Report Preparation Assistant

Role Summary

The assistant will support the preparation, organization, checking, updating and review of reports related to relative bioavailability and bioequivalence studies. You will work on processing and organizing information, contributing to the quality, accuracy and meeting deadlines of demands, in addition to providing support to the area's activities and the teams involved in the studies.

Training

Completed higher education or studying Statistics or related areas.

Knowledge

• Computer knowledge;
• Office Package;
• Intermediate Excel;
• Programming skills;
• Basic English;

Knowledge of statistics and/or statistical software is desirable.

• Salary + Benefits;
• Hiring information
• Type of contract: Temporary – 6 months

Reason: Maternity leave coverage.

Requirements

• Assist in the preparation, checking, printing and organization of statistical reports on relative bioavailability/bioequivalence studies, in accordance with current technical standards.
• Assist in the preparation, checking and updating of spreadsheets with pharmacokinetic data from studies, according to established models and procedures.
• Support research into bibliographic references related to determining sample size, using websites, scientific articles and specialized literature.
• Support the performance of statistical analyzes and simulations, using appropriate statistical software, under the guidance of the responsible team.
• Keep study databases updated, ensuring organization and ease of consultation of information.
• Assist in reviewing sections of clinical protocols related to the statistical stage, including information on sample size, design and statistical methods.
• Assist in sending results, spreadsheets and simulations by email to the departments involved, according to requests received.
• Assist in preparing and checking randomization lists for different study designs.
• Support the completion of documents and forms requested by clients, including documents related to budgets and post-study activities.
• Provide statistical support to the Protocol sector, carrying out research, surveys and simulations under guidance.
• Make notes and update studies in the Microsiga management system, as well as organize and attach the relevant documents.
• Support the organization and control of documents and statistical information from studies, ensuring that records are updated and available for consultation.
• Perform other related activities, as directed by the immediate superior.

About the Company

QIMA Life Sciences (ICF) is a fast-growing division of the QIMA Group dedicated to providing end-to-end services for the life sciences industry – from R&D to market launch.

In Brazil, we operate through 5 entities – ICF, Apex Science, Labmass, Lychnoflora and CP Quali – with 450 talented professionals who provide services ranging from clinical trials to quality control.

QIMA is more than a testing, inspection, certification and compliance company. We are on a mission to provide customers with smart solutions to create products that consumers can trust. With a global reach spanning more than 100 countries, QIMA serves the consumer products, food and life sciences industries, supporting more than 30,000 brands, retailers, manufacturers and food producers. The company combines local expertise with digital solutions to bring accuracy and visibility to quality, security and compliance data. What sets QIMA apart is its unique culture: 6,000 employees live and make decisions every day according to QIMA's values. With customer passion, integrity and a commitment to making things simple, QIMA continues to revolutionize the testing, inspection and certification industry.