Associate Laboratory Project Services Manager

IQVIA Inc; Livingston; Híbrido; GBP 55.000 - 75.000; Jornada completa

Ventajas ofrecidas por este puesto de trabajo

Global exposure

Therapeutic areas

Collaborative team

In-house tech

Career progression

Work-life balance

Descripción de la vacante

IQVIA is seeking a Project Manager to support study setup, budgeting, and lifecycle management across global clinical trial programs. The role collaborates with multi-disciplinary teams to ensure timely delivery and quality, coordinating database setup, data management, and lab operations across Phase I–IV studies.

You should bring a Life Sciences degree, 1.5+ years PM experience in a customer-facing environment, and strong timelines and budgets skills to drive successful trial execution.

Formación

• Bachelor's degree in Life Sciences or related field preferred.
• Knowledge of project management methodologies, processes, and best practice technology.
• Minimum of 18 months experience in a project management and customer-facing environment preferred.
• Over 2 years of experience in the clinical or research industry preferred.
• Skill in creating and maintaining project timelines to ensure deadlines are met.
• Experience in managing project budgets to avoid cost overruns.
• Ability to achieve results through collaborative efforts with others.
• Knowledge of Laboratory Operations, and Central Laboratory Functions (kits/supplies, logistics, specimen storage, data reporting, site alerts, etc.).
• Ability to identify potential risks and develop mitigation strategies.
• Experience in successfully leading large, global, and complex Phase I-IV clinical trials preferred.

Responsabilidades

• Facilitate study setup, including protocol and budget review, leading meetings, and developing project plans.
• Partner with the Study Setup team for quality database set up and oversee protocol documentation.
• Prepare and present protocol-specific materials at Kick Off and Investigator meetings.
• Monitor project plans, timelines, and deliverables, manage documentation, and oversee study monitoring and reporting.
• Manage study scope changes and budget monitor quality of the study and any service-related issues, implementing changes as required.
• Collaborate with project management to improve processes and service quality.
• Coordinates company services, such as but not limited to, database setup, data management, and lab operations, and serves as a resource for internal departments.

Conocimientos

Project management

Timeline management

Budget management

Cross-functional collaboration

Clinical trials knowledge

Educación

Bachelor's degree in Life Sciences

Descripción del empleo

IQVIA Laboratories is a global leader in drug discovery and development, offering comprehensive central and specialty biomarker services. Our expertise includes genomics, immunoassays, flow cytometry, anatomic pathology, precision medicine, vaccine assays, ADME, and bioanalytical services. We also specialize in antibody and biomarker discovery and decentralized clinical trial solutions. Committed to scientific rigor and operational excellence, we support all phases of drug development, ensuring high data integrity and accelerating transformative therapies.

Join us on our exciting journey!

Work Arrangement

Home-based, office-based, hybrid options available

Job Overview

• Facilitate study setup, including protocol and budget review, leading meetings, and developing project plans.
• Partner with the Study Setup team for quality database set up and oversee protocol documentation.
• Prepare and present protocol-specific materials at Kick Off and Investigator meetings.
• Monitor project plans, timelines, and deliverables, manage documentation, and oversee study monitoring and reporting.
• Manage study scope changes and budget monitor quality of the study and any service-related issues, implementing changes as required.
• Collaborate with project management to improve processes and service quality.
• 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 Equivalent combinations of education, training, and experience may be considered.
• Knowledge of project management methodologies, processes, and best practice technology.
• Minimum of 18 months experience in a project management and customer-facing environment preferred.
• Over 2 years of experience in the clinical or research industry preferred.
• Skill in creating and maintaining project timelines to ensure deadlines are met.
• Experience in managing project budgets to avoid cost overruns.
• Ability to achieve results through collaborative efforts with others.
• Knowledge of Laboratory Operations, and Central Laboratory Functions (kits/supplies, logistics, specimen storage, data reporting, site alerts, etc.).
• Ability to identify potential risks and develop mitigation strategies.
• Experience in successfully leading large, global, and complex Phase I-IV clinical trials preferred.

Benefits

• 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.

Join IQVIA to see where your skills can take you.

IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com

IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.