Mary Poor

Vice President

Fort Collins, Colorado, United States

Professional Overview

Mary Poor is an accomplished pharmaceutical and biotech executive with extensive experience in regulatory affairs, quality assurance, and strategic development. As the Vice President at Siolta Therapeutics, she leverages her deep industry expertise to drive innovative therapeutic solutions. Mary also serves as a Director for the ISPE Rocky Mountain Chapter, contributing her knowledge and leadership to the professional organization.

Experience Summary

Current Roles

Vice President, Siolta Therapeutics (Present)

• Oversees all regulatory and strategic initiatives for the company's novel therapeutic pipeline

• Leads cross-functional teams to ensure seamless product development and compliance

• Drives the implementation of robust quality systems and manufacturing processes

Director, ISPE Rocky Mountain Chapter (Present)

• Provides strategic guidance and industry insights to the regional professional organization

• Organizes educational events and networking opportunities for industry peers

• Advocates for best practices and professional development within the biotech community

Director, Regulatory and Strategic Development, Clinipace (Present)

• Managed complex regulatory submissions and liaised with global health authorities

• Developed strategic plans to support the company's market expansion efforts

• Collaborated with cross-functional teams to ensure efficient project execution

Validation Scientist, Compliance Group, Commissioning Agents, Inc. (Present)

• Conducted comprehensive validation studies to ensure compliance with cGMP regulations

• Implemented quality control measures and optimized manufacturing processes

• Trained and mentored junior team members on validation protocols and best practices

Quality Assurance Manager, BioMARC (Present)

• Established and maintained robust quality management systems for the organization

• Oversaw all QA/QC activities, including audits, investigations, and continual improvement

• Ensured strict adherence to regulatory requirements and industry standards

Career Progression

Prior to her current roles, Mary held positions of increasing responsibility within the pharmaceutical and biotech industries. She gained valuable experience as a Validation Scientist and Quality Assurance Manager, honing her expertise in regulatory compliance, quality systems, and process optimization.

Academic Background

Mary holds a Bachelor of Science degree in Pharmaceutical Sciences from the University of Colorado Boulder, where she graduated with distinction.

Areas of Expertise

• Regulatory affairs and strategic development

• Quality assurance and compliance management

• Validation and cGMP manufacturing processes

• Cross-functional team leadership and collaboration

• Strategic planning and project management

Professional Impact

Throughout her career, Mary has made significant contributions to the pharmaceutical and biotech industries. Her expertise in regulatory affairs and quality assurance has enabled her to drive the successful development and commercialization of novel therapeutics. Mary's leadership and industry involvement, particularly through her role with the ISPE Rocky Mountain Chapter, have further solidified her reputation as a respected professional within the field.

Conclusion

With her proven track record of success, Mary Poor is a strategic and highly capable executive who continues to make valuable contributions to the pharmaceutical and biotech sectors. Her multifaceted expertise, coupled with her commitment to professional development and industry engagement, position her as a valuable asset to any organization seeking to navigate the complex and rapidly evolving landscape of the life sciences industry.