Tanya Mustacchio Email & Phone Number | Over 16 years of experience in clinical data management and over 15 years of experience in line management. I have worked on more than 50 clinical trials, including Phase I, II, III, OLE, LTFU, pediatric and natural history/observation studies. A strong leader, experienced with establishing CDM departments - including: - Growing teams - hiring, training, mentorship and professional development; - Developing process (SOPs, WIs, etc.), templates, and standards (including global library creation); - Selecting, implementing and validating systems (EDC, ePRO, sFTPs, etc.); - Evaluating and implementing resourcing models (in-source, outsourced - FSP/CRO), including development of vendor oversight processes; - Setting goals, vision and overall project management for the department; - Budget planning and oversight; - Liaising and establishing relationships with cross-functional teams and vendors; and - Leveraging my established knowledge of the entire life cycle of a clinical trial and my disease area experience including: oncology (solid tumors, multiple myeloma, and lymphoma) and rare disease (TTR amyloidosis, HAE, hemophilia, and AAT deficiency).

Tanya Mustacchio

Over 16 years of experience in clinical data management and over 15 years of experience in line mana...
Greater Boston, Greater Boston, United States

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Tanya Mustacchio’s Location Greater Boston, Greater Boston, United States

Tanya Mustacchio’s Current Industry Intellia Therapeutics

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Senior Director, Clinical Data Management

2024-01-01 00:00:00 - Present

Associate Director, Clinical Data Management Oncology

2019-12-01 00:00:00 - 2021-05-01 00:00:00

Associate Director, CDM

2018-10-01 00:00:00 - 2019-11-01 00:00:00

Associate Manager of Clinical Data Management

2016-09-01 00:00:00 - 2018-10-01 00:00:00

Manager, Data Management

2015-06-01 00:00:00 - 2016-09-01 00:00:00

Consultant

2015-06-01 00:00:00 - 2015-12-01 00:00:00

Project Coordinator for GI-GU Trials

2009-04-01 00:00:00 - 2014-02-01 00:00:00

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Tanya Mustacchio is a Over 16 years of experience in clinical data management and over 15 years of experience in line management. I have worked on more than 50 clinical trials, including Phase I, II, III, OLE, LTFU, pediatric and natural history/observation studies. A strong leader, experienced with establishing CDM departments - including: - Growing teams - hiring, training, mentorship and professional development; - Developing process (SOPs, WIs, etc.), templates, and standards (including global library creation); - Selecting, implementing and validating systems (EDC, ePRO, sFTPs, etc.); - Evaluating and implementing resourcing models (in-source, outsourced - FSP/CRO), including development of vendor oversight processes; - Setting goals, vision and overall project management for the department; - Budget planning and oversight; - Liaising and establishing relationships with cross-functional teams and vendors; and - Leveraging my established knowledge of the entire life cycle of a clinical trial and my disease area experience including: oncology (solid tumors, multiple myeloma, and lymphoma) and rare disease (TTR amyloidosis, HAE, hemophilia, and AAT deficiency).

Tanya Mustacchio has prior
experience in the following industries:
Bluebird Bio | Array Biopharma | Gilead Sciences | Alnylam Pharmaceuticals | Ecog Acrin Cancer Research | Eastern Cooperative Oncology

Tanya Mustacchio has the following professional experience:
Intellia Therapeutics | Bluebird Bio | Array Biopharma | Gilead Sciences | Alnylam Pharmaceuticals | Ecog Acrin Cancer Research | Eastern Cooperative Oncology