Clinical Supply Support Associate (Contract)

The role of the Clinical Supply Support Associate (CSSA) – Clinical Supply Operations (CSO) is to provide support for Clinical Supply Operations (CSO) in the areas related to the receipt, packaging, labeling, warehouse, distribution and logistics (P/L/D) operations of clinical supplies. They will also provide support in document management, metrics, order request and completion and other items required to support this area. The position also requires providing support across different global time zones.

Roles and Responsibilities

Support the implementation of operational strategies for effective and efficient execution of P/L/D operations.

Execute P/L/D operations ensuring quality, regulatory compliance, and exemplary customer service. Apply project management skills to strategically plan, implement, and assess risks to ensure operational success, and exercise sound judgment when resolving basic issues from limited alternatives, maintaining minimal or no impact on P/L/D outcomes.

Leverage knowledge of supply chain processes and systems to assist in implementing operational strategies that enable the effective and efficient execution of P/L/D operations, including managing receipt processes to ensure accurate documentation and timely reconciliation of all incoming goods and materials

Maintain systems and documentation for P/L/D operations.

Liaise with internal stakeholders, including, but not limited to Operational Strategy Leads (OSLs), CSO Planners and Schedulers, and Label Operations to support and execute P/L/D operations using technology and supply chain systems.

Utilize CSO enterprise systems (e.g., EMD365, CSDS, Clementine, Prisym360) to perform P/L/D operations.

Ensure timely completion of system-related tasks for assigned P/L/D jobs.

Design clinical labels in the label system/software based on requirements and procedures.

Support CSO operational compliance and inspection readiness.

Ensure all P/L/D activities comply with regulatory requirements and quality standards.

Manage receipts and shipment tracking.

Prepare reports on P/L/D activities and performance and maintain accurate records & documentation.

Provide occasional coverage for team members on high-priority activities and studies.

3 REQUIREMENTS

Qualifications and Education

BA/BS in supply chain, scientific, computer science or business field with at least 2 years experience in pharmaceutical industry and/or supply chain management.

Knowledge and experience working in a Good Manufacturing Practices (GMP) / Good Clinical Practices (GCP) environment.

Adaptable to non-standard work schedule or environment requirements.

o May require periodic attendance at team meetings across time zones and occasional after-hours support, particularly on software release dates.

Skills

Must be proficient in Microsoft Office programs.

Comfortable preparing and presenting ideas and information in a variety of settings.

Knowledgeable about Clinical Supply Packaging and/or Labelling and/or Distribution (e.g. technical, process, plan or system).

Articulate in both verbal and written communication.

Excellent customer focused communication and listening skills.

Proven interpersonal, facilitation, customer relations and negotiation skills.

Demonstrated ability to learn fast and foster a culture of innovation.

Possess strong analytical and problem-solving abilities, with a proven capacity to work collaboratively with colleagues and customers in a matrix environment.

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.