📑 Quanticate is seeking a talented and experienced Senior Medical Writer to join our Medical Writing team in India. As a leading global clinical research organization, Quanticate works with pharmaceutical, biotechnology, and medical device companies to support their regulatory and scientific communication needs. The Senior Medical Writer will be r ...
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📑 Job DescriptionOur client, are a well-established and multi-disciplined law firm known for putting its people first. With a strong commitment to client service and a reputation for excellence, they are currently experiencing significant growth in their clinical negligence department. As part of their ambit ...
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📑 Description Job Description: Senior Business Analyst with Clinical Data Management Experience We are currently seeking a highly skilled and experienced Business Analyst with a strong background in clinical data management to join our team at Saama. This role is ideal for someone who is passionate about leveraging their expertise in clinical d ...
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📑 Description Job Description: Senior Business Analyst with Clinical Data Management Experience We are currently seeking a highly skilled and experienced Business Analyst with a strong background in clinical data management to join our team at Saama. This role is ideal for someone who is passionate about leveraging their ex ...
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📑 Senior Medical Writer (India) (FSP) At Thermo Fisher Scientific, you will 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 ...
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📑 This position manages the performance and workload of Medical Writers and provides short-term and long-term resource planning in order to assign projects to appropriate and available staff. Supervises the preparation of Medical Writing deliverables. Organizes processes for completion of projects within established timelines. Evaluates ...
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📑 Cytel provides unrivaled biostatistics and operations research knowledge to our customers in the life sciences industries in the form of both software and services. At Cytel, we work hard to create successful careers with significant professional growth for our employees, as a result of which they work hard to make Cytel successful. Cytel is a pla ...
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📑 Job DescriptionA top-notch fertility center is looking to hire a qualified medical officer to join their medical team. In this role, your duties will include serving as a clinical advisor, overseeing clinical trials, conducting procedures on clients using the HIFU machine (training will be provided), and maintain ...
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📑 As a leading global contract research organization (CRO) with a passion for scientific rigor and decades of clinical development experience, Fortrea provides pharmaceutical, biotechnology, and medical device customers a wide range of clinical development, patient access and technology solutions across more than 20 therapeutic areas. With over 19,0 ...
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📑 <p><p>PRIMARY PURPOSE :<br><br>The Lead Clinical SAS Programmer designs, develops, evaluates and modifies computer programs to analyze and evaluate clinical data, recognizes inconsistencies and initiates resolution of data problems. The Clinical Programmer typically creates programs using SAS to support th ...
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📑 Cytel provides unrivaled biostatistics and operations research knowledge to our customers in the life sciences industries in the form of both software and services. At Cytel, we work hard to create successful careers with significant professional growth for our employees, as a result of which they work hard to make Cytel successful. Cytel is a ...
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📑 Senior Biostatistician (6+ Years of Exp)Location: RemoteRoles and Responsibilities:Provide statistical leadership support for clinical studies including study design, sample size calculations, patient randomization, case report form (CRF) review, statistical analyses, interpretation of data, and reporting of results.Coordinate the development of an ...
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📑 Senior Biostatistician (6+ Years of Exp)Location: RemoteRoles and Responsibilities:Provide statistical leadership support for clinical studies including study design, sample size calculations, patient randomization, case report form (CRF) review, statistical analyses, interpretation of data, and reporting of results.Coordinate the development of an ...
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📑 Responsible for contributing to the planning, coordination, development and timely delivery of high quality Clinical submission documents to Regulatory Affairs (RA) for1) New Drug Applications (NDA), Biologic Licensing Applications (BLA), Marketing Authorization Applications (MAA) and supplemental NDAs/BLAs/ Type II variations, 2) for related follo ...
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📑 As a leading global contract research organization (CRO) with a passion for scientific rigor and decades of clinical development experience, Fortrea provides pharmaceutical, biotechnology, and medical device customers a wide range of clinical development, patient access and technology solutions across more than 20 therapeutic areas. With over 1 ...
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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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📑 LCC Senior Programmer Join Cytel’s enthusiastic and collaborative Biometrics team by contributing to the overall success of one of our major pharma clients. Cytel provides unrivalled biostatistics and operations research to improve drug development success rates, crucial for human welfare. Focused on using innovative applicati ...
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📑 Job Description<spa ...
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📑 Cytel provides unrivaled biostatistics and operations research knowledge to our customers in the life sciences industries in the form of both software and services. At Cytel, we work hard to create successful careers with significant professional growth for our employees, as a result of which they work hard to make Cytel successful. Cytel is a pla ...
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📑 Job DescriptionOur client, a leading national law firm specialising in Clinical Negligence, are seek an adept Clinical Negligence Solicitor to join their team as a Senior Associate, with prospects for advancement to Head of Department. In this role, you'll oversee a varied caseload of high-value medical ne ...
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📑 As a leading global contract research organization (CRO) with a passion for scientific rigor and decades of clinical development experience, Fortrea provides pharmaceutical, biotechnology, and medical device customers a wide range of clinical development, patient access and technology solutions across more than 20 therapeutic areas. With over 19,0 ...
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📑 Position Overview:Title: Competitive Intelligence - Senior AnalystCore Responsibilities:Serve as the primary authority on healthcare industry dynamics, comprehensive competitive intelligence, and advanced secondary research.Systematically scrutinize internal data, vendor reports, and external sources to discern emergent trends, potential opportunit ...
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📑 Position Overview:Title: Competitive Intelligence - Senior AnalystCore Responsibilities:Serve as the primary authority on healthcare industry dynamics, comprehensive competitive intelligence, and advanced secondary research.Systematically scrutinize internal data, vendor reports, and external sources to discern emergent trends, potential opportunit ...
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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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📑 Position Title : Submission ManagerAbout The RoleResponsible for contributing to the planning, coordination, development and timely delivery of high quality Clinical submission documents to Regulatory Affairs (RA) forNew Drug Applications (NDA), Biologic Licensing Applications (BLA), Marketing Authorization Applications (MAA) and supplemental NDAs/ ...
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📑 Senior Biostatistician (6+ Years of Exp) Location: Remote Roles and Responsibilities: Provide statistical leadership support for clinical studies including study design, sample size calculations, patient randomization, case report form (CRF) review, statis ...
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📑 Principal Medical Writer (India) (FSP) At Thermo Fisher Scientific, you will 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 nee ...
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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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📑 Position Title : Submission Manager About The Role Responsible for contributing to the planning, coordination, development and timely delivery of high quality Clinical submission documents to Regulatory Affairs (RA) for New Drug Applications (NDA) , Biologic Licensing Applications (BLA), Marketing Authorization Applications (MAA) and supplemental ...
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📑 As a leading global contract research organization (CRO) with a passion for scientific rigor and decades of clinical development experience, Fortrea provides pharmaceutical, biotechnology, and medical device customers a wide range of clinical development, patient access and technology solutions across more than 20 therapeutic areas. With over 19,00 ...
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📑 At Cytel, we work hard to create successful careers with significant professional growth for our employees, as a result of which they work hard to make Cytel successful. Cytel is a place where talent, experience and integrity come together to advance the state of clinical development. Working under the direction of Senior Statistical Programmer/T ...
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📑 Cytel provides unrivaled biostatistics and operations research knowledge to our customers in the life sciences industries in the form of both software and services. At Cytel, we work hard to create successful careers with significant professional growth for our employees, as a result of which they work hard to make Cytel successful. Cytel is a pla ...
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📑 Position Title : Submission ManagerAbout The RoleResponsible for contributing to the planning, coordination, development and timely delivery of high quality Clinical submission documents to Regulatory Affairs (RA) forNew Drug Applications (NDA) , Biologic Licensing Applications (BLA), Marketing Authorization Applications (MA ...
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📑 Position Title : Submission ManagerAbout The RoleResponsible for contributing to the planning, coordination, development and timely delivery of high quality Clinical submission documents to Regulatory Affairs (RA) forNew Drug Applications (NDA) , Biologic Licensing Applications (BLA), Marketing Authorization Applications (MA ...
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📑 Position Title : Submission ManagerAbout The RoleResponsible for contributing to the planning, coordination, development and timely delivery of high quality Clinical submission documents to Regulatory Affairs (RA) forNew Drug Applications (NDA) , Biologic Licensing Applications (BLA), Marketing Authorization Applications (MA ...
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📑 Job Description Position Title, Responsibility Level Executive, Senior Executive Nurse Level 1 or 2A Function Nurse Abstractor Reports to Assistant Manager Permanent/ Temporary Permanent Span of Control None Location Kochi Basic Function Responsible for the review and evaluation of clinical information an ...
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📑 Job Description Position Title, Responsibility Level Executive, Senior Executive Nurse Level 1 or 2A Function Nurse Abstractor Reports to Assistant Manager Permanent/ Temporary Permanent Span of Control None Location Kochi Basic Function Responsible for the review and evaluation of clinical information an ...
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📑 Company DescriptionBeasyFit is a team of highly skilled nutritionists, fitness trainers and clinical dieticians who work together to help busy working professionals in India improve their confidence and life longevity without having to resort to strict diets and endless exercises. Our mission is to help individuals get into their best body shape wh ...
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📑 Precision for Medicine is a precision medicine CRO. Our uniquely integrated offering enables the science of precision medicine by combining novel clinical trial designs, industry-leading operational and medical authorities, advanced biomarker and data analytics solutions, and an unequivocal real passion for rare diseases and oncology.Due to growth ...
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📑 As a leading global contract research organization (CRO) with a passion for scientific rigor and decades of clinical development experience, Fortrea provides pharmaceutical, biotechnology, and medical device customers a wide range of clinical development, patient access and technology solutions across more than 20 therapeutic areas. With over 19,0 ...
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📑 Excelya is one of the leading CROs in Europe, founded in 2014 and headquartered in Paris. Our global team is composed of 900+ experts who understand the critical needs of clients and provide trial solutions across a broad spectrum of therapeutic areas.We take a one-team approach to work: our shared success is the result of collaboration at ...
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📑 Precision for Medicine are hiring an Investigator Grants Associate/Senior Investigator Grants Associate based in India to join our global team.Position Summary:The Investigator Grants Associate position is designed to provide grant administration processing and financial support to the Finance Team and applicable project teams. The position require ...
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📑 As a leading global contract research organization (CRO) with a passion for scientific rigor and decades of clinical development experience, Fortrea provides pharmaceutical, biotechnology, and medical device customers a wide range of clinical development, patient access and technology solutions across more than 20 therapeutic areas. With over 1 ...
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📑 At Cytel, we work hard to create successful careers with significant professional growth for our employees, as a result of which they work hard to make Cytel successful. Cytel is a place where talent, experience and integrity come together to advance the state of clinical development. Working under the direction of Senior Statistical Pr ...
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📑 Cytel provides unrivaled biostatistics and operations research knowledge to our customers in the life sciences industries in the form of both software and services. At Cytel, we work hard to create successful careers with significant professional growth for our employees, as a result of which they work hard to make Cytel successful. Cytel is a ...
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📑 About the jobAs a leading global contract research organization (CRO) with a passion for scientific rigor and decades of clinical development experience, Fortrea provides pharmaceutical, biotechnology, and medical device customers a wide range of clinical development, patient access and technology solutions across more than 20 therapeutic areas. Wi ...
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📑 Department Details Role Summary 1.Write, edit, review, format all regulatory (clinical and nonclinical) documents and dossier sections in a manner compliant with FDA, EMA, CDSCO and ICH guidelines. 2.Write, edit, review, clinical publications (systematic reviews, meta-analysis, manuscripts-primary and secondary, abstracts, posters, slide ...
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📑 When our values align, there's no limit to what we can achieve. The Senior Statistical Programmer provides technical expertise for the conduct of clinical trials, acts as an internal subject matter expert in specific areas providing technical support and expert advice and works independently to support various programing activities related to ...
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📑 Senior Statistical Programmer Analyst - 2406184143W **Description** The Senior Statistical Programmer Analyst is an individual contributor with in-depth knowledge of statistical programming methods, languages and data structures who supports data analysis and reporting activities within the Statistical Programming functional area ...
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📑 Department Details Role Summary 1.Write, edit, review, format all regulatory (clinical and nonclinical) documents and dossier sections in a manner compliant with FDA, EMA, CDSCO and ICH guidelines. 2.Write, edit, review, clinical publications (systematic reviews, meta-analysis, manuscript ...
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