📑 we are hiring Education CounsellorExperience : 1 - 2 year as counsellor is mustQualification : GraduatesGender : FemaleLocation **:AHMEDABAD**303 K 158 Complex, Sindhu Bhavan Road, Ahmedabad - 380054.Responsibilities:Skills : Good communication skills as well as convincing skills. Must be Aggressive & ...
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📑 As a Clinical Research Associate, you'll play a pivotal role in ensuring the successful execution of clinical trials. From monitoring trial progress to ensuring regulatory compliance and participant safety, you'll be at the forefront of cutting-edge medical research.Key Responsibilities:Conduct site visits to monitor trial activities and ensure com ...
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📑 **Add Validity: 10/4/2024****Position**:Postdoctoral Fellow**No. of positions**:1**Appointing Organisation**:Tata Translational Cancer Research CentreTata Medical Center, Kolkata**The Tata Medical Center and the Tata Translational Cancer Research Centre**The Tata Medical Center (TMC) is a multispecial ...
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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 Trial Delivery Support is a core GDO team responsible for supporting study startup for clinical study teams along providing support with analytics to development and study level teams for the purpose of trial optimization. Position Summary / Objective The Digital Architect role will be at the center of a dynamic technology mo ...
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📑 **Position: Post-Doctoral Fellow in Genomics****No. of positions: 1****Validity: 6/4/2024****Appointing Organisation**Tata Translational Cancer Research CentreTata Medical Center, Kolkata**The Tata Medical Center and the Tata Translational Cancer Research Centre**The Tata Medical Center (TMC) ...
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📑 Description OBJECTIVES : ACCOUNTABILITIES: EDUCATION, BEHAVIOURAL COMPETENCIES AND SKILLS: TRAVEL REQUIREMENTS: Locations India Worker Type Employee Worker Sub-Type Regular Time Type Full time ...
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📑 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 goals while taking science a step beyo ...
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📑 SDC is a team of diversified professionals who deliver exceptional Biometric Services, Consulting, and Technology Solutions to pharmaceutical, biologic, and medical device/diagnostic companies. Since 2005 our purpose has been to partner with sponsors to provide high quality and experienced team members to develop great medicines that save lives and ...
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📑 Job DescriptionPosition: Wellness Center Physician Location: (Chennai, Tamil Nadu) At (AIWO WELLNESS CENTRE) located in (CHENNAI), we are committed to enhancing the health and well-being of our community through integrative and holistic practices. We are looking for a dedicated and compassionate Wellness Center Physician to join our team and help o ...
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📑 Job Overview Provide Trial Master File (TMF) related assistance to study teams. Ensure all work is conducted in accordance with Standard Operating Procedures (SOPs), policies, practices, good clinical practices, applicable regulatory requirements, and meets quality and timeline metrics. Ensure that project timelines are met and facilitate the orde ...
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📑 Job Overview Provide Trial Master File (TMF) related assistance to study teams. Ensure all work is conducted in accordance with Standard Operating Procedures (SOPs), policies, practices, good clinical practices, applicable regulatory requirements, and meets quality and timeline metrics. Ensure that project timelines are met and facilitate the orde ...
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📑 Clinical SAS Programmer (India) India CRO - Biometrics Full-time 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 prod ...
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📑 Job Title: Clinical Data Manager II (CDM II)Job Location: Home-based Job Overview: The Clinical Data Manager II participates in the clinical data management activities for a project within a data management project team; including processing of case report form (CRF) and electronic data in accordance with Caiya SOPs, Good Clinical Practice, ICH Gu ...
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📑 Job Title: Clinical Data Manager II (CDM II)Job Location: Home-based Job Overview: The Clinical Data Manager II participates in the clinical data management activities for a project within a data management project team; including processing of case report form (CRF) and electronic data in accordance with Caiya SOPs, Good Clinical Practice, ICH Gu ...
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📑 Job Title: Clinical Data Manager II (CDM II)Job Location: Home-based Job Overview: The Clinical Data Manager II participates in the clinical data management activities for a project within a data management project team; including processing of case report form (CRF) and electronic data in accordance with Caiya SOPs, Good Clinical Practice, ICH Gu ...
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📑 Job OverviewProvide Trial Master File (TMF) related assistance to study teams.Ensure all work is conducted in accordance with Standard Operating Procedures (SOPs), policies, practices, good clinical practices, applicable regulatory requirements, and meets quality and timeline metrics.Ensure that project timelines are met and facilitate ...
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📑 Job OverviewProvide Trial Master File (TMF) related assistance to study teams.Ensure all work is conducted in accordance with Standard Operating Procedures (SOPs), policies, practices, good clinical practices, applicable regulatory requirements, and meets quality and timeline metrics.Ensure that project timelines are met and facilitate ...
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📑 : Coordinates, oversees and completes functions on assigned trials activities detailed on the task matrix. Performs department, Internal, Country and Investigator file reviews as assigned and documents findings in appropriate system. Ensures allocated tasks are performed on time, within budget and to a high quality standard. Brings up cases o ...
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📑 Together, we can beat cancer. At Varian, a Siemens Healthineers Company, we bring together the world's best talent to realize our vision of a world without fear of cancer. Together, we work passionately to develop and deliver easy-to-use, efficient oncology solutions. We are part of an incredible community of scientists, clinicians, developers ...
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📑 JOB DETAILS 1) Creating and writing trial protocols, and presenting these to steering committee. 2) Identifying, evaluating and establishing trial sites, and closing sites down on completion of trial. 3) Training site staff on therapeutic areas, protocol requirements, proper source documentation and case report form completion. 4) Liaise with ...
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📑 JOB DETAILS 1) Creating and writing trial protocols, and presenting these to steering committee. 2) Identifying, evaluating and establishing trial sites, and closing sites down on completion of trial. 3) Training site staff on therapeutic areas, protocol requirements, proper source documentation and case report form completion. 4) Liaise with ...
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📑 JOB DETAILS 1. Ensure that clinical research studies are conducted in accordance with the protocol, standard operating procedures, good clinical practice (GCP) guidelines, and other applicable regulatory requirements. 2. Perform site selection, initiation, monitoring and close-out visits in accordance with contracted scope of work and GCP gui ...
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📑 JOB DETAILS 1 Performing routine data collection from patients, 2 Verifying data sources, and reviewing regulatory documents/files to ensure that documents are in compliance with protocols, regulatory requirement 3 SOPs (standard operating procedures), and are aligned with the Monitoring Plan. 4 Some clinical research associates assist in rev ...
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📑 Clinical Research CoordinatorAbout the jobRole DescriptionThis is a full-time hybrid role for a Clinical Research Coordinator with Client. The Clinical Research Coordinator will be responsible for day-to-day tasks related to clinical research, including informed consent, protocols, research, clinical research experience, and clinical trials. This r ...
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📑 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 goals while taking science a step beyo ...
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📑 JOB DETAILS 1. Ensure that clinical research studies are conducted in accordance with the protocol, standard operating procedures, good clinical practice (GCP) guidelines, and other applicable regulatory requirements. 2. Perform site selection, initiation, monitoring and close-out visits in accordance with contracted scope of work and GCP gui ...
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📑 Job OverviewProvide Trial Master File (TMF) related assistance to study teams.Ensure all work is conducted in accordance with Standard Operating Procedures (SOPs), policies, practices, good clinical practices, applicable regulatory requirements, and meets quality and timeline metrics.Ensure that project timelines are met and facilitate ...
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📑 Principal Duties Responsibilities Perform and implement, under supervision, the following for clinical studies: (i) the SAS programming, testing, and documentation of statistical programs for use in creating statistical tables, figures, listings, and graphs and (ii) the programming of analysis datasets (derived datasets) and tra ...
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📑 Principal Duties & Responsibilities Perform and implement, under supervision, the following for clinical studies: (i) the SAS programming, testing, and documentation of statistical programs for use in creating statistical tables, figures, listings, and graphs and (ii) the programming of analysis datasets (derived datasets) and transfer files f ...
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📑 Principal Duties & Responsibilities Perform and implement, under supervision, the following for clinical studies: (i) the SAS programming, testing, and documentation of statistical programs for use in creating statistical tables, figures, listings, and graphs and (ii) the programming of analysis datasets (derived datasets) and transfer files f ...
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📑 Role DescriptionThis is a full-time hybrid role for a Clinical Research Coordinator with Learning Lab. The Clinical Research Coordinator will be responsible for day-to-day tasks related to clinical research, including informed consent, protocols, research, clinical research experience, and clinical trials. This role is located in Bengaluru but offe ...
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📑 ICON plc is a world-leading healthcare intelligence and clinical research organisation. From molecule to medicine, we advance clinical research providing outsourced services to pharmaceutical, biotechnology, medical device and government and public health organizations. With our patients at the center of all that we do, we help to accelerate the de ...
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📑 ICON plc is a world-leading healthcare intelligence and clinical research organisation. From molecule to medicine, we advance clinical research providing outsourced services to pharmaceutical, biotechnology, medical device and government and public health organizations. With our patients at the center of all that we do, we help to accelerate the de ...
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📑 Role DescriptionThis is a full-time hybrid role for a Clinical Research Coordinator with Learning Lab. The Clinical Research Coordinator will be responsible for day-to-day tasks related to clinical research, including informed consent, protocols, research, clinical research experience, and clinical trials. This role is located in Bengaluru but ...
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📑 Role DescriptionThis is a full-time hybrid role for a Clinical Research Coordinator with Learning Lab. The Clinical Research Coordinator will be responsible for day-to-day tasks related to clinical research, including informed consent, protocols, research, clinical research experience, and clinical trials. This role is located in Bengaluru but ...
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📑 Role DescriptionThis is a full-time hybrid role for a Clinical Research Coordinator with Learning Lab. The Clinical Research Coordinator will be responsible for day-to-day tasks related to clinical research, including informed consent, protocols, research, clinical research experience, and clinical trials. This role is located in Bengaluru but ...
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📑 JOB DETAILS 1. Ensure thatclinical researchstudies are conducted in accordance with the protocol, standard operating procedures, goodclinicalpractice (GCP) guidelines, and other applicable regulatory requirements. 2. Perform site selection, initiation, monitoring and close-out visits in accordance with contracted scope of work and GCP guideli ...
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📑 Description Performs review of clinical monitoring visit reports for allocated projects ensuring consistency across protocols and/or regions and escalates any protocol, site, and/or CRA issues or trends noted during the report review process to CTM. Liaises with clinical monitoring staff for prompt trip report review submission and approval a ...
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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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📑 Proposal & Contract Manager (India) India Corporate - Business Development and Marketing Full-time Proposal and Contract Manager The Proposal and Contract Manager manages all phases of the proposal development process in response to requests for proposals (RFP) from Innovaderm’s clients, as well as all contractual aspects of a proje ...
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📑 Job DescriptionScope of Work:· Development of an LLM product focused on clinical trial study start up.· Team is forming and needs ground up UX design support.· Potential 3rd product focused on clinical trial matching. Requirements:· 3+ year’s experience designing for complex internal software, 7+ years of UX experience· ...
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📑 JOB DETAILS 1.Collaborating with Project Manager to set targets for clinical monitoring staff, and ensuring recording of trial in compliance with project goals. 2.Creating and implementing study-specific clinical monitoring tools and documents. 3.Creating and overseeing trial budget. 4.Identifying, enlisting and choosing sites, and coordinati ...
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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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📑 ICON plc is a world-leading healthcare intelligence and clinical research organisation. From molecule to medicine, we advance clinical research providing outsourced services to pharmaceutical, biotechnology, medical device and government and public health organisations. With our patients at the centre of all that we do, we help to accelerate the de ...
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📑 ICON plc is a world-leading healthcare intelligence and clinical research organisation. From molecule to medicine, we advance clinical research providing outsourced services to pharmaceutical, biotechnology, medical device and government and public health organisations. With our patients at the centre of all that we do, we help to accelerate the de ...
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📑 Principal Duties & Responsibilities Perform, plan, co-ordinate and implement the following for complex studies: (i) the SAS programming, testing, and documentation of statistical programs for use in creating statistical tables, figures, listings, and graphs and (ii) the programming of analysis datasets (derived datasets) and transfer files for ...
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📑 Principal Duties & Responsibilities Perform, plan, co-ordinate and implement the following for complex studies: (i) the SAS programming, testing, and documentation of statistical programs for use in creating statistical tables, figures, listings, and graphs and (ii) the programming of analysis datasets (derived datasets) and transfer files for ...
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📑 Job Overview Provide Trial Master File (TMF) related assistance to study teams. Ensure all work is conducted in accordance with Standard Operating Procedures (SOPs), policies, practices, good clinical practices, applicable regulatory requirements, and meets quality and timeline metrics. Ensure that project timelines are ...
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📑 Job Overview Provide Trial Master File (TMF) related assistance to study teams. Ensure all work is conducted in accordance with Standard Operating Procedures (SOPs), policies, practices, good clinical practices, applicable regulatory requirements, and meets quality and timeline metrics. Ensure that project timelines are ...
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