Working with pharma company Abbvie hiring manager. Looking for data manager candidate but role is listed project lead. Role is located either Chicago, Irvine, San Fran, or New Jersey. Please reach out if interested.

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I know someone who might be interested! I'll send them a link to here.

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I will ask around! Sounds like a great opportunity.

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Any opportunity for WFH?

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How often is it necessary to into the office?

So I’ll give you the straight forward answer. If the Individual does the job without the need of supervision the fully remote is an option.

It is flexible.

Yes.

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: immunology, oncology, neuroscience, eye care, virology, women’s health and gastroenterology, in addition to products and services across its Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com. Follow @abbvie on Twitter, Facebook, Instagram, YouTube and LinkedIn.

This role can be hired at a PL Ior a PL II level, dependent on years of relevant experience; previous work, education, training, and clinical research capabilities

AbbVie Clinical Data strategy and Operations (CDSO) 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 Data and Statistical Sciences (DSS).

Represents DSS as the CDSO Program Lead within the cross-functional study team; aligning study teams with program and study-level strategies from the CDSO perspective.
Provides expertise on Data Management ensuring quality and timely delivery of all CDSO deliverables
For assigned programs and studies, the CDSO PL acts as single point of contact and is accountable for data management activities and timelines, collaborating with the cross-functional teams as needed.
Responsible for ensuring the quality of all CDSO deliverables; working in conjunction with our clinical technology teams and external partners (e.g. clinical database development (e.g. EDC, IRT, eCOA), data quality review, trending, Data Management Plan, etc.)
Utilizes operational analytics and project management tools to optimize execution of programs and studies, to manage internal and external resources, track study progress, and 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, as well as industry trends, data standards, and clinical technologies of importance for data management and contribute to enhancing capabilities and operational efficiencies.
If assigned, participates as the CDSO study owner in regulatory inspections and internal quality audits
Conducts study execution “lessons learned”
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, which may include indirect supervision of employee as well as supervising the work of contract resources
Leads DSS innovation and process improvement initiatives and participates in cross-functional initiatives

Qualifications
Must Have for PL I:

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
Must Have for PL II:

Bachelor’s degree degree in business, management information systems, computer science, life sciences or equivalent.
6+ years of data management / pharma or biotech / clinical research / health care experience
In-depth understanding of clinical trial processes and clinical technologies (e.g. EDC, IRT, eCOA), preferably RAVE
Working knowledge of electronic document management systems
Management of a clinical trial from initiation through to completion in a data management lead role
Understanding of ICH and GCP guidelines
Demonstrated performance as a functional leader
Demonstrated ability to influence others without direct authority
Demonstrated ability to successfully coach / mentor
Demonstrated effective communication skills
Demonstrated effective analytical skills
Nice to have:

Master’s degree
PMP Certification or Lean Six Sigma Green Belt
Understanding of relevant regulatory requirements and CDISC Standards

Let me know Jon description below. Reach out if interested. Taking you directly to the hiring manager

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