Regulatory and Start Up Manager Germany (m/w/d) Home Based
Regulatory and Start Up Manager Germany (m/w/d) Home Based
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Job Description
Job Overview
Direct and manage the delivery of all required site activation maintenance and regulatory activities for selected studies or multiprotocol programs including preaward activities oversight of the scope of work budget and resources.
Home Based requires fluent German language skills.
Essential Functions
- Oversee the execution of Site Activation (including preaward/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 multiregional and multiprotocol programs during initial startup 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 maintenance of clinical study approvals authorizations and review/ negotiation of contracts and essential documents.
- Work with Quality Management to ensure appropriate quality standards for the duration of site activation (or Maintenance as applicable).
- Mentor and coach colleagues as required. Ensure accurate completion and maintenance of internal systems (with emphasis on CTMS) databases tracking tools timelines and project plans with project specific information.
- May take a lead role in developing long standing relationships with preferred IQVIA customers. Deliver presentations/training to clients colleagues and professional bodies as required.
- May be involved in activities related to monthly study budget planning and reviews.
Qualifications
Bachelors Degree Life sciences or related field Req
7 years relevant experience in a scientific or clinical environment including demonstrable experience in an international role. Equivalent combination of education training and experience.
- Thorough understanding of regulated clinical trial environment and indepth knowledge of drug development process
- Demonstrated proficiency in using systems and technology to achieve work objectives
- Good regulatory and/or technical writing skills
- Strong knowledge and ability to apply Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines and applicable regulatory guidelines
IQVIA is a leading global provider of clinical research services commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at
Required Experience:
Manager
Employment Type
Full-Time
