IQVIA

RegulatoryandStartUpManager

€44–67k Kaunas, Lithuania FULL TIME
Market Sentiment
HIGH DEMAND

Neural analysis suggests this role is
optimal for Manager candidates.

The Brief

“Regulatory and Start Up Manager at IQVIA. Skills: Site activation, Regulatory strategy, Project management. Manage delivery of site activation. Manage maintenance activities”

Industry & Context.

Problems you'll solve

Issue resolution; Problem solving

What They're Looking For.

Must Have

Bachelor's Degree Life sciences, 7 years’ relevant experience, experience in an international role, knowledge of GCP, knowledge of ICH guidelines

What You'll Do.

Manage delivery of site activation

Manage maintenance activities

Manage regulatory activities

Oversee execution of Site Activation

Develop Management Plan

Implement Management Plan

Maintain Management Plan

Ensure collaboration across Regulatory & Site Activation

Create technical documentation

Review technical documentation

Create administrative documentation

Review administrative documentation

Provide regulatory support

Provide technical scientific support

Provide guidance of multi-regional programs

Provide oversight of multi-protocol programs

Determine regulatory strategy

Determine parameters for submissions

Identify regulatory complexity

Identify regulatory challenges

Offer creative solutions

Offer practical solutions

Assess regulatory landscape

Review regulatory landscape

Contribute to 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

Take lead role in developing relationships

Deliver presentations to clients

Deliver training to clients

Deliver presentations to colleagues

Deliver training to colleagues

Deliver presentations to professional bodies

Deliver training to professional bodies

Involve in budget planning

Involve in budget reviews

How You'll Work.

Team & Collaboration

Study management team; Cross-functional teams

Communication Scope

Negotiation skills; Communication skills; Technical writing skills; Regulatory writing skills; Scientific support

Process & Methodology

Project planning, Scope management, Budget management

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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