Senior Clinical Process Associate/ Lead Assistant

Real-World Evidence

Hybrid: Bulgaria

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.

PURPOSE      

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.      

RESPONSIBILITIES     

• 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 or French 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?

• Global exposure

• Collaborative and supportive team environment

• Access to cutting-edge in-house technology

• Excellent career development and progression opportunities

• Work-Life Balance

JOIN US

• 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!      

#LI-Hybrid #LI-ELISSAVETSANDALIDOU

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