Associate Clinical Project Manager, Netherlands

Join us on our exciting journey!

Remote/Hybrid/Office based working options.

Our Sponsor Dedicated (cFSP) team are growing, join us on our mission to drive healthcare forward!

Associate Clinical Project Managers are an integral part of clinical trial delivery, liaising with clinical teams to improve patients’ lives by bringing new drugs to the market faster. You will be a member of the core project team responsible for project delivery of clinical studies to meet contractual requirements in accordance with SOPs, policies and practices. Clinical Project Management is focused on project delivery, productivity and quality resulting in strong financial performance and customer satisfaction.

Job Overview:

Monitor progress against contract and prepare/present project and/or sub-team information proactively to internal stakeholders. Support the project leader to prepare/present project and/or sub-team information proactively to external stakeholders.

Accountable for assigned portion of clinical studies as per the contract while optimizing speed, quality and cost of delivery and ensuring consistent use of study tools and training materials and compliance with standard processes, policies, and procedures.

Provide input into the development of integrated study management plans with the core project team and/or sub-team.

Achieve project quality by identifying quality risks and issues, responding to issues raised by project sub-team members and partner with project leader planning/implementing appropriate corrective and preventative action plans.

Lead the efforts of a project sub-team, responsible for managing cross-collaboration of the sub-team to support milestone achievement and to manage issues and obstacles.

 Requirements:

• Bachelor's Degree In life sciences or related field required.
• 3-4 years clinical research experience.
• Knowledge of clinical trial conduct, and skill in applying applicable clinical research regulatory requirements i.e. ICH GCP and relevant local laws, regulations, and guidelines, towards clinical trial conduct You’ve handled multiple protocols and sites across a variety of drug indications.
• Flexibility and ability to travel.
• Strong communication, written and presentation skills.

What is in it for you?

• The chance to work on cutting edge medicines at the forefront of new medicines development.
• IQVIA has access to significant data pools allowing better site selection and recruitment.
• We offer genuine career development opportunities for those who want to grow as part of the organisation.
• We invest in keeping our teams stable, so workload is consistent.

#LI-REMOTE

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