Principal Analyst, Statistical Programming

About This Role

The Principal Analyst Statistical Programming reporting to Associate Director of Statistical Programming Biogen West Coast Hub. leads and oversees statistical programming activities of internally and externally through vendors in the in the application of data standards production of analysis datasets analysis dataset specifications tables listings figures electronic submission components ( and XPTs) and ad hoc analyses. He / she partners with Biostatistics to deliver high quality submission ready statistical outputs.

What Youll Do

Leads coordinates and manages timely creation oversight review completion and delivery of statistical programming activities and deliverables of projects via internal and / or external staff oversight.

Authors CDISC ADaM (analysis data model) analysis dataset specifications including the identification of potential data issues or areas of critical data examination. Works with statistics on defining and documenting programming endpoint algorithms.

Manage the end-to-end programming of deliverables through from CRF collections through electronic submission including preparation of electronic submissions (ESUB) components (input to reviewers guides annotated CRF define and XPTs) works with SMEs to ensure compliance to eSUB standards

Identifies process inefficiencies and lead efforts to remedy the inefficiencies and train the department on the new processes.

Serves as the Statistical Programming Lead to achieve milestones for a study; evaluates task objectives collaborates with PL and / or manager on issues or resource needs.

Verifies program consistency and usage of data analysis and submission standards across the department in consultation with data standards statistical submissions management and the data strategy plan.

Informs internal and external project team members of statistical programming requirements deliverable status and resource needs.

Who You Are

You love analytics and are passionate about using data to drive key business decisions. You love learning new technological skills and working through collaboration.

Required Skills

7 years relevant work experience within an organization with a focus on data management and analysis

7 years SAS Base programming with 7 years using SAS STAT GRAPH and MACRO

7 years relevant pharmaceutical / biotech industry experience

7 years clinical trial experience

5 years clinical database experience

CDISC and / or submissions experience

Knowledge of drug development process and clinical trials

Knowledge of drug submission requirements relevant ICH and FDA / EMEA / ROW guidelines

Familiarity with UNIX as well as software development packages (R Imaging and Genomics software packages)

Management skills and ability to effectively lead and collaborate across functions

Attention to detail including proven ability to manage some competing priorities

Preferred Skills

Experience with ISS / ISE and NDA / BLA submission

R Programming skill

Job Level : Management

Additional Information

The base compensation range for this role is : $122000.00-$163000.00

Base salary offered is determined through an analytical approach utilizing a combination of factors including but not limited to relevant skills & experience job location and internal equity.

Regular employees are eligible to receive both short term and long-term incentives including cash bonus and equity incentive opportunities designed to reward recent achievements and recognize your future potential based on individual business unit and company performance.

In addition to compensation Biogen offers a full and highly competitive range of benefits designed to support our employees and their families physical financial emotional and social well-being ; including but not limited to :

• Medical Dental Vision & Life insurances
• Fitness & Wellness programs including a fitness reimbursement
• Short- and Long-Term Disability insurance
• A minimum of 15 days of paid vacation and an additional end-of-year shutdown time off (Dec 26-Dec 31)
• Up to 12 company paid holidays 3 paid days off for Personal Significance
• 80 hours of sick time per calendar year
• Paid Maternity and Parental Leave benefit
• 401(k) program participation with company matched contributions
• Employee stock purchase plan
• Tuition reimbursement of up to $10000 per calendar year
• Employee Resource Groups participation

Why Biogen

We are a global team with a commitment to excellence and a pioneering spirit. As a mid-sized biotechnology company we provide the stability and resources of a well-established business while fostering an environment where individual contributions make a significant impact. Our team encompasses some of the most talented and passionate achievers who have unparalleled opportunities for learning growth and expanding their skills. Above all we work together to deliver life-changing medicines with every role playing a vital part in our mission. Caring Deeply. Achieving Excellence. Changing Lives.

At Biogen we are committed to building on our culture of inclusion and belonging that reflects the communities where we operate and the patients we serve. We know that diverse backgrounds cultures and perspectives make us a stronger and more innovative company and we are focused on building teams where every employee feels empowered and inspired. Read on to learn more about our DE&I efforts.

All qualified applicants will receive consideration for employment without regard to sex gender identity or expression sexual orientation marital status race color national origin ancestry ethnicity religion age veteran status disability genetic information or any other basis protected by federal state or local law. Biogen is an E-Verify Employer in the United States.

Required Experience :

Staff IC

Key Skills

Business Development,Customer Service,Attorney,CISSP,Data Analysis

Employment Type : Full-Time

Experience : years

Vacancy : 1

Monthly Salary Salary : 122000 - 163000