IQVIA
Life sciences
RegulatoryandStartUpManager-Bulgaria
Neural analysis suggests this role is
optimal for Manager candidates.
“Regulatory and Start Up Manager - Bulgaria at IQVIA. Skills: Regulatory affairs, Site activation, Clinical trials. Direct and manage site activation. Manage regulatory activities”
Industry & Context.
Problem resolution
What They're Looking For.
Must Have
Bachelor's Degree Life sciences, 7 years relevant experience, Experience in a scientific or clinical environment, Demonstrable experience in an international role, Knowledge of GCP, Knowledge of ICH guidelines
Nice to Have
Experience in clinical trial management
What You'll Do.
Direct and manage site activation
Manage regulatory activities
Oversee execution of Site Activation
Oversee Maintenance for assigned projects
Develop Management Plan
Implement Management Plan
Maintain Management Plan
Resolve project related issues
Ensure collaboration across Regulatory & Site Activation
Communicate with regions and countries
Create technical documentation
Review technical documentation
Create administrative documentation
Review administrative documentation
Provide specialist regulatory support
Provide technical scientific support
Provide overall guidance
Provide oversight of multi-regional programs
Determine regulatory strategy
Determine parameters for submissions
Determine necessary authorizations
Identify regulatory complexity
Identify regulatory challenges
Offer creative solutions
Offer practical solutions
Assess regulatory landscape
Review regulatory landscape
Contribute to collection of regulatory intelligence
Contribute to interpretation of regulatory intelligence
Contribute to analysis of regulatory intelligence
Contribute to dissemination of regulatory intelligence
Execute operational strategy
Maintain clinical study approvals
Maintain authorizations
Review essential documents
Negotiate essential documents
Ensure appropriate quality standards
Ensure accurate completion of internal systems
Maintain internal systems
Complete tracking tools
Maintain tracking tools
Complete project plans
Maintain project plans
Take a lead role in developing relationships
Deliver presentations to clients
Deliver presentations to colleagues
Deliver presentations to professional bodies
Deliver training to clients
Deliver training to colleagues
Deliver training to professional bodies
Involve in monthly study budget planning
Involve in monthly study budget reviews
How You'll Work.
Team & Collaboration
Study management team; Cross-functional teams
Communication Scope
Communication skills; Negotiation skills; Presentation skills; Training delivery
Process & Methodology
Project planning, Scope management, Budget management, Resource planning
Full Job Description
_**Job Overview**_ Direct and manage the delivery of all required site activation, maintenance and regulatory activities for selected studies or multi-protocol programs, including pre-award activities, oversight of the scope of work, budget and resources. _**Essential Functions**_ * Oversee the execution of Site Activation (including pre-award/bid defense activities) and/or Maintenance for assigned projects in accordance with the agreed RSU site activation strategy, adhering to project timelines. * Develop, implement and maintain the Management Plan according to the Scope of Work and Project Plan, within the agreed project strategy, resolving project related issues where required. * Ensure collaboration across Regulatory & Site Activation, including communication with regions and countries, to successfully deliver the agreed project scope in compliance with the RSU Management Plan. * Create and/or review technical and administrative documentation to support business development and enable study initiation and maintenance, as required. Provide specialist regulatory and technical scientific support to facilitate efficient business development, initiation and maintenance of clinical trials, whilst enabling compliance with regulatory requirements. * Provide overall guidance and oversight of multi-regional and multi-protocol programs during initial start-up and maintenance phase as an integral member of the study management team. * Determine regulatory strategy/expectations and parameters for submissions and all necessary authorizations * Identify regulatory complexity and challenges and offer creative and practical solutions to support the bid process and subsequent execution of the site activation plan. * Assess and review the regulatory landscape and contribute to the collection, interpretation, analysis and dissemination of accurate regulatory intelligence to support assigned studies and wider company, as required. * Execute operational strategy/ expectations for mai
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