PROFESSIONAL SKILLS

• Clinical Trial Monitoring.

• AE/SAE Assessment.

• Human Ethics, Protocol Writing and clinical trials.

• Well versed with identification of adverse drug reactions and reporting the same to the ADR Monitoring Center / Pharmacovigilance centre;

• Reviewing prescriptions for medication errors, rational prescribing and drug-drug interactions during ward rounds / Case Studies / Case Assessments;

• Developing Databases, data management, Analysis and Interpretation of epidemiological studies;

• Handling Medical, Bio-statistical and Drug information and clinical trial databases like Medline, IBM Micromedex, IDIS, Toxicology Treatment, IBM SPSS, Clinion, Medrio and Inclinical.

• Well versed with the phases of clinical trials and study co-ordination.

• Good handling skill of BA/BE, Phase 2 and Phase 3 study of clinical trial.

CONCEPTUAL SKILLS

• Through knowledge about clinical trials, Pharmacotherapeutics, Pharmacology, Clinical pharmacy Clinical Pharmacokinetic and Bio- Pharmacokinetic.

• Awareness about the SOAP format and different Phases study of clinical trial.

• Awareness about ICH-GCP Guideline, CDSCO guideline for clinical trial, ICMR for Biomedical research, Ethical code of Helsinki, Belmont Report and various guidelines pertaining to the management of the disease.

• Well versed with IBM SPSS software and Cardiopulmonary resuscitation (CPR)