David Stock
Senior Clinical Trial Management Associate at Ionis Pharmaceuticals, Inc.
- Role
- Senior Clinical Trial Management Associate at Ionis Pharmaceuticals, Inc.
- Location
- San Diego, CA, US
- LinkedIn followers
- 500 followers
About David Stock
I’m a city dweller with roots in the Alaskan wilderness, passionate about exploring new places, creating music, and embracing outdoor adventures. With a background in environmental and life sciences, data analysis, and project management, I thrive in dynamic environments where I can contribute to meaningful solutions.I’m driven by the opportunity to connect with people, build strong relationships, and solve complex challenges. There’s nothing more fulfilling to me than playing a role in the growth and success of a business, all while fostering collaboration and innovation along the way.
Experience
Senior Clinical Trial Management Associate
Jul 2023 — Present · CA, US
Performs study tracking generates, reviews, and distributes management reports from internal tracking systems at requested intervals-Collaborates with the CTM and/or the CPL on the development of certain study-specific plans and/or processes-Presents at team meetings as needed -Supports TMF set-up, maintenance, ongoing quality review, and final reconciliation of study documents -Participates/leads in study specific tasks such as Investigator identification, recruitment, collection of Investigator regulatory documents and site activation-Contributes to or leads the development of the Monitoring Plan and assists with ensuring appropriate quality and timely monitoring of clinical sites-Assists/leads in development of study materials, case report forms (CRFs), informed consent documents for clinical studies -Prepares investigational site reference materials-Acts as primary contact for study contractors-Keeps the CPL informed of the progress of projects-Develops and maintains good working relationships with Investigators and study staff-Assists/leads in the organization and preparation of and participates in Investigator Meetings-Performs document tracking and signature/approval follow-up, where applicable, including Confidential Disclosure Agreements (CDAs), contracts, proposals, invoices, and other study documentation-Executes meeting logistics as needed-May assist with study entry and updates to ClinicalTrials.gov-Assists with or leads the design and preparation of study related materials for the training of internal and external staff-Participates in or leads co-monitoring activities and oversight of CRO or contract CRAs for pre-study, initiation, routine monitoring and closeout visits -Assists or leads with oversight of study vendors-Helps facilitate resolution of data queries and requests from Clinical Data Management-Assists with or leads with the tracking and management of study specific budgets
Education
North Kitsap High School
Diploma
2006 — 2010
Western Washington University
Bachelor of Science (B.S.), Environmental Science
2010 — 2015
Rome Business School
Master of Business Administration - MBA
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