Associate Project Manager – Centurion Associate Project Manager – Bellville Associate Project Manager – Bloemfontein Associate Consultant, Advisory Services CSEC – Centurion Consultant, Advisory Services CSEC – Centurion Contract Negotiator – Bellville Contract Negotiator – Centurion Manager, Clinical Data Management FSP – Bellville Manager, Clinical Data Management FSP – Bloemfontein Manager, Clinical Data Management FSP – Centurion Global Study Leadership – Clinical Project Manager – Oncology – Centurion Patient Support Program (PSP) Manager – Centurion Principal Clinical Database Designer – Bloemfontein Principal Clinical Database Designer – Bellville Principal Clinical Database Designer – Centurion Senior Statistical Programmer – Bellville Senior Statistical Programmer – Centurion Statistical Programmer 1 – Bloemfontein Statistical Programmer 1 – Bellville Statistical Programmer 1 – Centurion Statistical Programmer 2 – Bloemfontein Statistical Programmer 2 – Bellville Statistical Programmer 2 – Centurion

  • Full Time
  • Gauteng

Website IQVIA

Sharing a Vision to Drive Healthcare Forward Healthcare is an industry designed to help humans. As a global community, we continuously invest and commit to advancing human health. To deliver value and real outcomes. To rise to the challenge to find the next breakthrough by making the most of increa… read moresingly limited resources. We are inspired by the potential and propelled by the possibilities. We share the vision to drive healthcare forward. To see how we can help accelerate progress and achievements. Others are developing these medical breakthroughs. We do our part by using breakthroughs in insights, technology and human intelligence to reimagine and deliver ways to help make them a reality. It’s bigger than better clinical trials. Or advances in technologies and analytics. Or faster insights. It’s about exploring a new path to better health outcomes via Human Data Science. It’s about harnessing the power of the IQVIA COREâ„¢ to channel the insights, commercial and scientific depth, and executional expertise that drive maximum value for our customers. Motivated by the industry we help, we’re committed to providing solutions that enable life sciences companies to innovate with confidence, maximize opportunities, and, ultimately, drive human health outcomes forward. Southdown's Ridge Office Park 2nd Floor, Unit 5 Corner Nellmapius & John Vorster Drive Irene Ext. 54 Centurion Pretoria South Africa 0169

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.
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.

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Apply via company website ( https://www.iqvia.com ) or

 

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