Associate Regulatory & Start Up Manager Job Overview The Regulatory & Site Activation Manager leads the delivery of site activation, regulatory, and maintenance activities for assigned clinical studies and programs. This role ensures projects are delivered on time, within scope, and in compliance with regulatory requirements while providing leadership, strategic oversight, and support to study teams and clients. Why Join IQVIA? Join a global leader in clinical research and contribute to bringing innovative therapies to patients worldwide while developing your career in a collaborative and fast-paced environment. Key Responsibilities Lead site activation, maintenance, and regulatory activities for assigned studies. Develop and oversee project plans, timelines, budgets, and resources. Provide regulatory strategy and guidance to support study start-up and ongoing maintenance. Identify risks and regulatory challenges, implementing effective solutions. Collaborate with global, regional, and country teams to ensure successful project delivery. Support business development activities, including proposals and bid defenses. Ensure compliance with quality standards, regulatory requirements, and internal processes. Mentor and support team members, driving performance and development. Maintain accurate project documentation, systems, and tracking tools. Qualifications Bachelor's Degree in a relevant Life Sciences or Healthcare field. Minimum 3 years' clinical research experience, including at least 1 year in a leadership or project management capacity. Strong knowledge of clinical research, regulatory requirements, and clinical systems. Excellent communication, stakeholder management, and presentation skills. Proven ability to manage multiple priorities, lead teams, and work independently. Strong organizational skills, attention to detail, and problem-solving abilities. 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 https://jobs.iqvia.com IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism. IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create connections that accelerate the development and commercialization of innovative medical treatments. Everything we do is part of a journey to improve patient outcomes and population health worldwide. To get there, we seek out diverse talent with curious minds and a relentless commitment to innovation and impact. No matter your role, everyone at IQVIA contributes to our shared goal of helping customers improve the lives of patients everywhere. Thank you for your interest in growing your career with us.

Associate Regulatory and Start Up Manager - Hungary.

more at Iqvia.

Records Management Associate

Young Professionales (m/w/d) - Neueinsteiger (m/w/d)

Neueinsteiger und erfahrene Mitarbeiter im Pharma- und Apothekenaußendienst (m/w/d) - Großraum Würzburg/Nürnberg

similar roles.

Lead Climate Action Coordinator

Janitor

Deli Trainee