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📑 Clinical knowledge pertaining to clinical history taking, prescription and medicinesResponsible for coordinating Tele-consultations Responsible for registration, clinical history taking, remote examination of the patient and necessary documentation for effective teleconsultation and to ensure patient satisfaction. To provide nursing care to patient ...

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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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📑 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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📑 You will be a practitioner on our telehealth platform 'Intellect', where your role is to support our clients' mental health and personal growth based on the individual needs and goals. This is delivered primarily through scheduled 30-minute video sessions on our platform.This is a freelance remote role with the flexibility to decide your bu ...

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📑 You will be a practitioner on our telehealth platform 'Intellect', where your role is to support our clients' mental health and personal growth based on the individual needs and goals. This is delivered primarily through scheduled 30-minute video sessions on our platform.This is a freelance remote role with the flexibility to decide your ...

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📑 JOB DETAILS 1. Responsible for performing activities in compliance with applicable Corporate and Clinical Operations Policies, Standard Operating Procedures and Work Instructions 2. Assists Clinical Monitoring staff with site management activities, including serving as a Sponsor representative for sites on assigned studies, and communicating ...

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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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📑 We are seeking a motivated and detail-oriented Clinical Research Coordinator to join our dynamic team. As a Clinical Research Coordinator, you will play a crucial role in the planning, implementation, and coordination of clinical research studies. You will work closely with principal investigators, study participants, and other healthcare profes ...

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📑 We are seeking a motivated and detail-oriented Clinical Research Coordinator to join our dynamic team. As a Clinical Research Coordinator, you will play a crucial role in the planning, implementation, and coordination of clinical research studies. You will work closely with principal investigators, study participants, and other healthcare profes ...

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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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📑 Our commitment to developing our staff is only surpassed by our commitment to advancing treatment options available to patients. At Cytel, we work hard to create successful careers with significant professional growth for our employees and as a result work hard to make Cytel successful. Cytel is a place where talent, experience, and integrity come ...

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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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📑 <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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📑 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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📑 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 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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📑 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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📑 Our commitment to developing our staff is only surpassed by our commitment to advancing treatment options available to patients. At Cytel, we work hard to create successful careers with significant professional growth for our employees and as a result work hard to make Cytel successful. Cytel is a place where talent, experience, and integrity come ...

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📑 Our commitment to developing our staff is only surpassed by our commitment to advancing treatment options available to patients. At Cytel, we work hard to create successful careers with significant professional growth for our employees and as a result work hard to make Cytel successful. Cytel is a place where talent, experience, and integrity come ...

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📑 You will be a practitioner on our telehealth platform 'Intellect', where your role is to support our clients' mental health and personal growth based on the individual needs and goals. This is delivered primarily through scheduled 60-minute video sessions on our platform.This is a freelance remote role with the flexibility to decide your bu ...

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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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📑 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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📑 : 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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📑 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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📑 Job Summary:The Manager of Clinical Trials will lead and oversee all clinical trial activities for our medical device portfolio, ensuring compliance with international regulatory standards for markets including the U.S. and Japan. The role requires extensive experience in clinical trial management, a deep understanding of regulatory requirements in ...

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📑 Minimum 2 years of clinical experenceBSc Nurse / Post Basic NurseWill be working for US process from Kochi Office. Good Communication skills and clinical KnowlegdeMedical record /file review expereince is an advantage. Working hours : US/Evening shift. Transportation will be provided within company transportation limit.Job profileSupports identific ...

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📑 Our commitment to developing our staff is only surpassed by our commitment to advancing treatment options available to patients. At Cytel, we work hard to create successful careers with significant professional growth for our employees and as a result work hard to make Cytel successful. Cytel is a place where talent, experience, and integrity co ...

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📑 Our commitment to developing our staff is only surpassed by our commitment to advancing treatment options available to patients. At Cytel, we work hard to create successful careers with significant professional growth for our employees and as a result work hard to make Cytel successful. Cytel is a place where talent, experience, and integrity co ...

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📑 Our commitment to developing our staff is only surpassed by our commitment to advancing treatment options available to patients. At Cytel, we work hard to create successful careers with significant professional growth for our employees and as a result work hard to make Cytel successful. Cytel is a place where talent, experience, and integrity co ...

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📑 Job DescriptionJob Title: Clinical Lead -Nursing HomePosition Type: Full-timeHours: 40 hours per week, Monday to Friday with alternate ...

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📑 Job Summary:The Manager of Clinical Trials will lead and oversee all clinical trial activities for our medical device portfolio, ensuring compliance with international regulatory standards for markets including the U.S. and Japan. The role requires extensive experience in clinical trial management, a deep understanding of regulatory require ...

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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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📑 JOB DETAILS 1 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. 2 Provide expert medical/scientific advice for assigned ...

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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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📑 Minimum 2 years of clinical experenceBSc Nurse / Post Basic NurseWill be working for US process from Kochi Office. Good Communication skills and clinical KnowlegdeMedical record /file review expereince is an advantage.Working hours : US/Evening shift. Transportation will be provided within company transportation limit.<b ...

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📑 Minimum 2 years of clinical experenceBSc Nurse / Post Basic NurseWill be working for US process from Kochi Office. Good Communication skills and clinical KnowlegdeMedical record /file review expereince is an advantage.Working hours : US/Evening shift. Transportation will be provided within company transportation limit.<b ...

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📑 Minimum 2 years of clinical experenceBSc Nurse / Post Basic NurseWill be working for US process from Kochi Office. Good Communication skills and clinical KnowlegdeMedical record /file review expereince is an advantage.Working hours : US/Evening shift. Transportation will be provided within company transportation limit.<b ...

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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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📑 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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📑 Regional Medical Advisor- Oncology (Uro-Oncology), based out at Mumbai ABOUT ASTRAZENECA BUSINESS AREA What you’ll do As a Regional Medical Advisor, you will be responsible to engage medical / scientific experts in in-depth medical / scientific product or disease area dis ...

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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 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 for ...

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📑 Job DescriptionPrimary Purpose / Regulatory Responsibilities: • Establishment of robust, fit for purpose biological drug product manufacturing processes for the different development phases (FIM, Ph2, Ph3). • Definin ...

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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) ...

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📑 Position Title : Executive / Assistant Manager - Clinical Operations (Clinical Research Associate)Location : Bangalore At VIATRIS™, we see healthcare not as it is but as it should be. We act courageously and are uniquely positioned to be a source of stability in a world of evolving healthcare needs.Viatris empowers people worldwide to live healthie ...

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📑 Position Title : Executive / Assistant Manager - Clinical Operations (Clinical Research Associate)Location : Bangalore At VIATRIS™, we see healthcare not as it is but as it should be. We act courageously and are uniquely positioned to be a source of stability in a world of evolving healthcare needs.Viatris empowers people worldwide to live healthie ...

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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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📑 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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