1. on site clinical trial audits of phase II and III, global multicentric, clinical trials 2. Identification and preparation of SOPs which are missing in the system. 3. Periodic review, distribution, maintenance, withdrawal and archiving of SOPs. 4. Preparation of Internal Audit Policy for the QA department. 5. Induction and training of new employees and ongoing training of SOPs and GCP for the existing staff 6. Corrective action of the cited observations. 7.Participate in ComesAn ideal candidate wouldhave at least bachelor degree in medicine (MBBS/MD), or masters/PhD. in lifesciences with at least 3-5 years of experience in clinical trial auditing(Phase I-III) S/he would be familiar with GCP guidelines issued byNIH, NCI and ICH. Preference would be given to applications who havedemonstrated experience in Oncology. Candidatemust have excellent oral and written communication skills, proficientpresentations and good computer skills




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