8317 Clinical Research Jobs - Page 18

Profile Name : Project Reasearch Sientist II Medical Educational Qualification :- MBBS degree from a recognized University / Institution with three years experience OR MBBS with MPH/PhD from a recognized University / Institution OR BDS with MPH/PhD from a recognized University / Institution OR MBBS + Post Graduate Degree (MD /MS in Community Medicine/ Pediatrics/ Pathology/ ObGyn), including the integrated PG degrees from a recognized University / Institution OR BDS + Post Graduate Degree (MDS), including the integrated PG degrees from recognized University / Institution Desirable Qualification :- (i) MD/MS/DNB in Medicine/ Pediatrics/ Path ology/ Obstetrics and Gynecology/ from a recognized...

Job Summary We are looking for the Primary scientific face of the organization to ‘Thought Leaders’ & physicians for a given therapy area. You will be responsible for Identification, mapping and profiling of thought leaders of given geography and therapy area, on an ongoing basis. Roles & Responsibilities • You will be responsible for the engagement of identified key thought leaders through medical affairs activities, in alignment with the overall strategic plan • You will be responsible to execution of strategic medical affairs plan including but not limited to medical education, product education, medical evidence generation, advisory boards, pre-license activities and special projects • Y...

Clinical research and clinical supplies projects in functional and software areas Responsibilities include: Review & analyze project/study requirements Define and document the functional requirements mapping to business requirements into required documents (like specifications, user acceptance plans, test plans, etc). Propose clinical solutions to software development teams Participate in pre-project documents for the approved projects and any related documents Involve extensively in reviewing and testing clinical systems acting as subject expert from study perspective Write testing scenarios and impact scenarios for study changes to clinical systems Develop workflow and process diagrams & p...

Location: Kodambakkam / Gummidipoondi Department: Pharmacovigilance Position: Pharmacovigilance (PV) Associate Job Type: Full-time Role Overview : The Pharmacovigilance (PV) Associate is responsible for the timely and accurate processing of adverse event reports, ensuring compliance with global and local regulatory requirements for drug safety. Key Job Responsibilities 1. Case Management & Processing Receive and Triage: Intake and prioritize all incoming adverse event (AE) reports from various sources (e.g., spontaneous reports, literature, clinical trials, and regulatory authorities). Data Entry: Perform detailed and accurate data entry of AE reports ensuring complete case documentation. Ca...

Job Profile for a Trainer A. Conduct training sessions and assessments for employees at arrival and as & when required B. Develop training content to facilitate functioning of new employee considering his job description, experience and role in organization. That will include - D ocumentation training pertaining to every applicable SOP - Regulatory guidelines training C. Review and centralized finalization of all SOPs and Forms. D. Synchronization of systems and processes across locations, through training programs. E. Continuous up-gradation of training systems, as per updated requirements.

Ensure clinical research studies are conducted in compliance with protocol, SOPs, Good Clinical Practice (GCP) guidelines, and other regulatory requirements. Perform site selection, initiation, monitoring, and close-out visits in accordance with contracted scope of work and GCP guidelines. Review and oversee informed consent documents and procedures. Negotiate study budgets with investigators and assist in execution of site contracts. Provide site management and monitoring visits for multiple protocols and sites. Train site personnel on protocol and study-related procedures, and establish regular communication to manage project expectations. Evaluate the quality and integrity of study site p...

Collaborate with Project Manager to set targets for clinical monitoring staff and ensure trial documentation aligns with project goals. Create and implement study-specific clinical monitoring tools and documents. Develop and oversee trial budgets. Identify, enlist, and select trial sites, coordinating all site management activities. Supervise and coordinate the clinical monitoring team. Provide project-specific training to Clinical Research Associates and hold regular team meetings. Record and share interactions with clients and act as their representative. Arrange and oversee site visits for clinical trials. Gather, examine, and maintain trial documentation. Ensure compliance with SOPs, loc...

Create and write trial protocols and present them to the steering committee. Identify, evaluate, and establish trial sites, and close sites upon trial completion. Train site staff on therapeutic areas, protocol requirements, proper source documentation, and case report form completion. Liaise with ethics committees regarding the rights, safety, and well-being of trial subjects. Order, track, and manage investigational products (IP) and trial materials. Oversee and document IP dispensing, inventory management, and reconciliation. Protect subject confidentiality, update information, and verify that IP has been dispensed and administered according to protocol. Conduct regular site visits, coord...

Prevent payment of potentially fraudulent and/or abusive claims by utilizing medical expertise, knowledge of CPT/diagnosis codes, CMC guidelines, and client-specific policies. Ensure adherence to state and federal compliance policies and contract requirements. Assist the team with special projects and reporting as required. Identify discrepancies between medical records and billed services, including up-coding, duplication, and misrepresentation of services. Manage and report adverse events and serious adverse events. Review clinical study protocols, reports, and study documentation. Supervise study drug administration and activities performed by other clinical staff. Conduct clinical examin...

Create and write trial protocols and present them to the steering committee. Identify, evaluate, and establish trial sites, and close sites upon trial completion. Train site staff on therapeutic areas, protocol requirements, proper source documentation, and case report form completion. Liaise with ethics committees regarding the rights, safety, and well-being of trial subjects. Order, track, and manage investigational products (IP) and trial materials. Oversee and document IP dispensing, inventory management, and reconciliation. Protect subject confidentiality, update information, and verify that IP has been dispensed and administered according to protocol. Conduct regular site visits, coord...

Work to improve efficiency and quality in delivering healthcare services. Stay updated on laws and regulations to ensure the facility's compliance. Supervise assistant administrators in larger facilities. Manage facility finances, including patient fees and billing. Create and manage staff work schedules. Represent the facility at investor meetings or on governing boards. Maintain and organize records of facility services, such as inpatient bed usage. Communicate effectively with medical staff and department heads.

Develop and maintain in-depth knowledge of assigned product(s) and therapeutic area(s) via internal meetings, training sessions, congresses, seminars, and self-study of national/international literature. Provide expert medical/scientific advice for assigned products and therapeutic areas, responding to scientific/technical information requests and contributing to accurate medical dossiers (e.g., medical information packs, clinical expert reviews). Establish and maintain professional relationships with key opinion leaders and academic centers, participating in advisory boards, round-table meetings, discussion forums, and scientific congresses. Deliver scientific presentations and medical educ...

Develop and maintain in-depth knowledge of assigned product(s) and therapeutic area(s) via internal meetings, training sessions, congresses, seminars, and self-study of national/international literature. Provide expert medical/scientific advice for assigned products and therapeutic areas, responding to scientific/technical information requests and contributing to accurate medical dossiers (e.g., medical information packs, clinical expert reviews). Establish and maintain professional relationships with key opinion leaders and academic centers, participating in advisory boards, round-table meetings, discussion forums, and scientific congresses. Deliver scientific presentations and medical educ...

Serve as the medical expert for the therapy area and act as the medical lead within the brand team, providing strategic input. Support the Medical Director in day-to-day operations of the Medical Department. Review and approve promotional and non-promotional materials to ensure compliance with Codes of Practice. Provide input to global projects (e.g., Norgine Global) on a defined basis. Ensure compliance with all company procedures, including GxP standards, Codes of Practice, and medicines legislation. Support medical affairs projects and activities. Maintain high standards of technical and clinical proficiency. Develop relationships with key opinion leaders, patient organizations, and profe...

GREETINGS ! ARE YOU LOOKING FOR A CORE ENGINEERING JOB ? SEND YOUR UPDATED CV/ RESUMES TO RECRUIT@MEDIANALYTIKA.COM FOR AN IMMEDIATE RESPONSE. WOULD YOU LIKE TO HAVE YOUR CAREER IN TECHNICAL SALES, APPLICATION SUPPORT, INSTALLATION & TO PROVIDE SERVICE SUPPORT OF HIGH TECHNOLOGY IMPORTED EQUIPMENTS ? WELCOME TO JOIN ONE OF THE THE LARGEST INSTRUMENTATION COMPANIES IN INDIA MEDI ANALYTIKA - INDIA, ESTABLISHED DURING 1994 HAS SUCCESSFULLY COMPLETED 29 YEARS IN BUSINESS. WE ARE RECOGNIZED AS THE LARGEST INSTRUMENTATION COMPANY IN INDIA SUPPLYING HIGH TECHNOLOGY EQUIPMENTS FOR VARIOUS FIELDS FROM SEVERAL WORLD LEADING INSTRUMENTATION COMPANIES FROM USA - CANADA - UK - EUROPE - JAPAN - KOREA OUR ...

Influence government and industry policy, legislation, and regulations to optimize strategic growth opportunities. Engage with key government and industry stakeholders to advocate for favorable regulatory frameworks. Track and analyze global geopolitical developments and their impact on the company's India business strategy. Provide strategic advice on legislative and regulatory matters to internal stakeholders. Develop and implement advocacy strategies and initiatives aligned with business goals. Oversee sensitive business matters, ensuring aligned actions with corporate values and guidelines. Disclaimer: This job description has been sourced from a public domain and may have been modified ...

Administer standardized assessments and ensure data quality and consistency in stroke clinical trials. Review and evaluate assessments conducted by other raters for accuracy and adherence to protocol. Conduct live interactions with raters to provide feedback on scoring techniques and methodology. Participate in training, orientation, and calibration sessions to maintain certification and consistency. Prepare for rater discussions by reviewing case data and relevant documentation. Complete scheduled rater interactions and submit all required documentation promptly. Disclaimer: This job description has been sourced from a public domain and may have been modified by Naukri.com to improve clarit...

Prepare samples and specimens for lab tests to ensure accurate results. Execute routine tasks and follow strict methodologies for analyses to maintain quality standards. Maintain glassware by picking up, cleaning, washing, sterilizing, and distributing it to the team. Operate and maintain equipment by following operating instructions, troubleshooting breakdowns, maintaining supplies, performing preventive maintenance, and calling for repairs. Order, receive, and inventory glassware to ensure adequate stock levels. Document information by maintaining daily logs and equipment record books to track progress. Perform pharmacy/medical warehouse storing activities to keep pharmacy stock above secu...

Administer standardized assessments, ensuring data quality and consistency in stroke clinical trials. Review and evaluate assessments conducted by other raters for accuracy and adherence to protocol. Conduct live interactions with raters to provide feedback on scoring techniques and methodology. Participate in training, orientation, and calibration sessions to maintain certification and consistency. Prepare for rater discussions by reviewing case data and relevant documentation. Complete scheduled rater interactions and submit all required documentation promptly. Disclaimer: This job description has been sourced from a public domain and may have been modified by Naukri.com to improve clarity...

Implement local medical plans to execute the national Medical Affairs strategy within the region. Build and maintain scientific relationships with key opinion leaders, diabetes specialists, and other relevant stakeholders. Gather and communicate clinical insights from healthcare professionals to inform business decisions. Support brand and commercial strategy by collaborating with marketing and sales teams. Develop and deliver scientific training and educational activities for physicians, allied HCPs, and internal field and marketing personnel. Provide medical advice and support to the brand team and other internal stakeholders on clinical data interpretation, label information, and therapeu...

Conduct site/trial feasibility to identify and select the right sites and investigators for studies. Ensure timely compilation of all essential documents and assist in regulatory package preparation. Coordinate with sites for study initiation, review patient data base, pre-screening, and identify physician networks. Manage clinical trial supplies receipt, accountability, storage, dispensing, and related documentation. Prepare site teams for study initiation visits and coordinate with monitors for these visits. Assist in administering informed consent and discussing patient information sheets with potential objects. Maintain current, accurate, and complete site documentation. Coordinate lab s...

Utilize cloud-specific commands like kubectl to monitor and manage ECM containerized services. Participate in daily standups and Agile ceremonies for operational alignment. Possess deep functional knowledge of ECM product configuration entities, including Product Offer (PO), Product Specification (PS), Customer & Resource Facing Service Specifications (CFSS/RFSS), Product Offering Price & Charge Type (POP & CT), CCS offer templates, and Code Tables. Work with TMF Forum APIs for catalog querying, configuration, and integration. Configure products, update catalog items, and manage lifecycle changes using ACLT Tool. Understand ECM database schema and table relationships to execute validations a...

Assist in configuring and setting up clinical trial databases and electronic data capture (EDC) systems. Perform quality control checks on clinical trial data and study documentation to identify discrepancies and inconsistencies. Collaborate with cross-functional teams to address QC findings and ensure data integrity and reliability. Support the development and implementation of validation plans to assess EDC system functionality and performance. Provide training and support to end-users on system configuration, data entry guidelines, and QC processes. Identify and resolve data-related issues using strong analytical skills. Disclaimer: This job description has been sourced from a public doma...

Implement local medical plans to execute the national Medical Affairs strategy within the designated region. Build and maintain scientific relationships with key opinion leaders, diabetes specialists, and other relevant stakeholders. Gather and communicate clinical insights from healthcare professionals to capture clinical needs and practice trends. Support brand and commercial strategy by collaborating closely with marketing and sales teams. Develop and deliver scientific training and educational activities for physicians, allied HCPs, and internal field and marketing personnel. Provide medical advice and support to the brand team and other internal stakeholders on clinical data interpretat...

Fortis Healthcare Ltd is looking for Pharmacist to join our dynamic team and embark on a rewarding career journey Compounding and dispensing medications, as prescribed by physicians. Monitoring customers drug therapies, advising interventions, and informing customers of any potential side effects. Instructing customers on how and when to take prescribed medications. Conducting health and wellness screenings. Providing immunizations, and other medical services, such as taking blood pressure, temperature measurements, and checking blood sugar levels. Keeping accurate customer records. Ensuring a safe and clean working environment. Completing operational requirements of the pharmacy, including ...