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Clinical Process Coordinator cRSU office based in Bratislava
IQVIA
Place of work
Bratislava
Bratislava
Contract type
full-time
full-time
Wage (gross)
1000 €
1000 €
Information about the position
Job description, responsibilities and duties
PURPOSE
Provide project related assistance in core start-up processes: Project Budget Build and Inform Consent Form. Ensure all work is conducted in accordance with SOPs, policies and practices, good clinical practices and applicable regulatory requirements and meets quality and timeline metrics.
RESPONSIBILITIES
• Perform assigned complex administrative tasks to support team members with project execution
• Assist in updating and maintaining complex data in systems within project timelines and per project plans
• Establish and maintain effective project/ site communications
• Create and maintain relevant project documents
• Ensure accurate completion and maintenance of internal systems, databases, tracking tools and project plans
Provide project related assistance in core start-up processes: Project Budget Build and Inform Consent Form. Ensure all work is conducted in accordance with SOPs, policies and practices, good clinical practices and applicable regulatory requirements and meets quality and timeline metrics.
RESPONSIBILITIES
• Perform assigned complex administrative tasks to support team members with project execution
• Assist in updating and maintaining complex data in systems within project timelines and per project plans
• Establish and maintain effective project/ site communications
• Create and maintain relevant project documents
• Ensure accurate completion and maintenance of internal systems, databases, tracking tools and project plans
Information about the selection process
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™.
Whatever your career goals, we are here to ensure you get there!
We invite you to join IQVIA™.
Requirements for the employee
Candidates with education suit the position
Secondary with school-leaving examination
University education (Bachelor's degree)
University education (Master's degree)
University education (Bachelor's degree)
University education (Master's degree)
Language skills
English - Upper intermediate (B2)
Personality requirements and skills
REQUIRED KNOWLEDGE, SKILLS AND ABILITIES
• Good knowledge of applicable clinical research regulatory requirements; i.e., ICH GCP and relevant local laws, regulations and guidelines
• Strong written and verbal communication skills including good command of English language
• Results and detail-oriented approach to work delivery and output
• Good problem solving skills
• Good planning, time management and prioritization skills
• Attention to detail and accuracy in work
• Good software and computer skills, including MS Office applications including but not limited to Microsoft Word, Excel and PowerPoint
• Ability to establish and maintain effective working relationships with coworkers, managers and clients.
• Strong listening and phone skills
• Good data entry skills
MINIMUM REQUIRED EDUCATION AND EXPERIENCE
• Bachelor's degree in life sciences or related field and up to 2 years relevant experience; or equivalent combination of education, training and experience
Language requirements:
Fluent English in written and spoken form.
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.
• May require working in shifts.
• Good knowledge of applicable clinical research regulatory requirements; i.e., ICH GCP and relevant local laws, regulations and guidelines
• Strong written and verbal communication skills including good command of English language
• Results and detail-oriented approach to work delivery and output
• Good problem solving skills
• Good planning, time management and prioritization skills
• Attention to detail and accuracy in work
• Good software and computer skills, including MS Office applications including but not limited to Microsoft Word, Excel and PowerPoint
• Ability to establish and maintain effective working relationships with coworkers, managers and clients.
• Strong listening and phone skills
• Good data entry skills
MINIMUM REQUIRED EDUCATION AND EXPERIENCE
• Bachelor's degree in life sciences or related field and up to 2 years relevant experience; or equivalent combination of education, training and experience
Language requirements:
Fluent English in written and spoken form.
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.
• May require working in shifts.
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 offers a broad range of solutions that harness advances in healthcare information, technology, analytics and human ingenuity to drive healthcare forward.
ID: 3545386
Dátum zverejnenia: 23.11.2018
2018-11-23
lokalita: Bratislava Pozícia: Administrative Worker, Official, Pharmacist, Regulatory Affairs Specialist Spoločnosť: IQVIA
Základná zložka mzdy (brutto) a ďalšie odmeny: 1000 €