Experience

Cobu

• United States
• Real Estate
• 1 - 100 Employee

• Senior Manager, Innovation

  • Jul 2022 - Present

• Customer Success Director

  • Feb 2020 - Jul 2022

  Cobu makes it easy for residents to connect with their neighbors and neighborhood, turning apartments into homes. By creating a strong sense of community, Cobu helps leading building owners to increase resident satisfaction and retention.

• Director of Community

  • Nov 2017 - Feb 2020

  Cobu is the leading amenity activation platform built for multifamily housing. We supercharge apartment communities through our curated community event experiences and app.

• Community Manager

  • Jul 2017 - Nov 2017



Album of US

• Project Manager

  • Apr 2016 - Sep 2017

  Art & travel project consisting of 10k photographs and 20 hours of video. Designed and coded website visited by ~7k people from 95 countries. Managed community relationships while traveling over 40k miles through the 48 contiguous United States in a temperamental ‘83 Volkswagen Vanagon. Art & travel project consisting of 10k photographs and 20 hours of video. Designed and coded website visited by ~7k people from 95 countries. Managed community relationships while traveling over 40k miles through the 48 contiguous United States in a temperamental ‘83 Volkswagen Vanagon.



Premier Research

• United States
• Biotechnology Research
• 700 & Above Employee

• Project Specialist

  • Feb 2015 - Mar 2016

  - Facilitated study team and financial tracking, timeline adherence, and team communication.- Assisted in adherence to project budgets and scope of work to realize project profitability. - Assisted in ensuring project tasks were completed in accordance with project plans and SOPs.

• Clinical Trial Associate

  • Sep 2014 - Feb 2015

  - Oversaw document processing, timely delivery, filing, and archiving for a complement of clinical studies.- Performed QC checks to ensure documents complied with SOPs, GCPs, and other regulations.- Communicated with clients and team members to prioritize trials and document processing.



Doheny Eye Institute

• United States
• Non-profit Organizations
• 100 - 200 Employee

• Study Coordinator

  • Sep 2012 - Mar 2014

  - Reviewed study documents and images submitted by clinical centers to ensure protocol requirements were met.- Communicated with study sites to resolve any discrepancies, errors, or omissions before images were graded. - Performed QC reviews on grading materials and followed up with project managers and graders on any deficiencies.- Entered study data in eCRFs and resolved all queries. - Presented status updates regarding workflow at team meetings to optimize performance and address bottlenecks.



Brigham and Women's Hospital

• United States
• Hospitals and Health Care
• 700 & Above Employee

• Program Coordinator

  • Oct 2009 - Sep 2011

  - Managed all aspects of the Translational Pain Research group, including staff and finances. - Oversaw the conduct of two long-term, multi-center phase II-III clinical trials. - Negotiated an itemized budget of approximately $500K for an industry sponsored trial.- Created and submitted study materials to the hospital's IRB to obtain and maintain trial approval.- Oversaw the patient recruitment process, edited marketing materials, and established advertising contracts. - Managed internal AE/SAE documentation and reporting.- Maintained the trial master file and regulatory documents to ensure compliance with GCP.



Toxikon Corporation

• United States
• Medical Equipment Manufacturing
• 1 - 100 Employee

• Quality Assurance Associate

  • Sep 2006 - May 2009

  - Reviewed and edited reports, protocols, and SOPs to ensure compliance and accuracy in a GLP facility.- Performed raw data and phase audits across a range of pre-clinical medical device and pharmaceutical studies. - Reported findings on system audits to define weaknesses and propose corrective actions.- Contributed to protocol and report development, design, and data presentation.- Inspected in vivo studies conducted according to ISO, USP, MHLW, and OECD guidelines. - Reviewed and edited reports, protocols, and SOPs to ensure compliance and accuracy in a GLP facility.- Performed raw data and phase audits across a range of pre-clinical medical device and pharmaceutical studies. - Reported findings on system audits to define weaknesses and propose corrective actions.- Contributed to protocol and report development, design, and data presentation.- Inspected in vivo studies conducted according to ISO, USP, MHLW, and OECD guidelines.