Compliance Manager

Develops, supports and executes Governance, Risk and Compliance strategies and initiatives across PPD. Promotes awareness of quality and regulatory compliance standards and trends; participates in quality improvement activities. Oversees governance and compliance management processes; implements quality awareness objectives; develops and maintains quality and compliance guidance/reference materials and tools and provides any other support or knowledge necessary to advance the vision of the Global Quality and Compliance (GQ&C) group.

Develops, supports and executes Governance, Risk and Compliance strategies and initiatives across PPD. Promotes awareness of quality and regulatory compliance standards and trends; participates in quality improvement activities. Oversees governance and compliance management processes; implements quality awareness objectives; develops and maintains quality and compliance guidance/reference materials and tools and provides any other support or knowledge necessary to advance the vision of the Global Quality and Compliance (GQ&C) group.

Education and Experience: Bachelor's degree in a scientific or related discipline 6 years of clinical drug development experience including 4 years clinical operations or quality management experience in the pharmaceutical industry and/or CRO Or equivalent combination of education, training and experience that provides the individual with the required knowledge, skills and abilities

Knowledge, Skills and Abilities: Excellent oral and written communication skills Strong influencing and motivation skills Solid organization skills Extensive knowledge of the clinical trial process Thorough understanding of ICH GCP and other relevant regulations and guidelines Effective negotiation and problem solving skills Strong writing and computer skills Ability for frequent multi-tasking

Pharmaceutical Product Development, LLC is firmly committed to Equal Employment Opportunity (EEO) and prohibits employment discrimination for employees and applicants based on age, race, color, pregnancy, gender, gender identity, sexual orientation, national origin, religion, marital status, citizenship, disability or protected veteran or other status protected by federal, state, and/or local law.

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Education and Experience: Bachelor's degree in a scientific or related discipline 6 years of clinical drug development experience including 4 years clinical operations or quality management experience in the pharmaceutical industry and/or CRO Or equivalent combination of education, training and experience that provides the individual with the required knowledge, skills and abilities

Knowledge, Skills and Abilities: Excellent oral and written communication skills Strong influencing and motivation skills Solid organization skills Extensive knowledge of the clinical trial process Thorough understanding of ICH GCP and other relevant regulations and guidelines Effective negotiation and problem solving skills Strong writing and computer skills Ability for frequent multi-tasking

Pharmaceutical Product Development, LLC is firmly committed to Equal Employment Opportunity (EEO) and prohibits employment discrimination for employees and applicants based on age, race, color, pregnancy, gender, gender identity, sexual orientation, national origin, religion, marital status, citizenship, disability or protected veteran or other status protected by federal, state, and/or local law.

#LI-PA1