8317 Clinical Research Jobs - Page 13

About The Role Skill required: Clinical Data Services - Clinical Reports Management Designation: Clinical Data Svs Analyst Qualifications: BE/BTech/BSc Years of Experience: 3 to 5 years Language - Ability: English(Domestic) - Intermediate What would you do? You will be aligned with our Life Sciences R&D vertical. Our services span across the entire life sciences enterprise, from research laboratories, clinical trials support, and regulatory services, to pharmacovigilance and patient services solutions. Employees under this span will be a part of one of the sub-offerings - Clinical, Pharmacovigilance & Regulatory, helping the worlds leading biopharma companies bring their vision to life enabl...

At Johnson & Johnson, we believe health is everything Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity Learn more at Job Function: Data Analytics & Computational Sciences Job Sub Function: Biostatistics Job Category: Scientific/Technology All Job Posting Locations: Bangalore, Karnataka, India, Hyderabad, Andhra ...

Designs, analyzes, programs, debugs, and maintains system/web enhancements and/or new products Develops and executes test plans and scripts to confirm the quality and success of various technologies Manual and automated testing of applications and web resources works as specified; and that a system performs adequately on the platform on which it will be deployed Under broad guidance, executes and verifies software applications tests Understands and reviews requirements, creates test plans and/or contributes in test estimations, manual and automation planning/strategies Responsible for test case planning, authoring and execution of compliance products for client implementation projects Perfor...

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...

This position provides functional expertise, leadership and direction while ensuring adequate staffing, training, and delivery. Responsibilities: Onboarding of new employees, including training on procedures and systems Mentor, monitor, and supervise direct reports (including monitoring time reporting and training requirements) Responsible for the hiring, promotion, transfer, and release of staff; participate in candi interviews Conduct performance reviews and assist with goal setting of direct reports Provide input on resource planning and assignments Review metrics for department performance; identify and address risks or areas of concern Implement and maintain performance metrics Identify...

We are seeking a skilled and proactive Flexera Tool Administrator to manage and optimize our Flexera Software Asset Management (SAM) platform. This role is critical to ensuring software compliance, cost efficiency, and accurate IT asset tracking across the organization. The ideal candi will have hands-on experience with Flexera tools and a strong understanding of software licensing, IT asset lifecycle, and configuration management. Roles and responsibilities: Administer and configure Flexera SAM tools including FlexNet Manager Suite, Flexera One and related modules. Monitor and maintain the health, performance, and reliability of Flexera environments. Ensure software license compliance by im...

Provide comprehensive data management expertise (defined as efficient and quality data management products) to Data Management (DM) team to meet sponsor and company needs. Perform Clinical Data Management and/or Coding activities, and may provide leadership either in the role of the Lead Coder or in a specific CDM task (e. g. Data Operations Coordinator (DOC) or lead a coding related task on a mega trial). Essential Functions Serve independently as a Clinical Data Coder and/or Lead Coder or DOC for one or more protocols. Manage delivery of coding activities and/or stand alone coding projects through full study life-cycle (with minimal guidance). Validates/tests the coding application and pro...

Designs, analyzes, programs, debugs, and maintains system/web enhancements and/or new products. Develops and executes test plans and scripts to confirm the quality and success of various technologies. Manual and automated testing of applications and web resources works as specified; and that a system performs adequately on the platform on which it will be deployed. Under broad guidance, executes and verifies software applications tests. Understands and reviews requirements, creates test plans and/or contributes in test estimations, manual and automation planning/strategies. Responsible for test case planning, authoring and execution of compliance products for client implementation projects. ...

Roles and responsibilities: Administer and configure Flexera SAM tools including FlexNet Manager Suite, Flexera One and related modules. Monitor and maintain the health, performance, and reliability of Flexera environments. Ensure software license compliance by implementing policies and tracking usage across platforms. Collaborate with IT, procurement, and finance teams to optimize software spend and usage. Integrate Flexera tools with CMDB, SCCM, ServiceNow, and other enterprise systems. Generate and analyze reports on software usage, entitlements, and audit readiness. Troubleshoot and resolve issues related to Flexera tool performance or data accuracy. Support audits and vendor negotiation...

Technical & Operational Leadership Lead and manage clinical database programming activities for multiple studies of varying complexity , ensuring adherence to established processes, standards, timelines, and quality expectations. Design, develop, test, and maintain clinical databases including forms, folders, matrices, data dictionaries, unit dictionaries, edit checks, derivations, and custom functions . Provide study-level technical support and mentorship to junior team members, resolving complex technical issues and evaluating alternative solutions. Create, review, and approve technical specifications and develop complex programs and technical solutions for data management systems. Support...

What You Will Be Doing: Supporting Study Start-Up activities , including review of essential documents, green light process management, and site activation readiness. Handling maintenance tasks such as customization of site-specific Informed Consent Forms (ICFs), coordination of translations, EC/IRB submissions, and documentation in eTMF systems. Assisting in the contract process , including understanding site contract workflows, managing contract amendments, participating in negotiations, and ensuring finalization of executed agreements. Collaborating effectively with cross-functional teams and stakeholders to ensure timelines are met and compliance is maintained. Communicating clearly and ...

What you will be doing: Managing vendor data in the masterfile system, ensuring accuracy and completeness. Reviewing and verifying vendor information to ensure compliance with company policies and procedures. Communicating with internal stakeholders and vendors to gather necessary information and resolve discrepancies. Driving procurement processes by updating vendor records, including pricing and payment terms. Generating reports and performing data analysis to identify trends and opportunities for improvement in vendor management. Your Profile: Bachelor s degree in business administration, Finance, Accounting, or related field preferred. Previous experience in vendor management, data entry...

What You Will Do The Amgen Global Clinical Data Management team is looking for an experienced Director to lead our data management team on the aspiration of optimizing and delivering an industry admired clinical evidence platform to deliver innovative medicines to patients with unmet medical needs. The Director is accountable for leadership and oversight of the data management organization; ensuring operational excellence and consistency in clinical trial execution. They are accountable for building and developing a high performing internal data management team, as well as ensuring engagement and alignment of Amgens strategy and priorities with the Functional Service Provider (FSP). The Dire...

Roles and Responsibility Manage and oversee the daily activities of clinical research teams to ensure compliance with regulatory requirements. Develop and implement effective clinical trial management plans to achieve study objectives. Collaborate with cross-functional teams to resolve issues and improve processes. Conduct site visits and monitor clinical trials to ensure quality and adherence to protocols. Analyze data and prepare reports to track progress and identify areas for improvement. Ensure timely resolution of adverse events and serious protocol deviations. Disclaimer: This job description has been sourced from a public domain and may have been modified by Naukri.com to improve cla...

Roles and Responsibility Develop and implement effective teaching methods to educate nursing students. Provide guidance and support to students, ensuring their academic success. Collaborate with other faculty members to develop curriculum and programs. Conduct research and publish papers in reputable journals. Participate in departmental meetings and contribute to the development of the nursing program. Mentor and advise students on career paths and professional development. Disclaimer: This job description has been sourced from a public domain and may have been modified by Naukri.com to improve clarity for our users. We encourage job seekers to verify all details directly with the employer ...

Roles and Responsibility Assist in the planning, execution, and monitoring of clinical trials to ensure compliance with regulatory requirements. Collaborate with cross-functional teams to develop and implement study protocols and case report forms. Conduct site feasibility assessments and coordinate with investigators to ensure timely and accurate data submission. Develop and maintain study databases and track systems for timely updates on study progress. Coordinate with internal stakeholders to resolve issues related to study start-up, patient enrollment, and protocol deviations. Ensure adherence to Good Clinical Practice (GCP) guidelines and maintain high standards of quality control. Disc...

Roles and Responsibility Manage and oversee all aspects of clinical trial operations, including protocol development, site monitoring, and data management. Develop and implement effective clinical trial strategies to ensure successful study execution. Collaborate with cross-functional teams, including medical writing, biostatistics, and project management. Conduct risk assessments and develop mitigation plans to minimize risks associated with clinical trials. Ensure compliance with regulatory requirements and company policies. Provide training and guidance to staff members on clinical trial procedures and protocols. Disclaimer: This job description has been sourced from a public domain and m...

Align Prescription. Do IP Billing / OP Billing Check In house ware. Dispersal of medicines for OP and IP. Remove expiring items. Stock out monitoring. Discharge medicines handling

Roles and Responsibility Perform complex interventional cardiac procedures, including angioplasty, stenting, and other cardiovascular interventions. Diagnose and treat patients with cardiovascular diseases and conditions. Develop and implement treatment plans for patients with various cardiac conditions. Collaborate with other healthcare professionals to provide comprehensive patient care. Stay updated with the latest advancements and technologies in interventional cardiology. Participate in quality improvement initiatives to enhance patient outcomes and safety. Disclaimer: This job description has been sourced from a public domain and may have been modified by Naukri.com to improve clarity ...

Roles and Responsibility Provide expert guidance on medical matters, including diagnosis and treatment. Mentor junior staff members to enhance their knowledge and skills. Collaborate with cross-functional teams to achieve business objectives. Develop and implement effective medical strategies to improve outcomes. Stay updated with the latest medical research and advancements. Ensure compliance with regulatory requirements and industry standards. Disclaimer: This job description has been sourced from a public domain and may have been modified by Naukri.com to improve clarity for our users. We encourage job seekers to verify all details directly with the employer via their official channels be...

Roles and Responsibility Develop and implement effective strategies for clinical trial transparency, including data submission and reporting. Collaborate with cross-functional teams to ensure compliance with regulatory requirements and industry standards. Conduct thorough reviews of clinical trial protocols, informed consent forms, and other study-related documents. Provide guidance on clinical trial design, methodology, and statistical analysis plans. Ensure timely and accurate reporting of clinical trial results, including individual case narratives and aggregate reports. Stay up-to-date with changing regulatory requirements and industry trends related to clinical trial transparency. Discl...

Roles and Responsibility Lead and manage a team of clinical scientists to achieve project goals and objectives. Develop and implement clinical trial protocols and study designs. Collaborate with cross-functional teams to ensure successful project execution. Provide scientific guidance and mentorship to junior team members. Conduct peer reviews and quality control checks on clinical trial data. Ensure compliance with regulatory requirements and company policies. Disclaimer: This job description has been sourced from a public domain and may have been modified by Naukri.com to improve clarity for our users. We encourage job seekers to verify all details directly with the employer via their offi...

Roles and Responsibility Develop and implement comprehensive strategies for digital innovation, focusing on third-party oversight and risk management. Lead cross-functional teams to identify, assess, and mitigate potential risks associated with third-party vendors and partners. Collaborate with stakeholders to develop and implement effective risk management plans and procedures. Conduct regular audits and assessments to ensure compliance with regulatory requirements and industry standards. Provide expert guidance and support on digital innovation-related matters, including project management and team leadership. Foster a culture of innovation and continuous improvement within the organizatio...

Support 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 diagr...

To write, support and manage projects, to prepare high quality medical and scientific communications including, literature review, abstracts, posters, slide sets, manuscripts (complex) for publication/ presentation at congresses or internal medical and/or clinical teams. About the Role Senior Scientific Writer II Location - Hyderabad #LI Hybrid Major Responsibilities Prepares, literature review, abstracts, posters, and slide sets, and Manuscripts (complex) working from various data sources including clinical study reports, patient profiles, protocols etc. Performs quality control (QC) checking / proof reading of the above-mentioned deliverables to meet customer expectations. Manages multiple...