When you are in your twenties, the most important task is choosing a career which will not be confined within the boundaries of retirement. Irrespective of you being in finance, marketing, administration or engineering everybody will face retirement some or the other day. When you have chosen a career in healthcare segment then you might dare to think of working beyond retirement lines.

ICRI – The Pioneer in Healthcare and Clinical Research Field

ICRI being the best rated Institute in India in terms of clinical research gives you the option to work throughout your life and thereby defy the definition of retirement. The more experience you gather the better is your exposure in being a teaching staff in ICRI and you will enjoy providing knowledge and guidance to the young ones. A recent trend in ICRI shows that students from various fields want to undergo course and they can serve until the age they want to. Moreover, the people who are in the following segment can opt to undergo a course in ICRI.

Unique Features:

• India is going to be the hub of clinical trials
• Starting salary of ICRI’ians is 4 to 7 lacs
• 100% placement with ICRI
• Career progression in Clinical Research 

Career Prospects

• For Doctors: Who want to be the Principal Investigators, co-investigator, medical advisor, drug developers, regulatory affairs Manager or Clinical research physician can opt to study here. The course curriculum will provide a new dimension to their professional degree.

• For Paramedics, Pharmacists & Life Science Graduates: Students who want to be medical Writers , Clinical research Associates , site coordinators , clinical Research Manager , drug development associates , pharmacovigilance executive , clinical Trail analyst ,drug Reviewer , clinical data management drug Safety Physician & many more profession of desired specification must undergo a course designed by ICRI to get that cutting edge in their career.

• For Management Professionals: (with Life Science/Health Science background): Students who desire to be in fields like business development, clinical project management, clinical research management and regulatory affairs needs to study in ICRI so as to be a core professional in respective fields. 

• Some of the regular recruiters like Accenture, Cipla, Nicholas Piramal ,Clinigene, CliniRx, Clinisys, Cognizant, Novartis, Panacea, Excel Lifesciences, Global Spectrum, Jubilant, Siro Clinpharm ,iGate, Indegene Life Systems, Quintiles, Ranbaxy, Sanofi-Aventis  & TCS  more prefer candidates with ICRI degree so that they can contribute and excel in the respective companies.

• Clinical Research Associates: Who want to monitor clinical trials, ensure compliance with the clinical trial protocol, checks clinical sites activities, make on-site visits, CRFs, and other allied fields must undergo a course from ICRI and they will be deemed and the industry leaders in respective fields.

• Clinical Research Investigators: Who Conduct BA/BE studies, writing / revising SOP, review of protocols, ICF & CRFs Protocol, investigator’s brochures, CRF & ICF preparations plans and conduct of BA/BEIER/IRB affairs-GC prefer to take a degree from ICRI so that they can carve a permanent niche in the fields served by them.

• Study Coordinators: Who provides safety & protection while collecting & managing the study data prefer to undergo course from IRCI and include that cutting edge in their career.

• Data Manager / Biostatistician: Who design, study & predict the seriousness of disease, seriousness of disease, evaluate new treatment and effectiveness of medication, participate in research design, data collection, choosing & implementing appropriate methodologies, interpreting the results must opt for a course from ICRI to add perfection to the fields they want to serve.

• Regulatory Affairs Managers: Who wants review & register documents, evaluate technical data, liaison with regulatory authorities opts for ICRI in order to add excellence in their way of working.

• Clinical Trials Auditors: Who want to conduct audits for regulatory function within the trial department to assure compliance with GLP/GCP in accordance with established FDA regulations and company policies & standard operating procedure prefer to undergo a course from ICRI in order to enhance their knowledge in the said field.

• Clinical Research Managers: Who wants to manage, supervise, train, mentor clinical research staff, approve investigator’s study, budget & contract, review & approve regulatory documents, develop protocol, approve CRFs, review study data  must undergo course in ICRI so that their style of working be flawless and set examples in the industry.

• Business Development Manager: Who wants to identify potential clients, establish business relations, liaison meeting with new clients, follow up on leads and do market research opt o study from ICRI so that they might get that cutting edge in career and behave like industry leaders.

• Drug Safety Associate: Students who want to manage & relay drug safety information, maintain current knowledge of global drug safety regulations, summarize clinical safety data, write down narratives and critical inputs, report SADRs to the Regulatory Authorities, participate in training on drug safety issues & other tasks under drug safety prefer to undergo a course from ICRI so that it adds sharpness of mind and their career become impeccable.
• Medical Writer: Students who want to document, manuscript, abstract and specialize in external communication tools must undergo a course from ICRI and ensure impeccable edge in the career.

• Clinical Data Manager: Students who want to ensure the accuracy & consistency of data prepared for regulatory bodies for reporting purpose prefer to undergo studies in ICRI in order to ensure they have maverick in the industry they serve.

• Other professionals like auditors, quality assurers, patents & IP Related position must study from ICRI to ensure better grip in the subject they want to specialize.