3711 Clinical Research Jobs - Page 28

About The Role Skill required: Com.Bkg- Commercial Real Estate - Real Estate Due Diligence Designation: Banking Advisory Associate Qualifications: BCom/MCom/Master of Business Administration Years of Experience: 1 to 3 years What would you do? We help clients address quality and productivity issues, keep pace with customer expectations, navigate regulatory and operational pressures and ensure business sustainability by transforming their banking operations into an agile, resilient operating model.The Corporate banking /Wholesale banking team is responsible for helping clients and organizations processes trade finance transactions by providing superior service delivery to trade customers whil...

About The Role Skill required: AML fraud mgmt. Financial Crime & Fraud Management Designation: Regulatory Compliance Senior Analyst Qualifications: Any Graduation Years of Experience: 5 to 8 years What would you do? The Risk & Controls Analyst will be a key member of the Clients Operations Team, supporting the day-to-day management of the First Line of Defense risk management framework and related activitiesThis role involves working collaboratively across the bank to identify, assess, monitor, and mitigate operational risks.Strategize, architect, Analyse, design, implement and contribute to engagements involving tools and processes associated with the prevention (or management ) of fraud. W...

About The Role Skill required: AML fraud mgmt. Financial Crime & Fraud Management Designation: Regulatory Compliance Analyst Qualifications: Any Graduation Years of Experience: 3 to 5 years What would you do? Investigate Fraud and Disputes, review and determine the request and validate the chargeback.Looking for someone with AML and Fraud mgmt experience.Strategize, architect, Analyse, design, implement and contribute to engagements involving tools and processes associated with the prevention (or management ) of fraud. What are we looking for? Written and verbal communicationEnd to end knowledge in the areas of Fraud investigation, Fraud Detection, Dispute & Chargebacks.Understanding of Regu...

Medical Coding is the process of converting Verbal Descriptions into numeric or alpha numeric by using ICD 10-CM, CPT && HCPCS. As per HIPAA rules healthcare providers need efficient Medical Coders. Qualification & Specifications : MBBS,BDS,BHMS,BAMS,BSMS,PHARMACYB.Sc/M.Sc (Life Sciences / Biology / Bio Chemistry / Micro Biology / Nursing / Bio Technology), B.P.T, B.E BIOMEDIAL, B.Tech (Biotechnology/Bio Chemistry). Skills Required: * Candidates should have Good Communication & Analytical Skills and should be Good at Medical Terminology (Physiology & Anatomy). Role: To review US medical records Initial file review for identifying merits Subjective review and analysis to identify instances of...

We are looking for an Associate STEM Content Analyst to join our Biological Drugs team in Chennai (India). This is an amazing opportunity to work on content analysis for our Cortellis Drug Discovery Intelligence (CDDI) product. The team consists of 9 members based across Chennai, Hyderabad and Barcelona (Spain) and this role reports to the Biologicals Team Manager. We have a great skill set in Biology, Immunology, Pharmacology, Pharmacokinetics andcomplementary skill sets to address challenges in drug discovery, including new biological drugs identification and drug repositioning. We would love to speak with you if you have an understanding of biological drug products. About You experience, ...

Looking to onboard a highly motivated and detail-oriented individual with 0-1 years of experience to join our team as a Trainee Medical Reviewer in Bengaluru. Roles and Responsibility Conduct thorough medical reviews of patient records, including diagnoses, treatments, and test results. Analyze medical data to identify trends, patterns, and areas for improvement. Collaborate with healthcare professionals to develop and implement effective treatment plans. Maintain accurate and up-to-date records of patient information and review findings. Participate in quality improvement initiatives to enhance patient care and outcomes. Develop and maintain knowledge of medical terminology, regulations, an...

We are looking for a highly motivated and detail-oriented individual to join our team as a Trainee Medical Reviewer in Bengaluru. The ideal candidate should have 0-1 years of experience. Roles and Responsibility Conduct thorough medical reviews of patient records and reports to ensure accuracy and compliance with regulatory requirements. Collaborate with cross-functional teams to identify and resolve issues related to medical review. Develop and maintain expertise in medical terminology, regulations, and guidelines. Provide high-quality support to the medical review team through data entry, documentation, and other administrative tasks. Participate in ongoing education and training to enhanc...

Role Description Regulatory Reporting is responsible for establishing and maintaining control frameworks designed to manage regulatory - monitoring, surveillance, compliance, transaction monitoring and screening. As a Regulatory Reporting team member, you will be responsible for managing daily reporting tasks and remediation activities. Your key responsibilities Participate in change and BAU activities. Perform daily reviews of exceptions within the SLAs. Ensure accurate investigation and timely escalations. Identify opportunities to create efficiency in the current process. Liaise with internal stakeholders for issue resolutions Participate in new system implementation and projects Review a...

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The Associate Medical Expert in Translational Clinical Oncology (TCO) serves as the medical leader for global, roll-over, and long-term follow-up studies, as well as studies in the close-out phase. Additionally, they provide medical support for assigned components of active TCO studies under the guidance of a Clinical Program Leader (CPL) or Medical Expert. TCO, a department within the Biomedical Research division, specializes in designing and conducting early-phase clinical studies in cancer patients, bridging the gap between drug discovery and late-phase clinical development to deliver innovative oncology treatments. In this role, your major responsibilities include providing medical suppo...

As a DM/DNB Interventional Cardiologist at a reputed corporate multispecialty hospital in Bhilwara, Rajasthan, you will play a crucial role in the healthcare team. With 1 to 5 years of experience, your responsibilities will revolve around providing comprehensive care to patients with cardiovascular issues. Your expertise will be vital in diagnosing cardiac conditions, creating personalized treatment plans, and performing interventional cardiology procedures. Your key responsibilities will include conducting thorough assessments, managing chronic conditions, collaborating with healthcare professionals, and educating patients about cardiovascular health. Additionally, you will participate in c...

Our imaging services are expanding rapidly, and we are currently looking for a full-time Imaging Technologist - MRI or Nuclear Medicine to join our team in Hyderabad, India. If you are seeking an exciting career where you can utilize your previous expertise and further develop and advance your career, then this opportunity is for you. Responsibilities: - Perform quality assurance checks on medical imaging data to ensure protocol-specific requirements are met. - Utilize established image processing techniques (such as converting imaging formats, conducting preliminary measurements of lesions and volumes) across MRI or Nuclear medicine imaging modalities using proprietary software as well as o...

Inhouse CRA - India - Bangalore ICON plc is a world-leading healthcare intelligence and clinical research organization. We're proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development We are currently seeking an IHCRA (In-House Clinical Research Associate) to join our diverse and dynamic team. As an IHCRA at ICON, you will play a pivotal role in supporting the execution and management of clinical trials, contributing to the advancement of innovative treatments and therapies. What you will be doing Assisting in the planning, initiation, and execution of clinical trial activities Conducti...

CTA - India, Chennai Hybrid: Office/Remote ICON plc is a world-leading healthcare intelligence and clinical research organization. We're proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development 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 development of drugs and devices that save lives a...

Are you a life science/research graduate interested in medical writing Do you enjoy collaborating with peers in the medical field, interpreting and communicating scientific data Does interacting with global medical leaders interest you Then there is an opportunity within the Global Medical Affairs department at Novo Nordisk. Join a growing team in an international environment. Global Medical Affairs, GBS (GMA GBS) is an extension of the Global Medical Affairs unit in Headquarters in Denmark and Zurich, based out of Global Business Services (GBS) in Bangalore, India. The team comprises highly motivated medical advisors, project managers, and publication managers collaborating with HQ, regions...

As a visionary leader in the field of Ayurveda Clinical Research, you will play a crucial role in advancing the scientific credibility of Ayurveda and transforming traditional knowledge into evidence-based solutions that are globally recognized. Your primary responsibility will be to lead clinical studies aiming to validate Ayurvedic principles utilizing modern research methodologies. It will be imperative to publish research outcomes in peer-reviewed journals and present findings to international healthcare communities. You will be expected to identify and secure funding from both national and international bodies to support research and development activities. Building strategic partnershi...

You are invited to join our research team at SJRI as a Medical Technician. In this role, you will be involved in supporting a variety of research projects, particularly focusing on nutrition, public health, and health technology. Your responsibilities will include handling technical aspects of various studies, such as longitudinal, interventional, observational, cohort studies, and randomized controlled trials. As a Medical Technician at SJRI, you will be expected to manage the setup, installation, and configuration of advanced and sensitive equipment and devices. You will conduct systematic assessments using medical equipment, ensuring compliance with quality and safety standards in the lab...

Skill required: KYC Screening - Know Your Customer (KYC) Designation: Regulatory Compliance Associate Qualifications: Any Graduation Years of Experience: 1 to 3 years About Accenture Combining unmatched experience and specialized skills across more than 40 industries, we offer Strategy and Consulting, Technology and Operations services, and Accenture Song all powered by the worlds largest network of Advanced Technology and Intelligent Operations centers. Our 699,000 people deliver on the promise of technology and human ingenuity every day, serving clients in more than 120 countries. Visit us at www.accenture.com What would you do :Experience working in Client On-boarding, Account Maintenance...

Skill required: Pharmacovigilance Operations - Pharmacovigilance & Drug Safety Surveillance Designation: Pharmacovigilance Services Sr Analyst Qualifications: Bachelor of Pharmacy/Master of Pharmacy Years of Experience: 5 to 8 years About Accenture Combining unmatched experience and specialized skills across more than 40 industries, we offer Strategy and Consulting, Technology and Operations services, and Accenture Song all powered by the worlds largest network of Advanced Technology and Intelligent Operations centers. Our 699,000 people deliver on the promise of technology and human ingenuity every day, serving clients in more than 120 countries. Visit us at www.accenture.com What would you...

Skill required: Regulatory Services - Life Sciences Regulatory Affairs Designation: LifeScience Regulatory Svs Associate Qualifications: Bachelor of Pharmacy/Master of Pharmacy Years of Experience: 1 to 3 years About Accenture Combining unmatched experience and specialized skills across more than 40 industries, we offer Strategy and Consulting, Technology and Operations services, and Accenture Song all powered by the worlds largest network of Advanced Technology and Intelligent Operations centers. Our 699,000 people deliver on the promise of technology and human ingenuity every day, serving clients in more than 120 countries. Visit us at www.accenture.com What would you do You will be aligne...

Job Description: Johnson & Johnson is recruiting for Associate Medical Advisor Oncology, Medical Affairs located in Mumbai, India. The position reports to the Senior Medical Advisor Haematology, Medical Affairs, Janssen India. Position overview: Enable the associated franchise for all their scientific needs and partner with various stakeholders for all scientific purposes including clinical trial designs, publications, medical education initiatives . Key Responsibilities : As a associate Medical Advisor at J&J Innovative Medicine India, you will play a key role in leading and shaping one of the Hematology Portfolio strategy for one of the key molecules closely in collaboration with cross fun...

CTA - India, Chennai Hybrid: Office/Remote ICON plc is a world-leading healthcare intelligence and clinical research organization. We re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development 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 development of drugs and devices that save lives a...

CTA - India, Chennai Hybrid: Office/Remote 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 development of drugs and devices that save lives and improve quality of life. Our people are our greatest strength, are at the core of our culture, and the driving force behind our success. ICON people have a mission to succeed and a passion that ensures what we do, we do well. Clinical Trial Assistant. Loca...

Good Clinical Domain knowledge with understanding of clinical phases and Work experience must be in clinical / healthcare domain. Experience in Edit Check Listings programming using SAS. Experience in Data Import Programming using SAS, SAS Output Delivery system (ODS) for generating reports in specific output formats like RTF, PDF, and HTML. Handling missing values, Reading Raw data files, creating data structures, Handling programming errors, Accessing and Managing data, Appending, Concatenating of SAS data sets. Comprehensively prepared reports using SAS report generating procedures like PROC PRINT, PROC FREQ, PROC MEANS, PROC TRANSPOSE and PROC SQL. Well versed with coding in Macros and S...

Good Clinical Domain knowledge with understanding of clinical phases and Work experience must be in clinical / healthcare domain. Experience in Edit Check Listings programming using SAS. Experience in Data Import Programming using SAS, SAS Output Delivery system (ODS) for generating reports in specific output formats like RTF, PDF, and HTML. Handling missing values, Reading Raw data files, creating data structures, Handling programming errors, Accessing and Managing data, Appending, Concatenating of SAS data sets. Comprehensively prepared reports using SAS report generating procedures like PROC PRINT, PROC FREQ, PROC MEANS, PROC TRANSPOSE and PROC SQL. Well versed with coding in Macros and S...