Miriam Fogelson

Associate Director, Product Safety at Macrogenics, Inc

For over 19 years Miriam Fogelson has been working in different jobs. Recently, this expert worked as a Associate Director, Product Safety at Macrogenics, Inc in Macrogenics, Inc. enhancing knowledge. Miriam graduated from University of Maryland in 1992 where this person received all the knowledge and skills. You can find this expert in Rockville, Maryland, where he lives nowadays. SoftwareOfficial has all the information you need to connect Miriam Fogelson, such as this professional's phone or email. Feel free to send us the request to get more info.
Name variants:
Myriam Fogelson, Mimi Fogelson, Miri Fogelson, Mira Fogelson
Last updated Jun 08, 2024

Contact Information

Last Update
Jul 9, 2022
Email
fo**@macrogenics.com, mf**@kai-research.com
Location
Rockville, MD

Workplace

MacroGenics, Inc.
Associate Director, Product Safety at Macrogenics, Inc

Rockville, MD

Industry

Biotechnology, Internist

Work History

Associate Director, Product Safety at Macrogenics, Inc

9704 Medical Center Dr, Rockville, MD 20850
Provide operational and strategic pharmacovigilance/drug safety support to ensure alliance with company goals. Serve as a pharmacovigilance/drug safety expert and safety database business sy...
from Jul 2018

Director, Medical Affairs

11300 Rockville Pike SUITE 500, Rockville, MD 20852
Manage all activities relating to clinical trial safety, pharmacovigilance and medical communications. Serve as pharmacovigilance/drug safety subject matter expert. Establish and implement s...
Sep 1999 — May 2015

Associate Director, Product Safety

9704 Medical Center Dr, Rockville, MD 20850
Provide day-to-day direction to Product Safety Team members to ensure business needs and priority tasks are completed including management of CRO/contractor staff; development of standard op...
from May 2015

Project Manager

11300 Rockville Pike SUITE 500, Rockville, MD 20852
Develop informed consent forms, case report forms, administrative forms, and Manuals of Operating procedures for clinical trials. Trained study investigators and site staff with respect to c...
Apr 1996 — Sep 1999

Education

Occupations

Executive
Deputy Director
Owner
Sales Specialist
Supplier
Director
Subject Matter Expert
IT Professional
Software Tester
Deputy Manager
Chief Executive
Services Professional
Sales Representative
Operations Manager
Skilled Professional
Computer Specialist

Skills

Clinical Trials
Pharmacovigilance
Pharmaceutical Industry
Fda
Regulatory Affairs
Gcp
Clinical Research
Clinical Development
Ctms
Sop
Clinical Data Management
Cro
Edc
Medical Writing
Drug Development
Regulatory Submissions
Medical Devices
Clinical Monitoring
Infectious Diseases
Medical Affairs
Lifesciences
Life Sciences
Oncology
Quality Assurance
Therapeutic Areas
Biotechnology
Clinical Study Design
Ich Gcp
Pharmaceuticals
Standard Operating Procedures
Auditing
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