[TU-05] | Technical Study Designer Home Based Mexico Iqvia Biotech

[TU-05] | Technical Study Designer Home Based Mexico Iqvia Biotech

20 feb
|
Reconocida empresa
|
México

20 feb

Reconocida empresa

México

Technical Study Designer Home Based Mexico Iqvia Biotech



Technical Study Designer Home Based Mexico Iqvia Biotech



IQVIA Biotech is seeking a Technical Study Designer for a home based opportunity Mexico City Mexico br br BASIC FUNCTIONS br br Design of data collection forms and data validation checks within an electronic data capture EDC system for conducting clinical trials Coordinate tasks and resource allocation for a given project under the supervision of a manager of Project Programming Develop training materials and assist with the development of data collection work practices as needed br br ESSENTIAL JOB FUNCTIONS DUTIES AND RESPONSIBILITIES br br Interpret the study protocol for design in EDC br Create study build timeline with input from internal and sponsor teams br Plan and conduct internal and sponsor team meetings for determining data collection requirements and for review of study designs br Design and update data collection forms based on study protocol requirements corporate standards best practices and feedback from internal and sponsor study teams br Create and update data validation edit check specifications based on study protocol requirements corporate standards best practices and feedback from internal and sponsor teams br Coordinate edit checks and custom function programming with programming leads br Deploy study design to test and production environments br Communicate any project risks to the project manager including the potential for missing a planned timeline and working outside of the original budget or scope of work expectations br Escalate potential quality issues to management br Comply with all training and standard operating procedures SOPs for the position br Responsible for multiple study design projects at the same time br May work on projects across multiple trial EDC platforms br Identify areas for process improvement and actively participate in process improvement initiatives as assigned by manager br Train and support junior Technical Study Designers to ensure they have necessary skills to meet their deliverable br Support and develop standards ensuring alignment with other functional groups associated with EDC workspace br br KNOWLEDGE SKILLS AND ABILITIES br br Knowledge of clinical research process and methodology br Knowledge and understanding of current GCP ICH and FDA guidelines and regulations applicable to conduct of clinical research br Ability to supervise resources and plan tasks for EDC development with the support of management br Ability to work creatively and independently to carry out assignments of a complex nature br Ability to manage multiple project timelines and regularly switch between projects as required to meet timeline deliverable expectations br Ability to communicate and work effectively and cooperatively with fellow employees and with sponsors br Ability to learn new programming languages technology and tools that will facilitate the clinical trial process br Excellent interpersonal and organizational skills required br Ability to train other staff br br MINIMUM RECRUITMENT STANDARDS br br Bachelor s degree in computer or biological life sciences br 5 years of work experience as a lead data manager or lead EDC programmer br Experience with web page and database design preferred br Equivalent combination of education training and experience br br CLASSIFICATION br br This position is classified as exempt under the Fair Labor Standards Act employees are not eligible for overtime compensation br br LI BN3 br br LI Remote



Requirements: Professional Bilingual English 80% Minimum experience: 5 years Proven working experience in project management Excellent client-facing and...

El anuncio original lo puedes encontrar en Kit Empleo:
https://www.kitempleo.com.mx/empleo/16285573/tu-05-technical-study-designer-home-based-mexico-iqvia-biotech-mexico/?utm_source=html

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