8317 Clinical Research Jobs - Page 15

Manage end-to-end delivery of data management services for single/multi-service projects with minimal guidance, ensuring quality deliverables on time and within budget, to customer satisfaction Provide comprehensive data management expertise to Data Management (DM) team to provide high quality data management products that meet customer needs Provide leadership to the team in the areas of project planning, execution, and close-out; Overview of financial management for data management activities; communications; and milestone deliverables Perform role of Data Team Lead (DTL) Essential Functions Gather Study Set up requirements through discussion and communication with relevant stakeholders Wi...

Job Overview Manage end-to-end delivery of data management services for single/multi-service projects with minimal guidance, ensuring quality deliverables on time and within budget, to customer satisfaction. Provide comprehensive data management expertise to Data Management (DM) team to provide high quality data management products that meet customer needs. Provide leadership to the team in the areas of project planning, execution, and close-out; Overview of financial management for data management activities; communications; and milestone deliverables. Perform role of Data Team Lead (DTL). Essential Functions Gather Study Set up requirements through discussion and communication with relevan...

Job Overview Manages a team of professional-level employees. Develops and communicates plans and priorities to meet team performance and results requirements. Essential Functions Manages a team of professional-level employees. Develops and communicates plans and priorities to meet team performance and results requirements. Establishes team processes, goals, and procedures and tracks performance. Informs and influences decision-making at the management level. Provides coaching and guidance on job performance and career development to direct reports. Qualifications Bachelors Degree Computer Engineering, Computer Science or related field Req 5-7 years+ experience in software development 5+ year...

Educational Qualification/s Bachelor's degree in Lifesciences /medical, Biotech, public health required + Certification in Clinical Research & basic knowledge of GCP Experience - 0-2 Years Job Duties & Responsibilities: Coordinates with Principal Investigator, CRO, Sponsor and Fortis central administration to help ensure that clinical research and related activities are performed in accordance with Protocol, DCGI Schedule Y & FDA policies and procedures. Assists the PI in the conduct of the study around issues related to protocol requirements, Patient schedule of visits, execution of research plan. Essential study related documentation, Site setup, Patient database searching, assist in ICF a...

Educational Qualification/s Bachelor's degree in Lifesciences /medical, Biotech, public health required + Certification in Clinical Research & basic knowledge of GCP Experience - 0-2 Years Job Duties & Responsibilities: Coordinates with Principal Investigator, CRO, Sponsor and Fortis central administration to help ensure that clinical research and related activities are performed in accordance with Protocol, DCGI Schedule Y & FDA policies and procedures. Assists the PI in the conduct of the study around issues related to protocol requirements, Patient schedule of visits, execution of research plan. Essential study related documentation, Site setup, Patient database searching, assist in ICF a...

Educational Qualification/s Bachelor's degree in Lifesciences /medical, Biotech, public health required + Certification in Clinical Research & basic knowledge of GCP Experience - 0-2 Years Job Duties & Responsibilities: Coordinates with Principal Investigator, CRO, Sponsor and Fortis central administration to help ensure that clinical research and related activities are performed in accordance with Protocol, DCGI Schedule Y & FDA policies and procedures. Assists the PI in the conduct of the study around issues related to protocol requirements, Patient schedule of visits, execution of research plan. Essential study related documentation, Site setup, Patient database searching, assist in ICF a...

This position plays a role in the authoring, compilation and peer review of Amgens Periodic Aggregate Safety Reports (PASR) e.g. Development Safety Update Report (DSUR), Periodic Benefit Risk Evaluation Report (PBRER)/Periodic Safety Update Report (PSUR), Semi Annual Safety Update Report (SSUR), Periodic Adverse Drug Experience Report (PADER/PAER), Device PSUR, and country specific reports e g Korea PSUR, Brazil PSUR and Colombia Clinical Research Annual Safety Report Submission and Evaluation form In compliance with global regulatory requirements This role supports the end-to-end writing and documentation process and ensures timelines are met Key Responsibilities:Compilation and authoring o...

Roles & Responsibilities Develop and execute biocompatibility evaluation plans and reports. Assess material composition, manufacturing processes, and potential biological risks. Coordinate testing with external laboratories and review study protocols/reports. Support risk assessments and justification for biological safety. Ensure compliance with ISO 10993 series, FDA, and EU MDR requirements. Collaborate with R&D, Regulatory, and Quality teams for product development and change control. Maintain documentation and support regulatory submissions. Qualifications Bachelor’s/Master’s in Biomedical, Materials, or Chemical Engineering, or related field. 5+ years’ experience in biocompatibility or ...

Deliver industry-leading clinical trial excellence with scientific insights and external engagement. Partner with Clinical Operations Therapy Area Leads and Trial Managers on scientific and medical aspects of early trial planning, start-up, recruitment, and retention. Provide scientific inputs to trial portfolio review, country allocation, and site feasibility processes. Visit assigned sites periodically to discuss clinical trial conduct, strategies, and collect insights from site staff. Contribute to site selection criteria and assess medical capabilities and scientific training needs at sites. Engage relevant key opinion leaders who are investigators to optimize trial methodologies, mitiga...

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 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 interpretation, label ...

IQVIA Biotech is looking for Stat Programmer Scientist to join our team Develop and implement statistical programs for creating statistical tables, figures, and listing summaries. Program analysis databases and transfer data for internal and external clients. Plan and coordinate the development of integrated programming solutions for statistical programming needs. Provide technical expertise and leadership to the department. Perform, plan, and coordinate complex studies, including programming, testing, and documentation of statistical programs. Manage project budget and resource requirements, and provide revenue forecasts for single studies. Disclaimer: This job description has been sourced ...

Job Description: Biostatistician Location: [Bangalore / WFO] Experience: 6 - 12 Years Industry: Pharmaceutical / Clinical Research Employment Type: Full-time Role Summary We are looking for an experienced Biostatistician to support statistical planning, analysis, and reporting for clinical trials conducted within a pharmaceutical or clinical research organization . The role involves close collaboration with clinical development, data management, and regulatory teams to ensure high-quality statistical outputs for global studies. Key Responsibilities Develop Statistical Analysis Plans (SAPs) for clinical trials Perform statistical analyses for Phase IIV clinical studies Support protocol design...

Novartis Healthcare Pvt. Ltd. is looking for Senior Medical Information Manager I to join our team Create and deliver timely responses to unsolicited medical information inquiries from HCPs in a multi-media environment. Develop and review Medical Response Documents (MRDs) for product portfolio. Collaborate with cross-functional teams including global MI colleagues and Medical Strategy Teams (MSTs). Provide therapeutic area and product training to internal customers and partners. Support in development and implementation processes for internal departments as they relate to daily MI activities. Monitor, collect, and analyze metrics for MI activities and develop reports, identifying actionable ...

IQVIA Biotech is looking for Clinical Research Coordinator to join our team 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 the visit. Assist in administering informed consent and discuss patient information sheets in detail. Maintain current, ac...

IQVIA Biotech is looking for Senior Medical Safety Advisor to join our team Perform medical review and clarification of trial-related Adverse Events (AEs) and post-marketing adverse drug reactions (ADRs). Compose, edit, and medically review Analyses of Similar Events (AOSE) for expedited cases. Provide coding review of AEs, SAEs, SADRs, Past medical history, Concomitant medications, or other medical data listings. Serve as an internal consultant to pharmacovigilance case processing teams on projects being supported. Lead and participate in initiatives to ensure service delivery from productivity, compliance, and quality perspectives within regulatory/contracted timelines. Ensure update of wa...

Perform medical review and clarification of trial-related Adverse Events (AEs) and post-marketing adverse drug reactions (ADRs). Compose, edit, and medically review Analyses of Similar Events (AOSE) for expedited cases. Serve as an internal consultant to pharmacovigilance case processing teams on projects being supported. Provide aggregate reviews of safety information, including clinical data, to maintain oversight of a product's safety profile. Represent safety and clinical data review findings during client meetings. Review and sign off on both the Project Safety Plan and the Medical Monitoring Plan per medical safety scope agreed in contract. Act as Global Safety Physician or Assistant o...

Collaborate with cross-functional teams to achieve strategic outcomes. Apply subject expertise to support operations, planning, and decision-making. Utilize tools, analytics, or platforms relevant to the job domain. Ensure compliance with policies while improving efficiency and outcomes. 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 before applying.

Conduct site monitoring visits according to protocol requirements. Review case report forms and ensure compliance with regulatory guidelines. Collaborate with cross-functional teams to achieve study objectives. Develop and maintain relationships with investigators and other stakeholders. Ensure timely resolution of issues related to study conduct. Maintain accurate records of study activities and progress. 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 before applying.

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...

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...

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...

Fisher & Paykel Healthcare India Pvt. Ltd. is looking for Clinical Educator to join our team Deliver educational seminars to promote FPH products by educating clinicians on product applications, benefits, and best practices. Ensure the clinical community understands FPH's proprietary technologies and how our products differentiate from competitors. Support the sales team with post-sales education, troubleshooting, and complaint resolution to ensure correct equipment use and drive consumable sales. Identify, nurture, and collaborate with Key Opinion Leaders (KOLs) to drive therapy and clinical adoption. Build partnerships with nursing associations to enhance education, training, and protocol ...

The primary responsibility of this role is to perform quality control reviews of of Amgens Periodic Aggregate Safety Reports (PASR) e.g. Development Safety Update Report (DSUR), Periodic Benefit Risk Evaluation Report (PBRER)/Periodic Safety Update Report (PSUR), Semi Annual Safety Update Report (SSUR), Periodic Adverse Drug Experience Report (PADER/PAER), Device PSUR, and country specific reports e.g. Korea PSUR, Brazil PSUR and Colombia Clinical Research Annual Safety Report Submission and Evaluation form. The QC Reviewer will ensure accuracy, consistency, and compliance with regulatory and company standards. This role supports the end-to-end writing and documentation process and ensures t...

You will be joining CMCH, a leading 100-bedded healthcare institution dedicated to delivering advanced cardiovascular care with empathy and expertise. The institution is expanding its cardiology team due to the increasing number of over 300 cases. Your role as an Interventional Cardiologist will involve the following responsibilities: - Perform interventional procedures such as angioplasty, stent placement, and catheter-based diagnostics. - Interpret diagnostic studies including echocardiograms, stress tests, and angiograms. - Collaborate with cardiac surgeons, primary care physicians, and ancillary staff to manage complex cases. - Engage in call rotation, outpatient clinics, and hospital-ba...

As an R&D Biomedical Engineer, you will focus on the research and development of biomedical technologies to enhance healthcare delivery. Your role involves designing, developing, and optimizing medical devices and systems to contribute to the advancement of patient care while ensuring compliance with regulatory standards. By leading the development of innovative solutions, you will play a crucial role in improving the safety, functionality, and reliability of critical healthcare equipment. Key Responsibilities: - Lead research for developing new medical devices, ensuring compliance with regulatory standards such as CDSCO, FDA, ISO, and CE. - Design and implement preclinical and clinical stud...