Senior Vice President, Regulatory Affairs and Quality Assurance at Fulcrum Therapeutics, Inc.
Cambridge, Massachusetts
Pamela Strode is skilled in: Clinical Trials, Clinical Development, Regulatory Submissions, Pharmaceutical Industry, Regulatory Affairs, Oncology, CTMS, FDA, 21 CFR Part 11, Drug Development, Clinical Research, Therapeutic Areas, CRO, Lifesciences, Drug Discovery, Infectious Diseases, Medical Affairs, GCP, Life Sciences
Pamela Strode is skilled in: Clinical Trials, Clinical Development, Regulatory Submissions, Pharmaceutical Industry, Regulatory Affairs, Oncology, CTMS, FDA, 21 CFR Part 11, Drug Development, Clinical Research, Therapeutic Areas, CRO, Lifesciences, Drug Discovery, Infectious Diseases, Medical Affairs, GCP, Life Sciences
What industry does Pamela Strode work in?
Pamela Strode works in the industry.
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