Study Project Manager I - Oncology

Allergan; Irvine (CA); On-site; USD 110,000 - 140,000; Full time

Benefits offered by this job

Paid time off

Medical/dental/vision insurance

401(k)

Long-term incentive programs

Job summary

AbbVie in Irvine, CA is seeking a Study Project Manager I to drive the interface between science and operations for clinical studies across development stages. You will lead cross-functional Clinical Study Teams, ensuring quality, on-time delivery and budget adherence while applying ICH/GCP standards and AbbVie policies.

The role demands strategic thinking, strong communication, and ability to manage external vendors and stakeholders, with a focus on patient-centric study execution and

Qualifications

• Bachelor’s Degree or equivalent degree is required.
• 6 years of pharma-related and/or clinical research experience.
• Preferred exposure in Phase 1-4 studies and/or Medical Device trials.

Responsibilities

• 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).
• Proactively manages budget, timelines and study issues; brings scientific acumen and global mindset to drive study objectives.
• Leads the cross-functional Clinical Study Team and oversees vendor relationships.
• Coaches and supports cross-functional team members and contributes to Development Operations community.

Skills

Budget management

Cross-functional leadership

Stakeholder management

ICH/GCP knowledge

Education

Bachelor’s Degree or equivalent

Job description

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 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

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.

Responsibilities

• -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
  -Puts patients and customers at the center of what we do
  -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
  - study budget creation and oversight
  - vendor selection, scope development, management and oversight of external vendors
  - Proactively identifying risks and address and/or expand 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

Qualifications

• 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

Additional Information

Applicable only to applicants applying to a position in any location with pay disclosure requirements under state orlocal law:

• The compensation range described below is the range of possible base pay compensation that the Companybelieves ingood faith it will pay for this role at the timeof this posting based on the job grade for this position.Individualcompensation paid within this range will depend on many factors including geographic location, andwemayultimatelypaymore or less than the posted range. This range may bemodifiedin thefuture.
• We offer a comprehensive package of benefits including paid time off (vacation, holidays, sick),medical/dental/visioninsurance and 401(k) to eligibleemployees.
• This job is eligible toparticipatein our long-term incentiveprograms.

Note: No amount of payis considered to bewages or compensation until such amount is earned, vested, anddeterminable.The amount and availability of any bonus,commission, incentive, benefits, or any other form ofcompensation and benefitsthat are allocable to a particular employeeremainsin the Company's sole andabsolutediscretion unless and until paid andmay bemodifiedat the Company’s sole and absolute discretion, consistent withapplicable 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