Clinical Trial Operations Leader

**Lead Clinical Trials Data Specialist Role Summary**">The ideal candidate will be responsible for leading single and/or multiple clinical trials, ensuring the development, maintenance, and validation of annotated Case Report Forms (aCRFs) as well as specifications and statistical programming of Standard Data Tabulation Model (SDTM) datasets, Analysis Data...

Study Operations SpecialistThis role is responsible for spearheading the initiation of clinical trials at various sites. The ideal candidate will forge meaningful relationships with study personnel, serve as the primary point of contact, and provide regular reports on key metrics related to trial start-up activities.Key Responsibilities:Collaborate with...

Job OverviewAs a Central Monitoring Manager, you will be responsible for overseeing the development and execution of centralized monitoring plans across studies.Ensure consistency with RBQM strategy by reviewing and interpreting data quality trends and operational signals to identify emerging risks at the study, country, and site levels.Lead and manage a...

Statistical Programming LeadWe are seeking an experienced Senior Statistical Programmer to lead the development and maintenance of clinical trial data. As a key member of our team, you will be responsible for creating high-quality annotated Case Report Forms (aCRFs), specifications, and statistical programming of Standard Data Tabulation Model (SDTM)...

Senior Clinical Project LeadIn this pivotal role, you will spearhead the success of our clinical trials. Your expertise will ensure that all activities and deliverables are completed to the highest standards, within predetermined timelines and budgets.A successful Senior Clinical Project Lead excels at creating project plans, driving task completion, and...

Responsible for the clinical operations of a project within a defined regional/global level. Provides oversight of project deliverables, assigned Clinical Research Associate (CRAs) and Investigator sites in accordance with the Monitoring Plan, Protocol, Good Clinical Practice (GCP), ICH guidelines and local regulations. The COL acts as a primary liaison...

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...

The Senior Clinical Analyst and Programmer will lead the programming activities for various purposes including different data listings to be used for data review, Safety Review Listings, Centralized Monitoring Listings and Reports. The Senior Clinical Analyst and Programmer will be responsible to gather, understand and analyze the needs reported by the Data...

Clinical Operations DirectorThe primary focus of this role is to oversee the operational aspects of clinical projects, ensuring seamless execution and compliance with regulatory guidelines.Leadership Responsibilities:Oversee project deliverables, CRAs, and investigator sites in accordance with the monitoring plan, protocol, GCP, ICH guidelines, and local...

The Clinical Data Coder is primarily responsible for providing support to activities related to coding of Clinical data for ongoing clinical studies. The Clinical Data Coder will also participate in various clinical data management activities required to ensure that data captured are collected, managed and reported clearly, accurately and securely. In...