Senior Associate, Central Monitor, Risk Based Monitoring, CDS
1 week ago
BASIC QUALIFICATIONS:
Bachelor's degree or above of equivalent experience in a scientific or business related discipline required. 3 - 5 years working experience in the clinical development fields. Working knowledge of clinical development process, understanding concepts of Phase I-IV and principles of study design Previous experience within a data management role, understanding key processes and principles associated with role including CRF design, database set-up, edit check specification, DMPs and data cleaning activities Knowledge of clinical trial database and its applications Knowledge of Windows Environment and its applications (Word, Excel, PowerPoint, Project, etc.) Experience in Oracle, PL/SQL, SAS, Java, relational database design and database programming skills.Technical Skill Requirements:
Technical expertise and business experience in supporting clinical trials database development, data management, site monitoring, etc. Thorough understanding of the processes associated with clinical study management, data management, and regulatory operations. Project management skills and technical capabilities as well as effective verbal and written communication skills in relating to colleagues and associates both inside and outside the organization. Works independently, receives instruction primarily on unusual situations Ability to organize tasks, time and priorities; ability to multi-task Ability to communicate effectively and appropriately with internal & external stakeholders, locally and globally Strong understanding of the state-of-the-art technologies to evaluate and leverage them into improved business processes for worldwide deployment and adoption.Pfizer is an equal opportunity employer and complies with all applicable equal employment opportunity legislation in each jurisdiction in which it operates.
Medical#LI-PFE-
Senior Central Monitor
1 week ago
Chennai, Tamil Nadu, India Pfizer Full timeBASIC QUALIFICATIONS:7 years working experience in the Central Monitoring (RBM)Experience in Oracle, PL/SQL, SAS, Java, relational database design and database programming skills.Working knowledge of clinical development process, understanding concepts of Phase I-IV and principles of study designPrevious experience within a data management role,...
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Senior Central Monitor
1 week ago
Chennai, Tamil Nadu, India Pfizer Full timeBASIC QUALIFICATIONS: years working experience in the Central Monitoring (RBM)- Experience in Oracle, PL/SQL, SAS, Java, relational database design and database programming skills.- Working knowledge of clinical development process, understanding concepts of Phase I-IV and principles of study design- Previous experience within a data management role,...
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