Associate Project Manager

Associate Project Manager

IQVIA Laboratories

Home-based, office-based, hybrid options available

IQVIA Laboratories also specializes in antibody and biomarker discovery, as well as decentralized clinical trial laboratory solutions. Committed to scientific rigor and operational excellence, we support every phase of the drug development and discovery process across diverse regions and regulatory frameworks, ensuring the highest standards of data integrity and accelerating the delivery of transformative therapies to patients.

Join us on our exciting journey!

Job Overview:

Facilitate seamless study set-up including Protocol and Budget review, leading meetings, develop and implement project plans, milestone, risk, issue, and action logs.

Partner with Study Setup team to ensure quality database set-up, oversee preparation of protocol specific documentation.

Prepare and present protocol-specific materials at Kick Off and Investigator meetings.

Monitor the Project Management Plan, timelines, and deliverables, manage study documentation throughout the Project lifecycle including filing into eTMF, oversee study monitoring and reporting, conduct meetings to meet needs of the Study and Customer requirements.

Manage study scope changes and budget monitor quality of the study and any service-related issues, implementing changes as required.

Participates with project management team members to continuously review and upgrade processes, practices, and the quality of service provided to clients.

Coordinates company services, such as but not limited to, database setup, data management, and lab operations, and serves as a resource for internal departments.

Requirements:

• Bachelor’s degree in Life Sciences and/or related field preferred and minimum of 2 years of experience in the equivalent capacity to a Project Manager in a clinical trial related industry.
• A Project Management Professional (PMP) certificate is desirable.
• Demonstrated proficiency with Microsoft Office, including Excel is required.
• Smartsheet proficiency is desirable.
• Excellent attention to detail, organizational and communication skills.
• Ability to establish and maintain effective working relationships with colleagues and clients.
• Ability to achieve results through collaborative efforts with others.
• Strong knowledge of Project Services processes, laboratory processes, and/or equivalent working knowledge of central laboratory operations preferred.
• Experience in successfully leading large, global, and complex Phase I-IV clinical trials preferred.

• Global exposure
• Variety of therapeutic areas
• Collaborative and supportive team environment
• Access to cutting-edge and innovative, in-house technology
• Excellent career development and progression opportunities
• Work-Life Balance, with a strong focus on a positive well-being.

Learn more at https://jobs.iqvia.com