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CLINICAL RESEARCH TO FIT YOURS NEEDS
Senior Clinical Research Independent
Ø Stong experience of monitoring in clinical research phases I to IV
o Phase I : collaboration with CROs Aster (Paris), Biotrial (Rennes and Paris) and LCG Bioscience (Cambridge) ; bioavailibility and pharmacokinetics trials o Phase II : monocentric and multicentric efficacy trials o Phase III : many national and international trials in replacement hormonal therapy, contraception, infectiology, rheumatology… o Phase IV : implementation and follow-up of questionnaires ; respect of the medical reps' Charter for epidemiologic studies Ø Selection, initiation, implementation of trials in investigation centres(private offices and hospital services) Ø Investigators meetings for pre-study and study visit Ø Trial Master Files updating, in prevision of site's audits Ø Privileged contact with investigators, good relationship
Services offered to conduct your studies in clinical research Ø Procedures in clinical research
Freelance cra - Senior CRA - Monitoring in clinical research - Clinical trial coordination - Regulatory submission of clinical trial - Writing and implementation of procedures in clinical research - Training in clinical research - clinical research associate - clinical research indenpendent - Clinical Research Independent - Senior Clinical Research - links |
| Monitoring in Clinical Research |

