Study Project Manager I Oncology
Study Project Manager I Oncology
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Job Description
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 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 escalate study related issues and opportunities for efficiency Empowered decision maker on operational aspects of study .
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
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Qualifications :
- Bachelors Degree or equivalent degree is required
- 6 years of demonstrated pharmarelated and/or clinical research related experience or equivalent required.
- Preferred exposure in study initiation through study completion in Phase 14 and/or Medical Device Trial Experience
- Hybrid model based in the office 3 days per week onsite)
Key Stakeholders:
Clinical Study Team members which includes TA MD/SD DSS Lead Data Mgmt Lead GSML Start Up Lead. Program Leads
Additional Information :
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 AbbVies 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 & Puerto Rico applicants seeking a reasonable accommodation click here to learn more:
No
Employment Type :
Fulltime
Employment Type
Full-time
