Cindy Garrison

Cindy Garrison Email and Phone Number

Senior Manager, Clinical Operations at SpringWorks Therapeutics, Inc. @ SpringWorks Therapeutics, Inc.
Raleigh, NC, US
Cindy Garrison's Location
Raleigh, North Carolina, United States, United States
Cindy Garrison's Contact Details

Cindy Garrison personal email

n/a

Cindy Garrison phone numbers

About Cindy Garrison

I have extensive pharmaceutical research experience in the management and coordination of clinical trials. This includes management of clinical operations for three trials that were successfully submitted to regulatory authorities. Some of my core competencies include:• Clinical Research Organization (CRO)/vendor management• Good Clinical Practice (GCP)/International Conference on Harmonization (ICH)/Regulatory requirements• Institutional Review Board (IRB)/Independent Ethics Committee (IEC) requirements• Protocol development• Management status reporting• Process development• Data analysis• Trial Master File (TMF) reconciliation• Training/mentoringI am known for my excellent organizational and communication skills and I collaborate effectively with multi-disciplinary global study teams. Additionally, I have led departmental process improvement initiatives.My experience includes multiple therapeutic areas, including CNS, respiratory, oncology, liver disease, women's health and immunology.I can be contacted at cindygB22@yahoo.com, 919-614-1948.

Cindy Garrison's Current Company Details
SpringWorks Therapeutics, Inc.

Springworks Therapeutics, Inc.

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Senior Manager, Clinical Operations at SpringWorks Therapeutics, Inc.
Raleigh, NC, US
Employees:
418
Cindy Garrison Work Experience Details
  • Springworks Therapeutics, Inc.
    Springworks Therapeutics, Inc.
    Raleigh, Nc, Us
  • Springworks Therapeutics, Inc.
    Senior Manager, Clinical Operations
    Springworks Therapeutics, Inc. Jan 2019 - Present
    Provide oversight and management of day-to-day clinical operations, ensuring successful execution of clinical trials and completion of trial deliverables.
  • Protrials Research Inc.
    Lead Clinical Research Associate
    Protrials Research Inc. Jan 2017 - Jan 2019
    Los Gatos, California, Us
    Assisted with the coordination of operational aspects of global clinical studies for pharmaceutical sponsors. Acted as liaison between sites, CRO(s), vendors and sponsor, supported data finalization and submission activities, facilitated study launch and closure activities, monitored performance of clinical operations activities including review of CRA visit reports, provided study metrics reports to management team, trial master file review/reconciliation.
  • Ucb Biosciences, Inc
    Associate Clinical Project Manager
    Ucb Biosciences, Inc Apr 2001 - Oct 2016
    Brussels, Be
    Functioned as a clinical team lead to assist project manager in clinical operations oversight. Accountable for planning, coordination and supervision of site-related and monitoring activities, which included visit report review, Clinical Research Associate (CRA) training, assessment visits, in accordance with quality and compliance standards.Responsibilities included preparation/review/submission of clinical documents, Clinical Research Organization (CRO) and vendor management and training, data review and analysis, project tracking and reporting, CRO and site performance review, trial master file review/reconciliation, essential document review/approval.
  • Resource Solutions, Inc
    Senior Clinical Research Associate
    Resource Solutions, Inc 1996 - 2001
    As member of Clinical Research Organization (CRO) study teams, performed site qualification, initiation, monitoring and close-out visits in multiple therapeutic areas. Managed study site activities, ensuring quality and integrity of data, and compliance with regulatory requirements and Good Clinical Practice (GCP). Conducted study start-up activities, including investigator recruitment, budget and contract negotiation, essential document review and submission, study forms and manual development.
  • Clintrials Research, Inc.
    Clinical Research Associate
    Clintrials Research, Inc. 1989 - 1996

Cindy Garrison Skills

Clinical Trials Clinical Development Pharmaceutical Industry Cro Clinical Monitoring Ich Gcp Ctms 21 Cfr Part 11 Clinical Data Management Informed Consent Trial Master File Epilepsy Diabetic Neuropathy Sops Study Start Up Activities Cro Management Clinical Operations Ccra Regulatory Document Review Gcp Sop Regulatory Affairs Regulatory Submissions Drug Development Systemic Lupus Erythematosus Standard Operating Procedure Good Clinical Practice Clinical Research Clinical Trial Management System Project Management Vendor Management

Cindy Garrison Education Details

  • University Of North Carolina At Greensboro
    University Of North Carolina At Greensboro
    Speech-Language Pathology/Pathologist

Frequently Asked Questions about Cindy Garrison

What company does Cindy Garrison work for?

Cindy Garrison works for Springworks Therapeutics, Inc.

What is Cindy Garrison's role at the current company?

Cindy Garrison's current role is Senior Manager, Clinical Operations at SpringWorks Therapeutics, Inc..

What is Cindy Garrison's email address?

Cindy Garrison's email address is ci****@****ucb.com

What is Cindy Garrison's direct phone number?

Cindy Garrison's direct phone number is (866) 664*****

What schools did Cindy Garrison attend?

Cindy Garrison attended University Of North Carolina At Greensboro.

What skills is Cindy Garrison known for?

Cindy Garrison has skills like Clinical Trials, Clinical Development, Pharmaceutical Industry, Cro, Clinical Monitoring, Ich Gcp, Ctms, 21 Cfr Part 11, Clinical Data Management, Informed Consent, Trial Master File, Epilepsy.

Who are Cindy Garrison's colleagues?

Cindy Garrison's colleagues are Leah Delong, Chris Mauney, Annamaria Sprague, Michael Rohrer, Patrick Kivlin, Jess White, Christopher Shrader.

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