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Online Resumes with "Clinical Studies"
Regulatory Affairs- Manager
to contribute to the expansion of the company
Tags for this Online Resume: Regulatory affairs, Pharmacist, Pharmacovigilance, CTD & e-CTD, Clinical Studies, Bioequivalence
Registered Dietitian, Certified Diabetes Educator
High-powered, compassionate, and versatile healthcare professional equipped with more than 20 years of experience in Clinical Research, Diabetes Education, and Program Coordination. Show competency to manage delivery of clinical study protocols, clinical study reports, study agreements, applications, and other study documentation. Demonstrate strong analysis, research, documentation, and advocacy expertise, coupled with eff...
VP, CIO, Sr Director, SVP, EVP
I am an IT transformation leader driven to improve bottom line, develop high performance teams, security and compliance with agility along with advancing the company’s strategic objectives. I have extensive services experience in customer CRM multi-channel experience working Telecom, Financial, CPG, Medical Devices, MCO, Pharmaceuticals on DTC, OCT, grant processing, continuity programs, physician meetings, AE/PQC, Patient...
Tags for this Online Resume: Siebel CRM, MS/SQL, & Oracle, Avaya & Aspect VoIP , Cognos, BI, .Net, Web Portals, ISO/27002, PCI, HIPAA and CFR 21-par 11 regulatory compliance
Clinical Research Manager, 19 years experience in Medical Device Industry
Looking for an opportunity to contribute and expand my skills in clinical research study management.
Tags for this Online Resume: study management, clinical research associate, clinical research, site management, Clinical research monitor, clinical study monitoring
Clinical Study Coordinator
I have over 30n years experience with clinical trials I would like to advanc
Tags for this Online Resume: Study Coordinator, Clinical trials, Research Assistant, Cosmetic Clinical trials
Clinical Research Associate
Highly motivated and experienced biomedical professional with expert knowledge and proficiency in clinical research monitoring. A certified CRA. Hands-on experience in the clinical investigations of novel pharmacological products. Eager to translate expertise gained in research and monitoring to measurable success in the field clinical studies. A demonstrated record of academic achievement and recognition, accompanied by e...
Tags for this Online Resume: Clinical Site Monitoring , Identification and interviewing of potential investigators, ICH GCP Training , Adverse Event Reporting, Study Planning Activities
Statistical Programmer
SAS programming for clinical study reporting, e.g. data and TLG programming; CDISC; PK/PD
VP, Medical and Clinical
Drug development, clinical study, medical affairs, safety, pharmacovigilance, regulatory affairs, translational medicine, modelling, simulation, preclinical research, IIS and ISS
