Calogera McCormick

Senior Manager, Clinical Development Operations @Viridian Therapeutics, Inc.

West Orange, NJ, US
EMAILS
c••••••••@viridiantherapeutics.com
MOBILE NUMBERS
+19•••••••71

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WORK HISTORY

Mar 2025 — Present

Senior Manager, Clinical Development Operations @Viridian Therapeutics, Inc.

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EDUCATION

N/A

University of Pennsylvania

Bachelor of Arts - BA, 1) Economics and 2) Biological Basis of Behavior

N/A

Rutgers Business School

Executive Master of Business Administration (MBA), Marketing

2028

Brown University School of Public Health

Master of Public Health - MPH

ABOUT CALOGERA MCCORMICK

Passionate about transforming research into clear information for patients, caregivers, physicians & researchers *Strategic medical affairs and clinical development professional with over 20 years experience (including 10 years leadership in medical writing and 15 years in clinical trial operations) at domestic and global Fortune 50 and smaller pharma and biotech companies, as well as CRO and academic research organizations, providing solutions to design, implement, analyze and report data for on-time and on-budget clinical trials and producing a broad range of scientific and clinical communication deliverables. Organizational leader with experience in building and turning around teams, collaborating and partnering cross-functionally (business development, data management, biostatistics, field science team, medical affairs, regulatory and market access.Strategic clinical trial professional with a track record of producing a broad range of regulatory writing and scientific communication deliverables for Phase 0 to Phase IV studies and expertise in communicating meaningful scientific data in a clear way for patients, caregivers and healthcare providers. Skilled at project, customer relationship, and account management, trial design, budget development and negotiation, financial forecasting, training, feasibility, monitoring, data review, electronic clinical outcomes assessments (eCOA), patient reported outcomes (PROs), digital health, decentralized research, patient engagement, regulatory writing, medical writing, and publication planning of Phase 0 to Phase IV studies, clinical operations process improvement, and oversight of research programs in Clinical Development, Medical Affairs, and Real World Evidence.Experience across over 10 therapeutic categories including:Cardiovascular (cardiovascular disease), CNS (Alzheimer\'s, migraine, narcolepsy), Dermatology (atopic dermatitis, psoriasis), Immunology (allergies, osteoarthritis, rheumatoid arthritis, psoriatic arthritis), Infectious Disease (hepatitis), Metabolism (obesity), Oncology (AML, breast cancer, Gorlin syndrome), Pain, Rare Disease (hATTR amyloidosis, Duchenne muscular dystrophy), Respiratory (asthma, COPD), RNA therapeutics, Urinary (Lower Urinary Tract Symptoms, Benign Prostatic Hyperplasia), Tobacco/vaping-Reach out to me to discuss ways I can help with your clinical study design, operational process improvement or reporting c••••••••@persimmoncommunications.comphone: 19•••••••71

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