Associate Project Manager, Centurion

Centurion, South Africa | Full time | Home-based | R1546331

Home-based, office-based, hybrid options available

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.

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 setup 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.

Coordinate company services, such as but not limited to, database setup, data management, and lab operations, and serve 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.

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