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Latest Clinical Research Jobs

pharmiweb.com has added 244 opportunities in Clinical Research in the last 6 days.

CLINICAL OPERATIONS PROJECT MANAGER - Surrey, United Kingdom

Company: PRA Health Sciences
Location: Surrey, United Kingdom
Salary: Competitive
Benefits: Excellent Salary and Benefits
Closing Date: 22 Jul 17More Details
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 Clinical Operations Project Manager and help realize your career potential.

CLINICAL RESEARCH ASSOCIATE (CRA) - Poland

Company: PRA Health Sciences
Location: Poland
Salary: Competitive
Benefits: Excellent Salary and Benefits
Closing Date: 22 Jul 17More Details
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 Clinical Research Associate (CRA) and help realize your career potential.

Graduate Internal Recruiter

Company: Skills Alliance
Location: London
Salary: Negotiable
Closing Date: 06 Jul 17More Details
Skills Alliance, a leading global life science executive recruitment business is looking for a Graduate Internal Recruiter to assist with our European growth.This role...

Project Manager - Clinical Pharmacology

Company: Skills Alliance
Location: East Anglia
Salary: 30,000 - 40,000
Benefits: bonus + extensive benefits
Closing Date: 06 Jul 17More Details
A great opportunity for an ambitious Project Manager to join a leading UK based Bio-Pharma with a strong reputation in the industry.The company is...

CRA II / SCRA –Rare Disease – Biotech

Company: i-Pharm Consulting
Location: London
Salary: Negotiable
Closing Date: 06 Jul 17More Details
CRA II / SCRAMidsized Biotech Rare Disease Low protocol load LOCATIONLondon and Greater London RESPONSIBILITIES • Conduct site initiation visits, routine monitoring visits, and close-out visits• Work across Rare Disease Trials • Liaise with site personnel REQUIREMENTS• Bachelor of Science or Bachelor of Nursing Degree• 2+ years UK monitoring experience• Entitlement to work in the UK• Full UK drivers licenceBENEFITS• Excellent Salary• Healthcare• 25 days’ annual leave• PensionABOUT i-PHARM CO ...

Senior Clinical Research Associate

Company: i-Pharm Consulting
Location: London
Salary: Negotiable
Closing Date: 06 Jul 17More Details
Job TitleSenior Clinical Research AssociateJob Summaryi-Pharm Consulting are delighted to share this new SCRA opportunity within an exciting mid-sized CRO. This ever-developing organisation are continuing to build on their recent successes with the acquisition of a driven Senior Clinical Research Associate who is looking for longevity and career progression in a modern, positive family-feel team culture. ...

European Project Manager / Clinical Site Manager - Uxbridge

Company: inVentiv Health Clinical
Location: Uxbridge
Salary: Negotiable
Benefits: Benefits
Closing Date: 06 Jul 17More Details
European Project Manager / Clinical Site Manager Office based - Uxbridge Pharmaceutical company We are currently recruiting for a European Project Manager/ Clinical Site Manager to be fully dedicated to our client, a global pharmaceutical company. This position requires an experienced Clinical Research professional who is looking to undertake a great opportunity leading clinical studies and working across the UK, Ireland and the Benelux regions. inVentiv Health: Work Here. ...

Clinical Research Associate

Company: Chiltern
Location: Italy
Salary: On Application
Benefits: Excellent and competitive benefits
Closing Date: 25 Jul 17More Details
The Chiltern Source department is currently looking for a CRA to work for one of our clients, a top leading pharmaceutical company. This position is office based in Milan.

Clinical Project Manager

Company: CROMSOURCE
Location:  ITALY
Salary: On Application
Benefits: Excellent and Comprehensive Benefits – see below
Closing Date: 25 Jul 17More Details
Job Title: Project Manager     Office based, Verona Italy       Schedule: Full time, 37.5 hours a week         CROMSOURCE is a family owned international, full-service Contract Research Organisation who, since 1994, has been supporting our clients with outstanding clinical research and staffing solutions services.  We are currently recruiting for Project Manager.

Study Delivery Associate / Budget Specialist

Company: SynteractHCR Deutschland GmbH
Location: Brussels, Belgium
Salary: On Application
Benefits: Excellent
Closing Date: 25 Jul 17More Details
Study Delivery Associate / Budget Specialist (f/m) Overview The Study Delivery Associate / Budget Specialist  provides operational and administrative support for project, study delivery activities and budget management with main responsibilities in the area of budget management including: Responsibilities Ensure all information is kept up to date in planning and tracking tools for project and study level data Close cooperation with study team members to resolve...

CTM - Clinical Trial Manager - Netherlands

Company: i-Pharm Consulting
Location: Netherlands
Salary: Negotiable
Closing Date: 06 Jul 17More Details
If you are a CTM or Study Manager for two years + and you are looking for a new challenge in a multinational company this is the perfect opportunity for you!JOB TITLE CTM – Clinical Trial Manager – Study Manager LOCATION NetherlandsSALARY & BENEFITS +/- €70k+13th month+Car or Car allowance +Reimbursement of Mileage +Pension+Healthcare +Life insurance +Meal vouchers ROLE/DESCRIPTION Coordinating all aspects of clinical activities on a national basis, as well as the implementation of internati ...

HEOR Project Manager, Poland

Company: inVentiv Health Clinical
Location: Poland
Salary: 0 - 20,000
Benefits: Negotiable
Closing Date: 29 Jun 17More Details
Here at inVentiv Health Clinical we are currently recruiting for a Worldwide Health Economics and Outcomes Research Project Manager to be based in Poland.inVentiv Health: Work Here. Matters Everywhere. Job Details:We are currently recruiting for a Project Manager to be fully dedicated to our client, a global pharmaceutical company. ...

Associate Director, Biostatistics Manager

Company: Roche
Salary: On Application
Closing Date: 25 Jul 17More Details

The Biostatistics Manager is responsible for managing a group of Biostatisticians in order to provide excellent strategic partnership and execution for pre-approval and post-approval development and product portfolio programs across Roche. Typically their accountabilities extend across multiple marketed medicines, portfolio projects and disease areas. He/She may serve as (Deputy) Biostatistics Site Head. ...

PV Scientist I - 12 month rotation/FTC

Company: Roche
Salary: On Application
Closing Date: 25 Jul 17More Details

Who we areWe’re innovation, curiosity and diversity – multiplied by 80,000 professionals in 150 countries. As a global leader in research-focused healthcare, we’re constantly learning and growing – and seeking people who share these goals.
The PositionRoche is a global leader in pharmaceutical research and in order to uphold our high standards and commitment to delivery in respect to drug safety, we are looking to develop our Pharmacovigilance team. ...

Clinical Research Associate - Madrid-141050

Company: PPD
Location: Europe, Middle East & Africa-Spain-Community of Ma
Salary: On Application
Closing Date: 25 Jul 17More Details
PPD is recruiting for a Clinical Research Associate to join the established and growing clinical management team working home-based in Barcelona, Spain.
 
 
PPD is a leading global contract research organization providing comprehensive, integrated drug development, laboratory  and lifecycle management services. ...

Remote Site Monitor-140951

Company: PPD
Location: Europe, Middle East & Africa-Israel-Tel Aviv Metro
Salary: On Application
Closing Date: 25 Jul 17More Details
The clinical development services group is expanding our remote monitoring and site management capabilities.  Due to this expansion we are opening up the opportunity to apply for the position of Remote Site Monitor (RSM) in our Tel Aviv office.Responsibilities:Performs remote site management activities on assigned project(s) in accordance with FDA and/or local regulations and guidelines, ICH GCPs and PPD procedural documents.Reviews study data from various sources remotely. ...

Country Approval Specialist (FTC 1 year)-139165

Company: PPD
Location: Europe, Middle East & Africa-Israel-Tel Aviv Metro
Salary: On Application
Closing Date: 25 Jul 17More Details
PPD is recruiting a Senior/Country Approval Specialist (S/CAS) for our Site Intelligence & Activation (SIA) department in our Tel Aviv office. The Country Approval Specialist will manage the preparation, review and coordination of Ethics Committee and Regulatory submission in Israel and will coordinate all activities to get investigational sites ready to enroll patients in our clinical trials.This is a fixed term contract for one year. ...

Medical Affairs Supervisor

Company: Docs Global (Continental Europe)
Location: BUdapest,Hungary
Salary: Competitive
Benefits: Excellent & Comprehensive
Closing Date: 26 Jun 17More Details
As a driven person who has the ambition to achieve you will be given the opportunity to gain more responsibilities and enhance your professional profile. Please send yu application Orsolya.Berke@docsglobal.com Contact 0036703831286

Site Manager

Company: Docs Global (Continental Europe)
Location: IDF - 92,France
Salary: Competitive
Benefits: Excellent & Comprehensive
Closing Date: 26 Jun 17More Details
Vous êtes à la recherche d'une nouvelle opportunité de poste, ou d'un nouveau challenge professionnel ? DOCS vous accompagne dans ce changement en vous proposant des missions qui vous correspondent et participe au développement de votre carrière. Partenaire privilégié des acteurs de l'industrie pharmaceutique, nous vous proposons de rejoindre nos équipes en France.

Clinical Trial Manager Neuroscience LD

Company: Docs Global (Continental Europe)
Location: Belgium,Belgium
Salary: Competitive
Benefits: Excellent & Comprehensive
Closing Date: 26 Jun 17More Details
A challenging position as Clinical Trial Manager in a major Pharma company. The position is responsible for the regional/global coordination of clinical trial management activities for internally managed and/or outsourced trials.

Clinical Trial Associate

Company: Docs Global (Continental Europe)
Location: Prague 4,Czech Republic
Salary: Competitive
Benefits: Excellent & Comprehensive
Closing Date: 26 Jun 17More Details
DOCS has partnered with a highly prestigious organization with one of the most robust pipeline within the industry. A fantastic opportunity for an experienced clinical research professional that is ready to take on a new challenge and further develop their career!

Senior Safety Reporting Officer (m/w)

Company: Docs Global (Continental Europe)
Location: Düsseldorf,Germany
Salary: Competitive
Benefits: Excellent & Comprehensive
Closing Date: 26 Jun 17More Details
Our client is one of the world's leading pharmaceutical companies operating in various therapeutic areas as well as in the field of medical devices. For our client we are currently hiring a Senior Safety Reporting Officer (m/f) under Clinical Trail Safety Reporting Unit office-based near Düsseldorf.

Specialist Central Monitoring

Company: Docs Global (Continental Europe)
Location: Netherlands / Belgium,Netherlands
Salary: Competitive
Benefits: Excellent & Comprehensive
Closing Date: 26 Jun 17More Details
The Specialist executes and manages the day-to-day activities of Analytical Risk-Based Monitoring (ARBM) for approximately three low to medium complexity or two high complexity clinical trials in accordance with standard operating procedures, all relevant laws, regulations, guidelines, policies and good clinical practices.

Site Manager - Cardiology

Company: Docs Global (Continental Europe)
Location: Madrid,Spain
Salary: Competitive
Benefits: Excellent & Comprehensive
Closing Date: 26 Jun 17More Details
DOCS has grown to become the premier resourcing provider of global strategic resourcing and FSP services to the biopharmaceutical and medical device industries. Founded in 1997 we are driven by our core values that guide our culture and support our goal to become a Trusted Partner. Our five core values are: Our People, Excellence, Accountability, and Integrity.

IIS Trial Manager

Company: Docs Global (Continental Europe)
Location: Italy
Salary: Competitive
Benefits: Excellent & Comprehensive
Closing Date: 26 Jun 17More Details
We are looking for talented and motivated candidates to join the team and take part in this dynamic project!

Associate Director Clinical Trial Safety

Company: Docs Global (Continental Europe)
Location: Warszawa,Poland
Salary: Competitive
Benefits: Excellent & Comprehensive
Closing Date: 26 Jun 17More Details
DOCS is supporting highly prestigious and one of the world’s top pharmaceutical company that is bringing innovative ideas, products and services continuously improving people’s health. This is a fantastic opportunity for an experienced clinical research professional that is ready to take on a new challenge, further develop their career and enjoy working culture in vibrant Client's office in Warsaw.

Health Economics & Outcomes Research (HEOR) Project Manager / Home Based (m/f)

Company: Docs Global (Continental Europe)
Location: Anywhere in Europe,Germany
Salary: Competitive
Benefits: Excellent & Comprehensive
Closing Date: 26 Jun 17More Details
Location: Europe Position type : Initially fix term contract for 12 months, extension very probable, no freelance. Job Summary: DOCS/ICON is looking for global sponsor for a HEOR Project Manager. If you are an experienced HEOR Manager in the pharmaceutical industry or you are an established Project Manager with understanding of the HEOR work space and interested to change in that direction, we are looking forward to hearing from you.

Study Start Up Associate Freelance - H/F - Démarrage: 01/08/2017 - 0.9FTE

Company: Docs Global (Continental Europe)
Location: Nanterre,France
Salary: Competitive
Benefits: Excellent & Comprehensive
Closing Date: 26 Jun 17More Details
Vous êtes à la recherche d'une nouvelle opportunité de poste, ou d'un nouveau challenge professionnel ? DOCS vous accompagne dans ce changement en vous proposant des missions qui vous correspondent et participe au développement de votre carrière. Partenaire privilégié des acteurs de l'industrie pharmaceutique, nous vous proposons de rejoindre nos équipes en France.

Regulatory Affairs Specialist M/W - South IDF - 6 months' contract

Company: Docs Global (Continental Europe)
Location: Buc,France
Salary: Competitive
Benefits: Excellent & Comprehensive
Closing Date: 26 Jun 17More Details
We offer an exciting and challenging work environment for clinical research professionals looking for an opportunity to contribute to the success of a company dedicated to researching, developing, manufacturing and marketing pharmaceuticals that improve health and quality of life.

Regulatory Affairs Specialist M/W - South IDF - 6 months' contract

Company: Docs Global (Continental Europe)
Location: Buc,France
Salary: Competitive
Benefits: Excellent & Comprehensive
Closing Date: 26 Jun 17More Details
We offer an exciting and challenging work environment for clinical research professionals looking for an opportunity to contribute to the success of a company dedicated to researching, developing, manufacturing and marketing pharmaceuticals that improve health and quality of life.


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