Ľutujeme, spoločnosť ponúkajúca danú pracovnú pozíciu ukončila zverejnenie ponuky na stránke.
Ďakujeme za porozumenie.
Zobraziť podobné ponuky
Ďakujeme za porozumenie.
Zobraziť podobné ponuky
(Sr) Site Management Coordinator with English and German or Polish or Spanish language
IQVIA RDS Slovakia, s. r. o.
Place of work
Vajnorská 100/B, Bratislava
Vajnorská 100/B, Bratislava
Contract type
full-time
full-time
Wage (gross)
min. 1200EUR/gross. Our offer to you may be higher based on your experience.*
min. 1200EUR/gross. Our offer to you may be higher based on your experience.*
Information about the position
Job description, responsibilities and duties
PURPOSE
Support the delivery of activities as determined by the appropriate country, regional lead, global lead or team. May conduct specific tasks under guidance of senior staff. Responsibilities may include all or some of the activities listed at any one time.
RESPONSIBILITIES
Assist the team in the preparation, handling, distribution, filing and archiving of documentation according to the scope of work and standard operating procedures
Review documents for completeness, consistency and accuracy, under guidance of senior staff
Prepare client deliverable documents using appropriate tools and draft text for straightforward documents, under guidance of senior staff
Completion of relevant Clinical Trial Management System (CTMS) fields, databasess, tracking tools, timelines and project plan with project specific information
Provide support for administrative tasks, e.g. meeting coordination, minute taking, travel arrangements, faxing, copying, couriers
Interact with internal and external clients, under guidance of senior staff
Perform IP release activities on small, straightforward projects or support reviews for larger projects
REQUIRED KNOWLEDGE, SKILLS AND ABILITIES
Good interpersonal communication and organizational skills.
Fluency in English is required plus additional language French/ German/ Italian/ Spanish/ Polish
Good word processing skills and knowledge of MS Office applications.
Good attention to detail.
General awareness clinical trial environment and drug development process.
Ability to work on multiple projects.
Ability to establish and maintain effective working relationships with co-workers, managers and sponsors.
MINIMUM REQUIRED EDUCATION AND EXPERIENCE
Bachelors degree with 0-2 years experience in an administrative environment or equivalent combination of education, training and experience.
PHYSICAL REQUIREMENTS
Extensive use of keyboard requiring repetitive motion of fingers.
Extensive use of telephone and face-to-face communication requiring accurate perception of speech.
Regular sitting for extended periods of time
Support the delivery of activities as determined by the appropriate country, regional lead, global lead or team. May conduct specific tasks under guidance of senior staff. Responsibilities may include all or some of the activities listed at any one time.
RESPONSIBILITIES
Assist the team in the preparation, handling, distribution, filing and archiving of documentation according to the scope of work and standard operating procedures
Review documents for completeness, consistency and accuracy, under guidance of senior staff
Prepare client deliverable documents using appropriate tools and draft text for straightforward documents, under guidance of senior staff
Completion of relevant Clinical Trial Management System (CTMS) fields, databasess, tracking tools, timelines and project plan with project specific information
Provide support for administrative tasks, e.g. meeting coordination, minute taking, travel arrangements, faxing, copying, couriers
Interact with internal and external clients, under guidance of senior staff
Perform IP release activities on small, straightforward projects or support reviews for larger projects
REQUIRED KNOWLEDGE, SKILLS AND ABILITIES
Good interpersonal communication and organizational skills.
Fluency in English is required plus additional language French/ German/ Italian/ Spanish/ Polish
Good word processing skills and knowledge of MS Office applications.
Good attention to detail.
General awareness clinical trial environment and drug development process.
Ability to work on multiple projects.
Ability to establish and maintain effective working relationships with co-workers, managers and sponsors.
MINIMUM REQUIRED EDUCATION AND EXPERIENCE
Bachelors degree with 0-2 years experience in an administrative environment or equivalent combination of education, training and experience.
PHYSICAL REQUIREMENTS
Extensive use of keyboard requiring repetitive motion of fingers.
Extensive use of telephone and face-to-face communication requiring accurate perception of speech.
Regular sitting for extended periods of time
Requirements for the employee
Candidates with education suit the position
Secondary without school-leaving examination
University education (Bachelor's degree)
University education (Master's degree)
Postgraduate (Doctorate)
University education (Bachelor's degree)
University education (Master's degree)
Postgraduate (Doctorate)
Language skills
English - Advanced (C1) or French - Advanced (C1) or German - Advanced (C1) or Spanish - Advanced (C1) or Italian - Advanced (C1) or Polish - Advanced (C1)
Other knowledge
Business correspondence - Advanced
Microsoft Word - Advanced
Microsoft Excel - Advanced
Microsoft Outlook - Advanced
Microsoft PowerPoint - Advanced
Microsoft Word - Advanced
Microsoft Excel - Advanced
Microsoft Outlook - Advanced
Microsoft PowerPoint - Advanced
The position is suitable for a fresh graduate
Yes
Advertiser
Brief description of the company
IQVIA™ is The Human Data Science Company™, focused on using data and science to help healthcare clients find better solutions for their patients. Formed through the merger of IMS Health and Quintiles, IQVIA offices a broad range of solutions that harness advances in healthcare information, technology, analytics and human ingenuity to drive healthcare forward.
We know that meaningful results require not only the right approach but also the right people. Regardless of your role, we invite you to reimagine healthcare with us. You will have the opportunity to play an important part in helping our clients drive healthcare forward and ultimately improve human health outcomes.
Whatever your career goals, we are here to ensure you get there!
We invite you to join IQVIA™
We know that meaningful results require not only the right approach but also the right people. Regardless of your role, we invite you to reimagine healthcare with us. You will have the opportunity to play an important part in helping our clients drive healthcare forward and ultimately improve human health outcomes.
Whatever your career goals, we are here to ensure you get there!
We invite you to join IQVIA™
Number of employees
1000 and more employees
ID: 3592858
Dátum zverejnenia: 8.4.2019
2019-04-08
lokalita: Bratislava Pozícia: Administrative Worker, Official, Pharmacist, Regulatory Affairs Specialist Spoločnosť: IQVIA RDS Slovakia, s. r. o.
Základná zložka mzdy (brutto) a ďalšie odmeny: min. 1200EUR/gross. Our offer to you may be higher based on your experience.*