Project Programming Manager, Mexico, IQVIA Biotech

IQVIA Biotech is seeking a Project Programming Manager to join our growing team in Mexico. This role can be home-based or office-based in Mexico

BASIC FUNCTIONS:

Provide management, leadership, and training for the project programming group.  Manage staffing of projects and coordinate task assignments with other IQVIA Biotech departments and/or external vendors.  Manage the Clinical Data Processing System (CDPS) development process and set appropriate standards for development and testing.   Develop internal tools and add-ons to facilitate the processes and work flow for Data Management, Clinical Reporting, and Quality Control.  Maintain responsibility for the quality and completion of all projects within the programming group. 

ESSENTIAL JOB FUNCTIONS, DUTIES AND RESPONSIBILITIES:

• Supervise and train Project Programming staff.
• Oversee all programming activities related to EDC development.
• Coordinate training to enable Project Programming staff to take on Lead Programmer responsibilities for projects.  Oversee and mentor the Leads in their activities.
• Ensure adequate staffing of all project teams and coordinate requests for support from other IQVIA Biotech departments and/or external vendors.
• Assist other peer managers (Quality Control, Clinical Reporting, and Data Management) in the development and documentation of processes and procedures to improve the efficiency and quality of Project Programming activities.
• Manage the development of templates and libraries for eCRFs and validation.
• Review proposals and budgets to ensure that tasks and budget allocations are aligned with customer requests.  Once projects are awarded, work with Programming staff to ensure that budget allocations are adhered to.
• Identify areas for Project Programmer contribution to corporate activities and goals, and assist in the implementation of any necessary training, programs, or assignments.
• Manage the development and validation of internal tools and add-ons for use with EDC to increase efficiency and facilitate the workflow for Quality Control, Clinical Reporting, and Data Management.

KNOWLEDGE, SKILLS AND ABILITIES:

• Knowledge of clinical research process and methodology.
• Understanding of current GCP, ICH, and FDA guidelines and regulations applicable to conduct of clinical research.
• Ability to utilize electronic data processing systems in gathering, storing, retrieving, and analyzing data.
• Knowledge of programming and validation methods.
• Detailed technical knowledge of one or more relevant EDC packages.
• Ability to plan long-range needs with a high degree of accuracy while assuming responsibility for daily details.
• Ability to work creatively and independently to carry out assignments of a complex nature.
• Ability to work effectively and cooperatively with other professional staff members.
• Excellent organizational and program documentation skills, highly detail-oriented.
• Commitment to state-of-the-art data management & reporting procedures, as well as technologies and relevant advancements in research methodology.
• Willingness to learn new programming languages, new technology, and new tools that will facilitate the clinical trial process.

CRITICAL JOB FUNCTIONS IN ACCORDANCE WITH ADA CRITERIA:

• Very limited physical effort required to perform normal job duties.

MINIMUM RECRUITMENT STANDARDS:

• BS or Associate Degree in Computer Science or related field, with a minimum of 3 years of relevant programming or data processing experience; or Bachelor’s degree in a non-computer field with a minimum of 5 years of relevant programming or data processing experience  
• Minimum 5 years of external management experience, or 3 years internal experience as a senior-level Programmer.  
• Excellent interpersonal and organizational skills required.

#LI-VW1

#LI-REMOTE

At IQVIA, we believe in pushing the boundaries of human science and data science to make the biggest impact possible – to help our customers create a healthier world. The advanced analytics, technology solutions and contract research services we provide to the life sciences industry are made possible by our 67,000+ employees around the world who apply their insight, curiosity and intellectual courage every step of the way. Learn more at jobs.iqvia.com.