Data Science Program Lead I - Neurology

Allergan; Irvine (CA); On-site; USD 110,000 - 160,000; Full time

Job summary

AbbVie is seeking a CDSO Lead to coordinate study-level operational activities within the Clinical Data Strategy and Operations group in Irvine, CA. You will align study teams with program strategies and serve as the primary operational contact from DSS, connecting global teams to drive timely, compliant trial execution.

The role requires 3+ years in pharma/clinical data and strong leadership, communication, and analytical skills, with a focus on continuous improvement and adherence to

Qualifications

• 3+ years pharma/clinical research/data management/healthcare experience or 5+ years of project management experience.
• Strong understanding of clinical trial process and clinical technology.
• Leadership and ability to influence without direct authority.
• Effective communication and analytical skills.

Responsibilities

• Align CDSO study teams with program- and study-level strategies and lead the CDSO Study Team.
• Act as single point of contact and operational lead from DSS for assigned studies.
• Coordinate DSS study teams to meet objectives and engage global cross-functional teams.
• Use operational analytics and project management tools to optimize execution and track study progress.
• Ensure adherence to GCP, ICH Guidelines, AbbVie SOPs and local regulations.
• Participate in CDSO and cross-functional innovation and process improvement initiatives.
• Mentor Data Science Associates; may include indirect supervision of contract resources.
• Contribute to study execution lessons learned across functions.

Skills

Leadership

Influence without authority

Communication

Analytical skills

Project management

Education

Bachelor's degree in business, MIS, CS, life sciences or equivalent

Master's preferred

PMP or Lean Six Sigma Green Belt desired

Job description

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 atwww.abbvie.com. Follow @abbvie onLinkedIn,Facebook,Instagram,XandYouTube.

Job Description

AbbVie Clinical Data Strategy and Operations 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 key to ensuring successful delivery against the program- and study-level accountabilities assigned to Clinical Data Strategy and Operations (CDSO).

Responsibilities

• Aligns CDSOstudy teams with program- and study-level strategies. For assigned studies, leads the CDSOStudy Team and represents DS as a member of the cross-functional study team
• For assigned studies, 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
• Interacts with and influences cross-functional team members to achieve program and study objectives
• 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 or quality and develops options and solutions
• Ensures 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
• Participates in oversight of vendors and provides feedback related to study operations, issues, and trends in performance
• Responsible for coaching and mentoring Data Science Associates. May include indirect supervision of work for contract resources
• Participates in CDSOand cross-functional innovation and process improvement initiatives
• Contributes to study execution “lessons learned” across functions

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 at 3+ years of pharma / clinical research / data management / health care experience or 5+ years of project management experience (and / or applicable work experience)
• Strong understanding of clinical trial process and clinical technology. Experience in managing a clinical trial from initiation through to completion is preferred
• Demonstrated effective leadership skills
• Demonstrated ability to influence others without direct authority
• Demonstrated effective communication skills
• Demonstrated effective analytical skills

Additional Information

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

• The compensation range described below is the range of possible base pay compensation that the Company believes ingood faith it will pay for this role at the time of this posting based on the job grade for this position.Individualcompensation paid within this range will depend on many factors including geographiclocation,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 short-term incentiveprograms.

Note: No amount of payis considered to bewages or compensation until such amount is earned, vested, anddeterminable.Theamountandavailabilityof anybonus,commission, incentive, benefits, or any other form ofcompensation and benefitsthat are allocable to a particular employeeremainsin the Company'ssoleandabsolutediscretion 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, visithttps://www.abbvie.com/join-us/equal-employment-opportunity-employer.html

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