📑 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 guidelines 2. Completin ...
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📑 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 accord ...
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📑 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: 1. Act as monitor of specific sites on a clinical study, under supervision, as appropriate. 2. Facilitate preparation and collection of site level ...
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📑 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: 1. Act as monitor of specific sites on a clinical study, under supervision, as appropriate. 2. Facilita ...
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📑 JOB DETAILS 1.To Generate business leads from assigned territories primarily by cold calls and cold mails 2.Identify potential clients by researching industry and related events, publications, and announcements, generate RFPs and finalization of agreements. 3.To respond to RFI & RFP received from sponsors. 4.To follow up with assigned/develop ...
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📑 JOB DETAILS 1.To Generate business leads from assigned territories primarily by cold calls and cold mails 2.Identify potential clients by researching industry and related events, publications, and announcements, generate RFPs and finalization of agreements. 3.To respond to RFI & RFP received from sponsors ...
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📑 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 ...
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📑 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 ...
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📑 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 ...
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📑 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 ...
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📑 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 . Tri ...
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📑 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 ...
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📑 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 ...
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📑 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 ...
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📑 Are you interested in a leadership opportunity to bring ground-breaking cancer therapies to patients by working with a team that unites science, technology, and talent? If so, this role may be for you! The Clinical Scientist will report to the Clinical Science Program Lead in Oncology Clinical Development. As a Clinical Scientist, you will be res ...
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📑 We’re excited to be moving to our vibrant new home on New Oxford Street in central London from the end of June 2024. At GSK HQ, we’re building an energising space where we can connect, collaborate and get ahead of disease together. Designed especially for us, it’ll be one of the healthiest workplaces in the world, with best-in-class tech and bright ...
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📑 JOB DETAILS -Clinical Leader is primarily responsible for providing clinical leadership -Clinical Leader will provide clinical support and guidance to clinical staff -Multi-tasking & experienced & innovative professional with experience in mental health service. FUNCTIONAL AREA clinical psychology, medical psychology, healthcare psychology ...
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📑 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 pro ...
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📑 We’re excited to be moving to our vibrant new home on New Oxford Street in central London from the end of June 2024. At GSK HQ, we’re building an energising space where we can connect, collaborate and get ahead of disease together. Designed especially for us, it’ll be one of the healthiest workplaces in the world, with best-in-class tech and bright ...
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📑 JOB DETAILS -Clinical Leader is primarily responsible for providing clinical leadership -Clinical Leader will provide clinical support and guidance to clinical staff -Multi-tasking & experienced & innovative professional with experience in mental health service. FUNCTIONAL AREA clinical psych ...
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📑 Are you interested in a leadership opportunity to bring ground-breaking cancer therapies to patients by working with a team that unites science, technology, and talent? If so, this role may be for you! The Clinical Scientist will report to the Clinical Science Program Lead in Oncology Clinical Development. As a Clinical Scientist, you w ...
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📑 The Sr. Manager, Regulatory Affairs will be responsible for overseeing regulatory activities related to clinical trials conducted by the clinical research organization. This position will play a crucial role in ensuring compliance with regulatory requirements and providing strategic regulatory guidance to internal teams and clients. The Sr. Manager ...
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📑 The Sr. Manager, Regulatory Affairs will be responsible for overseeing regulatory activities related to clinical trials conducted by the clinical research organization. This position will play a crucial role in ensuring compliance with regulatory requirements and providing strategic regulatory guidance to internal teams and clients. The Sr. Manager ...
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📑 The Sr. Manager, Regulatory Affairs will be responsible for overseeing regulatory activities related to clinical trials conducted by the clinical research organization. This position will play a crucial role in ensuring compliance with regulatory requirements and providing strategic regulatory guidance to internal teams and clients. The Sr. Manager ...
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📑 The Sr. Manager, Regulatory Affairs will be responsible for overseeing regulatory activities related to clinical trials conducted by the clinical research organization. This position will play a crucial role in ensuring compliance with regulatory requirements and providing strategic regulatory guidance to internal teams and clients. The Sr. Manager ...
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📑 The Sr. Manager, Regulatory Affairs will be responsible for overseeing regulatory activities related to clinical trials conducted by the clinical research organization. This position will play a crucial role in ensuring compliance with regulatory requirements and providing strategic regulatory guidance to internal teams and clients. The Sr. Manager ...
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📑 The Sr. Manager, Regulatory Affairs will be responsible for overseeing regulatory activities related to clinical trials conducted by the clinical research organization. This position will play a crucial role in ensuring compliance with regulatory requirements and providing strategic regulatory guidance to internal teams and clients. The Sr. Manager ...
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📑 The Sr. Manager, Regulatory Affairs will be responsible for overseeing regulatory activities related to clinical trials conducted by the clinical research organization. This position will play a crucial role in ensuring compliance with regulatory requirements and providing strategic regulatory guidance to internal teams and clients. The Sr. Manager ...
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📑 The Sr. Manager, Regulatory Affairs will be responsible for overseeing regulatory activities related to clinical trials conducted by the clinical research organization. This position will play a crucial role in ensuring compliance with regulatory requirements and providing strategic regulatory guidance to internal teams and clients. The Sr. Manager ...
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📑 **Job Description** At Thermo Fisher Scientific, you’ll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life - enabling our customers to make the world healthier, cleaner and safer. We provide our teams with the resources needed to achieve individual career g ...
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📑 The Sr. Manager, Regulatory Affairs will be responsible for overseeing regulatory activities related to clinical trials conducted by the clinical research organization. This position will play a crucial role in ensuring compliance with regulatory requirements and providing strategic regulatory guidance to internal teams and clients. The Sr. Mana ...
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📑 Department – Clinical Medical Regulatory (CMR)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 yo ...
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📑 Job Description :-Monitoring of clinical and BA/BE studies.Review of clinical study reports and documents.Coordination with internal stakeholders like formulation, regulatory, purchase and finance teams.Coordinating with external vendors including CROs, packaging vendors, consultants etc.Skill Requirements :-Well versed with ICH GCP and regulatory ...
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📑 Job Description :-Monitoring of clinical and BA/BE studies.Review of clinical study reports and documents.Coordination with internal stakeholders like formulation, regulatory, purchase and finance teams.Coordinating with external vendors including CROs, packaging vendors, consultants etc.Skill Requirements :-Well versed with ICH GCP and regulatory ...
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📑 Job Description :-Monitoring of clinical and BA/BE studies.Review of clinical study reports and documents.Coordination with internal stakeholders like formulation, regulatory, purchase and finance teams.Coordinating with external vendors including CROs, packaging vendors, consultants etc.Skill Requirements :-Well versed with ICH GCP and regulatory ...
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📑 Main role of the scribe is to create medicolegally compliant, clinically sound high quality outpatient visit documentation for some of the best US Hospitals across multiple specialties . Listen and comprehend recorded patient physician interactions, develop an impression about the clinical condition and document clinical history, exam ...
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📑 Department – Clinical Medical Regulatory (CMR)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? I ...
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📑 Department –Clinical Medical Regulatory (CMR)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 yo ...
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📑 Department – Clinical Medical Regulatory (CMR) 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? I ...
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📑 Job Description :-Monitoring of clinical and BA/BE studies.Review of clinical study reports and documents.Coordination with internal stakeholders like formulation, regulatory, purchase and finance teams.Coordinating with external vendors including CROs, packaging vendors, consultants etc.Skill Requirements :-Well versed with ICH GCP ...
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📑 Job Description :-Monitoring of clinical and BA/BE studies.Review of clinical study reports and documents.Coordination with internal stakeholders like formulation, regulatory, purchase and finance teams.Coordinating with external vendors including CROs, packaging vendors, consultants etc.Skill Requirements :-Well ver ...
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📑 Job Description :-Monitoring of clinical and BA/BE studies.Review of clinical study reports and documents.Coordination with internal stakeholders like formulation, regulatory, purchase and finance teams.Coordinating with external vendors including CROs, packaging vendors, consultants etc.Skill Requirements :-Well versed with ...
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📑 Job Description :-Monitoring of clinical and BA/BE studies.Review of clinical study reports and documents.Coordination with internal stakeholders like formulation, regulatory, purchase and finance teams.Coordinating with external vendors including CROs, packaging vendors, consultants etc.Skill Requirements :-Well ver ...
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📑 Department – Clinical Medical Regulatory (CMR) 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 worki ...
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📑 • Excellent understanding of the statistical principles underlying clinical trials • Excellent statistical skills. • candidates that are Statistical SAS, R programmers, and separately, we need pharmaceutical clinical trial statisticians. • Excellent understanding of the regulatory issues associated with the reporting of clinical data in the submiss ...
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📑 Job Description :- Monitoring of clinical and BA/BE studies. Review of clinical study reports and documents. Coordination with internal stakeholders like formulation, regulatory, purchase and finance teams. Coordinating with external vendors including CROs, packaging vendors, consultants etc. </l ...
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📑 • Excellent understanding of the statistical principles underlying clinical trials • Excellent statistical skills. • candidates that are Statistical SAS, R programmers, and separately, we need pharmaceutical clinical trial statisticians. • Excellent understanding of the regulatory issues associated with the reporting of clinical dat ...
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📑 **Primary Job Function**:- Manage the quality, accuracy, compliance with internal & external standards and the timely production of documents- Point of Contact for all medical writing/publishing activities for affiliate.- Responsible for quality and timelines of all publications.- Develop, implement and manage templates & docume ...
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📑 • Develop and maintain in-depth knowledge for assigned product(s) / relevant therapeutic area(s) through attendance/ participation at key internal meetings/training sessions, relevant congresses, and seminars and by regular self-study of the national/international literature. • Provide expert medical/scientific advice for assigned prod ...
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📑 Integrated Data Analytics and Reporting (IDAR) Position Title*: Statistical Programming Lead Position Summary The Statistical Programming Lead is an experienced Statistical Programmer with advanced knowledge of statistical programming methods, languages and data structures and capabilities in leading analysis and reporting activities and ...
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Great News! We have discovered exciting live Clinical clinical job opportunities in Mumbai just for you at India Jobs Expertini. You can even download the search results for Clinical clinical jobs in mumbai here.
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There are currently 752 live jobs available for Clinical clinical in Mumbai according to India Jobs Expertini.
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There are currently 750,462 total jobs available in India according to India Jobs Expertini.
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