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Trial Supplies Manager

2+ years
Not Disclosed
10 Sept. 11, 2024
Job Description
Job Type: Full Time Education: B.Sc./ M.Sc./ M.Pharm/ B.Pharm/ Life Sciences Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

Work Schedule:
Standard, Monday to Friday

Environmental Conditions:
Office-based environment

Job Description:

Oversees the daily operations of the Import and Export department, managing activities related to commercial products, ancillary supplies, investigational products, and biological samples. Ensures that all import/export processes are compliant with CRG, Client requirements, and local regulations. Serves as the primary point of contact for all Import & Export matters, addressing current and future project needs as well as any CRG-led initiatives. Works to seamlessly integrate import/export activities within the clinical supply chain to support each project's logistics strategy.

Maintains effective communication with regulatory bodies and internal departments to prevent any disruptions during the import/export process and ensures adherence to all relevant regulations. Participates in bid and bid defense processes, contributing to the offering of import/export services for the assigned region.

Regularly interacts with internal teams and external representatives at various levels, presenting and addressing operational or scheduling concerns during meetings with stakeholders.