Clinical Data Manager II

Join to apply for the Clinical Data Manager II (Argentina) role at Indero (formerly Innovaderm) Continue with Google Continue with Google Join to apply for the Clinical Data Manager II (Argentina) role at Indero (formerly Innovaderm) Get AI-powered advice on this job and more exclusive features. As a Clinical Data Manager II, you will ensure that data captured in multiple clinical trials undertaken or managed by Indero is collected, managed, and reported clearly, accurately and securely.This role will be perfect for you if:You want to work on studies end-to-end (involved from protocol review to database lock) You have the experience and confidence to lead multiple concurrent studies successfully as a Data Manager You enjoy working directly with clients and forming recommendations as needed ResponsibilitiesData Management leadMonitor study status (ie. enrollment, CRFs monitored/approved, etc.) on an ongoing basis Present deliverables to clients, gather feedback and propose solutions. Provide regular data status reports to the project team Oversee work of the Clinical Data Coordinator as required (quality, timeliness) Oversee vendors to ensure that timelines and deliverables meet sponsor and protocol requirements Is responsible for ongoing maintenance of the clinical database, including data review/cleaning during study conduct and during preparation for database lock/close. Conduct reconciliation between external data and data in the EDC system to ensure consistency, including reconciliation with sponsor safety databases for adverse events/SAE (Serious adverse events) data Study setup – TechnicalDevelop the data management plan (DMP) Build a study-specific clinical database using the EDC system: Design the electronic case report form (eCRF) Build the clinical database in the chosen EDC independently or with the support of an EDC programmer (determined based on the complexity of the system and study. Coordinate the validation and testing (UAT) of the clinical database Support the study team with the development of external systems capturing clinical data (ePRO or IWRS), ensuring that any data transfer requirements between these systems and the EDC are documented and tested appropriately. User training and supportDevelop eCRF completion guidelines and other training material Conducts training for site users/monitors on the clinical database Activate/de-activate new users in the clinical database in response to requests from the project manager and maintain records of such request Respond to users requiring assistance with the EDC system Database close/lockGenerate data listings and reports needed for data review in preparation for database close/lock Ensure that data management documentation is complete and up to date in the trial master file (TMF) Archive the clinical database and related documents Requirements:EducationB.Sc. or M.Sc, or in a related field of study Experience10 years of clinical data management experience in the pharmaceutical industry or in a CRO environment 5 years of experience as a lead data manager Extensive experience working with EDC systems (experience with Medrio and Medidata Rave preferred) Knowledge And SkillsHighly organized and detail-oriented Project planning and time management skills Strong verbal and written communication skills in English Understanding of the drug development process and of applicable regulations, including Good Clinical Practices (GCP), ICH Guidelines Good understanding of CDISC SDTM/CDASH standards Knowledge of MedDRA and WHODrug dictionaries, an asset Our company:The work environmentAt Indero, you will work with brilliant and driven colleagues. Our values are collaboration, innovation, reliability and responsiveness. We offer a stimulating work environment and attractive advancement opportunities.In this position, you will be eligible for the following perks:Flexible work schedule / work schedule : Home-based position Ongoing learning and development About InderoA Global Clinical Leader In DermatologyFormerly known as Innovaderm, Indero is a world-renowned expert and clinical research leader in dermatology. We have more than two decades of experience serving a broad range of indications, patient populations, administration routes, and drug classes, and a global footprint.Indero is a dual-focus CRO for dermatology and rheumatology, with 25+ years’ experience in clinical research and trial delivery. Our full-service approach – which includes everything from protocol design and patient recruitment to trial monitoring and biometrics – provides biotech and pharmaceutical sponsors with the rigorous scientific foundation and tailored expertise their studies need to reach the finish line efficiently and effectively. With capabilities in North America, Europe, Asia Pacific and Latin America; vast, continuously growing relationships with investigators and patients; and a dedicated research clinic through which we design and execute our own studies, Indero is the ideal CRO partner for clinical needs at global scale.Indero is committed to providing equitable treatment and equal opportunity to all individuals. As such, Indero will provide accommodations throughout the recruitment and selection process to applicants with disabilities, upon request. Indero only accepts applicants who can legally work in Argentina Seniority level Seniority level Not Applicable Employment type Employment type Full-time Job function Job function Research, Analyst, and Information Technology Industries Research Services Referrals increase your chances of interviewing at Indero (formerly Innovaderm) by 2x Sign in to set job alerts for “Clinical Data Manager” roles. CRA II or Sr CRA I - Argentina Home Based Sr CRA - Ophthalmology Experience Required (Home-based, Argentina) We’re unlocking community knowledge in a new way. Experts add insights directly into each article, started with the help of AI. #J-18808-Ljbffr