Team Leader Regulatory Editor - Madrid, España - Iqvia Llc

Descripción

Team Leader Regulatory Editor page is loaded Team Leader Regulatory Editor Apply locations Madrid, Spain time type Full time posted on Posted Today job requisition id R Join us on our exciting journey

We are looking for a Team Leader Regulatory Editor, this could be your chance to start a new adventure in a company with the best Regulatory Talents.

In this role you will be joining part of a new team of experienced regulatory intelligence analysts during a period of strong growth.

Working in a team that creates intelligence for one of the leading regulatory teams in the industry.


POSITION PURPOSE:

Proactive monitoring and surveillance on changes in the global regulatory landscape covering the drug development lifecycle starting from preclinical through commercialization as well as the medical devices from concept stage to market.

This position will provide broad support on clinical, pharmacovigilance and manufacturing quality activities and requests.


MAIN RESPONSABILITIES:

Managerial Skills:
Support project objectives. Provide direction, support and feedback within the Business Analysis team. Perform team lead duties including scheduling, reporting to management, supervising analysts, delegating and prioritizing workloads. Resolve issues within and across teams.


Editorial Skills:

Monitor and analyse the changes and evolution of the local regulatory environment, including guidance and regulations from regulatory authorities, trade organizations, working groups, and relevant industry thought leaders for both drug and medical devices.

Assess regulatory intelligence information for relevance and impact to industry's internal processes, drug development projects and/or regulatory strategies to create and enrich the IQVIA proprietary documents.

Monitoring agency and professional websites, local specialized press, conferences and selecting documents to be integrated in line with the IQVIA scope, editorial and intelligence management processes Identify business critical aspects and communicate effectively to internal and external stakeholders.

This includes regular updates on new information that could impact clinical trial execution, pharmacovigilance activities, manufacturing quality as well as other ad hoc requests.

Synthesize information from regulatory documentation as well as interaction with local country experts as needed. Share/Input data into systems or tools to enable effective knowledge management of country level operational intelligence data.

Develop and refine regulatory intelligence processes and procedures to build efficiencies Our ideal candidate:

Key Responsibilities Scientific degree in pharmacy, chemistry, pharmacology, biology Proficient in proof reading and editing in English language Proficient in at least one more language other than English Capability to work remotely with peers in an international environment Good understanding of the drug development and commercialization process Ability to research, analyse and extrapolate critical regulatory information Highly organized and able to work independently to meet deliverable on time and on target Team-oriented and strong relationship builder, ability to effectively collaborate with a range of individuals across the organization and externally Attentive to details and focused on quality output Effective communicator - - both written and oral - in a multi-discipline team environment Proficient in the navigation of intelligence database(s) IQVIA is an equal opportunity employer .

We make employment decisions based on qualifications and merit.

We prohibit discrimination based on any unlawful consideration such as age, race, national origin, gender or other "protected status." We invite you to join IQVIA We know that meaningful results require not only the right approach but also the right people.

Regardless of your role, we invite you to reimagine healthcare with us . You will have the opportunity to play an important part in helping our clients drive healthcare forward and whatever your career goals, we are here to ensure you get there

IQVIA is a leading global provider of advanced analytics, technology solutions and clinical research services to the life sciences industry.

We believe in pushing the boundaries of human science and data science to make the biggest impact possible – to help our customers create a healthier world.

Learn more at

About UsIQVIA is a world leader in using data, technology, advanced analytics, and expertise to help customers drive healthcare – and human health – forward.

Together with the companies we serve, we are enabling a more modern, more effective and more efficient healthcare system, and creating breakthrough solutions that transform business and patient outcomes.

To get there, it takes diverse skills and a curiosity to explore new possibilities.

No matter your role, everyone at IQVIA, including our colleagues at Q2 Solutions, contributes to our shared goal of improving human health.

Thank you for your interest in growing your career with us.
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