IQVIA
Life sciences
RegulatoryandStartUpSpecialist-Poland
Neural analysis suggests this role is
optimal for Mid+ candidates.
“Regulatory and Start Up Specialist - Poland at IQVIA. Skills: Site Activation, Regulatory compliance, Clinical trials. Serve as Single Point of Contact. Ensure adherence to SOPs”
Industry & Context.
Home Based opportunity, Fluency in Polish
What They're Looking For.
Must Have
3 years clinical research experience, Bachelor’s Degree in life sciences
What You'll Do.
Serve as Single Point of Contact
Ensure adherence to SOPs
Perform start up activities
Distribute completed documents
Prepare site regulatory documents
Review documents for completeness
Ensure accurate completion of systems
Review site performance metrics
Establish project timelines
Implement contingency plan
Inform team of document completion
Track progress of documents
Provide local expertise
Perform quality control of documents
How You'll Work.
Team & Collaboration
Investigative sites; Site Activation Manager; Project Management team; Other departments; Sponsors
Process & Methodology
Project timelines
Full Job Description
_**Job Overview**_ Perform tasks at a country level associated with Site Activation (SA) activities in accordance with applicable local and/or international regulations, standard operating procedures (SOPs), project requirements and contractual/budgetary guidelines. May also include maintenance activities. __**Home Based opportunity requiring experience with local submissions and contracts. Fluency in Polish language.**__ _**Essential Functions**_ * Under general supervision, serve as Single Point of Contact (SPOC) in assigned studies for investigative sites, Site Activation Manager (SAM), Project Management team, and other departments as necessary. * Ensure adherence to standard operating procedures (SOPs), Work Instructions (WIs), quality of designated deliverables and project timelines. * Perform start up and site activation activities according to applicable regulations, SOPs and work instructions. * Distribute completed documents to sites and internal project team members. * Prepare site regulatory documents, reviewing for completeness and accuracy. * Ensure accurate completion and maintenance of internal systems, databases and tracking tools with project specific information. * Review and provide feedback to management on site performance metrics. * Review, establish and agree on project planning and project timelines. * Ensure monitoring measures are in place and implement contingency plan as needed. * Inform team members of completion of regulatory and contractual documents for individual sites. * Review, track and follow up the progress, the approval and execution of documents, regulatory, ethics, Informed Consent Form (ICF), and Investigator Pack (IP) release documents, in line with project timelines. * Provide local expertise to SAMs and project team during initial and on-going project timeline planning. * Perform quality control of documents provided by sites. * May have direct contact with sponsors on specific initiatives. **Qualifications** **Bachelor’
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