Data Science Program Lead III- Oncology

AbbVie Inc.; Irvine (CA); In loco; USD 150.000 - 230.000; Tempo pieno

Vantaggi offerti da questo lavoro

Paid time off

Medical/dental/vision insurance

401(k)

Long-term incentive programs

Descrizione del lavoro

AbbVie Inc. is seeking a Data Science lead to ensure successful delivery of program- and study-level accountabilities within the Data and Statistical Sciences group. You will align DSS study teams with strategic goals and coordinate cross-functional efforts to accelerate clinical program delivery.

The role emphasizes regulatory compliance, use of analytics to optimize timelines, and mentoring of team members in a matrix environment. Strong communication and leadership are required.

Competenze

• 8+ years pharma/clinical research/data management/healthcare experience or 10+ years project management experience

Mansioni

• Aligns DSS study teams with program- and study-level strategies.
• Acts as single point of contact and operational lead from DSS for assigned programs.
• Coordinates DSS study teams to meet operational objectives and timelines.
• Uses operational analytics and project management tools to optimize study execution.
• Ensures adherence to GCP, ICH guidelines, AbbVie SOPs, and regulatory standards.
• Coaches and mentors team members; leads continuous improvement initiatives.
• May supervise staff or contract resources as needed.

Conoscenze

Project management

Cross-functional leadership

Regulatory knowledge

Analytical skills

Communication skills

Formazione

Bachelor’s degree in business / MIS / computer science / life sciences or equivalent

Master’s degree preferred

Strumenti

SAS

Python

R

Tableau

Descrizione del lavoro

Company Description

About AbbVie

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 including immunology, oncology and neuroscience - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com. Follow @abbvie on LinkedIn, Facebook, Instagram, Xand YouTube.

Job Description

AbbVie Data Science is the best-in-class team within its cross-industry peer group and is responsible for bringing people, process, and technology together to generate business value from clinical trials data. Our operational model is exemplified through execution and innovation. This role is a key to ensuring successful delivery against the program- and study-level accountabilities assigned to Data and Statistical Sciences.

Responsibilities

• Aligns DSS study teams with program- and study-level strategies. Supports governance of assigned programs and studies, both within and outside DSS. Assigned programs may include programs of any size or any complexity
• For assigned programs, acts as single point of contact and accountable operational lead from DSS. Coordinates associated DSS study teams to meet operational objectives. Engages and connects global functional and cross-functional teams at both the program and study levels
• Interacts with and influences all levels of management and cross-functional team members to achieve program objectives. Represents DS in cross-functional forums and, if assigned, leadership meetings
• Utilizes operational analytics and project management tools to optimize execution of programs and studies, to manage internal and external resources, to track study progress, and to prepare study status reports. Anticipates and identifies issues that could affect timelines of own, as well as studies managed by the team. Anticipates and identifies issues that could affect timelines or quality and develops options and solutions
• Ensure adherence to federal regulations and applicable local regulations, Good Clinical Practices (GCPs), ICH Guidelines, AbbVie Standard Operating Procedures (SOPs), and to functional quality standards. Stays abreast of new and/or evolving local regulations, guidelines and policies related to clinical development. Coordinates and participates as the DS study owner in regulatory inspections and internal quality audits
• Participates in oversight of vendors and provides feedback related to clinical trial operations, issues, and trends in performance
• Responsible for coaching and mentoring team members, as well as providing input into their development
• Leads DSS and cross-functional innovation and process improvement initiatives
• If assigned, responsible for identifying training needs and standardizing and facilitating training solutions for DS roles. Conducts "lessons learned" across functions
• May include direct and/or indirect supervision of staff, as well as contract resources

Qualifications

• Bachelor’s degree in business, management information systems, computer science, life sciences or equivalent. Master’s preferred. PMP Certification or Lean Six Sigma Green Belt desired.
• Must have 8+ years of pharma / clinical research / data management / health care experience or 10+ years of project management experience (and / or applicable work experience).
• In-depth understanding of clinical trial processes and involved functional stakeholders, and clinical technology. Management of a clinical trial from initiation through to completion in a lead role is required.
• Demonstrated performance as a cross-functional leader.
  Demonstrated ability to influence others without direct authority.
  Demonstrated ability to successfully coach / mentor in a matrix environment.
  Demonstrated effective communication skills.
  Demonstrated effective analytical skills.

Additional Information

• The compensation range described below is the range of possible base pay compensation that the Companybelieves ingood faith it will pay for this role at the timeof this posting based on the job grade for this position.Individualcompensation paid within this range will depend on many factors including geographic location, andwemayultimatelypaymore or less than the posted range. This range may bemodifiedin thefuture.
• We offer a comprehensive package of benefits including paid time off (vacation, holidays, sick),medical/dental/visioninsurance and 401(k) to eligibleemployees.
• This job is eligible toparticipatein our long-term incentiveprograms.

Note: No amount of payis considered to bewages or compensation until such amount is earned, vested, anddeterminable.The amount and availability of any bonus,commission, incentive, benefits, or any other form ofcompensation and benefitsthat are allocable to a particular employeeremainsin the Company's sole andabsolutediscretion unless and until paid andmay bemodifiedat the Company’s sole and absolute discretion, consistent withapplicable 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