Sr Programmer Analyst II

This is a lead position contributing to functions of the programming roles within the Biostatistics and Programming Departments.Responsibilities include:Acts as the lead programmer on multiple studiesManages project timelines, budgets, and resourcesEffectively assigns and communicates priorities and work direction to ensure completion of assigned tasks on time and within budgetOversees the programming aspects of clinical trials from data extraction from trial databases through analysis and reporting, including integration of studies and submission data filesActively contributes to process improvement efforts including the leadership of solution teamsRepresents the department within the company and with interactions with client companies and regulatory agencies, as requiredInvolved in hiring, training, and mentoring staffLeads multiple projects including mentoring programming team members and may be assigned direct reports including Senior Programming Analyst, Programmer Analyst, and Associate Programmer AnalystThis is a lead position contributing to functions of the programming roles within the Biostatistics and Programming Departments.Responsibilities include:Acts as the lead programmer on multiple studiesManages project timelines, budgets, and resourcesEffectively assigns and communicates priorities and work direction to ensure completion of assigned tasks on time and within budgetOversees the programming aspects of clinical trials from data extraction from trial databases through analysis and reporting, including integration of studies and submission data filesActively contributes to process improvement efforts including the leadership of solution teamsRepresents the department within the company and with interactions with client companies and regulatory agencies, as requiredInvolved in hiring, training, and mentoring staffLeads multiple projects including mentoring programming team members and may be assigned direct reports including Senior Programming Analyst, Programmer Analyst, and Associate Programmer AnalystEducation and Experience:BA/BS degree in statistics, computer science, biostatistics, mathematics or related field5 years of SAS programming experience4 years clinical research or related experienceDemonstrated ability to successfully lead the programming elements of multiple clinical projects simultaneouslyMust have experience mentoring personnel and coordinating the work of project teamsMust have experience serving as a lead programmer on multiple projectsOr equivalent combination of education, training, and experience that provides the individual with the required knowledge, skills and abilities Knowledge, Skills and Abilities:Advanced SAS programming skills and understanding of database structuresGood organizational skills across individual projects. Ability to effectively organize, manage own and team work loads, and complete multiple assignments with challenging timelinesAbility to adapt and adjust to changing prioritiesExcellent written and verbal communication skillsAbility to work in a multi-disciplinary team settingBasic understanding of statistical principles applied to the design and analysis of clinical trialsAbility to contribute to development of policies. Ability to make decisions regarding programming on company policies and proceduresExcellent problem solving skillsAbility to supervise and mentor as shown by leadership of projects and team membersDemonstrated strong attention to detailAbility to facilitate communications with clients, project teams, departments and staffAwareness for project budget creation, including modifying for project updatesAbility to manage project budgets and risksKnowledge of clinical trials, ICH Statistical and reporting guidelines and GCPDelivery and Quality drivenWorking ConditionsWork is performed in an office environment with exposure to electrical office equipment. Frequently drives to site locations and frequently travels both domestic and internationalPhysical DemandsFrequently stationary for 6-8 hours per day. Repetitive hand movement of both hands with the ability to make fast, simple, repeated movements of the fingers, hands, and wrists. Moderate mobility required. Occasional crouching, stooping, bending and twisting of upper body and neck. Light to moderate lifting and carrying (or otherwise moves) objects including luggage and laptop computer with a maximum lift of 15-20 lbs. Ability to access and use a variety of computer software developed both in-house and off-the-shelf.Able to communicate information and ideas so others will understand; with the ability to listen to and understand information and ideas presented through spoken words and sentences.Frequently interacts with others, relates sensitive information to diverse groups both internally and externally. Ability to apply basic principles to solve conceptual issues. Performs a wide range of variable tasks as dictated by variable demands and changing conditions with little predictability as to the occurrence. Ability to perform under stress. Ability to multi-task. Regular and consistent attendance.Pharmaceutical Product Development, LLC is firmly committed to Equal Employment Opportunity (EEO) and prohibits employment discrimination for employees and applicants based on age, race, color, pregnancy, gender, gender identity, sexual orientation, national origin, religion, marital status, citizenship, disability or protected veteran or other status protected by federal, state, and/or local law.Education and Experience:BA/BS degree in statistics, computer science, biostatistics, mathematics or related field5 years of SAS programming experience4 years clinical research or related experienceDemonstrated ability to successfully lead the programming elements of multiple clinical projects simultaneouslyMust have experience mentoring personnel and coordinating the work of project teamsMust have experience serving as a lead programmer on multiple projectsOr equivalent combination of education, training, and experience that provides the individual with the required knowledge, skills and abilities Knowledge, Skills and Abilities:Advanced SAS programming skills and understanding of database structuresGood organizational skills across individual projects. Ability to effectively organize, manage own and team work loads, and complete multiple assignments with challenging timelinesAbility to adapt and adjust to changing prioritiesExcellent written and verbal communication skillsAbility to work in a multi-disciplinary team settingBasic understanding of statistical principles applied to the design and analysis of clinical trialsAbility to contribute to development of policies. Ability to make decisions regarding programming on company policies and proceduresExcellent problem solving skillsAbility to supervise and mentor as shown by leadership of projects and team membersDemonstrated strong attention to detailAbility to facilitate communications with clients, project teams, departments and staffAwareness for project budget creation, including modifying for project updatesAbility to manage project budgets and risksKnowledge of clinical trials, ICH Statistical and reporting guidelines and GCPDelivery and Quality drivenWorking ConditionsWork is performed in an office environment with exposure to electrical office equipment. Frequently drives to site locations and frequently travels both domestic and internationalPhysical DemandsFrequently stationary for 6-8 hours per day. Repetitive hand movement of both hands with the ability to make fast, simple, repeated movements of the fingers, hands, and wrists. Moderate mobility required. Occasional crouching, stooping, bending and twisting of upper body and neck. Light to moderate lifting and carrying (or otherwise moves) objects including luggage and laptop computer with a maximum lift of 15-20 lbs. Ability to access and use a variety of computer software developed both in-house and off-the-shelf.Able to communicate information and ideas so others will understand; with the ability to listen to and understand information and ideas presented through spoken words and sentences.Frequently interacts with others, relates sensitive information to diverse groups both internally and externally. Ability to apply basic principles to solve conceptual issues. Performs a wide range of variable tasks as dictated by variable demands and changing conditions with little predictability as to the occurrence. Ability to perform under stress. Ability to multi-task. Regular and consistent attendance.Pharmaceutical Product Development, LLC is firmly committed to Equal Employment Opportunity (EEO) and prohibits employment discrimination for employees and applicants based on age, race, color, pregnancy, gender, gender identity, sexual orientation, national origin, religion, marital status, citizenship, disability or protected veteran or other status protected by federal, state, and/or local law.