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📑 JOB DETAILS 1. Prevent the payment of potentially fraudulent and/or abusive claims utilizing medical expertise, knowledge of CPT/diagnosis codes, CMC guideline along with referring to client specific guidelines and member policies 2. Adhere to the state and federal compliance policies and contract compliance 3. Assist the prospective team wit ...

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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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📑 Are you a board-certified rheumatologist in India looking to expand your impact within the realm of immunology? Sense7ai Healthcare Division seeks a professional like you for a pivotal role with a prestigious yet confidential US-based client. This contract-based opportunity is focused on transforming patient care by shifting from broad immunosuppre ...

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📑 Are you a board-certified rheumatologist in India looking to expand your impact within the realm of immunology? Sense7ai Healthcare Division seeks a professional like you for a pivotal role with a prestigious yet confidential US-based client. This contract-based opportunity is focused on transforming patient care by shifting from broad immunosuppre ...

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📑 Are you a board-certified rheumatologist in India looking to expand your impact within the realm of immunology? Sense7ai Healthcare Division seeks a professional like you for a pivotal role with a prestigious yet confidential US-based client. This contract-based opportunity is focused on transforming patient care by shifting from broad immunosuppre ...

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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) 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 Coordinate and supervise the activities of clinical team members engaged in clinical care for patients under the supervision of a Physician or provider for the diagnosis, treatment and prevention of disease. 2 Organize and assign duties and tasks to clinical team members. 3 Establish clinical team member work schedules monthly a ...

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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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📑 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 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. 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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📑 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 1)Research potential vendors 2)Compare and evaluate offers from suppliers 3)Negotiate contract terms of agreement and pricing 4)Track orders and ensure timely delivery 5)Review quality of purchased products 6)Enter order details (e.g. vendors, quantities, prices) into internal databases 7)Maintain updated records of purchased prod ...

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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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📑 Are you a board-certified rheumatologist in India looking to expand your impact within the realm of immunology? Sense7ai Healthcare Division seeks a professional like you for a pivotal role with a prestigious yet confidential US-based client. This contract-based opportunity is focused on transforming patient care by shifting from broad immunosup ...

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📑 JOB DETAILS JD - Publication Planning * Support the development of Global publication strategy and integration with GMA strategy, global medical and scientific communication strategy * Plan, manage and execute publication plan activities KOL Engagement * Manage and track author engagements ...

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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 -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 1 To provide timely inputs in the protocol and Informed Consent (for e.g. dosing information, contraindications, warnings, precautions, adverse events, and drug interactions) and thus ensure it is scientifically sound and gives a clear detailed description of trial related activities. 2 To submit protocol and other required study ...

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📑 Are you a board-certified rheumatologist in India looking to expand your impact within the realm of immunology? Sense7ai Healthcare Division seeks a professional like you for a pivotal role with a prestigious yet confidential US-based client. This contract-based opportunity is focused on transforming patient care by shifting from broad imm ...

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📑 JOB DETAILS 1.writing drug trial methodologies (procedures) 2.identifying and briefing appropriate trial investigators (clinicians) 3.setting up and disbanding trial study centres 4.designing trial materials and supplying study centres with sufficient quantities 5.providing clinicians with instructions on how to conduct the trials 6.collectin ...

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📑 Join a team that is changing millions of lives. Transforming smiles, changing lives. At Align Technology, we believe a great smile can transform a person’s life, so we create technology that gives people the confidence to take on whatever’s next. We revolutionized the orthodontic industry with the introduction of the Invisalign system, and we have ...

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📑 Join a team that is changing millions of lives. Transforming smiles, changing lives. At Align Technology, we believe a great smile can transform a person’s life, so we create technology that gives people the confidence to take on whatever’s next. We revolutionized the orthodontic industry with the introduction of the Invisalign system, and we have ...

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📑 Prudential’s purpose is to be partners for every life and protectors for every future. Our purpose encourages everything we do by creating a culture in which diversity is celebrated and inclusion assured, for our people, customers, and partners. We provide a platform for our people to do their best work and make an impact to the business, and we s ...

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📑 Excelya is one of the leading independent CRO in Europe, it is founded in 2014 and it is a people-centered Contract Research Organization (CRO) that excels with care. In Excelya, our mission is to offer our collaborators a human and authentic experience within a young and ambitious healthcare company that is becoming a leader in clinica ...

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📑 (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 to achieve individua ...

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📑 JOB DETAILS 1. Prevent the payment of potentially fraudulent and/or abusive claims utilizing medical expertise, knowledge of CPT/diagnosis codes, CMC guideline along with referring to client specific guidelines and member policies 2. Adhere to the state and federal compliance policies and contract compliance<b ...

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📑 India Audiologist - Hyderabad Hearing Care ProfessionalAndhra Pradesh, India Job Purpose: Deliver all clinical audiology services in Amplifon clinics audiology diagnostics to hearing aid fitting and verification. Job Specification: Strong and effective communica ...

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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 ass ...

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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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📑 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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📑 Prudential’s purpose is to be partners for every life and protectors for every future. Our purpose encourages everything we do by creating a culture in which diversity is celebrated and inclusion assured, for our people, customers, and partners. We provide a platform for our people to do their best work and make an impact to the business, and w ...

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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, e ...

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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 ...

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📑 PHP Developer 0-4 years of experience. Extensive knowledge of working experience in OOPs, Javascript, Database. Hands on experience in PHP, MYSQL, Jquery, Ajax. Candidate should have experience in any framework (Cake PHP, Zend, Codeigniter, Laravel, Yii, Symphony.etc) Experience and knowledge Angular JS & Node JS. Strong knowledge of HTML, CSS, ...

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📑 PHP Developer 0-4 years of experience. Extensive knowledge of working experience in OOPs, Javascript, Database. Hands on experience in PHP, MYSQL, Jquery, Ajax. Candidate should have experience in any framework (Cake PHP, Zend, Codeigniter, Laravel, Yii, Symphony.etc) Experience and knowledge Angular JS & Node JS. Strong knowledge of HTML, CSS, ...

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📑 JOB DETAILS 1) Evaluate health message scripts and content for clinical accuracy. 2) Check documents (mentioned above) developed by copywriters for clinical and scientific, reporting errors by checking the developed material against annotated references, clinical guidelines, other published sources data 3 ...

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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 ...

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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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📑 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 Title: Clinical Data Manager III (CDM III)Job Location: India (Remote)Job Overview: The Clinical Data Manager III is responsible to participate the clinical data management activities for a project within a data management team; including processing of Case Report form and electronic data, processing and reconciliation of external data, SAE rec ...

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📑 Job Title: Clinical Data Manager III (CDM III)Job Location: India (Remote)Job Overview: The Clinical Data Manager III is responsible to participate the clinical data management activities for a project within a data management team; including processing of Case Report form and electronic data, processing and reconciliation of external data, SAE rec ...

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📑 JOB DETAILS 1.approval of the Clinical Risk Management Plan, to confirm that the plan is appropriate and achievable in the context of Meds Companion 2.ensuring that clinical risk management activities are completed in accordance with the Clinical Risk Management Plan 3.reviewing and approving of safety do ...

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📑 JOB DETAILS 1 Coordinate and supervise the activities of clinical team members engaged in clinical care for patients under the supervision of a Physician or provider for the diagnosis, treatment and prevention of disease. 2 Organize and assign duties and tasks to clinical team members. 3 Establi ...

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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 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 con ...

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📑 Position Title: Clinical Operations Lead - Diabetes (Insulin) Minimum Educational Requirements: MBBS, MD in Pharmacology As a Contract Research Organization (CRO), Must Have - experience in clinical trials across with a focus on Pharmacovigilance to look after clientele spans nationwide, conducting trials throughout India. The incumbent in this ro ...

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