Job-Clinical research associate-reputed clinical research company-Mumbai, Maharshtra, INDIA-upto 5 LPA-Chitra

JOB DETAILS One of our clients, a reputed company in clinical research, is looking out for a Clinical Research Associate for their office based in Mumbai.The job responsibilities are as follows:Act as monitor of specific sites on a clinical study, under supervision, as appropriate. Facilitate preparation and collection of site level documents.Participate...

JOB DETAILSOne of our clients, a reputed company in clinical research, is looking out for a Clinical Research Associate for their office based in Mumbai. The job responsibilities are as follows:1. Act as monitor of specific sites on a clinical study, under supervision, as appropriate.2. Facilitate preparation and collection of site level documents.3....

JOB DETAILSOne of our clients, a reputed company in clinical research, is looking out for a Clinical Research Associate for their office based in Mumbai.The job responsibilities are as follows:1. Act as monitor of specific sites on a clinical study, under supervision, as appropriate.2. Facilitate preparation and collection of site level documents.3....

JOB DETAILS One of our clients, a reputed company in clinical research, is looking out for a Clinical Research Coordinator for their office based in Mumbai. The job responsibilities are as follows:1. Maintaining the source documents, CRF s, Investigator Site File and other study related documents according to ICH -GCP guidelines2. Completing the...

JOB DETAILS One of our clients, a reputed company in clinical research, is looking out for a Clinical Research Coordinator for their office based in Mumbai. The job responsibilities are as follows:1. Maintaining the source documents, CRF s, Investigator Site File and other study related documents according to ICH -GCP guidelines2. Completing the...

JOB DETAILS One of our clients, a reputed company in clinical research, is looking out for a Clinical Research Coordinator for their office based in Mumbai.The job responsibilities are as follows:Maintaining the source documents, CRF s, Investigator Site File and other study related documents according to ICH -GCP guidelinesCompleting the eCRFMaintenance...

all Clinical Research Topic: - DRUG DEVELOPMENT: FROM MOLECULE TO PRESCRIPTION: PART 1 DRUG DEVELOPMENT: FROM MOLECULE TO PRESCRIPTION: PART 2 THE EVALUTION OF THE CLINICAL TRIAL PROCESS-A BRIEF HISTORY LESSON HISTORICAL BACKGROUND OF GCPINSTITUTIONAL REVIEW BOARD/INDEPENDENT ETHICS COMMITTEE (IRB/IEC)STAKEHOLDERS ENGAGEMENT TO ENSURE A SUCCESSFUL TRIAL...

JOB DETAILS One of our clients, a reputed biomedical research company, is looking out for a Research Scientist for their office based in Mumbai. The job responsibilities are as follows: Utilize your science backgrounds to discover new ways to prevent and treat all kinds of cancer.  Conducting laboratory studies on the role genetic markers play...

JOB DETAILS One of our clients, a reputed biomedical research company, is looking out for a Research Scientist for their office based in Mumbai. The job responsibilities are as follows: Utilize your science backgrounds to discover new ways to prevent and treat all kinds of cancer. Conducting laboratory studies on the role genetic markers play in...

JOB DETAILSOne of our clients, a reputed biomedical research company, is looking out for a Research Scientist for their office based in Mumbai. The job responsibilities are as follows:Utilize your science backgrounds to discover new ways to prevent and treat all kinds of cancer.Conducting laboratory studies on the role genetic markers play in predisposition...

JOB DETAILSOne of our clients, a reputed biomedical research company, is looking out for a Research Scientist for their office based in Mumbai.The job responsibilities are as follows:Utilize your science backgrounds to discover new ways to prevent and treat all kinds of cancer.Conducting laboratory studies on the role genetic markers play in predisposition...

Overview: As a Clinical Research Associate (CRA), you will play a pivotal role in the development and execution of clinical trials Working closely with research teams, regulatory bodies, and clinical sites, you will ensure compliance with protocols, regulatory requirements, and industry standards throughout the trial process. Responsibilities: 1 . Trial...

JOB DETAILSOne of our clients, a reputed company in medical & healthcare industry, is seeking a Drug Safety Associate to join their growing team. In this position, you will be responsible for1. processing and oversight ofa. (AE) adverse event/drug experience reports (serious and non-serious) andb. other safety-related data for Incite marketed products and...

**Department: Clinical Development Centre** Do you want to be a part of a high performing team in Novo Nordisk that plays a critical role in driving the success of the business? Do you have what it takes: the right drive, a sharp mind, customer orientation, openness and focus on what matters and a genuine interest in working with people? If you find...

Overview:As a Clinical Research Associate (CRA), you will play a pivotal role in the development and execution of clinical trials Working closely with research teams, regulatory bodies, and clinical sites, you will ensure compliance with protocols, regulatory requirements, and industry standards throughout the trial process.Responsibilities:1 . Trial...

Overview:As a Clinical Research Associate (CRA), you will play a pivotal role in the development and execution of clinical trials Working closely with research teams, regulatory bodies, and clinical sites, you will ensure compliance with protocols, regulatory requirements, and industry standards throughout the trial process.Responsibilities:1 . Trial...

JOB DETAILS One of our clients, a reputed company in medical & healthcare industry, is seeking a Drug Safety Associate to join their growing team. In this position, you will be responsible for 1. processing and oversight of  a. (AE) adverse event/drug experience reports (serious and non-serious) and  b. other safety-related data for Incite...

JOB DETAILS One of our clients, a reputed company in medical & healthcare industry, is seeking a Drug Safety Associate to join their growing team. In this position, you will be responsible for 1. processing and oversight of  a. (AE) adverse event/drug experience reports (serious and non-serious) and  b. other safety-related data for Incite...

JOB DETAILSOne of our clients, a reputed company in medical & healthcare industry, is seeking a Drug Safety Associate to join their growing team. In this position, you will be responsible for1. processing and oversight ofa. (AE) adverse event/drug experience reports (serious and non-serious) andb. other safety-related data for Incite marketed products and...

Overview:As a Clinical Research Associate (CRA), you will play a pivotal role in the development and execution of clinical trials Working closely with research teams, regulatory bodies, and clinical sites, you will ensure compliance with protocols, regulatory requirements, and industry standards throughout the trial process.Responsibilities:1.Trial...