IQVIA
life sciences
ClinProcessAnalyst1
Neural analysis suggests this role is
optimal for Mid candidates.
“Clin Process Analyst 1 at IQVIA. Skills: process management, cross-functional coordination, vendor/stakeholder management, operational metrics, resource planning, continuous improvement, clinical research regulatory, ICH GCP, document management, systems expert, process trainings. Provide project related assistance for assigned project(s), sites and project teams. Lead teams functionally, where assigned, including awareness of scope of work, budget, and resources”
What You'll Achieve.
meets quality and timeline metrics; high quality deliverables that are completed according to service level agreements (SLAs) and within project timelines
Industry & Context.
Good problem solving skills
What They're Looking For.
Must Have
Bachelor's Degree Life sciences or related field, Minimum 3 years of relevant experience, Good knowledge of, and skill in applying applicable clinical research regulatory i. e. , ICH GCP and relevant local laws, regulations and guidelines, 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, Ability to handle conflicting priorities, 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, Proven ability to work on multiple projects balancing competing priorities, Good leadership skills, Ability to work across cultures and geographies with a high awareness and understanding of cultural differences, Setting quality standards and reviewing deliverables to the same for process tasks
What You'll Do.
Provide project related assistance for assigned project(s)
sites and project teams
Lead teams functionally
including awareness of scope of work
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
Create and maintain relevant project documents
Ensure accurate completion and maintenance of internal systems
timelines and project plans with project specific information
evaluate and recommend modifications to designated processes
Participate in document management (creation
Participate in (study) team meetings and implement action items
Collaborate with the project lead/team members in creation/review of study documents
Setting quality standards and reviewing deliverables to the same for process tasks
Cordinate and collaborate with various project stake holders
Act as SME/mentoruddy for new joiners and support with system/process trainings
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 the trainings to the team and be available to address the quesries for the teams
How You'll Work.
Team & Collaboration
Lead teams functionally, where assigned; Establish and maintain effective project/ site communications; Participate in (study) team meetings; Collaborate with the project lead/team members; Cordinate and collaborate with various project stake holders; Act as SME/mentoruddy for new joiners; guiding teams on using of systems; Relaying the trainings to the team; address the quesries for the teams
Communication Scope
written and verbal communication skills; good command of English language; Establish and maintain effective project/ site communications
Process & Methodology
awareness of scope of work, budget, and resources, 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, Ensure accurate completion and maintenance of internal systems, databases, tracking tools, timelines and project plans with project specific information, Proven ability to work on multiple projects balancing competing priorities
Full Job Description
Job Overview Provide project related assistance for assigned project(s), sites and project teams. Lead teams functionally, where assigned, including awareness of scope of work, budget, and resources. 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. Essential Functions • 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 • Create and maintain relevant project documents • Ensure accurate completion and maintenance of internal systems, databases, tracking tools, timelines and project plans with project specific information • Review, evaluate and recommend modifications to designated processes • Participate in document management (creation, review, maintenance, storage, as applicable) • Participate in (study) team meetings and implement action items • Collaborate with the project lead/team members in creation/review of study documents • Setting quality standards and reviewing deliverables to the same for process tasks. • Cordinate and collaborate with various project stake holders. • Act as SME/mentor/buddy for new joiners and support with system/process trainings. • 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 the trainings to the team and be available to address the quesries for the teams. Qualifications • Bachelor's Degree Life sciences or related field Req • Typically requires Minimum 3 years of relevant experience. • Good knowledge of, and skill in applying applicable clinical research regulatory requirements; i.e., ICH GCP and relevant local laws, regulations and guidelines • Strong written and verbal
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