Parexel is in the business of improving the world’s health. We do this by providing a suite of biopharmaceutical services that help clients across the globe transform scientific discoveries into new treatments. From clinical trials to regulatory, consulting, and market access, our therapeutic, technical, and functional ability is underpinned by a deep conviction in what we do.  

Headquartered near Boston, Massachusetts and in Durham, North Carolina, and supporting clients in more than 100 countries, our almost 20,000 employees are united by one simple fact. We care. We’re not just the people with brains, we’re the people with heart.

As a global biopharmaceutical provider, each of us have the power to make real differences in people’s lives. We don’t take this responsibility lightly. Every project we touch could mean getting a life-changing medication to patients who need it as quickly as possible. It’s why we come to work every day. We’re not just the people with brains, we’re the people with heart. 

Parexel

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.

The Senior Statistical Programmer provides technical expertise for the conduct of clinical trials, acts as an internal subject matter expert in specific areas providing technical support and expert advice, and works independently to support various programming activities related to the analysis and reporting of clinical study data. In addition, the Senior Statistical Programmer can fill the Statistical Programming Lead role on projects, and liaise with sponsors, Biostatistics Leads, Data Management Leads, and other functional areas as required. Further, the Senior Statistical Programmer will monitor quality, timelines, resource allocation, and productivity in relation to budgets.

Skills: • Excellent analytical skills. • Proficiency in SAS. • Extensive knowledge and understanding of the programming and reporting process. • Knowledge of SOP's/Guidelines, ICH-GCP, and any other applicable local and international regulations such as 21 CFR Part 11. • Ability to learn new systems and function in an evolving technical environment. • Strong project management skills. • Strong organizational skills, ability to manage competing priorities, and flexibility to change. • Attention to detail. • Ability to successfully lead a global team. • Work effectively in a quality-focused environment. • Effective time management in order to meet daily metrics or team objectives. • Show commitment to and perform consistently high quality work. • Business/operational skills that include customer focus, commitment to quality management, and problem solving. • Demonstrate commitment to refine quality processes. • Good presentation skills. • Good business awareness/business development skills (including financial awareness). Knowledge and Experience: • Competent in written and oral English. • Excellent communication skills. Education: • Educated to degree level in a relevant discipline and/or equivalent work experience.

Senior Statistical Programmer

Are you ready to make your mark in the healthcare industry using your ingenuity and technical expertise? At Parexel, there's no limit to what you can accomplish. We work with the top 50 global pharmaceutical companies, the top global biotech companies, and hundreds of small and emerging companies. We've supported the development of some of the most important treatments of our time, including nearly all of the 50 top selling drugs currently on the market. Join us and you'll make a profound difference in millions of lives. With a role in our Information Technology group, you'll work with cutting-edge technology on internal and client-facing projects. Collaborating with people from all over the world and touching everything from enterprise systems and clinical applications to infrastructure and networking, you'll keep our data safe and confidential. You'll have the chance to develop your skills and pursue advancement opportunities that include managerial and technical tracks. If you have stellar coding and design experience and a passion to learn more about healthcare, Parexel invites you to discover our rewarding opportunities in Enterprise Architecture, Software Development, Project Management and Business Analysis, and more. In a global clinical trial environment, business-focused applications, connectivity, and data security are critical to a trial's outcome. Find out how you can be an invaluable part of our success story.

The Principal Database Programmer will be recognized as a subject matter expert, providing technical support and expert advice to internal and external sponsors. In addition, the Principal Database Programmer can fill the Database Primary (late phase) or Technical Lead role on projects; liaise with sponsors, Data Management Leads and other functional areas as required. General areas of responsibility also include eCRF design, edit check programming and integration of third party systems with the EDC databases.

• Proficiency in at least one programming environment (e.g., SAS, CDMS, EDC, SQL, VB, Java). • Experience working with at least one system used within the Clinical Trial process (e.g. SAS, CDMS, EDC (Inform, RAVE, DataLabs), CTMS, Medical Safety Reporting). • Relevant Clinical Trial industry experience. • Knowledge of the programming and reporting process within GDO. • Knowledge of SOPs/Guidelines/Work Instructions/System Life Cycle methodologies, ICHGCP and any other applicable local and international regulations such as 21 CFR Part 11 and proven practical application. • Team and Project leadership experience required. • Proven record of leading a team and a large scope of projects in a GDO, Technical, Clinical, Medical or Statistical environment.