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Career Opportunities in Clinical Research




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The medical and pharmaceutical industry brings attractive careers for science & pharmacy graduates with bright future growth. The clinical trial regulations, Good Clinical Practice guidelines, study designs and research methodology involved in bringing a potential drug from the laboratory to the market are the major things in clinical research. ...



Feature-img Clinical Research (CR)
The medical and pharmaceutical industry brings attractive careers for science & pharmacy graduates with bright future growth. Clinical research courses mainly deals with the efficiency and safety of a drug. India is becoming a major hub for clinical trials, due to increase in population and diseases; hence this course holds more importance and future. This is a responsible job which prepares the aspirants of the graduate Course with thoroughness, integrity, innovation, analytical thinking. Candidates should also be knowledgeable & have updates information about the techniques needed to diagnose and treat human injuries, diseases and deformities.

Prerequisites for Clinical Research Jobs
In order to pursue the course, the candidates needs to be graduated with pharmacy or in any life science stream with physics and chemistry as compulsory subject with any one of the Biology/Biotechnology. In addition candidates will also have to appear in Personal Interview. Job Opportunities: Pharmaceutical Industry is full of employment opportunities, although the industry needs skilled professionals to cater the demand of the industry.
Clinical research course mainly deals with the efficiency and safety of a drug. India is becoming a major hub for clinical trials, due to increase in population and diseases; hence this course holds more importance and future.This is a responsible job which prepares the aspirants of the graduate Course with thoroughness, integrity, innovation, analytical thinking. Candidates should also be knowledgeable & have updates information about the techniques needed to diagnose and treat human injuries, diseases and deformities.

Posted 2019-05-20 20:47:04


A Guide to become a Clinical Research Associate (CRA)




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Clinical Research Associate is one of the richest designations in clinical research. One must have to complete knowledge of the trial process or he / she must have done certificate course for clinical research. ...



How one can go for a Clinical Research Associate Profile?
After Successful Completion of Clinical Research Course the candidate need to work as an intern first to learn the clinical trial as clinical research co-coordinator. While working as clinical research coordinator one get the exact and hands-on knowledge of clinical trial and the exact knowledge of all regulatory guidelines and the clinical trial. This experience is very fruitful for the career in clinical research and which is mandatory to grab further levels of job opportunities in clinical research. After taking an experience of research coordinator or trial monitor candidates are eligible to go for a research associate profile and they can directly switch to CRA position according to their capabilities. Candidates can switch to CRA profile after getting an experience in any core clinical research profile. Feature-img Roles and Responsibilities of Clinical Research Associate A clinical research associate is a health care or life sciences professions who oversees clinical trials on behalf of pharmaceutical companies, medical research institutes, and government agencies. They are sometimes called clinical monitors or trial monitors or trial monitors. A key part of the job is to monitor the study trial while it’s going according to GCP guidelines which are developed by ICH.The CRA is an in charge of verifying the safety rights and wellbeing of patients enrolled in a trial, as well as checking that all the reported clinical data is accurate and verifiable. CRA manages a trial at several sites around the state or country and is the main point of contact for any site conducting a trial. One can eventually move up the ladder to a managerial position within a company or the other organization. They are the in-charge for verifying the safety, rights, and wellbeing of patients enrolled in a trial as well as checking that all the reported clinical trial data is accurate and verifiable. CRA manages the several trial sites around a state or country. They are main person of getting details of any other sites conducting a trial so one can eventually move up the stages to a managerial position within the company or in another organization. CRA is the only person holding special authorities to handle site activity along with CRO and SPONSOR. CRA has the detailed knowledge of regulatory requirement, site information, ICH-GCP, clinical data management knowledge for reviewing the clinical data and the data entry, including AE/SAE, reporting and ETHICS COMMITTEE.

Posted 2019-08-13 19:40:06


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