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Contract Clinical Monitors uniquely qualified to required to support your clinical development efforts. • Clinical Research Focus. Clinical experience with medical devices and therapeutics. Medical Writing. Onsite and remote monitoring. • Disease Areas. Interventional cardiology and radiology, orthopedics, rare diseases, vaccines, bioanalytical sciences, biomarkers, immunology, cell & molecular biology. Oncology research. Biopharmaceuticals and nucleic acid-based therapeutics. • Biomedical Industry. Contract Research Organizations (CRO), Biotech, MedTech, Pharma. Study-related activities in a matrix environment for internal & external clients within timelines & budget. • Medical Writing Experience. CSR, CER (EU), Clinical Protocols, Monitoring Plans, Agreements, Budgets, SOPs, Ligand Binding Assays, Bioanalytical Method Validation Reports and Protocols. • Communications. HCP interactions, Presentations, Conferences, Marketing Material, Posters, Contract Negotiation, Peer-reviewed Scientific Publications. Executive Focus, Governance Committees.