Clinovo’s mission is to empower healthcare and life science companies by providing expertise in sourcing and placing top clinical research professionals across a multitude of diverse opportunities. We have a proven track record with pharmaceutical, biotechnology, diagnostic, medical device, and CRO customers. Leading companies have chosen Clinovo as their preferred partner for its quality of customer service, excellent candidate profile, and its long-term relationships.

SUMMARY:

Our valued Client is currently seeking a highly skilled and motivated and experienced technical expertise to develop a process methodology for the department to meet internal and external clients’ needs. Planned and coordinated the development of integrated programming solutions serving the full spectrum of statistical programming needs. Provide technical expertise and leadership to the department. Provide internal consulting services, including specifications and user needs analysis for a complex project or client requirements.

RESPONSIBILITIES:
• Perform, plan coordinate, and implement the following for complex studies: (i) the programming, testing, and documentation of statistical programs for use in creating statistical tables, figures, and listing and (ii) the programming of analysis datasets (derived datasets) and transfer files for internal and external clients and (iii) the programming quality control checks for the source data and report the data issues periodically.
• Ability to interpret project-level requirements and develop programming specifications, as appropriate, for complex studies.
• Provide advanced technical expertise in conjunction with internal and external clients, and independently bring project solutions to SP teams and the Statistical Programming department, for complex studies.
• Fulfil project responsibilities at the level of technical team lead for single complex studies or groups of studies.
• Directly communicate with internal and client statisticians and clinical team members to ensure an appropriate understanding of requirements and project timelines.
• Estimate programming scope of work, manage resource assignments, communicate project status, and negotiate/re-negotiate project timelines for deliverables.
• Use and promote the use of established standards, SOP, and best practices.
• Provide training and mentoring to SP team members and Statistical Programming department staff.
Preferred Skills and Experience:
• Statistical programming in SAS within the CRO/Pharmaceutical/Biotechnology/Healthcare industries
• Experience as technical team lead directly engaging clients and coordinating tasks within a programming team
• In-depth knowledge of applicable clinical research regulatory requirements, i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines
• Knowledge of statistics, programming, and/or clinical drug development process
• Advanced knowledge of Base SAS, SAS/STAT, SAS Graph, and SAS Macro Language
• Good organizational, interpersonal, leadership, and communication skills
• Ability to independently manage multiple tasks and projects
• Ability to delegate work to other members of the SP team
• Excellent accuracy and attention to detail
• Ability to delegate work to other members of the SP team [SPM]
• Exhibits routine and occasionally complex problem-solving skills
• Recognizes when negotiating skills are needed and seeks assistance.
• Ability to lead teams and projects and capable of managing at a group level
• Ability to establish and maintain effective working relationships with co-workers, managers, and clients
REQUIREMENTS: Master’s degree in computer science or related field and 3 years relevant experience; bachelor’s degree or educational equivalent in computer science or related field and 5 years relevant experience; or equivalent combination of education, training and experience
* Please note, that the compensation offered to the final candidate depends on relevant work experience, skills, and years of experience.

Location: Remote Role


Clinovo is an Equal Opportunity Employer and prohibits discrimination and harassment of any kind.

Clinovo’s mission is to empower healthcare and life science companies by providing expertise in sourcing and placing top clinical research professionals across a multitude of diverse opportunities. We have a proven track record with pharmaceutical, biotechnology, diagnostic, medical device, and CRO customers. Leading companies have chosen Clinovo as their preferred partner for its quality of customer service, excellent candidate profile, and its long-term relationships.

SUMMARY:

Our valued Client is currently seeking a highly skilled and motivated and experienced technical expertise to develop a process methodology for the department to meet internal and external clients’ needs. Planned and coordinated the development of integrated programming solutions serving the full spectrum of statistical programming needs. Provide technical expertise and leadership to the department. Provide internal consulting services, including specifications and user needs analysis for a complex project or client requirements.

RESPONSIBILITIES:
• Perform, plan coordinate, and implement the following for complex studies: (i) the programming, testing, and documentation of statistical programs for use in creating statistical tables, figures, and listing and (ii) the programming of analysis datasets (derived datasets) and transfer files for internal and external clients and (iii) the programming quality control checks for the source data and report the data issues periodically.
• Ability to interpret project-level requirements and develop programming specifications, as appropriate, for complex studies.
• Provide advanced technical expertise in conjunction with internal and external clients, and independently bring project solutions to SP teams and the Statistical Programming department, for complex studies.
• Fulfil project responsibilities at the level of technical team lead for single complex studies or groups of studies.
• Directly communicate with internal and client statisticians and clinical team members to ensure an appropriate understanding of requirements and project timelines.
• Estimate programming scope of work, manage resource assignments, communicate project status, and negotiate/re-negotiate project timelines for deliverables.
• Use and promote the use of established standards, SOP, and best practices.
• Provide training and mentoring to SP team members and Statistical Programming department staff.
Preferred Skills and Experience:
• Statistical programming in SAS within the CRO/Pharmaceutical/Biotechnology/Healthcare industries
• Experience as technical team lead directly engaging clients and coordinating tasks within a programming team
• In-depth knowledge of applicable clinical research regulatory requirements, i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines
• Knowledge of statistics, programming, and/or clinical drug development process
• Advanced knowledge of Base SAS, SAS/STAT, SAS Graph, and SAS Macro Language
• Good organizational, interpersonal, leadership, and communication skills
• Ability to independently manage multiple tasks and projects
• Ability to delegate work to other members of the SP team
• Excellent accuracy and attention to detail
• Ability to delegate work to other members of the SP team [SPM]
• Exhibits routine and occasionally complex problem-solving skills
• Recognizes when negotiating skills are needed and seeks assistance.
• Ability to lead teams and projects and capable of managing at a group level
• Ability to establish and maintain effective working relationships with co-workers, managers, and clients
REQUIREMENTS: Master’s degree in computer science or related field and 3 years relevant experience; bachelor’s degree or educational equivalent in computer science or related field and 5 years relevant experience; or equivalent combination of education, training and experience
* Please note, that the compensation offered to the final candidate depends on relevant work experience, skills, and years of experience.

Location: Remote Role


Clinovo is an Equal Opportunity Employer and prohibits discrimination and harassment of any kind.