Anna Rodriguez Email and Phone Number
Anna Rodriguez work email
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Anna Rodriguez personal email
Experienced in Regulatory Affairs and Project Management with a demonstrated history of working in the healthcare, biotechnology, and pharmaceutical industry. Strong leadership skills having managed 10+ direct reports. Skilled in regulatory submissions to US/EU health authorities and ethics committees (IRB). Received a Master’s Degree focused in Health Care Management and Interprofessional Leadership from University of California, San Francisco.
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Director Global Regulatory AffairsCalico Life Sciences Jul 2024 - PresentSouth San Francisco, Ca, Us
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Associate Director Regulatory AffairsCalico Life Sciences Aug 2021 - Jul 2024South San Francisco, Ca, Us
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Senior Manager Regulatory Strategy (Promoted)Beigene Jun 2018 - Aug 2021Cambridge, Ma, Us• Manage the preparation, review, and submission of all components of regulatory submissions including INDs and amendments, BLAs/NDAs and supplements, annual reports, safety reports, etc. Participate on project teams and provide expertise on regulatory matters.• Serve as the Regulatory liaison with health authorities and manage regulatory activities related to assigned projects that span technical areas including clinical, non-clinical, and CMC.• Assist in developing and implementing strategies for the earliest possible approvals/clearance of regulatory submissions associated with assigned projects.• Develop and maintain current regulatory knowledge and advise management on significant developments -
Manager Sr Regulatory Affairs And Project Management Support (Promoted)University Of California, San Francisco Apr 2013 - Jun 2018San Francisco, California, Us• Responsible for the hiring and development of Regulatory Affairs and Project Management Support team with the goal of training future leaders.• Develop strategic plan for coverage across disease programs through cross-training and staff management• Spearhead the Investigational Trials Resource Volunteer Program that provides an introductory overview of clinical trials operation and management. • Work with disease programs to resolve complex project issues while monitoring program timelines and milestones.• Utilizes regulatory expertise and knowledge of regulatory requirements to ensure regulatory approvals are acquired.• Serves as a Project Manager for groups that require assistance and coverage -
Research AssistantUc Davis Jun 2011 - Jun 2012Davis, California, UsDr. Jorge Dubcovsky's Laboratory • Assisted researcher in conducting experiments and projects• Knowledge of basic laboratory skills and safety to perform the necessary tasks• Formulated chemical solutions by following lab protocols• Experience in making agarose and polyacrylamide gels for electrophoresis -
Clinical Research CoordinatorUc Davis Sep 2010 - Oct 2011Davis, California, Us• Assisted the principal investigator in refining the research methodology of the experiments.• Facilitated in the consent review process and research execution • Guided research participants to important aspects of the protocol
Anna Rodriguez Education Details
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University Of California, San FranciscoHealth/Health Care Administration/Management And Interprofessional Leadership -
University Of California, DavisCell/Cellular And Molecular Biology
Frequently Asked Questions about Anna Rodriguez
What company does Anna Rodriguez work for?
Anna Rodriguez works for Calico Life Sciences
What is Anna Rodriguez's role at the current company?
Anna Rodriguez's current role is Director, Global Regulatory Affairs at Calico Life Sciences.
What is Anna Rodriguez's email address?
Anna Rodriguez's email address is an****@****ene.com
What schools did Anna Rodriguez attend?
Anna Rodriguez attended University Of California, San Francisco, University Of California, Davis.
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