📑 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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📑 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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📑 Your responsibilities include, but are not limited to:• Lead and contribute to Clinical Data Standards planning, definition, development, validation and support within assigned standards discipline (domain) including the development and maintenance of associated metadata, documents, business rules and guidelines where applicable.• Serves as the pri ...
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📑 Your responsibilities include, but are not limited to:• Lead and contribute to Clinical Data Standards planning, definition, development, validation and support within assigned standards discipline (domain) including the development and maintenance of associated metadata, documents, business rules and guidelines where applicable.• Serves as ...
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📑 Your responsibilities include, but are not limited to:• Lead and contribute to Clinical Data Standards planning, definition, development, validation and support within assigned standards discipline (domain) including the development and maintenance of associated metadata, documents, business rules and guidelines where applicable.• Serves as ...
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📑 Your responsibilities include, but are not limited to:• Lead and contribute to Clinical Data Standards planning, definition, development, validation and support within assigned standards discipline (domain) including the development and maintenance of associated metadata, documents, business rules and guidelines where applicable.• Serves as the pri ...
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📑 Your responsibilities include, but are not limited to:• Lead and contribute to Clinical Data Standards planning, definition, development, validation and support within assigned standards discipline (domain) including the development and maintenance of associated metadata, documents, business rules and guidelines where applicable.• Se ...
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📑 Who we areTogether, we’re on a mission to make good health more affordable and accessible, to help millions around the world enjoy healthier lives. It’s a mission that bonds our people across nearly 60 countries and a rich, diverse variety of nationalities and backgrounds. Working here means working with the world’s l ...
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📑 Purpose of the role:This role will be responsible for Medical affairs activities for assigned existing Products / therapy and disease areas, collaborate with Commercial teams, training etc to drive medico-marketing activities, actively contribute to Medial activities with external experts,/ KOLs, implement Product/TA specific approved medical initi ...
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📑 Purpose of the role:This role will be responsible for Medical affairs activities for assigned existing Products / therapy and disease areas, collaborate with Commercial teams, training etc to drive medico-marketing activities, actively contribute to Medial activities with external experts,/ KOLs, implement Product/TA specific approved medical initi ...
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📑 Purpose of the role:This role will be responsible for Medical affairs activities for assigned existing Products / therapy and disease areas, collaborate with Commercial teams, training etc to drive medico-marketing activities, actively contribute to Medial activities with external experts,/ KOLs, implement Product/TA specific approved medical initi ...
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📑 Purpose of the role:This role will be responsible for Medical affairs activities for assigned existing Products / therapy and disease areas, collaborate with Commercial teams, training etc to drive medico-marketing activities, actively contribute to Medial activities with external experts,/ KOLs, implement Product/TA specific approved medical i ...
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📑 Purpose of the role:This role will be responsible for Medical affairs activities for assigned existing Products / therapy and disease areas, collaborate with Commercial teams, training etc to drive medico-marketing activities, actively contribute to Medial activities with external experts,/ KOLs, implement Product/TA specific approved medical i ...
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📑 Purpose of the role:This role will be responsible for Medical affairs activities for assigned existing Products / therapy and disease areas, collaborate with Commercial teams, training etc to drive medico-marketing activities, actively contribute to Medial activities with external experts,/ KOLs, implement Product/TA specific approved medical i ...
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📑 Purpose of the role:This role will be responsible for Medical affairs activities for assigned existing Products / therapy and disease areas, collaborate with Commercial teams, training etc to drive medico-marketing activities, actively contribute to Medial activities with external experts,/ KOLs, implement Product/TA specific approved medical i ...
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📑 Purpose of the role:This role will be responsible for Medical affairs activities for assigned existing Products / therapy and disease areas, collaborate with Commercial teams, training etc to drive medico-marketing activities, actively contribute to Medial activities with external experts,/ KOLs, implement Product/TA specific approved medical i ...
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📑 Purpose of the role: This role will be responsible for Medical affairs activities for assigned existing Products / therapy and disease areas, collaborate with Commercial teams, training etc to drive medico-marketing activities, actively contribute to Medial activities with external experts,/ KOLs, implement Product/TA specific approved me ...
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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 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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📑 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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📑 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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📑 Overview Medpace is a full-service clinical contract research organization (CRO). We provide Phase I-IV clinical development services to the biotechnology, pharmaceutical and medical device industries. Our mission is to accelerate the global development of safe and effective medical therapeutics through its scientific ...
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📑 OverviewMedpace is a full-service clinical contract research organization (CRO). We provide Phase I-IV clinical development services to the biotechnology, pharmaceutical and medical device industries. Our mission is to accelerate the global development of safe and effective medical therapeutics through its scientific and disciplined approac ...
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📑 OverviewMedpace is a full-service clinical contract research organization (CRO). We provide Phase I-IV clinical development services to the biotechnology, pharmaceutical and medical device industries. Our mission is to accelerate the global development of safe and effective medical therapeutics through its scientific and disciplined approach. We le ...
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📑 Overview Medpace is a full-service clinical contract research organization (CRO). We provide Phase I-IV clinical development services to the biotechnology, pharmaceutical and medical device industries. Our mission is to accelerate the global development of safe and effective medical therapeutics through its scientific and disciplined approac ...
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📑 OverviewMedpace is a full-service clinical contract research organization (CRO). We provide Phase I-IV clinical development services to the biotechnology, pharmaceutical and medical device industries. Our mission is to accelerate the global development of safe and effective medical therapeutics through its scientific and disciplined approach. We le ...
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📑 OverviewMedpace is a full-service clinical contract research organization (CRO). We provide Phase I-IV clinical development services to the biotechnology, pharmaceutical and medical device industries. Our mission is to accelerate the global development of safe and effective medical therapeutics through its scientific and disciplined approach. We le ...
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📑 Overview Medpace is a full-service clinical contract research organization (CRO). We provide Phase I-IV clinical development services to the biotechnology, pharmaceutical and medical device industries. Our mission is to accelerate the global development of safe and effective medical therapeutics through its scientific and disciplined approac ...
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📑 Overview Medpace is a full-service clinical contract research organization (CRO). We provide Phase I-IV clinical development services to the biotechnology, pharmaceutical and medical device industries. Our mission is to accelerate the global development of safe and effective medical therapeutics through its scientific ...
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📑 Overview Medpace is a full-service clinical contract research organization (CRO). We provide Phase I-IV clinical development services to the biotechnology, pharmaceutical and medical device industries. Our mission is to accelerate the global development of safe and effective medical therapeutics through its scientific ...
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Great News! We have discovered exciting live Clinical clinical job opportunities in Navi mumbai just for you at India Jobs Expertini. You can even download the search results for Clinical clinical jobs in navi mumbai here.
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There are currently 752 live jobs available for Clinical clinical in Navi mumbai according to India Jobs Expertini.
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