Clinical Data Manager

Our Client, an American Biotechnology company, is looking for a Clinical Data Manager for their Sunnyvale, CA/Hybrid location.Responsibilities:The candidate will manage design, develop, implement, validate, maintain, and support clinical databases related premarket or post market clinical studies/registries.The candidate will have an understanding of data design, development, implementation processes to develop EDC systems.The candidate will be responsible for adhering to the required departmental operating procedures regarding Data Management for clinical investigationsEssential Job Duties (Specific responsibilities and tasks an individual would be expected to perform in the role.Additional job duties may be determined by functional people manager)Develop project specific data management plan that includes design, creation and lifecycle management of data collection, validation, reporting specification and usage guidelines.Understand CRF design and interpret protocol requirements to efficient EDC design.Create clinical databases design specifications including edit check specifications.Experience with validation of EDCs at a study level including experience developing study requirements, test scripts, and UAT documentation.Administration of existing EDC systems for multiple studies simultaneously.Provide clinical data management support for study operations and analysis groups including the following.Assist in defining and creation of data listings, including programming software to generate listings.Data specifications and/or process data transfers in preparation for statistical review.Training users on EDC systems.Includes create of training documentation and running training sessions for end users.Data cleaning and review of clinical data. Including query management and data listing review.Manage postgo live issues and requests.Managing activities for multiple studies simultaneously in a dynamic environment.Contribute to development and/or maintenance of departmental operating procedures for data management.Proactive in understanding company needs/objectives and able to independently seek solutions.Works on significant and unique issues in critical situations and able to provide solutions proactively.Requirements:Required Skills and Experience: (Specific skills, knowledge, and experience that an individual must possess in order to successfully perform in job)Minimum of 35 years of data management experience with a proven track record working in a medical device/pharmaceutical industry.EDC system(s) experience (Preferably Medrio)Knowledge of Good Clinical Practices, Clinical research, Clinical trial process and related regulatory requirements and terminology.Required Education and Training: (As applicable Specific education and training that an individual must possess in order to successfully perform in job)BSc/BA in a scientific or medical fieldPreferred Skills and Experience: (As applicable Specific skills, knowledge, and experience that are not required to perform the job, but are desirable to have)Desired to have experience with SAS software.Desired to have medical knowledge as pertaining to medical devices for surgery.Excellent Interpersonal skillsWork well in a team environment.Work independently to carry out tasks with minimal guidance.Effective written communication and interpersonal skills.Why Should You Apply?Excellent growth and advancement opportunitiesICONMA is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to any status protected by applicable law.