Clinical Research comprises of Pharma Research, Drug Development Process, ICH-GCP Regulatory Affairs, Pharmacovigilance & Clinical Data Management-CDM for the effective management of clinical data related to the domains of investigational product and market available drug, Multicentrical data manipulation, tracking of Adverse events, Placebo, Active and Control Group Pharmacovigilance reports in accordance with 21 CFR USFDA Guidelines with Project.

You can be a part of Clinical Research as Clinical Research Associate, Clinical Research Coordinator, Principal Investigator, Co-investigator, Medical Writer, SOP Writer, Clinical Data Management Associate, Clinical Data Coordinator, Clinical Data Monitor, Clinical Data Auditor, Clinical Pharmacovigilance Associate, Regulatory Affairs Associate, Clinical Drug Safety Associate, Clinical CRF Designer, Clinical Data Design Analyst, Clinical Data Coder, Clinical Data Validator.

OPPORTUNITIES:

According to Mc Kinsey Report, more than 50,000 Clinical Trials professionals are needed shortly in successful completion of USFDA/DCGI Investigational New Drug Applications (INDs).

The report by Ernst & Young states that globalization of Clinical Trials to newer options for the Indian clinical research industry. Excellent Opportunities are available in Abroad / India in this emerging field. In India alone, the clinical trials market of $ 35 million is expected to grow to nearly $ 300 million shortly.