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 at www.abbvie.com. Follow @abbvie on LinkedIn, Facebook, Instagram, X and YouTube.
Job Description
Purpose:
This position reports into the Clinical Sciences (CS) Product Office within the Clinical Science organization’s Global Strategic Operations. The CS Product Office, Product Safety Team (PST) and Epidemiology organizations work collaboratively and strategically with colleagues across the product lifecycle to identify, evaluate, understand and communicate the safety profile of our drugs to protect patients worldwide.
The PST is a high-profile high-impact team that leads and owns safety decisions and strategy across the product lifecycle. The team partners with stakeholders across the product lifecycle to provide innovative safety-driven strategies, which will maximize product benefit-risk for patients. The CS Product Office plays a critical role in shaping and driving the priorities of the PST by providing strategic and operational leadership oversight of the PST model.
As an Epidemiology Study Operations Manager within the CS Product Office, you will support and partner with the Global Epidemiology organization to achieve its mission in managing the lifecycle of studies utilizing real world evidence and to ensure compliance with quality standards (Global Regulations and AbbVie policies and procedures).
Responsibilities:
- Strategic management and oversight of Epidemiology-led non interventional studies with progressive autonomy
- Provide support to the Study Leader for vendor selection, scope development, management, and oversight of external vendors/CROs
- Manage and coordinate the development of study-related deliverables including development of project plans/timelines, confirming accountabilities, document quality, driving completion of actions and escalating obstacles/risks
- Drive study-related deliverables to ensure regulatory and process timelines are met
- Responsible for relevant updates to the cross-functional team and stakeholders on study status
- Leverage applicable systems and processes to enable successful tracking and completion of the study and study-related deliverables
- Coordinate the development, review and approval of study protocol and other study-related documents
- Maintain study-related documents (e.g., meeting minutes, IRB/EC approvals) in the appropriate document repository
- Responsible for oversight of funds spent against approved budget
- Proactively identify, address and escalate, as appropriate, project-related issues
- Identify opportunity areas for efficiency and participate in department related projects in order to achieve operational excellence within Global Epidemiology and the CS Product Office
- Build solid foundation in understanding regulations and applies knowledge or regulations to guide the development study-related deliverables
- Collaborate effectively to build and leverage relationships across functions and organizations to achieve business results
- Participate in audit and inspection preparation and execution activities
Qualifications
- Bachelor’s degree in biological/medical science or healthcare professional
- 6+ years of experience working in healthcare, research institution, or pharmaceutical industry
- A minimum of 2 years driving project management activities or operational experience within global companies
- Preferred experience in one of the following areas: drug development, non-interventional study lifecycle management, risk management, and/or Pharmacovigilance
- Demonstrated ability to work and collaborate with others to build/leverage relationships
- Ability to adopt process and technology changes
- Familiarity with medical and study terminology and concepts is desirable
- Proficiency in computer skills (Windows, Word, Excel) and in databases (e.g., clinical trial management system)
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.
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 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
Recruitment Fraud Alert
We have recently become aware of various recruitment phishing scams targeting job seekers. Please be advised:
- AbbVie will never request sensitive personal information (such as bank account details, social security numbers, or payment of any kind) during the recruitment process.
- If you suspect you have received a fraudulent offer or communication claiming to be from AbbVie, please do not respond, open any attachments, or click on any hyperlinks.
If you have any questions or concerns regarding the authenticity of a communication alleged to have been made by or on behalf of AbbVie, please contact us immediately.
Protect yourself by verifying job offers and communications. Your safety is important to us.
Where We Work
Role is not performed at a site or office and requires limited or no travel to a site or office.
Bachelor's degree in biological/medical science or healthcare; 6+ years in healthcare, research, or pharma; 2+ years project management; proficiency in Windows, Word, Excel, and clinical trial management systems.
Key Responsibilities
- managing study operations
- overseeing vendors
- coordinating deliverables
Skills & Tools
Microsoft Windows, Microsoft Word, Microsoft Excel, clinical trial management system
Job Details
- Category: Project and Program Management
- Seniority: Mid Level
- Commitment: Full Time
- Workplace: Remote — Chicago, Illinois, United States
- Salary: USD 109,500 – 208,500 / year
- Languages: English
Benefits
- Generous paid time off
- Retirement plan
About AbbVie
A biopharmaceutical company discovering and delivering innovative medicines across key therapeutic areas. — Industry: Healthcare