Study Project Manager II Oncology

AbbVie Inc; Maidenhead; Hybrid; GBP 50,000 - 70,000; Full time

Job summary

A leading biopharmaceutical company is seeking a Study Project Manager II for oncology studies in Maidenhead. This role involves strategic planning and execution of clinical research while ensuring compliance with quality standards. Candidates must have a Bachelor's degree and extensive experience in clinical operations and project management. This position promotes innovation and effective stakeholder management in a cross-functional environment.

Qualifications

• Extensive experience in pharma-related and clinical research required.
• Experience in Project Management for interventional trials.
• Exposure in Phase 1-4 studies or Medical Device trials.

Responsibilities

• Define and drive the study level operational strategies.
• Lead clinical operations planning through to execution.
• Effectively present and contribute in cross-functional meetings.

Skills

Project Management

Clinical Operations Management

Stakeholder Management

Innovative Problem Solving

Cross-Functional Collaboration

Education

Bachelor's Degree or equivalent

Job description

Company Description

The Study Project Manager II Oncology drives the connection between the asset and operational delivery and execution of one or more clinical research studies. Leading the delivery of clinical operational strategies to ensure studies are executed with quality and efficiency, on-time, within budget, and meet company objectives. The Study Project Manager II achieves these objectives by bringing scientific acumen, strategic asset level thinking, innovation, expertise in clinical study operations management and stakeholder management to address risks and challenges.

Job Description

• Defines and drives the study level operational strategies and deliverables – linking these to asset level goals
• Brings strategic, asset level thinking and innovative problem solving to study planning and execution
• Responsible for executing clinical studies in compliance with quality standards (ICH/GCP, Global Regulations, and AbbVie policies and procedures).
• Effectively present and contribute to discussions on study operations at asset level strategic meetings
• Leads clinical operations planning through to execution via cross functional matrix environment and influences cross functional stakeholders to drive milestone achievement
• Demonstrates the skills, experience and critical thinking to lead cross functional teams with minimal supervision.
• Expertise in end-to-end clinical study operations management (all phases, set up to close out)
• Coaches and mentors team members, delegates and empowers to the right level, actively contributes to Development Operations community
• Demonstrates leadership with high level cross functional stakeholder management and influencing skills
• Lead operational efficiencies and foster a culture of innovation

Qualifications

• Bachelor’s Degree or equivalent degree is required
• Extensive demonstrated pharma-related and/or clinical research related experience or equivalent required.
• Exposure in study initiation through study completion in Phase 1-4 and/or Medical Device Trial Experience.
• No direct reports, but matrix management.
• Required experience in Project Management interventional trials
• Experience in Oncology studies in the lastyears of experience.
• Homebased.

Additional Information

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, visithttps://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