Project Manager, Study I

The Study Project Manager I drives the connection between science and operational delivery and ensures operational excellence in planning and execution of clinical research studies across all development stages. The Study Project Manager I is responsible for and ensures clinical research studies are executed with quality and efficiency, on-time, within budget, and meet company objectives.

The Study Project Manager I achieves these objectives by bringing scientific acumen, strategic thinking, innovation, experience in clinical study operations management and stakeholder management to address risks and challenges. The Study Project Manager I serves as leader of one or more cross functional Clinical Study Teams, leading clinical operations from planning through to execution in a cross functional matrix environment.

- -Defines and drives the operational strategies and deliverables for one or more clinical studies

-Responsible for executing clinical studies in compliance with quality standards (ICH/GCP, Global Regulations, and AbbVie policies and procedures).

-Proactively manages budget, timelines and study issues; brings scientific acumen, technical expertise and global mindset to drive achievement of study objectives

-Leader of the cross functional Clinical Study Team - -Leads clinical operations planning through to execution via cross functional matrix environment and influences cross functional stakeholders to drive milestone achievement

-Effectively manages vendors and a diverse set of external stakeholders including site staff, Key Opinion Leaders and patient groups

-Brings a growth mindset, demonstrated by a willingness to continuously learn, grow and adapt, give and receive feedback, see challenges as opportunities - -Coaches and effectively supports cross functional team members, delegates and empowers to the right level, actively contributes to Development Operations community

-Contributes towards operational efficiencies and brings innovative ideas to their teams and studies

-Demonstrates excellent communication and problem solving skills

-Navigates ambiguity and thrives even when not having all the information - On a given study responsible for (but not limited to) :

- the development of the clinical study design and associated systems, tools and documents

- vendor selection, scope development, management and oversight of external vendors - Proactively identifying risks and address and/or escalate study related issues and opportunities for efficiency - Empowered decision maker on operational aspects of study execution. - - creating an inclusive and innovative environment where staff and studies/programs will succeed - Provide leadership to Study Management Associates - lead, delegate and support activities to deliver on study milestones

6 years of demonstrated pharma-related and/or clinical research related experience or equivalent required.

Preferred exposure in study initiation through study completion in Phase 1-4 and/or Medical Device Trial Experience

- 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 thisposting 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.

- 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 anduntil paid and may be modified at the Company's sole and absolute discretion, consistent with applicable law.

https://www.abbvie.com/join-us/reasonable-accommodations.html

• Bachelor’s Degree or equivalent degree is required,

6 years of demonstrated pharma-related and/or clinical research related experience or equivalent required.

Preferred exposure in study initiation through study completion in Phase 1-4 and/or Medical Device Trial Experience The Study Project Manager I drives the connection between science and operational delivery and ensures operational excellence in planning and execution of clinical research studies across all development stages.

The Study Project Manager I is responsible for and ensures clinical research studies are executed with quality and efficiency, on-time, within budget, and meet company objectives. The Study Project Manager I achieves these objectives by bringing scientific acumen, strategic thinking, innovation, experience in clinical study operations management and stakeholder management to address risks and challenges.

The Study Project Manager I serves as leader of one or more cross functional Clinical Study Teams, leading clinical operations from planning through to execution in a cross functional matrix environment.

• -Defines and drives the operational strategies and deliverables for one or more clinical studies

-Responsible for executing clinical studies in compliance with quality standards (ICH/GCP, Global Regulations, and AbbVie policies and procedures).

-Proactively manages budget, timelines and study issues; brings scientific acumen, technical expertise and global mindset to drive achievement of study objectives

-Leader of the cross functional Clinical Study Team

• -Leads clinical operations planning through to execution via cross functional matrix environment and influences cross functional stakeholders to drive milestone achievement

-Effectively manages vendors and a diverse set of external stakeholders including site staff, Key Opinion Leaders and patient groups

-Brings a growth mindset, demonstrated by a willingness to continuously learn, grow and adapt, give and receive feedback, see challenges as opportunities

• -Coaches and effectively supports cross functional team members, delegates and empowers to the right level, actively contributes to Development Operations community

-Contributes towards operational efficiencies and brings innovative ideas to their teams and studies

-Demonstrates excellent communication and problem solving skills

-Navigates ambiguity and thrives even when not having all the information

• On a given study responsible for (but not limited to) :

- the development of the clinical study design and associated systems, tools and documents

- vendor selection, scope development, management and oversight of external vendors

• Proactively identifying risks and address and/or escalate study related issues and opportunities for efficiency
• Empowered decision maker on operational aspects of study execution.
• - creating an inclusive and innovative environment where staff and studies/programs will succeed
• Provide leadership to Study Management Associates – lead, delegate and support activities to deliver on study milestones