Bruno Colla Email & Phone Number

State Of São Paulo, Brazil

São Paulo, São Paulo, Brasil

• Complete appropriate therapeutic, protocol and clinical research training to perform job duties.• Gain experience in study procedures by working with experienced clinical staff.• Under close supervision, perform site monitoring visits (selection, initiation, monitoring and close out visits) in accordance with contracted scope of work and good clinical practices.• Under close supervision, administer protocol and related study training to assigned sites and establishes regular lines of communication with sites to manage ongoing project expectations and issues.• Under close supervision, evaluate the quality and integrity of study site practices related to the proper conduct of the protocol and adherence to applicable regulations. Escalate quality issues as appropriate.• Manage the progress of assigned studies by tracking regulatory submissions and approvals, recruitment and enrollment, Case Report Form (CRF) completion and submission,and data query generation and resolution.• Under close supervision, ensure copies/originals (as required) site documents are available for filing in the Trial Master File (TMF) and verify that the Investigator's Site File (ISF) is maintained in accordance with Good Clinical Practice (GCP) / International Conference on Harmonization (ICH) and local regulatory requirements.• Under close supervision may support start-up phase.• Under close supervision,create and maintain appropriate documentation regarding site management,monitoring visit findings and action plans by submitting regular visit reports, generating follow-up letters and other required study documentation.• Collaborate and liaise with study team members for project execution support as appropriate.• If applicable, learn key facets for successful development of project subject recruitment plan on a per site basis. Suggest ideas for improving site recruitment plan in line with project needs to enhance predictability. Assist in tracking subject site recruitment progress.

São Paulo, São Paulo, Brasil

- Assist Project Managers (PMs) and Clinical Research Associates (CRAs) in the administrative tasks related to studies under their responsibility in accordance with GCP-ICH, local regulatory requirements, SOPs and Intrials quality standards;- Organization and maintenance of project / clinical study documents (TMF);- Support and manage site communication in post-trials;- Provide support on study feasibility activities – first approach with sites per phone call or e-mail.- Support CRAs during monitoring visits to perform activities related to Investigational Product accountability and inventory review or ISF review- Remote contact with sites to follow up regarding study related matters, as requested by PM / CRAs;- Preparation and maintenance of spreadsheets with study contacts, including sites, vendors, and Sponsor- Preparation and maintenance of spreadsheets with study contacts, including sites, vendors, and Sponsor;- Assist in the review of clinical operations SOPs;- Assist study team during audit;- Assist QAM and IT during implantation of internal systems (training, e-learning, eTMF, CTMS, etc.).

São Bernardo Do Campo, São Paulo, Brazil

Analysis and completion of feasibility questionnaires, assistance in the preparation of initial package for submission of studies in Brazil Platform, filling and meeting of documents sources intermediating principal investigator and sponsor of the study. Assistance in the training of the research center team, control of CVs and certificates of the Investigator as well as the entire delegated team to participate in the study in question, scheduling, and monitoring of qualification visits, and initiation visits from CROs and Sponsors.

São Paulo, São Paulo, Brasil

Neuroproteomic analysis from the venom of the dark brown scorpion (Tityus Bahiensis) by biochemical techniques of separation and identification of molecules, fractionation and isolation of toxins by HPLC (High-Performance Liquid Chromatography), determination of the purity of toxins and molecular masses by mass spectrometry in MALDI-TOF (matrix-assisted laser desorption/ionization-time of flight) method, manipulation of animals, stereotactic surgery for the implantation of cannulas and electrodes in the hippocampus, intracerebral injection, recording of brain electrical activity, perfusion for removal of the encephalon, and histology for tissue analysis, slide preparation, and histopathological evaluation.

Barueri, São Paulo, Brasil

Follow-up and issued Pharmacovigilance reports for patients who were in treatment with the immunobiological Risanquizumab for moderate to severe plaque psoriasis.

São Paulo, São Paulo, Brasil

I performed front-line RT-PCR immunochromatographic analysis for rapid SARS-CoV-2 testing in a field laboratory at Expo Center Norte.

Chácara Santo Antônio - São Paulo

I developed personalized work in the publication of corporate acts and financial statements and offered our customers all the necessary assistance and support. With an experienced and dynamic team, it was responsible for the negotiation, layout, proofreading, and publication, in addition to the follow-up and execution of the registrations at the State Boards of Trade, including the Basic Entry Document (DBE). Perfect execution of the necessary actions, with perfect compliance with deadlines and excellence in all stages of the activities.

São Paulo E Região, Brasil

I worked as a Capital Markets commercial assistant, performing the mandatory publications of IPOs for our client portfolio. Prospecting, follow-up, quotes, and textual revision of the publications were part of my daily routine at this company.

Postgraduate Degree, Pesquisa Clinica E Medical Affairs

- Medical development and Pharmacology; - Dermocosmetics; - Herbal medicine; - Epidemiology and Biostatistics; - Management in Clinical.

Bacharelado, Biomedicina