Clinical Data Strategy & Operations Program Lead II (Remote Possible)

AbbVie; North Chicago (IL); Remote; USD 106,000 - 203,000; Full time

Job summary

A leading pharmaceutical company is seeking a Clinical Data Strategy & Operations Program Lead II to enhance their data management processes. This position emphasizes project management, compliance within clinical trials, and effective communication across teams to drive program success. Candidates should have substantial experience in the clinical research field and be capable of leading cross-functional initiatives.

Benefits

Comprehensive benefits package

Paid time off

401(k) plan

Short-term and long-term incentive programs

Qualifications

• Must have 6+ years of pharma/clinical research experience or 8+ years of project management experience.
• In-depth understanding of clinical trial processes preferred.

Responsibilities

• Leads DSS Study Team and aligns with program strategies.
• Acts as the single point of contact for operational leads.
• Ensures adherence to regulations and quality standards.

Skills

Project management

Communication

Analytical skills

Influencing others

Education

Bachelor’s degree in business, management information systems, computer science, life sciences or equivalent

Master’s degree

Job description

Clinical Data Strategy & Operations Program Lead II (Remote Possible)

Join to apply for the Clinical Data Strategy & Operations Program Lead II (Remote Possible) role at AbbVie

Clinical Data Strategy & Operations Program Lead II (Remote Possible)

Join to apply for the Clinical Data Strategy & Operations Program Lead II (Remote Possible) role at AbbVie

This range is provided by AbbVie. Your actual pay will be based on your skills and experience — talk with your recruiter to learn more.

Base pay range

$106,500.00/yr - $202,500.00/yr

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 X, Facebook, Instagram, YouTube, LinkedIn and Tik Tok.

Job Description

AbbVie Data Science is a 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 Data and Statistical Sciences, and includes the following job responsibilities:

• Aligns DSS study teams with program- and study-level strategies. Assigned programs may include programs that are of low complexity and size. For assigned programs and studies, leads the DSS Study Team and represents DS as a member of the cross-functional study team.
• For assigned programs and 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 at the study level
• Interacts with and influences cross-functional team members to achieve program 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. If assigned, 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
• Leads DSS innovation and process improvement initiatives and participates in cross-functional initiatives
• Conducts study execution “lessons learned” across functions
• May include indirect supervision of employee as well as supervision of work of contract resources
  
  

Qualifications

To be successful in this role, you should have a Bachelor’s degree in business, management information systems, computer science, life sciences or an equivalent. A Master’s degree is preferred. PMP Certification or Lean Six Sigma Green Belt desired.

Qualified candidates must also have/demonstrate:

• 6+ years of pharma / clinical research / data management / health care experience or 8+ years of project management experience (and / or applicable work experience).
• In-depth understanding of clinical trial processes and clinical technology. Management of a clinical trial from initiation through to completion in a lead role is preferred.
• Performance as a functional leader
• Ability to influence others without direct authority
• Ability to successfully coach / mentor in a matrix environment
• Effective communication skills
• Effective analytical skills
  
  

While there is a preference to have someone who can work from one of our sites, remote work is possible.

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. Salary: $106,500 - $202,500
• 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

Seniority level

• Seniority level

  Mid-Senior level

Employment type

• Employment type

  Full-time

Job function

• Job function

  Research, Analyst, and Information Technology

• Industries

  Pharmaceutical Manufacturing and Biotechnology Research

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