Project Manager Study I
Project Manager Study I
Employer Active
Job Alert
You will be updated with latest job alerts via email
Share
Job Alert
You will be updated with latest job alerts via email
Not Disclosed
Salary Not Disclosed
1 Vacancy
Job Description
The Study Project Manager I drives the connection between science and operational delivery and ensures operational excellence in planning and 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 ontime 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 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 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
*This position is preferred in Lake County IL or Irvine CA. Remote candidates may be considered.
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
.
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 shortterm incentive programs.
This job is eligible to participate in our longterm 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 Companys sole and absolute discretion unless and until paid and may be modified at the Companys 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 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
