Since 2019, Iman Barilero has been working in Poxel located None, None. This person is a well-qualified Senior Vice President, Global Head Regulatory Affairs with over 32 years of work experience. According to Iman's CV and work profile, this expert has worked at more than 14 places with numerous backgrounds and got different skills. Iman Barilero can be found in Washington, DC – where this professional currently lives. You can search for the professional's phone and email. We can also provide you with detailed contact information upon request.
Name variants:
Iman Barilero
Last updated May 15, 2024
Contact Information
Workplace
Colleagues
Work History
Vice President, Regulatory Science and Pharmacovigilance
3 Forbes Rd, Lexington, MA 02421
Sep 2017 — Feb 2019
Member of Teaching Faculty at Tufts Center For Study of Drug Development: Regulatory Science
Medford, MA
from Oct 2018
Senior Vice President, Chief Regulatory Science, Patient Advocacy and Pharmacovigilance Officer
840 Memorial Dr, Cambridge, MA 02139
Served as Senior Vice President and charged with bringing global regulatory leadership to the development of innovative products . Guided the development and executing of a vision and long t...
Jan 2017 — May 2017
Vice President, Global Regulatory Development Strategy, Science, Intelligence and Policy, Corporate R and D
Creation and management of GRDSP organization and recruit 25 people with 2 departments focusing on development projects and regulatory intelligence and policy and advocacy. Develop and imple...
Feb 2007 — 2016
Associate Director, Global Regulatory Affairs, Policy and Qa
New Brunswick, NJ
2002 — 2006
Global Director Training and Education, Gcp and Regulatory Compliance, International Medical Science
Led clinical practice training program for Clinical Science and Drug Safety Departments on Pharma Development Standard Operating Procedures (PD SOP) to ensure regulatory and ethical complian...
Mar 2001 — Dec 2002
Global Head, Product and Medical Information Group, Pharmacovigilance
Creation and management of PMIG organization (30 people) composed of product labelling and medical information departments in view of leading global development and maintenance of CDSs and g...
Aug 1997 — Feb 2001
Manager, International Product Information International Drug Regulatory Affairs
Managed scientific assessment of changes to local Prescribing Information worldwide for all Roche products in CNS, dermatology, oncology, virology
Medical advisor to affiliates on labellin...
Jul 1995 — Jul 1997
International Clinical Coordinator, Pharmacovigilance, Oncology
Charged with assessment and declaration of Serious Adverse Events for PI, PII, and PIII studies of Taxotere® in Europe, Canada, Australia, South Africa, and Latin America; achieved MAA appro...
1994 — 1995
International Clinical Research Coordinator, Clinical Research, Oncology
Organized, monitored, and coordinated PI studies (under IND) of anti-cancer drug Intoplicine in Europe (Holland, Denmark, and Switzerland); wrote Comprehensive Medical Report and US IND annu...
1993 — 1994
Clinical Research Associate and Cns and Internal Medicines
Organized, monitored, and finalized PIII study for antidepressant drug Effexor® in France; monitored and finalized PIII study of contraceptive drug Alesse® in France.
1992 — 1993
Clinical Research Assistant and Cardiovascular
New Jersey
Planned PII studies (under IND) of hyperlipemic drug Prevastin®; wrote protocol and designed CRFs.
1991 — 1992
Researcher Pre-Clinical, Clinical Ressearch and Pharmacokinetics, Oncology
Conducted in-vivo and in-vitro studies for metabolism of Ditercalinum, an anticancer drug, as part of research program Developed and executed pre-clinical research program and clinical Phase...
1985 — 1991
Education
2017 — 2018
2016 — 2016
1991 — 1994
1992 — 1992
1991 — 1992
1986 — 1990
1985 — 1986
upto
Occupations
Executive
Senior Vice President
Scientist
Biotechnology Professional
Vice President
Chief Executive
Biologist
Biological Scientist
Skills
Regulatory Affairs
Clinical Trials
Pharmaceutical Industry
Clinical Development
Life Sciences
Biotechnology
Pharmaceutics
Drug Development
Pharmacovigilance
Oncology
Clinical Research
R&D
R&D Experience
Regulatory Submissions
Fda
Strategy
Management
Senior Management Experience
Organizational Development
Stakeholders Management
Leadership
Strategic Competencies and Leadership
Strategies To Influence Health Care and Policy Environment
Cns Disorders
Health Technology/Regulatory Interface
Neurology
Market Access
Strategic Leadership
Pre Clinical and Clinical Research
Gcp
Therapeutic Areas
Biopharmaceuticals
Good Clinical Practice
Ema
Global Regulatory Development Strategy
Well Established Relationships With Health Authorities
FAQs about Iman Barilero
What is the main profession of Iman Barilero?
Iman is a Senior Vice President, Global Head Regulatory Affairs.
What are the main profession of This expert?
These person's professions are Executive and Senior Vice President
Where does Iman Barilero currently live?
Iman Barilero currently lives in Washington, DC.
What is Iman Barilero's email?
Iman's email is db**@lundbeck.com.
How many companies did Iman Barilero work at?
The professional worked at 14 jobs.
What education does Iman Barilero have?
Iman studied at the from 2017 to 2018.
What languages does Iman Barilero speak?
Iman Barilero speaks English, Arabic, and French.
What is professional industry that Iman Barilero worked in?
This professional works in Biotechnology industry.