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Are You looking for a events job? We have 311 vacancies. Choose the job that best matches your profile in our job board. Alcobendas Terrassa Sant Feliu de Llobregat Madrid Barcelona Murcia and Madrid.

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Empresa

Sell and deliver sustainability projects - from strategy to execution    · Complex project deliveries on client engagements, where linkage between corporate and sustainability strategy is key and where value creation is the focus  · Coordinating responses to proposals on a variety of industries and topics    Position Accenture in the market as a leading provider of Sustainability Service  · Identifying opportunities to grow Accenture's Sustainability Services' market share  · Creating networks of customers across existing and potential clients  · Representing Accenture at industry events     Strengthen sustainability services ...

Sustainability Strategy Manager Madrid 21-09-2014
Empresa

Chat, Physical and Online Events -Reach out to set of leads in specific <b>verticals</b> defined by Territory Managers and qualify them -Collaboration with Territory...

Spanish or Portuguese Enterprise Management Demand Representative Barcelona 20-09-2014
Empresa

Chat, Physical and Online Events -Reach out to set of leads in specific <b>verticals</b> defined by Territory Managers and qualify them -Collaboration with Territory...

Turkish or Russian Enterprise Demand Management Representative Barcelona 20-09-2014
Empresa

Chat, Physical and Online Events -Reach out to set of leads in specific <b>verticals</b> defined by Territory Managers and qualify them -Collaboration with Territory...

Arabic /Nigerian Enterprise Demand Management Representative Barcelona 20-09-2014
Empresa

Attend events as requested in a PR/Hostess capacity Requirements Excellent <b>English</b> communication skills, both written and verbally Good knowledge of Microsoft...

Senior Secretary Madrid 19-09-2014
Empresa

What will you be doing? Participating in departmental meetings in order to revise events, brainstorm and discuss practical matters Welcoming guests at...

Trabajo estudiantes, Prácticas y Becas: Internship in a Youth hostel in reception & events department en Barcelona Sant Feliu de Llobregat 18-09-2014
Empresa

team Analyze daily reports which include traffic report, busy hour report, and <b>etc</b> Get involved in software &amp; hardware upgrade Coordinate planned events with...

VAS Engineer Alcobendas 18-09-2014
Empresa

ClinTec International is actively recruiting for a Senior Clinical Research Associate to join our expanding global company in Spain - this is a permanent contract, home based opportunity in Madrid. By working for ClinTec you can further your career in a dynamic, fast-paced environment and you can be assured of rewarding benefits. Role Description The Senior Clinical Research Associate will perform all the duties expected of a CRA and additionally will be responsible for the supervision, mentoring and performance of a team of assigned CRAs. The position encompasses all the activities required of a CRA i.e. to successfully identify, select, initiate monitor and close-out appropriate investigational sites for clinical studies plus a supervisory role in reviewing monitoring activities of his/her team to ensure that clinical trials are carried out according to the study protocol and in accordance with Standard Operating Procedures and all applicable regulations as well as principles of ICH-GCP. The Senior CRA will be responsible for ensuring the quality and integrity of data, recruitment and eligibility of subjects and study completion on time and within budget. Responsibilities of the Senior Clinical Research Associate: - Supervise and monitor clinical trials to ensure absolute adherence to Good Clinical Practice in accordance with ICH-GCP standards, Declaration of Helsinki, Federal Regulatory Requirements and study procedures - Monitor activities of assigned CRAs to ensure early identification and resolution of issues, timely completion and reporting of tasks and communication of important study findings - Review and help assigned CRAs in addressing comments raised by sites regarding clinical trial agreements, both in terms of legal aspects and financial ones and liaise with sponsor and site as appropriate to achieve a mutually agreed outcome - Review monitoring visit reports before these are released to the sponsor or internally - Track recruitment across assigned sites, identify key issues with slow recruiting sites and suggest/take corrective action to sponsor and CRAs - Perform pre-study initiation, interim monitoring and close out visits as required - Ensure during site visits proper adherence by study sites to protocol, verify integrity of the data submitted on CRFs by source document verification, assist CRAs and investigative sites with timely and accurate resolution of data queries, documented ongoing site staff training and maintenance of essential documents in the ISF - Report promptly and in accordance with sponsor SOPs, ICH-GCP and local regulatory requirements any Serious Adverse Events reported by sites to relevant sponsor contact and/or Regulatory Authority contact as appropriate - Distribute SUSARs (Suspected unexpected serious adverse reaction) in accordance with IEC & local regulatory requirements - Ensure adequacy of drug shipment and drug accountability (and storage times and conditions are acceptable or in compliance with GMP) - Ensure that assigned team of CRAs attend diligently all sponsor required team meetings, keep a record of attendance and action items assigned to team members and track progress with completion of assigned action items - Provide mentoring, training and support to less experienced members of the team and identify and raise with Line Manager training and development needs for assigned CRAs that require additional expertise from other parts of the organisation or via the use of external providers - Develop, review and edit clinical trial related documentation including but not limited to: Case Report Forms, Informed Consent Forms, study specific handbooks, guidelines and checklists - Compile if appropriate local Competent Authority /IEC applications according to national regulations - Assist with study protocol design, development and/or review when required Essential Criteria: - Bachelors degree, equivalent or higher qualification within Medicine, Biological Science, Pharmacology, Nursing or a relevant life sciences discipline - Clear understanding of the drug development process - Significant experience in performing a Clinical Research Associate role - Work experience within either a hospital, medical / research centre environment, Contract Research Organisation or Pharmaceutical company - Previous experience working on clinical trials in the area of Oncology - Proven track record of adherence to ICH-GCP and applicable local regulatory requirements during the conduct of clinical trials - Ability to contribute to the development of clinical trial related documents and materials - Ability to independently perform pre-study initiation, interim monitoring and close out visits as required - Knowledge and understanding of local Regulatory and Ethical requirements - Experience and ability to mentor, train, supervise and inspire confidence in newcomers to the industry - Good communication skills including the ability to present complex information to both clinical and non

Senior Clinical Research Associate Madrid 18-09-2014
Empresa

As an intern (m/f) in our Community Management department you will be tasked with dealing with inquiries from our players, organizing community events and...

Internship - Community Management Spanish (m/f) Murcia 17-09-2014
Empresa

and participation at industry trade shows and events, together with other <b>marketing</b> activities.brbrAdvanced degree.Native English language, spoken and written...

Director comercial Terrassa 17-09-2014