6710 Clinical Research Jobs - Page 32

UG Training Academy is looking for Freshers Trainee Medical coders to join our dynamic team and embark on a rewarding career journey. Assisting experienced employees with their daily tasks and responsibilities. Observing and gaining hands - on experience in various aspects of the job. Receiving feedback and guidance from supervisors and mentors. Completing assigned projects and tasks under the supervision of experienced employees. Collaborating with team members and contributing to team projects. Demonstrating a strong work ethic, positive attitude, and a willingness to learn and grow. Disclaimer : This job description has been sourced from a public domain and may have been modified by Naukr...

Aster Medcity is looking for Pharmacist - Pharmacy to join our dynamic team and embark on a rewarding career journey. Dispense medication to patients, ensuring accuracy and compliance with applicable laws and regulations. Counsel patients on the safe and effective use of medication, including dosage, side effects, and potential drug interactions. Manage medication inventory, including ordering, receiving, and storing medication in a safe and secure manner. Maintain accurate and complete medication records, including patient information, medication orders, and dispensing records. Monitor patient health status and medication therapy outcomes, and make appropriate recommendations for changes in...

Aster Medcity is looking for Pharmacist - Pharmacy to join our dynamic team and embark on a rewarding career journey. Dispense medication to patients, ensuring accuracy and compliance with applicable laws and regulations. Counsel patients on the safe and effective use of medication, including dosage, side effects, and potential drug interactions. Manage medication inventory, including ordering, receiving, and storing medication in a safe and secure manner. Maintain accurate and complete medication records, including patient information, medication orders, and dispensing records. Monitor patient health status and medication therapy outcomes, and make appropriate recommendations for changes in...

Aster Medcity is looking for Associate - Fetal Medicine to join our dynamic team and embark on a rewarding career journey. Assist in performing detailed fetal scans, diagnostic tests, and procedures under supervision of a senior fetal medicine specialist. Support doctors during prenatal counseling and follow - up sessions, ensuring accurate documentation and adherence to clinical protocols. Collaborate with sonographers and obstetricians to maintain patient data accuracy and assist in generating fetal anomaly reports. Monitor patients during invasive procedures such as amniocentesis and provide post - procedure support and education for expectant mothers, maintaining high clinical and ethica...

Essential Functions Interprets the study protocol. Design and update the eCRF using third party or in house CDMS tools in alignment with industry standards like SDTM, CDASH as applicable. Create and update Edit Specification Document. Generate specifications for EDC build components (e.g., Rights and Roles, System Settings and Home Page) Complete the Study Authorization Form and Trial Capacity Request Form (InForm) Attend the Pre-Design Meeting, Online Screen Review Meeting, Unblinded Data review meeting. Attend and present comments at the Internal Design Review Meeting. May lead Online Screen Review Meeting. Facilitate the internal Edit Specification Review Meeting and leads the discussions...

Provides high quality, on-time input to client projects in the life sciences field. Assignments typically require analysis and problem solving within an established framework. Essential Functions Under direct supervision, assists with the review and analysis of client requirements or problems and assists in the development of client solutions. Assists in the development of detailed documentation and specifications. Under close supervision, performs quantitative or qualitative analyzes to assist in the identification of client issues and the development of client specific solutions. Assists in the design and structure of presentations that are appropriate to the characteristics or needs of th...

Lead the strategic design, delivery and maintenance of the CRMA dashboards that will support organizational priorities. Identify data sources, create dataflows and recipes, define dataset granularity, build the data model, design the dashboard layout, testing, deploy, and maintenance of enterprise level dashboards. Collaborate with cross-functional stakeholders to gather requirements and develop reporting around relevant Clinical Systems, IT and other ERP applications. Own the design of analytics dashboards and KPI reports in Novotech BI tool starting from requirements gathering across departments, system owners and senior leadership teams to the delivery of final, polished reports/dashboard...

Project Name :- Molecular analysis and genotype-phenotype correlation of Diamong-Blackfan anemia in Indian Patients Name of Post :- Project Research Scientist-I (Non-Medical) No. of Vacancy :- 1 Emoluments :- Rs. 56,000/- Per Month + 30% HRA Essential qualifications :- M.Sc. in Applied Biology/Biotechnology/Biochemistry/Microbiology Desirable Qualification :- Research experience in molecular biology, NGS for rare haemolytic anemia anmd bioinformatic analysis Job Responsibilities:- To carry out biochemical and molecular techniques independently Age limit :- Under 35 years Duration :- Till 21st February 2026 Postig Location :- Parel Mumbai

Be a therapeutic area scientific expert where you will be scientific face of the company engaging in interactions with Key Opinion Leaders (KOL) discussing treatment trends, clinical trial data of our molecules and seeking insights that support the medical strategy. Key Responsibilities : Primary scientific face of the organization to KOL s for Immunology therapy area, responsible for: Identification, mapping and profiling of KOL s of the given geography and therapy area on an ongoing basis Engagement of identified KOL s through medical affairs initiatives in alignment with the overall franchise plan Represent the TA for medical & scientific affairs on all relevant cross functional teams and...

Monitor and manage network environments Ensure optimal performance and update of critical network infrastructure Provide technical support to end users Resolve issues relating to hardware, software and mobile telephony across our end userbase Perform routine maintenance and updates Maintain and update network and compute environments Collaborate with other functions and teams within IT and the wider business unit Troubleshoot and resolve complex technical issues Maintain knowledge documentation Document network configurations, procedures and known issues Assist in the implementation of new technologies Implement and upgrade new services and platforms, adhering to appropriate change controls ...

Role Summary: Intake Coordinator is responsible for reviewing the fax that we receive and understand the medical terminology on each page of the fax. Should be able to identify the type of fax and provide authorization within TAT. Essential Responsibilities: Build cases based on the documentation on the fax after thorough review and complete the case build with in the TAT based on SLA. Ensure login timings are adhered to as the process is time-bound and the TAT is 4-6 hours. Ensure cases are built based on updated and current tip sheets following all essential rules. To ensure quality and productivity is met based on our SLAs. Flexible enough to meet overtime requirements and take responsibi...

Who we want: Hard-working winners. Confident, competitive and results-oriented professionals who create a track record of success. Dedicated achievers. People who thrive in a fast-paced environment and will stop at nothing to ensure a project is complete and meets regulations and expectations. Effective communicators. People who can interpret information clearly and accurately to concisely communicate results and recommendations to stakeholders. Collaborative partners. People who build and leverage cross-functional relationships to bring together ideas, information, use cases, and industry analyses to develop best practices. What you will do: Relationship management skills in a sales/marketi...

Responsible for study build design, edit specifications, system configurations and is accountable for associated study design components. This role will collaborate with various stakeholders- DTL, Programmer, Validation Team, vendors, statisticians, and client representatives. In addition to project deliveries, the role also would be responsible for the project financials from programming shared services perspective. Essential Functions Interprets the study protocol. Design and update the eCRF using third party or in house CDMS tools in alignment with industry standards like SDTM, CDASH as applicable. Create and update Edit Specification Document. Generate specifications for EDC build compon...

Essential Functions Assists with the review and analysis of client requirements or problems and assists in the development of proposals and client solutions. Assists in the development of detailed documentation and specifications. Performs quantitative or qualitative analyses to assist in the identification of client issues and the development of client specific solutions. Assists in the design/structure and completion of presentations that are appropriate to the characteristics or needs of the audience. Develops, and may present, complete client deliverables within known/identified frameworks and methodologies. Proactively develops a basic knowledge of consulting methodologies and the life ...

Location Hyderabad, India Step into a role where your expertise drives innovation in clinical research. As an Associate Clinical Study Manager, you ll play a pivotal part in shaping the future of patient care by ensuring our studies are executed with precision, quality, and compassion. At Novartis, your contributions will directly impact lives, and you ll be empowered to grow in a collaborative, purpose-driven environment. About the Role Key Responsibilities Maintain and update Clinical Trial Management Systems (CTMS) and Trial Master File (TMF), and related platforms to ensure accuracy and compliance. Assist in planning, tracking, and reporting clinical study budgets accurately Monitor stud...

THE OPPORTUNITY The RMA (Regional Medical advisor) will be a valued representative of our company India working in the field to interact and engage key stakeholders. Our medical affairs team objective is to provide scientific expertise across their identified regions/products/therapy areas to these valued customers. WHAT YOU WILL DO: The RMA will have the following key responsibilities: Developing and implementing medical strategies: Scientific leader identification development and engagement to build regional, national or international relationships to contribute to understanding of diseases, scientific trends, practice guidelines, and treatment patterns in areas relevant to our business Su...

Collect, evaluate, and process adverse event (AE) and serious adverse event (SAE) reports from various sources (clinical trials, literature, healthcare professionals, patients). Perform case processing including data entry, coding (using MedDRA/WHO-DRL), and narrative writing in the safety database. Ensure compliance with regulatory timelines (e.g., 15-day or 7-day expedited reporting). Conduct quality checks on case reports to ensure accuracy and completeness. Assist in preparation of Periodic Safety Update Reports (PSURs) and Risk Management Plans (RMPs). Monitor literature and scientific publications for potential safety signals. Support signal detection and analysis activities. Maintain ...

Role & responsibilities Analyzing and summarizing medical records for pre and postsettlement projects. Interpreting clinical data in terms of medical terminology and diagnosis. Adhering to company policies/ principles and hence taking good care of Archer culture. Adhere to Health Insurance Portability and Accountability Act (HIPPA) all the time. Daily reporting to Medical team lead for productivity & quality Preferred candidate profile Knowledge of basic level of health care data analysis and clinical review. Sound knowledge of medical terminology, assessments, patient evaluation, and clinical medicine. Ability to work proficiently with Microsoft Word, Adobe, and Excel. Perks and benefits

Choosing Capgemini means choosing a place where youll be empowered to shape your career, supported by a collaborative global community, and inspired to reimagine whats possible. Join us in helping leading healthcare and life sciences organizations unlock the value of data and drive evidence-based, impactful research. Your Role As a Statistical Programmer II at Capgemini, you will be responsible for programming and validating clinical trial data displays, datasets, and documentation in alignment with regulatory standards. Youll collaborate with cross-functional teams and contribute to the delivery of high-quality statistical outputs for clinical research. In this role, you will: Program table...

Clinical trials is a crucial field in the pharmaceutical industry focused on drug safety. Professionals in this area monitor, assess, and prevent adverse drug reactions to protect public health. 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). 2020 -2024 passed out Skills Required: Scientific Background: Degree in Pharmacy, Life Sciences, or Medicine. Attention to Detail: Meticulous accuracy in data entry and documentation. Analytical Skills: Ability to analyze data and identify safety signals. Regulatory Knowledge: Unders...

Clinical trials is a crucial field in the pharmaceutical industry focused on drug safety. Professionals in this area monitor, assess, and prevent adverse drug reactions to protect public health. 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). 2020 -2024 passed out Skills Required: Scientific Background: Degree in Pharmacy, Life Sciences, or Medicine. Attention to Detail: Meticulous accuracy in data entry and documentation. Analytical Skills: Ability to analyze data and identify safety signals. Regulatory Knowledge: Unders...

Clinical trials is a crucial field in the pharmaceutical industry focused on drug safety. Professionals in this area monitor, assess, and prevent adverse drug reactions to protect public health. 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). 2020 -2024 passed out Skills Required: Scientific Background: Degree in Pharmacy, Life Sciences, or Medicine. Attention to Detail: Meticulous accuracy in data entry and documentation. Analytical Skills: Ability to analyze data and identify safety signals. Regulatory Knowledge: Unders...

Clinical trials is a crucial field in the pharmaceutical industry focused on drug safety. Professionals in this area monitor, assess, and prevent adverse drug reactions to protect public health. 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). 2020 -2024 passed out Skills Required: Scientific Background: Degree in Pharmacy, Life Sciences, or Medicine. Attention to Detail: Meticulous accuracy in data entry and documentation. Analytical Skills: Ability to analyze data and identify safety signals. Regulatory Knowledge: Unders...

Clinical trials is a crucial field in the pharmaceutical industry focused on drug safety. Professionals in this area monitor, assess, and prevent adverse drug reactions to protect public health. 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). 2020 -2024 passed out Skills Required: Scientific Background: Degree in Pharmacy, Life Sciences, or Medicine. Attention to Detail: Meticulous accuracy in data entry and documentation. Analytical Skills: Ability to analyze data and identify safety signals. Regulatory Knowledge: Unders...

Clinical trials is a crucial field in the pharmaceutical industry focused on drug safety. Professionals in this area monitor, assess, and prevent adverse drug reactions to protect public health. 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). 2020 -2024 passed out Skills Required: Scientific Background: Degree in Pharmacy, Life Sciences, or Medicine. Attention to Detail: Meticulous accuracy in data entry and documentation. Analytical Skills: Ability to analyze data and identify safety signals. Regulatory Knowledge: Unders...