RWE Senior Clinical Process Associate, Slovakia based
Senior Clinical Process Associate/ Lead Assistant
Join us on our exciting journey!
IQVIA Real-World Evidence (RWE) teams work with clients to help them collect and use real-world data to generate evidence to meet the needs of regulators, payers, providers, and patients.
Our approach is unique in the industry and is defining the way companies develop and apply real-world evidence for healthcare decision making.
We are collaborative, intellectually curious, entrepreneurial, and constantly looking for opportunities to harness the value of real-world evidence in an evolving industry.
Due to continued growth, we are seeking new brave minds to join our award winning and innovative department.
Provide project related assistance for assigned complex project(s), sites and project teams. 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.
Provide project related assistance for assigned complex project(s), sites and project teams.
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.
Perform complex processes and tasks that eventually result in high quality deliverables that are completed according to service level agreements (SLAs) and within project timelines
Establish and maintain effective project/ site communications
Ensure accurate completion and maintenance of internal systems, databases, tracking tools, timelines and project plans with project specific information and recommend modifications to designated processes if necessary.
May be assigned role of systems expert - guiding teams on using of systems, creating guidance documents, updating relevant trainings and any new updates available in the systems.
Relaying training to the team and be available to address queries.
REQUIRED KNOWLEDGE, SKILLS AND ABILITIES
Good knowledge of applicable clinical research regulatory requirements; i.e ICH GCP and relevant local laws, regulations and guidelines
Excellent written and verbal communication skills including good command of English & German or Spanish orFrench language (C1 level).
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 co-workers, managers and clients
Proven ability to work on multiple projects balancing competing priorities
Ability to coach / mentor junior colleagues
MINIMUM REQUIRED EDUCATION AND EXPERIENCE
Bachelor’s degree in life sciences or related field
Minimum 2 - 3 years relevant experience in Clinical Trials
WHAT IS IN IT FOR YOUu?
Collaborative and supportive team environment
Access to cutting-edge in-house technology
Excellent career development and progression opportunities
Embrace your curiosity and grow your career in an exciting environment where development is a priority.
Think boldly and disrupt conventional thinking.
Enjoy what you do.
Whatever your career goals, we are here to ensure you get there!
IQVIA is a leading global provider of advanced analytics, technology solutions and clinical research services to the life sciences industry. We believe in pushing the boundaries of human science and data science to make the biggest impact possible – to help our customers create a healthier world. Learn more at https://jobs.iqvia.com
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