Sr Manager, Stat Programming
About the role
This vacancy has now expired. Please see similar roles below...
Looking for a Sr Manager Stat Programming for ICON, Trivandrum.
If you are someone with around 10 years of experience in SAS Programming (early phase preferred) coupled with line management experience this might be the right opportunity for you.
Job Responsibilities
- As a Manager, the employee is expected to embrace and contribute to our culture of process improvement with a focus on streamlining our processes adding value to our business and meeting client needs.
- Read, ensure understanding and adhere to all assigned ICON SOPs and working procedures.
- Ensure team compliance with ICON systems and procedures.
- Collaborate with Biostatistics/Programming management team to review and assess existing SOPs/WPs and provide input into the revision process, as appropriate.
- Record all billable and non-billable time accurately into the appropriate time management system. Review/approve time sheets for assigned staff on a timely and accurate basis.
- Complete all assigned training, including any mandatory training courses in ICON's Training Management System (i earn) in compliance with ICON and departmental policies.
- Address any gaps identified by ICON's Corporate Training Department (CTD) in the completion of essential training for direct reports on a timely basis.
- Proactively assess, revise and improve the programming group's training process and requirements to meet changing industry standards and requirements.
- Identify and organize training needs of staff in coordination with ICON's CTD,as appropriate.
- Manage assigned programming team deliverables to ensure project objectives are met within budget, to agreed timelines and to the highest standard of quality.
- Develop and foster client relationships through the implementation of effective communication, project management and solution-based approaches for assigned programming teams.*Represent and/or offer significant contributions for the statistical programming function on specific sponsor partnerships/alliances that are considered large-scale and/or complex in nature.
- Develop and maintain resource projections for global teams in accordance with contract requirements to ensure appropriate planning and utilization of programming staff and to plan for competing priorities.
- Continually monitor assigned study team productivity and performance through utilization of systematic reporting to ensure approved KPls and quality standards are met consistently.
- Ensure senior level review, quality control and approval of programming deliverables for assigned studies, and implemenUfollow through on corrective action plans, as appropriate
- Ensure timely and realistic project and study-level programming plans are in place and maintained for assigned projects.
- Review and assess new technologies, industry standards and procedures with a view towards implementation across the global statistical programming organization.
- Lead process improvement initiatives assigned at a department and/or company level including scope, charter, project budget management and coordinate activities of a cross-functional team.
- Provide input into revenue forecasting and recognition and out-of-scope and change order documentation in a timely and efficient manner.
- Represent the Statistical Programming around internal/external audits and manage findings through resolution both operationally and within the Quality Management System.
- Complete assigned Business Development tasks, including timely review of statistical programming inputs into RFPs/RFls. In addition, to represent the Statistical Programming function in sponsor bid defence and/or capability meetings, as applicable.
- Liaise effectively with other managers in the Statistical Programming group to improve the effectiveness of the organization.
- Srive for excellence and act in a proactive and responsive manner to internal and sponsor needs.
- Demonstrate a constructive and flexible approach in managing project delivery, including problem solving, handling changing priorities and meeting study timelines.
- Proactively participate and contribute towards department goals, including sharing of technical knowledge and expertise, current literature reviews and process improvement initiatives.
- Preparation and delivery of presentations and attendance at appropriate scientific meetings and conferences.
- Keep Senior Management informed of project status in relation to quality, timelines and staff issues.
- Perform other tasks and duties as assigned by Senior Management.
A better career. A better world. A better you.
Our people are our greatest strength, are the core of our culture and the driving force behind our success. Throughout all levels of the company, our people have a drive to succeed and a passion that ensures what we do, we do well. We help you build exciting and rewarding careers, deliver results to help bring life-changing medicine and devices to market and maintain ICON’s success as an industry leader. See all locations Read more
Day in the life
Teaser label
Our PeopleContent type
BlogsPublish date
05/20/2024
Summary
Deepak is a Clinical Data Management Project Manager at ICON Strategic Solutions, the largest global provider of Functional Service Provision (FSP). He works as a dedicated resource within one of o
Teaser label
Career ProgressionContent type
BlogsPublish date
05/10/2024
Summary
Overcoming Resume Gaps In an ideal world, resumes would neatly showcase an uninterrupted career progression. However, In today's dynamic job market, it's not uncommon for professionals to encoun
Teaser label
Career ProgressionContent type
BlogsPublish date
05/10/2024
Summary
The Art of Customisation: How to Tailor Your CV for Any Role or Industry In today's competitive job market, a one-size-fits-all CV often misses the mark. To truly stand out and position yourself a
Who we are
Similar jobs at ICON
Salary
Location
Mexico, Mexico City
Department
Full Service - Corporate Support
Location
Mexico City
Remote Working
Office Based
Business Area
ICON Full Service & Corporate Support
Job Categories
Corporate Support
Job Type
Permanent
Description
ICON plc is a world-leading healthcare intelligence and clinical research organization. From molecule to medicine, we advance clinical research providing outsourced services to pharmaceutical, biotech
Reference
JR118122
Expiry date
01/01/0001
Author
Daniela GuerreroAuthor
Daniela GuerreroSalary
Location
Regional United States (PRA)
Department
Clinical Trial Management
Location
Multiple US Locations
Remote Working
Hybrid: Office/Remote
Business Area
ICON Full Service & Corporate Support
Job Categories
Clinical Trial Management
Job Type
Permanent
Description
At ICON, it’s our people that set us apart. Our diverse teams enable us to become a better partner to our customers and help us to fulfil our mission to advance and improve patients’ lives. Our ‘Own I
Reference
JR119792
Expiry date
01/01/0001
Author
Tina GeerAuthor
Tina GeerSalary
Location
Mexico, Mexico City
Location
Mexico City
Remote Working
Hybrid: Office/Remote
Business Area
ICON Full Service & Corporate Support
Job Categories
Study Start Up
Job Type
Permanent
Description
At ICON, it’s our people that set us apart. Our diverse teams enable us to become a better partner to our customers and help us to fulfill our mission to advance and improve patients' lives.ICON plc i
Reference
JR117178
Expiry date
01/01/0001
Author
Diego ToniniAuthor
Diego ToniniSalary
Location
Mexico, Mexico City
Location
Mexico City
Remote Working
Office Based
Business Area
ICON Full Service & Corporate Support
Job Categories
Drug Safety
Job Type
Permanent
Description
ICON plc is a world-leading healthcare intelligence and clinical research organization. From molecule to medicine, we advance clinical research providing outsourced services to pharmaceutical, biotech
Reference
JR119371
Expiry date
01/01/0001
Author
Florencia PistolesiAuthor
Florencia PistolesiSalary
Location
Belgium
Department
Clinical Monitoring
Location
Belgium
Remote Working
Remote
Business Area
ICON Strategic Solutions
Job Categories
Clinical Monitoring
Job Type
Permanent
Description
Voor 1 van z'n sponsors is ICON op zoek naar een Study Start Up Clinical Research Associate.Als SSU CRA ben je verantwoordelijk voor het hele proces voor 'green light'. Waar houdt onze sponsor zich me
Reference
2024-110108
Expiry date
01/01/0001
Author
Vanessa VerdicktAuthor
Vanessa VerdicktSalary
Location
Canada
Department
Clinical Trial Management
Location
Canada
Remote Working
Remote
Business Area
ICON Strategic Solutions
Job Categories
Clinical Trial Management
Job Type
Permanent
Description
ICON plc is a world-leading healthcare intelligence and clinical research organisation. From molecule to medicine, we advance clinical research providing outsourced services to pharmaceutical, biotech
Reference
2024-110505
Expiry date
01/01/0001
Author
Jonathan HolmesAuthor
Jonathan Holmes