Job Details

ID #53733887
Estado Illinois
Ciudad Northchicago
Full-time
Salario USD TBD TBD
Fuente AbbVie
Showed 2025-03-28
Fecha 2025-03-28
Fecha tope 2025-05-27
Categoría Etcétera
Crear un currículum vítae
Aplica ya

Study Management Associate (SMA) II

Illinois, Northchicago, 60064 Northchicago USA
Aplica ya

Company DescriptionAbbVie'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 Twitter, Facebook, Instagram, YouTube and LinkedIn. Job DescriptionKey Responsibilities

Contribute to global clinical trials from inception to closure, with support from the Study Project Manager (SPM) & in compliance with quality standards.

Responsibilities include, but are not limited to:

Drive deliverables & timelines;

lead & manage meetings with stakeholders;

Manage vendors, recruitment, CTMS & eTMF; Maintain Inspection Readiness;

identify, mitigate & manage risks;

Develop & manage study materials;

provide training to stakeholders;

Support EDC, IRT, & ePRO design specifications, user acceptance testing, plans & key risk indicators, & system management activities;

manage IP & study supplies;

Support process improvement initiatives & serve as a subject matter expert &/or mentor.

QualificationsEducation & ExperienceMust have a Bachelor’s or foreign education equivalent, & 2 years of clinical research work experience. Of work experience required, must have 2 years in each of the following: (i) applying standard quality procedures to full clinical trials, including SOP, ICH/GCP, Global Regulations; (ii) working with ICFs, protocols, & amendments; (iii) functioning independently in a matrixed environment with teams in multiple time zones; (iv) using 1 or more of the following clinical trial systems or vendors: EDC, IRT, TMF, ePRO, CTMS, central labs, &/or central imaging; (v) analyzing & evaluating complex issues to accelerate study timelines & enable a well-run study; (vi) managing meetings (creating agendas, preparing minutes, or presenting); & (vii) ensuring data is clean, documents are accurate to maintain inspection readiness.Work experience may be gained concurrently. 100% Telecommuting permitted.Additional InformationSalary Range: $106,296 - $153,000 per year.(Multiple/3 positions available)Apply online at https://careers.abbvie.com/en. Refer to Req ID: REF37788PWe 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 and long-term incentive programs.AbbVie is committed to operating with integrity, driving innovation, transforming lives, serving our community, and embracing diversity and inclusion. It is AbbVie’s policy to employ qualified persons of the greatest ability without discrimination against any employee or applicant for employment because of race, color, religion, national origin, age, sex (including pregnancy), physical or mental disability, medical condition, genetic information, gender identity or expression, sexual orientation, marital status, status as a protected veteran, or any other legally protected group status.AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives, serving our community and embracing diversity and inclusion. It is AbbVie’s policy to employ qualified persons of the greatest ability without discrimination against any employee or applicant for employment because of race, color, religion, national origin, age, sex (including pregnancy), physical or mental disability, medical condition, genetic information, gender identity or expression, sexual orientation, marital status, status as a protected veteran, or any other legally protected group status.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.htmlSalary: $0 - $0

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