Erica Powers

Erica Powers Email and Phone Number

Founder and Principal Advisor @ Ethical Path Advisors, LLC
Boston, MA, US
Erica Powers's Location
Boston, Massachusetts, United States, United States
Erica Powers's Contact Details
About Erica Powers

Dynamic leader and compliance professional with 20 years of biopharmaceutical industry experience. Collaborative business partner who supports the achievement of desired goals while adhering to global compliance standards. Proven ability to develop strategic vision, motivate teams, and deliver complex global programs requiring cross-functional support.Key attributes include:• Excellent communicator with strong interpersonal skills and public speaking abilities in settings ranging from large audiences to meetings with senior executives• Inspirational leader with a strong focus on employee development• Motivates teams to perform effectively, even while under intense time and resource constraints • Strong work ethic and drive to deliver high quality work products• Creative and open-minded problem solver• Broad knowledge of pharmaceutical business operations• Ability to communicate complex compliance requirements to a wide variety of stakeholders• Recognized globally as a thought leader and expert in the areas of Compliance training, data analytics, monitoring & auditing, risk assessments, data privacy, and global spend transparency

Erica Powers's Current Company Details
Ethical Path Advisors, LLC

Ethical Path Advisors, Llc

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Founder and Principal Advisor
Boston, MA, US
Erica Powers Work Experience Details
  • Ethical Path Advisors, Llc
    Founder And Principal Advisor
    Ethical Path Advisors, Llc
    Boston, Ma, Us
  • Sage Therapeutics
    Vice President, Chief Compliance Officer
    Sage Therapeutics Nov 2024 - Present
    Cambridge, Ma, Us
  • Sage Therapeutics
    Head Of Us Commercial Compliance, Collaboration Compliance, & Compliance Ops (Exec. Director)
    Sage Therapeutics Oct 2022 - Nov 2024
    Cambridge, Ma, Us
  • Sage Therapeutics
    Head Of Us Commercial Compliance And Compliance Operations
    Sage Therapeutics Nov 2021 - Oct 2022
    Cambridge, Ma, Us
  • Sage Therapeutics
    Compliance Officer For Scientific Exchange Functions And Head Of Compliance Operations, Sr. Dir
    Sage Therapeutics Jun 2020 - Mar 2022
    Cambridge, Ma, Us
  • Sage Therapeutics
    Compliance Officer, Director, Head Of Compliance Operations
    Sage Therapeutics Jul 2018 - Jun 2020
    Cambridge, Ma, Us
  • Vertex Pharmaceuticals
    Director Corporate Compliance
    Vertex Pharmaceuticals May 2016 - Jul 2018
    Boston, Ma, Us
    GDPR Program Lead and Head of Global Compliance Operations
  • Vertex Pharmaceuticals
    Associate Director, Corporate Compliance
    Vertex Pharmaceuticals Oct 2011 - May 2016
    Boston, Ma, Us
    Head of Global Compliance Operations:¯¯¯¯¯¯¯¯¯¯¯¯¯¯¯¯¯¯¯¯¯¯¯¯¯¯¯¯¯¯¯¯¯¯¯¯¯¯¯¯¯¯¯¯¯¯¯¯¯¯¯¯¯Program Manager for Global Spend Transparency initiative: Designed and implemented global multi-year strategy to adhere to disclosure laws and codes which require the reporting of payments and transfers of value to a broad set of recipients in the healthcare industry (e.g., healthcare professionals, healthcare organizations, patient organizations). This entailed: • Performing detailed stakeholder needs, process gap assessment, and system inventory • Leading cross-functional teams to define overall program objectives • Managing priorities, budget, timelines and both internal and external resources • Driving company interpretation of over 30 global disclosure laws/codes in partnership with legal        counsel • Development and deployment of enterprise wide program governance, processes, and systems • Championing Global Spend Transparency program adoption throughout the organizationManagement of Compliance team responsible for Global Compliance operations initiatives, including: • End-to-end process and system development related to the engagement of critical parties         (Fair Market Value, Contracting processes, etc.) • Investigation Support • Internal Auditing and Monitoring • Development and maintenance operational strategies through ongoing evaluation of trends • Design and maintenance of systems to capture relevant data points for compliance monitoring,         auditing, and transparency reporting • Development and delivery of Global Compliance training and education • Supporting the development of guidelines, procedures, and policies • Data analysis and compliance dashboard development • Global Data Privacy initiativesOctober 2011 - September 2013: Manager, Corporate ComplianceOctober 2013 - January 2015: Senior Manager, Corporate Compliance
  • Genzyme
    Principal Business Process Analyst, Finance
    Genzyme Dec 2009 - Oct 2011
    Paris, France, Fr
    • Responsible for the design and implementation of system, process, and policy changes to meet federal and state reporting requirements on interactions with health care professionals and organizations• Responsible for implementing a robust customer master data solution and the process for ensuring ongoing data integrity within• Managed data validation efforts for Aggregate Spend• Key player on various process improvement changes throughout the organization• Developed tracking tool and related processes for Global Meetings Management team
  • Genzyme
    Senior Business Systems Analyst, Corporate Development
    Genzyme Apr 2007 - Dec 2009
    Paris, France, Fr
    • Designed, built, and maintained databases for the Business Development, Legal, Program Management and Science departments• Designed tracking system for physician spend and was subsequently appointed as key member of Aggregate Spend Steering Committee to address the growing requirements to report interactions with health care professionals• Developed and managed process for external collaboration using secure data rooms• Collaborated with Business Development teams to design best practices for due diligence processes• Worked with senior management on a broad range of corporate goals• Designed knowledge management practices for the Business Development department
  • Genzyme
    Regulatory Affairs Information Coordinator
    Genzyme Jun 2004 - Mar 2007
    Paris, France, Fr
    • Developed and executed a methodology for integrating information from acquisitions and mergers into the Genzyme environment• Trained staff worldwide on the use of the Global Regulatory information system and the process for tracking Chemical, Manufacturing, and Control Change Information• Managed data steward staff and coordinated process for maintaining CMC Change Data• Managed IT consultants to develop an XML conversion tool to support FDA’s Structured Product Labeling rule• Prepared product submissions for the FDA and EMEA• Database administrator for Genzyme’s Global Regulatory information system

Erica Powers Skills

Fda Pharmaceutical Industry Regulatory Affairs Biotechnology Process Improvement Biopharmaceuticals Aggregate Spend Project Management 21 Cfr Part 11 Program Management Life Sciences Technology Transfer Cross Functional Team Leadership Mergers And Acquisitions Management Medical Devices Regulatory Submissions Lifesciences Business Development Capa Clinical Development Gcp Global Spend Transparency Mergers Business Process Development Business Process Improvement Good Clinical Practice U.s. Food And Drug Administration Compliance Compliance Monitoring System Administration Quality System Drug Development Regulatory Requirements Auditing Fcpa Corporate Development Systems Analysis Oracle Applications Sap

Erica Powers Education Details

  • Harvard University
    Harvard University

Frequently Asked Questions about Erica Powers

What company does Erica Powers work for?

Erica Powers works for Ethical Path Advisors, Llc

What is Erica Powers's role at the current company?

Erica Powers's current role is Founder and Principal Advisor.

What is Erica Powers's email address?

Erica Powers's email address is er****@****rtx.com

What schools did Erica Powers attend?

Erica Powers attended Harvard University.

What skills is Erica Powers known for?

Erica Powers has skills like Fda, Pharmaceutical Industry, Regulatory Affairs, Biotechnology, Process Improvement, Biopharmaceuticals, Aggregate Spend, Project Management, 21 Cfr Part 11, Program Management, Life Sciences, Technology Transfer.

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