- Conducting and internal monitoring of patient visits and documentation, ensuring that documents are reviewed in accordance with the protocol study and Good Clinical Practices (GCP/ICH);- Corrective actions highlighted in monitoring letters by sponsors;- Pharmacovigilance activities through the identification of adverse events related or not to the product under investigation, in order to guarantee the safety of the patient and that the benefits are greater than the risks;- Responsible for the medical evaluation of reported adverse events, as well as on the Case Report Form system;- Focus on attention to detail, dealing with different tasks and unexpected situations;- Flexibility in prioritizing activities according to the study and schedule of the project clinical research center.

• Conducting clinical trials in accordance with GCP/ICH, applicable SOPs and clinical trial protocols sponsored by CROs and pharmaceutical industries;• Assistance to the study coordinator in activities of research projects of phases II and III in the areas of proctology, gastroenterology, endocrinology and rare diseases;• Support in conducting clinical monitoring, such as communication with CRA to schedule visits, provision of data and documentation for review and meetings with sponsor and actions to correct findings monitoring;• Monitoring, scheduling and support of initiation and close-out visits of clinical studies;• Participation in meetings with principal investigators and study sponsors;• Review, collecting and filling in data, solving queries in CRFs (Medidata, Veeva and Laptec) to be in order in the anticipated schedule;• Monitoring the medication administration process in some study protocols;• Pending control of study activities in spreadsheets;• Document control: storage of electronic and physical documents (Binder, patient folders andfrom the pharmacy);• Activities for receiving and processing clinical trial supplies;• Completion and submission of adverse events that occurred during the studies;• Recruitment, reimbursement and scheduling of visits for research participants.

• Prepare and review of regulatory documentation (Protocol, Informed Consent, budget, study calendar, among others) for activation of the research center;• Completion of feasibility questionnaires with information from center;• Submit submissions to ethics and regulatory to the Ethics Committee (EC) via Brazil Platform within specific deadlines;• Contact with the Regulatory & Study Start-Up and Study Start-Up Specialist team;• Preparation of document forwarding letter and review of documents for submission;• Completing and updating spreadsheet submissions;• Verification of expired documents and charge for updating (team resume, GCP certificate anddocument of the respective Council of the professional).

• Consumer Technical Insights Intern - Personal Care for Unilever Latin America;• Innovation projecs with brands: Seda, Dove and Tresemmé;• Claims development for Hair Care LatAm;• Participation in new product development projects;• Insertion of agile methodology (Scrum) for project execution;• Work with multi-functional teams based in Latin America and global development centers in the UK;• Interface with multifunctional teams based in Latin America and Global Development Centers;• Use of digital tools for analyzing ingredients and consumer preference;• Studies of understanding routine and consumer habits;• Participation in meetings with global teams.

• Consumer Technical Insights Intern - Home Care and Pet Care Products for Unilever Latin America;• Innovation projecs with brands: OMO, Brilhante, CIF and Cafune;• Development of behavioral research and analysis through social media;• Opportunities to improve the brand's performance;• Interface with the Consumer Marketing Insights (CMI) team for communication through data intelligence and behavioral insights;• Data organization, analytical and strategic vision, analysis of consumer behavioral data;• Monitoring the context of connection between the technician and the final consumer;• Support in claims validation and product demonstrations; •Interface with regulatory affairs teams to evaluate legal requirements of regulatory agencies such as ANVISA and Ministry of Agriculture and Livestock and approval of product benefits;• Support area coordinators in the activities of project to assist in your knowledge;• Support in development activities in the laboratory.

• Recruitment of research participants for clinical studies;• Organization and archiving of documents, such as informed consent, study protocols, contracts and receipts of compensation to participants;• Participation of health education events for the population.