Kahina Lamrani
In house Clinical Research Associate
Driving License
Bagneux (92220) France
Employed
Available
Holding a master’s degree in Biology and a Certificate in Clinical Research from Institute Léonard De Vinci in Paris, I have handled growing responsibilities with my first experience as a Study Coordinator. Actually, I am part of a clinical trial team and responsible to make sure that rights and well-being of subjects are protected and also that a quality control of clinical data are accurate, complete and verifiable from source documents during a trial.
My numerous responsabilities as a Study Coordinator have allowed me to develop communication skills and thus to work efficiently as a team member .I have also had the opportunity to acquire leadership qualities. With my strong management and organizational skills, and my ability to adapt to new environments.I will be quickly independant and operational.
My numerous responsabilities as a Study Coordinator have allowed me to develop communication skills and thus to work efficiently as a team member .I have also had the opportunity to acquire leadership qualities. With my strong management and organizational skills, and my ability to adapt to new environments.I will be quickly independant and operational.
Senior hospital CRA, Department of IBD (Inflammatory Bowel Diseases) l . CTA and Study Coordinator missions
Beaujon hospital
January 2016
to December 2016
- Involvement in several clinical trials phase II-III on behalf of big pharmaceutical companies in the context of chronic inflammatory bowel disease (IBD)
- Screening, randomization and monitoring of patient enrolled in different Trails
- Management of serious adverse events, queries
- Facilitated completion of clinical charts and Case report forms
- Prepare selection, monitoring and Close-Out Visits with monitor CRA
- Collaborated with Pharmacists and Medical Staffs to plan different event (patient visit, monitoring visits, WebEx conferences…)
- Managed Studies documents (TMF, ISF,DCF, patient files…)
- Management of IWRS system and studies materials ( eDiary, ePRO, ERT, Robarts et Bioclinica)
- Entered data in e-CRF (ERT, Mdsol ,eClinicalOS ,Medidata-Rave and OC-RDC. ..)
- Recruited and trained new CRA
- Participated to Investigator meeting (Madrid, Amsterdam, Prague…)
