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Senior Statistical Programmer

4 months ago

Montreal, Canada Altasciences Full time

Monday, April 29, 2024

Your New Company
At Altasciences we all move in unison to assist and work in the discovery, development, and manufacturing of new drug therapies to get them faster to people who need them.No matter your role, we all play an important part and you will have a significant impact on the health and well-being of people across the globe. By living our values of Employee Development, Customer Focus, Quality and Excellence, Respect and Integrity, we look to foster a passionate and collaborative work environment and we are looking for talented and enthusiastic people, like you, to join our growing team Whether you’re a recent college graduate or seeking your next career opportunity, it’s time to discover your future at Altasciences. We are better together and together We Are Altasciences.

You are an experienced Statistical Programmer that has understanding of clinical research and the role of data management, programming and statistics in the clinical study process and you want to make a difference by helping to improve people's quality of life, our opportunity will surely interest you At Altasciences, you will have the opportunity to develop your skills and advance your career. If you stand out for; your client-focused approach to work, your ability to prioritize workload and your superior attention to details; don't hesitate to send us your application

Your Role:

The Senior Statistical Programmer is responsible for developing high-quality programming that support sponsors’ research programs with a high level of proficiency. In addition, the Senior Statistical Programmer has an active role in continuous improvement and is expected to act as a leader in the department.

What you’ll do here:

  • Follow the department and company standard operating procedures (SOPs), policies, and standards.
  • Using SAS, perform SDTM, ADaM, and table figure, listing (TFL) programming, quality control (QC) review, and documentation of programs used in creating statistical outputs.
  • May perform role of Lead Statistical Programmer on studies, portions of studies, or programs.
  • Understand regulatory agency standards and provide final deliverables in accordance with these standards (ie, final Clinical Data Interchange Standards Consortium [CDISC] deliverables for studies to be included in Food and Drug Administration [FDA] submissions).
  • Collaborate with Lead Biostatisticians and study team to resolve any study-related questions to ensure that programming outputs represent the statistical analysis plan (SAP) and raw data from external sources and the clinical database.
  • Perform peer review and take accountability for ensuring programming accurately reflects the raw data.
  • Follow current SDTM standards and current ADaM Implementation Guides.
  • Lead studies or portions of studies from a programming perspective. Monitor study progress and quality of other assigned programmers to meet quality and timeline expectations, escalate to management as needed.
  • Perform review of the clinical database in regards to visit naming, Clinical Data Acquisition Standards Harmonization (CDASH), and accurate data collection to provide clinical data that is analyzable for and meets the needs of the Biostatistics team.
  • Understand timelines and milestones affecting work.
  • Create Biostatistics deliverables that follow the protocol and SAP.
  • Understand and update SAS programs to adapt to various study situations and perform self-review to ensure outputs are as expected .
  • Accurately import external data to be used in TFLs.
  • Reconcile external data and provide findings for non-reconcilable items to the Data Management team.
  • Interact with other staff members to understand and explain SAS programs accurately.
  • Analyze existing processes and explore improvement solutions.
  • Provide technical expertise for internal and external clients, and independently bring project solutions to the Biostatistics team and other departments.
  • Develop and lead intradepartmental and interdepartmental process and quality improvement initiatives.
  • Perform and plan the development, implementation, and validation of new process technologies, macros, and applications.
  • Mentor and train programmers or other team members and/or develop training materials as needed.
  • Other tasks as requested.

What you need to succeed

  • Bachelor’s Degree in programming, health-related sciences, or relevant field;
  • 7 to 10 years’ experience;
  • CRO experience an asset;
  • Excellent verbal and written communication skills;
  • Professional attitude and strong interpersonal skills;
  • Ability to work well with a multi-disciplinary team of professionals;
  • Flexible attitude with respect to work assignments and new learning;
  • Strong technical aptitude and ability to adapt to multiple data management platforms;
  • Good computer skills (Microsoft Word, Excel, and Power Point) and ability to understand and adapt to multiple information technology (IT) systems

What We Offer
Altasciences offers a wide variety of benefits to help our employees live healthy and fulfilling lives both at and outside of work.

Altasciences’ Benefits Package Includes:

  • Health/Dental/Vision Insurance Plans
  • 401(k)/RRSP with Employer Match
  • Paid Vacation and Holidays
  • Paid Sick and Bereavement Leave
  • Employee Assistance & Telehealth Programs
  • Telework when applicable
  • Training & Development Programs
  • Employee Referral Bonus Program
  • Annual Performance Reviews
MOVING IN UNISON TO DELIVER A BIG IMPACT WITH A PERSONAL TOUCH

MOVING IN UNISON TO DELIVER A BIG IMPACT WITH A PERSONAL TOUCH Altasciences is an equal opportunity employer committed to diversity and inclusion. Our goal is to attract, develop and retain highly talented employees from diverse backgrounds, allowing us to benefit from a wide variety of experiences and perspectives. All qualified applicants will receive consideration for employment without regard to age, race, color, religion, creed, sex, sexual orientation, gender identity, national origin, disability or any other protected grounds under applicable legislation. Reasonable accommodations for persons with disabilities during the recruitment process are available upon request. Join us at Altasciences

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