Training and Compliance Specialist

August 1

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Clinical Trials Design • Planning • Safety Management • Custom Services • Study Management

201 - 500

Description

• Drives a culture of compliance within Clinical Research. • Evaluates the quality status of project deliverables by reviewing applicable project quality metrics and documentation. • Identifies and evaluates potential risks and quality issues in collaboration with project team leadership and other relevant parties. • Determines appropriate mitigation measures. • Leads the development of relevant policies and procedures. • Leads training initiatives and acts as a resource for audits and inspections. • Supports or manages the CAPA process. • May include laboratory assay quality control (QC) for the histopathology laboratory.

Requirements

• The successful candidate should hold either an undergrad degree with 4-6 years of relevant experience, or a college diploma with 7-9 years of relevant experience. • Health Sciences, Sciences or Clinical Research specialty preferred. • Excellent interpersonal, verbal and written communication skills. • Customer focused approach to work. • A flexible attitude with respect to work assignments and new learning. • Ability to manage and prioritize tasks efficiently and accurately. • Ability to work in a matrix environment and to value the importance of teamwork. • Ability to analyze and interpret data. • Attention to detail and organizational skills. • Ability to work independently and take ownership of and responsibility for work assigned. • IT literate. Experience with Microsoft based applications and a general knowledge of PC functions. • Culturally aware and ability to think and work globally.