Luisa Campos

Luisa Campos Email and Phone Number

Clinical Trial Manager - partner with Boehringer Ingelheim @ IQVIA
State of São Paulo, Brazil
Luisa Campos's Location
São Paulo, São Paulo, Brazil, Brazil
Luisa Campos's Contact Details

Luisa Campos personal email

About Luisa Campos

Luisa Campos is a Clinical Trial Manager - partner with Boehringer Ingelheim at IQVIA. She possess expertise in pharmaceutical industry, clinical trials, gcp, ich gcp, clinical monitoring and 13 more skills. She is proficient in Inglês.

Luisa Campos's Current Company Details
IQVIA

Iqvia

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Clinical Trial Manager - partner with Boehringer Ingelheim
State of São Paulo, Brazil
Website:
iqvia.com
Employees:
52333
Luisa Campos Work Experience Details
  • Iqvia
    Clinical Trial Manager - Partner With Boehringer Ingelheim
    Iqvia
    State Of São Paulo, Brazil
  • Iqvia
    Assoc Clinical Project Manager
    Iqvia Feb 2023 - Present
    São Paulo, Brasil
  • Novartis
    Evidence Generation Monitor
    Novartis Mar 2021 - Feb 2023
    São Paulo, Brasil
    Site management (on-site and remote monitoring) for the observational and interventionist studies.Monitoring studies on pre-clinics phase, phases II, III or IV using primary or secondary data collection.Perform the quality review for studies conducted in collaboration, stablishing a relevant relationship with researchers and the company. Therapeutic areas: rheumatology, neurology, transplants, cardiology, Dermatology Coordinate the monitoring activities within the department and responsible for training the new CRAs.Additional activities:* support Study Manager in the eCRF review, * support Study Manager in the Monitoring Plan construction,* support Study Manager in the Protocol review,* support Department Manager in the Medical Writing of protocol synopsis.
  • Novartis
    Medical Affairs/Rwe Cra Jr.
    Novartis Dec 2018 - Mar 2021
    São Paulo, São Paulo
    CRA Jr. - Strategic Evidence Generation department at Novartis S.A Brasil (medical affairs).Job description:Site management (on-site and remote monitoring), observational or interventionist studies and monitoring RWE studies with primary and secondary data collection. Therapeutic areas: rheumatology, neurology, transplants, cardiology. Additional activities:* support Study Manager in the eCRF review, * support Study Manager in the Monitoring Plan construction,* support Study Manager in the Protocol review,* support Department Manager in the Medical Writing of protocol synopsis.
  • Boehringer Ingelheim
    Regulatory Affairs Associate (Clinical Research)
    Boehringer Ingelheim Sep 2017 - Nov 2018
    São Paulo, São Paulo
    - End-to-end of regulatory process to competent authorities (MoH - ANVISA) , ensuring they are in full compliance to international and local regulations for clinical trials, access programs, compassionated use and post- study drug supply in Brazil.- Regulatory inteligence - Process otimization
  • Johnson & Johnson
    Business Quality Analyst - Medical Devices
    Johnson & Johnson Aug 2015 - Aug 2017
    São José Dos Campos E Região, Brasil
    Member of the Center of Excellence for Product Complaints, specialist managing product complaints for all countries of Latin America in compliance with local regulations and the quality standards of Company.  Metrics specialist building data about general complaints, our and sales force timeliness, quantity of reported events, etc.  Training the Trainer - Trained by developers of the system used to manage the product complaints to train the local users of LATAM
  • Docs
    Clinical Trial Associate - Amgen Partner
    Docs Mar 2014 - Aug 2015
    São Paulo E Região, Brasil
    Support for all clinical trial and regulatory operations of Brazil, Argentina, Peru, Colombia and Chile (start-up and close-out of sites, contact with local and global clinical research teams), insert site ́s data in specific data-bases and update TMF with all documents. Experience with initiation process of studies in start-up preparing and collecting documents of submission in Ethic Committees and Regulatory Agencies, in compliance with GCP-ICH and other local regulations (FDA, ANVISA, ANMAT etc.).
  • Novartis
    Cra Jr.
    Novartis Mar 2012 - Mar 2013
    Argentina, Buenos Aires
    In charge of monitoring all documents/medicines, CRF, materials and equipments of sites, site staff trainings, to manage and correct problems (in case), initiation and closing out visits, making reports and follow up letters. Experience with cardiology, respiratory, transplants and reumatology areas in blinded or double-blinded studies.

Luisa Campos Skills

Pharmaceutical Industry Clinical Trials Gcp Ich Gcp Clinical Monitoring Clinical Research Cro Biotechnology Ich Guidelines Regulatory Affairs English Medical Devices Molecular Biology Regulatory Submissions Powerpoint Microsoft Excel Microsoft Office Product Complaints

Luisa Campos Education Details

Frequently Asked Questions about Luisa Campos

What company does Luisa Campos work for?

Luisa Campos works for Iqvia

What is Luisa Campos's role at the current company?

Luisa Campos's current role is Clinical Trial Manager - partner with Boehringer Ingelheim.

What is Luisa Campos's email address?

Luisa Campos's email address is bc****@****ail.com

What schools did Luisa Campos attend?

Luisa Campos attended Universidade De São Paulo / Usp, Harvard Medical School, Harvard Medical School.

What are some of Luisa Campos's interests?

Luisa Campos has interest in Poverty Alleviation, Children.

What skills is Luisa Campos known for?

Luisa Campos has skills like Pharmaceutical Industry, Clinical Trials, Gcp, Ich Gcp, Clinical Monitoring, Clinical Research, Cro, Biotechnology, Ich Guidelines, Regulatory Affairs, English, Medical Devices.

Who are Luisa Campos's colleagues?

Luisa Campos's colleagues are Ryan Clee, Pt, Dpt, Saurabh Tyagi, Chen Liang, Suchismita Sikdar, Purnima Gopinathan, Jenita Mascarenhas, Mba, Pmp, Kahina Mousi.

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