Altasciences

Senior Biostatistician

Altasciences  •  $80k - $110k/yr  •  United States (Onsite)  •  12 days ago
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Job Description

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.

About The Role
The Senior Biostatistician is responsible for having expert knowledge of all related processes with the ability to independently lead a study, support analysis, and provide high-quality documents to support sponsors' research programs, , and deliver a high level of quality and timeliness, resulting in high levels of client satisfaction.


What You’ll Do Here
• Follow department and company standard operating procedures (SOPs), forms, templates and policies.
• Act as Lead Biostatistician for simple to complex studies and be the central point of contact for the assigned Biostatistics team, extended internal project team and the client.
• Mentor, guide, and train other Biostatisticians in all aspects of the Lead Biostatistician role and all other tasks.
• Provide input for Biostatistics portion of project timelines.
• Review and provide statistical guidance for protocols for simple to complex studies.
• Create and provide Biostatistics-related training to create and sustain culture of continuous improvement.
• Generate randomization schedules using SAS or randomization-specific software.
• Develop and quality control (QC) review statistical analysis for simple to complex studies.
• Develop or assist in developing the Statistical Analysis Plans (SAPs) and related table, figure, and listing (TFL) shells for studies of simple to moderate complexity.
• Develop tables of summary statistics and graphics for clinical aspects of clinical trials.

• Develop Inferential Statistics.

• Potentially support some Statistical Analysis for our Preclinical group.

• Provide statistical analysis for PD subjective measures and PK endpoints.
• Responsible for answering deficiency letters from regulatory agencies, as required.
• Validate Biostatistician programs and results using SAS.
• Perform QC review of analyses and documents prepared by other team members for completeness, accuracy, consistency, and structure.
• Coordinate with internal team to deliver high-quality documents in accordance with agreed upon timelines.
• May represent Biostatistics in client and inter-departmental meetings.
• Conduct all work in compliance with SOPs, Good Clinical Practice (GCP), and all regulatory guidelines.
• Maintain familiarity with client and internal team expectations and produce analyses and documents consistent with these.
• Have awareness of regulatory guidelines of related authorities (Therapeutic Products Directorate [TPD], FDA, European Medicines Agency [EMA], etc) as well as ICH and GCP procedures.
• May lead or participate in departmental or interdepartmental quality improvement initiatives.
• Maintain and participate in the objectives of the department.
• Oversee direct reports as assigned.


What You’ll Need to Succeed
• Bachelor's Degree or higher in Statistics or related field.
• Excellent verbal and written communication skills.
• Professional attitude and strong interpersonal skills.
• Ability to work well with a multi-disciplinary team of professionals.
• Client-focused approach to work.
• Flexible attitude with respect to work assignments and new learning.
• Ability to prioritize workload.
• Superior attention to detail.
• Understanding of clinical research project life cycle and applicable regulatory guidelines.
• Good computer skills (Microsoft Word, Excel, and Power Point) and ability to understand and adapt to information technology (IT) systems as needed.
• Excellent SAS programming proficiency.

Altasciences strives to provide a French working environment for its employees in Quebec. Although as part of its francization program has taken all reasonable steps to avoid imposing the above-mentioned requirement. Fluency in English is an essential requirement for the position of Senior Biostatistician including, but not limited to, for the following reasons:

  • The requirement to have study protocols, designs and clinical research documents written and documented in English as required by industry regulatory agencies.

  • The employee communicates frequently with Altasciences employees across Canada and the United States. As such, English is the main language used to correspond between offices.

  • The employee frequently communicates with English-only customers outside the province of Quebec.

What We Offer
The salary range estimated for this position is $80,000 - $110,000. Please note that salaries vary within the range based on factors including, but not limited to, prior relevant experience, skills, education, certification, location as well as internal equity and market data.


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

Altasciences' Incentive Programs Include:

  • Training & Development Programs

  • Employee Referral Bonus Program

  • Annual Performance Review

#LI-TN1

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!

Altasciences

About Altasciences

Outsourcing made easy with a one-stop solution to early-phase drug development.

We are an integrated drug development solution company, offering pharmaceutical and biotechnology companies a proven, flexible approach that removes the need for multiple service providers during the early stages of drug development. Whether for one study or an end-to-end program, we help you reach critical decision-making milestones sooner by improving speed and ease from lead candidate selection to clinical proof of concept, and beyond. When partnering with Altasciences, you can experience up to 40% in time savings thanks to our integrated, one-stop solution offering.

We strive to create a true partnership with our clients, our partners, and our colleagues that enables a mutually supporting relationship built on a combination of excellent science and solid communication.

Helping sponsors get better drugs to the people who need them, faster, for over 25 years.

Our full-service offering is always tailored to your specific research needs:

- Preclinical research

- Clinical pharmacology

- Drug formulation

- Manufacturing and analytical services

- Bioanalysis

- Program management

- Medical writing

- Biostatics

- Data management

- And so much more!

Industry
Biotech & Life Sciences
Company Size
1,001-5,000 employees
Headquarters
Laval, CA
Year Founded
1995
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