📑 Clinical Data Management Job DescriptionWe are looking for a detail-oriented and organized Clinical Data Manager (CDM) to join our expanding clinical research team. The ideal candidate will be a passionate advocate for data accuracy and integrity, ensuring the smooth and efficient flow of clinical trial data from collection to analysis. You will pl ...
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📑 Clinical Data Management Job DescriptionWe are looking for a detail-oriented and organized Clinical Data Manager (CDM) to join our expanding clinical research team. The ideal candidate will be a passionate advocate for data accuracy and integrity, ensuring the smooth and efficient flow of clinical trial data from collection to analysis. You will pl ...
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📑 Clinical Data Management Job DescriptionWe are looking for a detail-oriented and organized Clinical Data Manager (CDM) to join our expanding clinical research team. The ideal candidate will be a passionate advocate for data accuracy and integrity, ensuring the smooth and efficient flow of clinical trial data from collection to analysis. You wil ...
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📑 Clinical Data Management Job DescriptionWe are looking for a detail-oriented and organized Clinical Data Manager (CDM) to join our expanding clinical research team. The ideal candidate will be a passionate advocate for data accuracy and integrity, ensuring the smooth and efficient flow of clinical trial data from collecti ...
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📑 DescriptionJob 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 data man ...
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📑 DescriptionJob 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 data man ...
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📑 DescriptionJob 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 ...
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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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📑 About Us:Our client is a multidisciplinary hospital in Pune offering a wide range of services in tertiary care. Having started operations in the year 2016, the hospital has blossomed to become a trusted provider of innovative yet affordable healthcare.The Hospital has a capacity of 250 beds and houses all specialties (Orthopedics, Obstetrics, emerg ...
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📑 Job DescriptionAbout Us: Our client is a multidisciplinary hospital in Pune offering a wide range of services in tertiary care. Having started operations in the year 2016, the hospital has blossomed to become a trusted provider of innovative yet affordable healthcare.The H ...
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📑 Job DescriptionAbout Us: Our client is a multidisciplinary hospital in Pune offering a wide range of services in tertiary care. Having started operations in the year 2016, the hospital has blossomed to become a trusted provider of innovative yet affordable healthcare.The H ...
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📑 About Us: Our client is a multidisciplinary hospital in Pune offering a wide range of services in tertiary care. Having started operations in the year 2016, the hospital has blossomed to become a trusted provider of innovative yet affordable healthcare.The Hospital has a capacity of ...
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📑 The Clinical SAS Programmer will lead the programming activities for various purposes including SAS Data Listings to be used for data review, Safety Review Listings, Centralized Monitoring Listings and Reports. The Clinical SAS Programmer will also be responsible for productions of Key Risk Indicators, working collaboratively across departments to ...
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📑 The Clinical SAS Programmer will lead the programming activities for various purposes including SAS Data Listings to be used for data review, Safety Review Listings, Centralized Monitoring Listings and Reports. The Clinical SAS Programmer will also be responsible for productions of Key Risk Indicators, working collaboratively across departments to ...
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📑 We have urgent opening for optometrist for Pune location Perform thorough routine eye inspections. Identify the patients visual alertness, field of vision, and hand-eye coordination. Diagnose sight problems, such as near sightedness and colour blindness. Prescribe corrective lenses and medications. Maintain accurate medical files for all pa ...
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📑 <p>Position : Clinical Data Analyst EPIC ClarityLocation : : 3+Job Description :We are seeking a skilled and experienced Clinical Data Analyst to join our team and support our Epic Systems implementation. The ideal candidate will have a strong background in healthcare data ana ...
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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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📑 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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📑 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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📑 SAS Certified professionals 3-8yrs 2 Experience in handling Clinical Data / Clinical Programming Exp in macros a must Good knowledge in Base SAS and SQL Hands on experience with SAS APIs will be an added advantageGraduateExperienced SAS Certified professionals 3-8yrs 2 • Experience in handling Clinical Data / Clinical Programming Exp ...
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📑 The Clinical SAS Programmer will lead the programming activities for various purposes including SAS Data Listings to be used for data review, Safety Review Listings, Centralized Monitoring Listings and Reports. The Clinical SAS Programmer will also be responsible for productions of Key Risk Indicators, working collaboratively across departments ...
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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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📑 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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📑 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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📑 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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📑 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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📑 The project manager has the overall responsibility for the successful initiation, planning, execution, monitoring, controlling and closure of assigned clinical trials. The project manager oversees and coordinates study resources to ensure compliance with the study budget, project scope and timelines and in accordance with applicable standard operat ...
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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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📑 ZS is a place where passion changes lives. As a management consulting and technology firm focused on transforming global healthcare and beyond, our most valuable asset is our people. Here you’ll work side-by-side with a powerful collective of thinkers and experts shaping solutions from start to finish. At ZS, we believe that making an impact dema ...
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📑 ZSis a place where passion changes lives. As a management consulting and technology firm focused on transforming global healthcare and beyond, our most valuable asset is our people. Here you’ll work side-by-side with a powerful collective of thinkers and experts shaping solutions from start to finish. At ZS, we believe that making an impact demands ...
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📑 ZS is a place where passion changes lives. As a management consulting and technology firm focused on transforming global healthcare and beyond, our most valuable asset is our people. Here you’ll work side-by-side with a powerful collective of thinkers and experts shaping solutions from start to finish. At ZS, we believe that making an impact dema ...
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📑 Description: -Act as the Lead Programmer overseeing technical planning for increasingly complex projects including global and multiple study projects, Integrated of Summary of Safety (ISS) and Integrated Summary of Efficacy (ISE)Work on complex problems where analysis of situations or data requires an evaluation of intangible variables; development ...
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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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📑 Description: - Act as the Lead Programmer overseeing technical planning for increasingly complex projects including global and multiple study projects, Integrated of Summary of Safety (ISS) and Integrated Summary of Efficacy (ISE)Work on complex problems where analysis of situations or data requires an evaluation of intangible variables; develop ...
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📑 About the jobRole: This role is an exciting opportunity for innovation in the field of Statistics and Data Science to help the Global Clinical Operations function and transform the way in which Client (Pharma company) uses data drive decision-making in RD clinical operations. Understanding of clinical data is an added advantage.Responsibilities:Imp ...
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📑 ZS is a place where passion changes lives. As a management consulting and technology firm focused on transforming global healthcare and beyond, our most valuable asset is our people. Here you’ll work side-by-side with a powerful collective of thinkers and experts shaping solutions from start to finish. At ZS, we believe that making an ...
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📑 Description1. Candidate must carry Clinical Knowledge. Either in the area of Data Management or Clinical Operations or Data Standardization ( SDTM, ADaM, TLF) or Healthcare domain2. Candidate must carry minimum of 7+ years of experience in writing user stories, prototyping tools, working on JIRA and other Product Roadmap tools ( AHA, ProductBoard)3 ...
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📑 Description1. Candidate must carry Clinical Knowledge. Either in the area of Data Management or Clinical Operations or Data Standardization ( SDTM, ADaM, TLF) or Healthcare domain2. Candidate must carry minimum of 7+ years of experience in writing user stories, prototyping tools, working on JIRA and other Product Roadmap tools ( AHA, ProductBoa ...
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📑 Description 1. Candidate must carry Clinical Knowledge. Either in the area of Data Management or Clinical Operations or Data Standardization ( SDTM, ADaM, TLF) or Healthcare domain 2. Candidate must carry minimum of 7+ years of experience in writing user stories, prototyping tools, working on JIRA and other Product Roadmap tools ( AHA, Produ ...
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📑 Description 1. Candidate must carry Clinical Knowledge. Either in the area of Data Management or Clinical Operations or Data Standardization ( SDTM, ADaM, TLF) or Healthcare domain 2. Candidate must carry minimum of 7+ years of experience in writing user stories, prototyping tools, working on JIRA and other Produ ...
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📑 Description1. Candidate must carry Clinical Knowledge. Either in the area of Data Management or Clinical Operations or Data Standardization ( SDTM, ADaM, TLF) or Healthcare domain2. Candidate must carry minimum of 7+ years of experience in writing user stories, prototyping tools, working on JIRA and other Product Roadmap tools ( AHA, Pr ...
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📑 About the jobRole: This role is an exciting opportunity for innovation in the field of Statistics and Data Science to help the Global Clinical Operations function and transform the way in which Client (Pharma company) uses data drive decision-making in RD clinical operations. Understanding of clinical data is an added advantage.Responsibili ...
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📑 About the jobRole: This role is an exciting opportunity for innovation in the field of Statistics and Data Science to help the Global Clinical Operations function and transform the way in which Client (Pharma company) uses data drive decision-making in RD clinical operations. Understanding of clinical data is an added advantage.Responsibili ...
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📑 Description: - Act as the Lead Programmer overseeing technical planning for increasingly complex projects including global and multiple study projects, Integrated of Summary of Safety (ISS) and Integrated Summary of Efficacy (ISE)Work on complex problems where analysis of situations or data requires an evaluation of intangible va ...
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📑 Description : - Act as the Lead Programmer overseeing technical planning for increasingly complex projects including global and multiple study projects, Integrated of Summary of Safety (ISS) and Integrated Summary of Efficacy (ISE) Work on complex problems where analysis of situations or data re ...
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📑 JOB DETAILS Manage Pharmaceutical and biological documentation & Registration application for chemical active substances, biological medicinal products & data control activities Schedule as per Drugs and Cosmetics Act, India GMP and USFDA CGMP Maintain Cell Therapy guidelines, USFDA guidelines, EMA Animal Safety & efficacy studies with GLP ce ...
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📑 About the jobRole: This role is an exciting opportunity for innovation in the field of Statistics and Data Science to help the Global Clinical Operations function and transform the way in which Client (Pharma company) uses data drive decision-making in RD clinical operations. Understanding of clinical data is an added adv ...
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📑 JOB DETAILS Manage Pharmaceutical and biological documentation & Registration application for chemical active substances, biological medicinal products & data control activities Schedule as per Drugs and Cosmetics Act, India GMP and USFDA CGMP Maintain Cell Therapy guidelines, USFDA guidelines, EMA A ...
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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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📑 The project manager has the overall responsibility for the successful initiation, planning, execution, monitoring, controlling and closure of assigned clinical trials. The project manager oversees and coordinates study resources to ensure compliance with the study budget, project scope and timelines and in accordance with applicable standard ope ...
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