Study Project Manager (Medical Affairs/Immunology/Oncology)

Benefits

Parental leave

12 weeks From the posting source

Non-birth-parent leave

12 weeks From the posting source

Family-building benefits

• Fertility benefits: Not verified
• Adoption assistance: Not verified
• Surrogacy assistance: Not verified

Mental health support

Not verified

Relocation assistance

Not verified

Childcare support

Not verified

Learning budget

Not verified

Verification

Source-linked checked May 7, 2026

Salary

$148K-$202K From the posting source

401(k) match

Reported from DOL Form 5500 industry filing (not employer-specific)

Was this benefit information wrong? Tell us.

Market context

U.S. role benchmark (BLS OEWS)

$61,842 U.S. median for this role

Projected growth (BLS Employment Projections)

+1.9% - Slower

183% above the BLS role benchmark for operations aggregate.

Matched to SOC 11-1021 - Operations aggregate by role bucket.

Source: U.S. Bureau of Labor Statistics, OEWS, May 2024 and Employment Projections, 2024-2034.

Role

Role function

Operations From the posting source

Seniority

Senior From the posting source

Schedule

Shift type

Not verified

Weekend work

Not verified

Company

Equity

Offered Verified - SEC 10-K source

Application

Cover letter

Not verified

Assessment

Not verified

Deadline

Not stated

Where they hire

State eligibility is not yet verified.

About this role

Study Project Manager (Medical Affairs/Immunology/Oncology) Mettawa, IL, United States 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: Key Responsibilities Independently lead Medical Affairs + Health Impact (MHI) funded research, including Externally Sponsored Collabs & Non-Interventional Studies (NIS) (single & multi-country) from inception to closure, in compliance with quality standards. Support strategic leadership of the Cross-Functional Team. 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. Qualifications: Education & Experience Must possess a Master'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: applying standard quality procedures to MHI research, including SOP, ICH/GCP, Global Regulations;

Read the full description at jobs.smartrecruiters.com. FewerJobs shows a preview and links to the original posting.