Let’s get started
By clicking ‘Next’, I agree to the Terms of Service
and Privacy Policy, and consent to receive emails from Rise
Jobs / Job page
Associate Director, Statistical Programming & Analysis - Oncology Early Development image - Rise Careers
Job details

Associate Director, Statistical Programming & Analysis - Oncology Early Development - job 4 of 4

Company Description

AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas – immunology, oncology, neuroscience, and eye care – and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com. Follow @abbvie on XFacebookInstagramYouTubeLinkedIn and Tik Tok.

Job Description

* Must be able to come onsite 3 days per week

Purpose:

The Associate Director, Statistical Programming leads the whole stat programming team within CDOR (Clinical Data Operation and Reporting) in OED (Oncology Early Development) clinical development organization.The stat programming team performs statistical programming and analysis oversight for OED all clinical projects conducted by CROs.  The associate Director leads the recruitment and training of new staff onboarding activities, manage the overall resource allocation and monitoring on regular basis, provide technical guidance for team members, performs ongoing and annual performance management and staff career development, initiate and lead stat programming related process improvement collaborating with CRO partners, create a collaborative team work environment for both internal staff as well as with CRO partners, build strong relationship with internal and external stakeholders management.  This person may also need to support clinical projects if needed, therefore strong hands on stat programming skills for both analysis datasets and TLFs in oncology therapeutics are fundamental to the success of this role.                                

Responsibilities:

•SAS Programming: Demonstrated extensive understanding of SAS programming concepts and techniques appropriate to the pharmaceutical industry. Demonstrated proficiency in applying SAS programming knowledge to solve problems related to non-routine situations. Standards: Oversees effort to determine and implement global company standards related to output design and programming conventions. Responsible for monitoring regulatory guidance and industry best practices.
•Case report forms and database definitions: Provides strategic guidance on the development of CRFs and database designs. Provides in-depth critical review of global standards related to CRF designs and database designs. Derivation Programming, Submission Data Sets and Programs: Demonstrated proficiency in interpreting statistical analysis plans and developing analysis data set specifications. Oversees effort to determine and implement global company standards related to derive data sets and subm
•Works collaboratively with multiple stakeholders to manage priorities and resources across therapeutic areas. Demonstrates an understanding of drug development principles. Anticipates potential problems within and across projects and develops appropriate contingency plans. Creates escalation plans to ensure resolution of all issues at the therapeutic and project levels. Participates in and is viewed as a key contributor to cross functional initiatives.
•Effectively and persuasively presents statistical programming concepts, assessment of risks and impacts and logical arguments to other statistical programmers, statisticians, scientists and non-scientists. Effectively presents information through planning and execution of meetings and presentations.
•Training and Mentoring: Provides appropriate background and motivation to staff. Arranges appropriate training opportunities for staff to facilitate their timely career development. Ensures that self and staff are compliant with training requirements. Effectively mentors statistical programming staff with regard to functional operations.
•Manages statistical programming staff by appropriate assignment of responsibilities, defining scope and reviewing activities/progress so that projects are delivered on time with suitable quality. Allocates resources to projects such that the correct balance of expertise and experience is maintained for all projects. Works collaboratively with the statistical programming management team to assess project resource requirements versus current staff
•Establishes high expectations and goals to ensure organizational success and leads staff to meet or exceed those goals. Creates an organization that executes efficiently and is committed to meeting goals. Encourages a culture of open, honest communication where all are encouraged to express their views. Provide all performance management activities for 4-10 statistical programmers
.

Qualifications

•MS in Statistics, Computer Science or a related field with 10+ years of relevant experience. OR BS in Statistics, Computer Science or a related field with 12+ years of relevant experience.
•High degree of technical competence and communication ability, both oral and written. Highly competent in SAS programming and Macro development. Pharmaceutical experience with clinical trials, including familiarity with expectations of regulatory agencies, especially FDA and EMEA. NDA/BLA or other regulatory filing experience, including ISS or ISE experience. Thorough understanding of ICH Guidelines and relevant regulatory requirements. A minimum of 2 yrs management experience required, 2-5 years preferred. 

Additional Information

Applicable only to applicants applying to a position in any location with pay disclosure requirements under state or local law: ​

  • The compensation range described below is the range of possible base pay compensation that the Company believes in good faith it will pay for this role at the time of this posting based on the job grade for this position. Individual compensation paid within this range will depend on many factors including geographic location, and we may ultimately pay more or less than the posted range. This range may be modified in the future.​

  • We offer a comprehensive package of benefits including paid time off (vacation, holidays, sick), medical/dental/vision insurance and 401(k) to eligible employees.​

  • This job is eligible to participate in our short-term incentive programs. ​

  • This job is eligible to participate in our long-term incentive programs​

Note: No amount of pay is considered to be wages or compensation until such amount is earned, vested, and determinable. The amount and availability of any bonus, commission, incentive, benefits, or any other form of compensation and benefits that are allocable to a particular employee remains in the Company's sole and absolute discretion unless and until paid and may be modified at the Company’s sole and absolute discretion, consistent with applicable law. 

AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community.  Equal Opportunity Employer/Veterans/Disabled. 

US & Puerto Rico only - to learn more, visit https://www.abbvie.com/join-us/equal-employment-opportunity-employer.html

US & Puerto Rico applicants seeking a reasonable accommodation, click here to learn more:

https://www.abbvie.com/join-us/reasonable-accommodations.html

AbbVie Glassdoor Company Review
3.9 Glassdoor star iconGlassdoor star iconGlassdoor star icon Glassdoor star icon Glassdoor star icon
AbbVie DE&I Review
No rating Glassdoor star iconGlassdoor star iconGlassdoor star iconGlassdoor star iconGlassdoor star icon
CEO of AbbVie
AbbVie CEO photo
Richard A. Gonzalez
Approve of CEO

Average salary estimate

$135000 / YEARLY (est.)
min
max
$120000K
$150000K

If an employer mentions a salary or salary range on their job, we display it as an "Employer Estimate". If a job has no salary data, Rise displays an estimate if available.

Similar Jobs
Photo of the Rise User

Lead quality assurance efforts for CMC product development at AbbVie, ensuring timely release and compliance of clinical supplies in a hybrid work model.

Photo of the Rise User

Support senior leaders at Allergan Aesthetics with administrative duties and coordination in a hybrid work setting.

Photo of the Rise User
Eurofins Hybrid West Point, PA, USA
Posted 9 days ago

Eurofins Scientific is seeking an experienced In-Vivo Scientist to design and perform animal model studies focused on infectious diseases and vaccines at their West Point, PA location.

Photo of the Rise User
Viatris Hybrid St. Albans, Vermont, USA
Posted yesterday

Viatris is looking for a 2nd shift Chemist to conduct analytical testing and support laboratory operations at their St. Albans facility.

Photo of the Rise User

Avison Young is looking for a Senior Market Intelligence Analyst to provide data-driven real estate market insights and support strategic client decision-making using advanced analytics technologies.

Photo of the Rise User
Brillio Hybrid Dallas, Texas, United States
Posted 9 days ago

Lead the design and development of multi-agent AI systems at Brillio, advancing enterprise AI automation through innovative Agentic AI solutions.

Photo of the Rise User

Palo Alto Networks is looking for a Threat Hunting Researcher to join their Unit 42 team, driving advanced threat detection and cybersecurity innovation remotely.

Photo of the Rise User
Waymo Hybrid Mountain View, CA, United States, San Francisco, CA, USA
Posted 10 days ago
Social Impact Driven
Empathetic
Collaboration over Competition
Growth & Learning

Lead the development and management of state-of-the-art evaluation methodologies and teams to enhance Waymo’s autonomous driving AI systems.

Photo of the Rise User

Experienced Nuclear Survivability Scientist/Physicist needed at Peraton to lead development of physics-based nuclear environment models supporting national security missions.

Photo of the Rise User
Posted 7 days ago

Lead clinical development strategies and execution for targeted radiopharmaceutical therapies in GU cancers at RayzeBio, a Bristol Myers Squibb company.

Photo of the Rise User
Eurofins Hybrid Kalamazoo, MI, USA
Posted 2 days ago

Experienced Analytical Chemist needed at Eurofins Scientific to perform HPLC, GC, and dissolution testing for drug substance and product characterization.

An opportunity to innovate in robotics simulation and AI by developing GPU-based simulation pipelines and collaborating across technical teams.

Photo of the Rise User

Seeking an Environmental Monitoring Sampler on 2nd shift to perform critical sampling and monitoring in biopharmaceutical cleanrooms at Eurofins Scientific.

Photo of the Rise User

Eurofins Scientific seeks a QC Microbiology Technician for 2nd shift environmental monitoring and sampling at their biopharmaceutical manufacturing site in Rensselaer, NY.

Photo of the Rise User
Insmed Hybrid NJ-Bridgewater
Posted 2 days ago

Join Insmed as an Associate Scientist to contribute to the development and analytical evaluation of lipid nanoparticle formulations for gene-based therapies.

AbbVie’s mission is to discover and deliver innovative medicines that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people’s lives across several key therapeutic areas: i...

3866 jobs
MATCH
VIEW MATCH
FUNDING
SENIORITY LEVEL REQUIREMENT
TEAM SIZE
EMPLOYMENT TYPE
Full-time, hybrid
DATE POSTED
May 23, 2025

Subscribe to Rise newsletter

Risa star 🔮 Hi, I'm Risa! Your AI
Career Copilot
Want to see a list of jobs tailored to
you, just ask me below!