Data Management Specialist

Job not on LinkedIn

🕒 June 24

Apply Now

Find Similar Remote Jobs

Set Up Email Alert For New Jobs

📊 Check your resume score for this job

Improve your chances of getting an interview by checking your resume score before you apply.

Upload Resume

SYNVIA

WebsiteLinkedInAll Job Openings

51 - 200 employees

Founded 1993

📦 Logistics

🚗 Transport

🤝 B2B

Logistics • Transport • B2B

SYNVIA is a logistics and transport company specializing in secure, compliant, and customized supply chain solutions for high‑value and sensitive industries. The company provides multimodal transport (road, air, maritime), temperature‑controlled and regulated warehousing (including ICPE), handling of dangerous goods, customs transit services, and value‑added operations like co‑packing, labeling and kitting. SYNVIA focuses on B2B clients in sectors such as chemistry, energy, agriculture, cosmetics and public hygiene, emphasizing traceability, regulatory compliance, and operational agility.

📋 Description

• Assist with data management activities in clinical research (Data Management); • Create, maintain, and manage Excel spreadsheets, Word documents, and PowerPoint presentations; • Prepare the Query Plan; • Perform database cleaning (Data Cleaning); • Manage queries (creation, tracking, and review of responses); • Program eCRF/IWRS in specialized software; • Provide support to study users (address questions, create user accounts, manage EDC access); • Prepare data management documentation (e.g., DMP, UAT, DBL, User Manual, IP Dispensing Manual); • Meet established deadlines for studies under your responsibility; • Complete all required training; • Serve as the point of contact (internal and external) for studies under your responsibility regarding data management; • Provide eCRF usage training when requested.

🎯 Requirements

• Bachelor's degree in Computer Science, Information Systems, Statistics, Business Administration, health-related fields (Biomedicine, Pharmacy, Nursing, Biology, Biological Sciences) or related areas; • Experience in data management for clinical research, preferably in CROs, research centers, or the pharmaceutical industry; • Experience in eCRF design and configuration (CRF design) within EDC systems; • Experience preparing Query Plans, performing Data Cleaning, and supporting Database Lock; • Knowledge of implementation and management of IWRS/IRT; • Familiarity with good clinical practice and regulatory requirements applicable to clinical research (ICH-GCP, ANVISA); • Intermediate to advanced English for reading protocols and regulatory documentation.

🏖️ Benefits

• Transportation allowance; • Parking (subject to availability); • Health insurance plan with no monthly premium for the employee; co-payment required for tests and consultations; • Dental plan with employee co-payment; • Life insurance at no cost to the employee; • Flexible meal/food allowance; • Pharmacy partnership/discount program; • Partnership with SESC; • Physical wellness program - TotalPass; • Day off for healthcare professionals; • Childcare assistance (per internal policy).