Catherine Colot work email
- Valid
Catherine Colot personal email
- Valid
- Valid
From a young age, I was captivated by the power of medicine to transform lives. This passion led me to earn my PharmD and embark on a global journey across the life sciences industry. With over 20 years of experience, I’ve had the privilege of leading global teams, driving strategic initiatives across pharmacovigilance, quality assurance, and clinical research, while building high-performing, resilient organizations. My passion lies in creating a culture of excellence, where compliance and innovation go hand in hand, empowering teams to deliver their best. I’m committed to advancing patient safety and improving healthcare quality through visionary strategy, operational excellence, and fostering a deep sense of ownership among my teams. I lead by example—not just telling but showing—and inspire those around me to challenge the status quo, driving transformation for the greater good. My Key Strengths: 1. Global Leadership: Proven success in managing multinational teams, steering complex projects, and implementing strategies across diverse therapeutic areas. I empower individuals to challenge conventional thinking, fostering a mindset where quality and innovation thrive. 2. Regulatory Expertise: Ensuring compliance with international standards and regulatory requirements while fostering continuous improvement. I approach regulatory challenges as opportunities to enhance processes and push for excellence. 3. People-Centric Approach: Promoting a culture of respect, where empathy, active listening, and personal growth are at the heart of leadership. I lead with purpose and positivity, inspiring my teams to take pride in their work and drive meaningful results.Strategic Collaboration: I cultivate a collaborative environment, engaging stakeholders across functions to achieve shared goals and solutions. I build cross-functional and trusting partnerships to drive innovation in drug safety, and risk management—ensuring sustainable impact for both patients and the organization.
-
Executive Director Head, Global Pharmacovigilance Quality Assurance & Head, Europe Quality AssuranceDaiichi Sankyo Europe Gmbh Aug 2021 - Sep 2023Munich, De Defined the Global Pharmacovigilance (PV) Medical Affairs (MA) Quality vision in collaboration with business units and senior leadership. Provided global leadership in defining and executing quality strategies for Global PV, Post Marketing and Research & Development (R&D) PV Quality Assurance (QA) to uphold the highest standards of patient safety and regulatory compliance. Ensured a fit-for-purpose PV Quality organization through strategic and operational collaborations with internal and external business partners, meeting set objectives and KPIs. Developed and implemented policies, processes and procedures that are compliant with applicable PV regulations and requirements, ICH guidelines, international standards, relevant regulatory requirements (such as FDA, EMA, MHRA, PMDA, NMPA), and expectations. -
Regional Head Of Pharmacovigilance, Uk & IrelandBoehringer Ingelheim Jan 2020 - Jun 2021Ingelheim Am Rhein, Rhineland-Palatinate, De Ensured patient safety through product safety reporting and surveillance, while maintaining the PV Systems for the UK, Ireland, and Malta in line with global / local PV legislation (e.g., MHRA and HPRA), supporting marketing authorisation of its products in the countries. Developed and maintained a strategic cross-functional network, actively contributing to patient safety and benefit/risk management. Oversaw pharmacovigilance operations and maintained high-performing PV and Quality systems. Provided strategic leadership to drive continuous improvement initiatives and enhance pharmacovigilance practices, ensuring PV system compliance and audit readiness. -
Regional Head Of Pharmacovigilance, South East Asia And South KoreaBoehringer Ingelheim Oct 2015 - Dec 2019Ingelheim Am Rhein, Rhineland-Palatinate, De Provided leadership for local PV managers and units, ensuring alignment with regional and global strategies. Established and maintained high-performing PV system compliant with international and local regulations. Developed and implemented PV training and knowledge strategies to facilitate safety data collection and reporting. Drove the development of a robust PV culture and implemented strategic initiatives to optimize PV activities, including effective management of non-compliances and CAPAs. -
Senior / Gcp Auditor, Global Quality Medicine AuditingBoehringer Ingelheim Apr 2012 - Sep 2015Ingelheim Am Rhein, Rhineland-Palatinate, De Maintained high standards of GCP compliance and quality assurance for assigned projects across Asia Pacific region, including India, China and Japan. Led and supported more than 70 internal process and system audits (CROs, Investigator Sites and Internal) including targeted audits and audits in collaboration with Corporate Division Internal Auditors. Identified, assessed, and categorised areas of risk on trials and programs, offering guidance for inspection readiness while driving continuous improvement in clinical practices and addressing complex compliance issues with a risk-based approach. Established and managed the regional outsourcing audit process and activities for external contract auditors. -
Regional Project ManagerBoehringer Ingelheim Jul 2010 - Mar 2012Ingelheim Am Rhein, Rhineland-Palatinate, De Delivered international trials in South-East Asia and Middle Eastern countries, overseeing site monitoring, preparation, and conduct. Managed budgets, CROs, and ensured compliance with internal and external standards. Proactively identified and addressed risks affecting study timelines, data quality, and patient safety, by designing and implementing targeted mitigation plans. -
Associate Clinical Project ManagerLundbeck May 2008 - Jun 2010Valby, Copenhagen, Dk Managed 2 multiple international clinical trials across Asia and Australia, overseeing all phases from site feasibility to study closure. Ensured compliance with ICH-GCP and relevant external regulations and implemented risk mitigation strategies. Conducted accompanied site visits and managed Clinical Research Associates (CRAs) on a project basis across regions.
Catherine Colot Skills
Catherine Colot Education Details
-
Faculty Of Pharmacy Chatenay- Malabry, Paris XiPharmaceutical Sciences -
Faculty Of Law Jean Monnet, Paris XiHealth Law
Frequently Asked Questions about Catherine Colot
What is Catherine Colot's role at the current company?
Catherine Colot's current role is Global Pharma Leader | Elevating Patient Safety & Healthcare QualityThrough Visionary Strategy and Operational Excellence.
What is Catherine Colot's email address?
Catherine Colot's email address is ca****@****ail.com
What schools did Catherine Colot attend?
Catherine Colot attended Faculty Of Pharmacy Chatenay- Malabry, Paris Xi, Faculty Of Law Jean Monnet, Paris Xi.
What skills is Catherine Colot known for?
Catherine Colot has skills like Ctms, Clinical Monitoring, Edc, Regulatory Affairs, Endocrinology, Regulatory Submissions, Clinical Data Management, Pharmaceutics, Pharmacovigilance, Therapeutic Areas, Drug Development.
Free Chrome Extension
Find emails, phones & company data instantly
Aero Online
Your AI prospecting assistant
Select data to include:
0 records × $0.02 per record
Download 750 million emails and 100 million phone numbers
Access emails and phone numbers of over 750 million business users. Instantly download verified profiles using 20+ filters, including location, job title, company, function, and industry.
Start your free trial