Clinical Supply Support Associate
3 days ago
Job Qualifications:
- 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.
- May require periodic attendance at team meetings across time zones and occasional after-hours support, particularly on software release dates.
- Design clinical labels in the label system/software based on requirements and procedures.
- Can start ASAP.
- Willing to work in Makati.
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.
Job Responsibilities:
The role of the Clinical Supply Support Associate – CSO (CSSA 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.
- Support the implementation of operational strategies for effective and efficient execution of P/L/D operations.
- 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.
- 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.
Job Type: Full-time
Pay: Php35, Php40,000.00 per month
Application Question(s):
- Do you have any working experience in Pharmaceutical Industry?
- Do you have knowledge or experience working in a Good Manufacturing Practices (GMP) / Good Clinical Practices (GCP) environment ?
- Are you knowledgeable about Clinical Supply Packaging and/or labelling and/or Distribution ?
- Do you have experience in designing clinical labels in the label system/software based on requirements and procedures?
Work Location: In person
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