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Senior Statistical Programmer
PAREXEL International Corporation
Own the challenges that lead to innovation and growth
Promoted to Head of Biotech Operations for Americas East, helping clients develop novel therapies with a focus on patient needs.
Advanced to Corporate VP Clinical Operations to lead Site Monitoring for Americas, Europe and SE Asia.
Streamlined Parexel’s clinical operations model; driving effectiveness, and increasing employee, client and site satisfaction.
Promoted to VP Clinical Operations, and relocated to the US in 2017.
Promoted to Senior Director of Clinical Operations for the Americas, consolidating both North and South American regions.
Joined Parexel as Director of Global Monitoring Operations for Latin America.
Create the solutions that drive global projects to success
Promoted to Senior Director, Project Management. Taking on management responsibilities for dedicated Enterprise accounts and enhancing his contributions to Parexel’s Global Project Leadership.
Managing Project Director role for dual Enterprise accounts, with a focus on client delivery and satisfaction in order to bring in new awards and expand growth.
Assumed the role of Global Project Leadership Training Coordinator, ensuring new PLs are properly inducted in all regions, while leading cross regional meetings to review and update training materials for PLs.
Promoted to Associate Director in Project Management at Parexel working on post-approval smoking cessation treatment.
Joined Parexel as a Senior Project Lead mentoring and managing 5 project managers working on a phase IV smoking cessation treatment.
Be part of a diverse team that drives healthcare innovation
Advanced into Senior Manager, Human Resources
Promoted to Manager, Human Resources Operations
Joined Parexel as a Human Resources Operations Partner.
Human Resources Business Partner at leading pharmaceutical company.
Manager of Diversity Resources.
Contribute to meaningful advances that benefit patients in need
Joined the Scientific Data Organization as Scientific Data Technology Director, creating agile access to real world data, bringing best in class technology solutions to Parexel services, and harnessing data to transform therapy development for patients.
Promoted to Director IT Project and Programme Office, leading engineering projects for Wearable and Sensor devices with a view to streamlining Clinical Trials patient engagement and approaches.
Promoted to Associate Director of IT Program and Project Management at Parexel.
Joined Parexel as a Project Manager in the IT Project Program Office.
Own the challenges that make you grow
Promoted to Senior Medical Writer, focusing on the development and support of clinical documents intended for regulatory submission.
Began a new role working remotely as a Medical Writer II, researching and coordinating the development of clinical documents intended for submission to the FDA or other regulatory authorities.
Director of Imaging Operations leading a team of 13 Project Managers and the imaging of over 130 clinical trials.
Senior Project Manager, overseeing standardization of program operations and deliverables while leading a team of Project and Imaging Research Managers.
Promoted to Project Manager for clinical oncology trials.
Joined Parexel as an Imaging Research Associate on clinical trials utilizing medical imaging.
Forge the relationships that elevate customer experience
Corporate Vice President, General Manager – Japan
Vice President, Growth Accounts
Senior Director of Business Development at Parexel.
Associate in the Proposal Development department at Parexel.
One of the founders and Marketing Director of an IT venture company developing web related systems
Voice the ideas that get treatments to patients faster
Promoted to Senior Director of Clinical Application Development and Technology.
Promoted to Associate Director of IT.
Promoted to Senior Programmer.
Joined Parexel in Clinical IT.
Received Master's in Computer Applications.
Own the challenges, program your future
Promoted to Senior Manager, Statistical Programming FSP, with increasing responsibilities for department development and team supervision.
Advanced to Statistical Programming Manager, responsible for a dynamic, multinational team of over 12 people.
Increased responsibility, leading projects and managing small teams as a Principal Statistical Programmer / Associate Manager.
Promoted to Senior Statistical Programmer, participating in high profile trials for diverse range of sponsors, as main programmer.
Referred by a friend to join Parexel as a Statistical Programmer, taking the opportunity to further develop my programming skills in 4GL language using SAS® .
Natalia – Head of Biotech Operations for Americas East
Ruben – Senior Director
Deborah – Senior Manager
Scientific Data Technology Director
Nicholas – Senior Medical Writer
Shigehiro – Corporate Vice President, General Manager – Japan
Naresh – Senior Director of Clinical Application Development
Pawel – Senior Manager
Senior Statistical Programmer
Chengdu, Sichuan, China
As a member of Parexel’s Statistical Programming group, you will be heavily involved in leading trials to successful completion, working in close collaboration with sponsor teams, and Parexel teams in differing locations. Depending on your career goals, you will be provided the opportunity to be exposed to a variety of different sponsors, products and therapeutic areas, or choose to focus your career on working with a specific sponsor and gaining in depth knowledge of a specific therapeutic area and compound.
You will become a part of a team with an inherent breadth of knowledge and expertise in small, single center Investigator studies to multi-site, multi-national trials in Phases I to IV of clinical development, as well as observational studies. From initial planning meetings at the study design stage through to implementation and execution, our team of skilled statistical programmers will employ industry-accepted statistical tools and techniques, as well as innovative consulting, to provide the quality and efficiency of projects.
Parexel develops and delivers cost effective, high-quality training programs for those employees that are directly involved with sponsor functional partnerships to ensure that our statistical programmers can quickly step in to make significant contributions to the success of a study. In addition, you will receive the opportunity to shape your development through quarterly conversations with your manager.
Glassdoor Reviews and Company Rating
Check out the top traits we’re looking for and see if you have the right mix.
"I have learned a great deal and developed my expertise. The management team here is open and honest and it is refreshing to be treated with a high degree of trust and flexibility. I have been fortunate to work on a wide variety of projects and partnerships and the work is always interesting."
Richard – Principal Statistical Programmer
We are one truly global team working together to propel each client´s journey ahead faster.
We value work-life balance. We try and keep regular hours and an emphasis on life outside the office.
Opportunity to learn and grow through a performance and development goal-setting program.
Work with industry leaders and subject matter experts.
Opportunity to work on a wide range of therapeutic areas and medical devices.
Deliver best value and high quality service.
Ability to fill Statistical Programming Coordinator role on projects. The Statistical Programming
o Input into and negotiate statistical programming timelines. Ensure that timelines are
o Coordinate and lead a statistical programming team to successful completion of a study
within given timelines and budget.
o Monitor project resourcing, project budgets, and identify changes in scope.
Interact with Sponsors as the key contact with regard to statistical programming issues.
Provide technical support and advice to the internal team.
Check own work in an ongoing way to ensure first-time quality
Ensure quality control (QC) on all process and technical activities related to derived dataset, table,
listing, and figure programming in accordance with corporate quality standards,
WSOPs/Guidelines, ICH-GCP and/or other international regulatory requirements are performed.
Coordinate project start-up activities, including Unix/PMED project area set-up, creation of global
programs (e.g. setup.sas, formats.sas, etc.), tracking spreadsheets, and required documentation.
Assist in the production and QC of analysis plans, produce and QC TLF mock-shells, derived
dataset specifications, programming specifications, and other process supporting documents.
Use efficient programming techniques to produce and/or QC derived datasets tables, figures and
Understand regulatory requirements concerning industry technical standards (e.g. CDISC, 21 CFR
Part 11, electronic submissions, etc.) and implications for the department.
Provide input into monthly PERFORM forecasts and monitor the completion of forecasted units.
Create standard macros and applications to improve the efficiency of the department.
Maintain all supporting documentation for studies in accordance with WSOPs/Guidelines to
ensure traceability and regulatory compliance.
Be trained in sponsor WSOP’s and disseminate knowledge to project team members as
Proactively participate in and/or lead process/quality improvement initiatives.
Work closely with the Quality Management Groups (QMG) to ensure compliance with
WSOPs/Guidelines, ICH-GCP and any other applicable local and international regulations and
participate in internal/external audits and regulatory inspections as required.
Develop wider knowledge of SAS and other relevant programming languages and processes
within the GRO, Biostatistics, and Medical arenas.
Maintain and expand local and international regulatory knowledge within the clinical industry.
Assist project teams in the resolution of problems encountered in the conduct of their daily work
Provide relevant training and mentorship to staff and project teams.
Lead and supervise and/or create, implement and execute import and export programs, in either
standard format, client specific format or CDISC compliant format depending on nature of
Develop mapping specifications for data exports in accordance with applicable standards.
Ability to successfully work together with a (“virtual”) team (including international teams as
required) as well as independently.
Demonstrate strong organizational skills, ability to manage competing priorities, and be flexible to
Business/Operational skills that include customer focus, commitment to quality management and
Good business awareness/business development skills (including financial awareness).
Ability to create, maintain and define strategies to improve the efficiency of running a clinical trial.
Work effectively in a quality-focused environment.
Demonstrate commitment to refine quality processes.
Effective time management in order to meet daily metrics or team objectives.
Shows commitment to and performs consistently high quality work.
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Meet Amrita: Associate Manager Statistical Programmer
Amrita tells us about how Parexel has helped her grow within her career with working flexibility and opportunities to learn.
Roles within Data Operations
Impact patients with a role in Biostatistics, Statistical Programming and Data Management.
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