  Munich, Germany.  PPD works in collaboration with this partner; you will be dedicated to the client projects and sites, working within their teams, systems and processes on behalf of PPD. ...
Study Start Up Manager - UK/EU home based - permanent.
Home based UK/Europe
Feb 7
Exciting opportunity to join new department within established global CRO. Novella Clinical, a Quintiles company, is seeking an experienced Study Start Up Manager with global experience in planning, oversight and driving projects in Study Start Up.
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...
(Senior) Clinical Study Manager
South East
Oct 17
A very exciting opportunity to join a fast growing Biotech. Permanent Clinical Study Manager or Senior Clinical Study Manager role based in Hertfordshire offering an...
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. ...
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Clinical Study Manager
Home Based Southeast of England Ideally, UK
May 19
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 as and when necessary so being a reasonable commute to junction 4 of the M3 may be an advantage. You would be employed by Chiltern and seconded to a Pharmaceutical Company.
Clinical Trial Manager/Clinical Study Manager - (Sponsor Dedicated) - UK-139810
Europe, Middle East and Africa-UK-England-Uxbridge
May 7
PPD has an exciting opportunity for a Clinical Trial Manager/Study Manager to join us dedicated to one of our strategic pharmaceutical partners in Uxbridge, West London.  PPD works in collaboration with this partner; you will be dedicated to UK clinical projects, 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
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 : 34
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