3474 Clinical Trials Jobs - Page 40

As a part of Medpace's newly launched office in Hyderabad, India, you have the opportunity to play a significant role in shaping the culture, building the team, and influencing the company's growth in India from the ground up. Your work will have a meaningful impact on global projects right from day one. **Responsibilities:** - Perform quality assurance checks on medical imaging data to ensure protocol specific requirements are met - Utilize established image processing techniques across MRI or Nuclear medicine imaging modalities using proprietary software and third-party software - Compile and maintain project-specific status reports and timelines associated with imaging studies - Execute p...

As a Clinical Research Coordinator based in Meerut, your role will involve managing and overseeing clinical trials, ensuring compliance with research protocols, and obtaining informed consent from participants. You will be responsible for monitoring and documenting clinical research activities, coordinating with research teams, and maintaining accurate records of all research data. Key Responsibilities: - Manage and oversee clinical trials - Ensure compliance with research protocols - Obtain informed consent from participants - Monitor and document clinical research activities - Coordinate with research teams - Maintain accurate and up-to-date records of research data Qualifications Required...

As a Clinical Data Associate / Clinical Data Coordinator at Imaging Endpoints, your role involves conducting all clinical data management activities for each assigned clinical study. This includes coordinating with study team members, management, and clients to complete work as detailed in the clients" work order. You will be responsible for maintaining audit readiness by ensuring study-related documents are in the study eTMF in a timely manner, effectively communicating project status to internal and external stakeholders, and conducting clinical data management activities per relevant standard operating procedures and work instructions as directed by management. Additionally, you will perf...

Concept Pharmaceuticals Ltd. is looking for Clinical Research Physician to join our dynamic team and embark on a rewarding career journey Provide medical leadership on project teamsProvide medical monitoring for clinical studiesReview and approve final study reports or other clinical documentsExcellent communication skills Excellent presentation skillsServe as medical team leader on assigned projects Ensure provision of all contracted activities and identification of out of scope activities on projects assigned 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 al...

Concept Pharmaceuticals Ltd. is looking for Clinical Data Manager to join our dynamic team and embark on a rewarding career journey Data Collection and Entry: Oversee the collection and entry of clinical trial data into electronic databases, ensuring accuracy, completeness, and compliance with regulatory requirements Data Cleaning: Perform data validation, verification, and quality control procedures to identify and resolve discrepancies or errors in the data Database Design: Contribute to the design and development of electronic data capture (EDC) systems and databases for data collection and management Data Standardization: Ensure data standardization and adherence to data collection stand...

Concept Pharmaceuticals Ltd. is looking for Clinical Research Associate to join our dynamic team and embark on a rewarding career journey As a Clinical Research Associate (CRA), you will be responsible for monitoring clinical trials and ensuring that they are conducted in accordance with regulatory requirements and ethical standards Ensure compliance with study protocols, regulatory requirements, and ethical standardsMonitor and review study data to ensure accuracy, completeness, and compliance with study protocolsStrong knowledge of clinical research protocols, regulations, and guidelines, including ICH-GCP and FDA regulations Proficiency in using clinical research software, such as EDC sys...

A Consultant / Senior Consultant at Axience is hired typically from peer groups or related backgrounds with a minimum of 3 years of experience (minimum one-year experience for Consultant, although graduate and post-graduate freshers from reputed institutions will also be considered). Detailed responsibilities may include (but not limited to): Be a part of the team working on various pharma / biotech / med devices business research projects aiding decision making for reputable large and medium-sized global corporates and consultancies, and be exposed to truly global professional standards Understand research objectives, design partial or full research strategies, interpret and analyse informa...

About You experience, education, skills, and accomplishments. An advanced degree in a relevant discipline (epidemiology, public health-with a focus on quantitative research- or biostatistics) 2+ years of experience in Epidemiology or Consulting within life sciences & healthcare Familiarity with observational/epidemiological or analytical methods. Strong analytical and critical-thinking skills with the ability to interpret complex data and draw evidence-based conclusions. A proven commitment to client service and competency to communicate technical concepts to a both technical/academic/clinical as well as non-technical audiences. Experienced with MS Office including MS Word, PowerPoint, and E...

Job Title: Clinical Product Owner/Scientist Location: Bangalore Experience: 10+ years Role Overview: We are seeking a visionary and accomplished Medical Device Clinical Product Owner to lead our new product development initiatives in Healthcare and Life sciences. This role combines deep functional expertise with strong leadership and business acumen. The ideal candidate will have a proven track record in conceptualizing, evaluating, and developing medical systems. You will liaison with medical practitioners, OEM partners and cross-functional engineering teams to guide solution development and implementations. This is a customer-facing role with a strong focus on innovation, solution developm...

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...

Core Purpose of the Role: To perform Biostatistical activities in Biometrics Department for Clinical Studies Phase 1-4 Role Accountabilities Reviewing protocol SAP & RAP preparation and implementation Sample size calculation Provides statistical consultations Preparing and reviewing randomization list Perform Statistical analysis as per SAP and Protocol Reviewing of SDTM and AdAM dataset Preparing and reviewing of tables, listing and graphs, as applicable Preparing and reviewing of statistical report, as applicable Provides support for blinding and unblinding documentations Preparing and reviewing standard operating procedures Training/Guiding/Mentoring associate biostatisticians and junior ...

MAIN PURPOSE OF ROLE Summarize the main purpose of the role. Specialist professional individual contributor with comprehensive knowledge in the area of Medical Affairs. Ability to execute highly complex or specialized projects. Adapts precedent and may make significant departures from traditional approaches to develop solutions. Main Responsibilities As the Specialist in the Medical Affairs Sub-Function, considered as highly experienced and knowledgeable resource within the organization in overseeing the direction, planning, execution, clinical trials/research and the data collection activities. Contributes to implementation of clinical protocols, and facilitates completion of final reports....

Role Overview: As a Clinical Data Standards Specialist at Novartis, you will strategically and tactically support the Director of Clinical Data Standards. Your responsibilities will include advising and leading the planning, development, and implementation of Industry compliant clinical data standards, infrastructure, and automation technologies. You will provide expert support to business users and teams on various aspects including data standard collection tools, data transfer specifications, analysis data standards, and automation solutions. Additionally, you may lead global teams to ensure alignment with the CDS strategy and drive efficient implementation of new standards and technologie...

The R2R Ops /Controllership Senior Manager for BMS will be a highly collaborative Fice team member. This exceptional leader will act as a player-coach, overseeing and supporting execution of R2R accounting activities in BMS s Hyderabad CoE, and demonstrate the following attributes: Exceptional expertise in record-to-report accounting processes Deep understanding of the business landscape, market trends, and industry dynamics Open communication and cooperation to ensure R2R activities are executed seamlessly Successful candidates will possess excellent leadership skills, inspiring and motivating team members to deliver exceptional results. A minimum of 7-9 years of experience is required, wit...

Project Role : Software Development Engineer Project Role Description : Analyze, design, code and test multiple components of application code across one or more clients. Perform maintenance, enhancements and/or development work. Must have skills : SAP HCM Payroll Good to have skills : NA Educational Qualification : 15 years of full time education Summary :As a Software Development Engineer, your typical day will involve analyzing, designing, coding, and testing various components of application code for multiple clients. You will engage in maintenance and enhancement tasks, ensuring that the applications function optimally and meet client requirements. Collaboration with team members will b...

The Associate pharmacovigilance specialist performs pharmacovigilance services such as biomedical literature monitoring and assessing for adverse events reporting, indexing, and abstracting by using broad knowledge of scientific terms and medical terminology, drugs and therapeutic areas, and pharmacovigilance regulations. About You - Education, Experience, Skills Masters Degree in life Sciences, Health, or Biomedical Sciences (Pharmacy, Microbiology, Biochemistry, Biotechnology, Biophysics etc.). A degree in Dentistry/physiotherapy/Nursing, which involves patient exposure in hospital-based environment, would be an advantage. At least 1-2 years of experience reviewing biomedical literature fo...

Responsibilities: Lead and oversee the entire Quality Control department operations. Ensure compliance with cGMP, regulatory guidelines, and company quality standards. Review and approve analytical methods, specifications, and validation protocols. Supervise raw material, in-process, and finished product testing. Ensure timely release of batches and materials. Manage laboratory investigations, OOS, OOT, deviations, and CAPA. Coordinate with QA, Production, and Regulatory teams for smooth operations. Handle audits (internal, external, and regulatory) and ensure readiness at all times. Provide training, mentoring, and performance evaluation of QC staff. Drive continuous improvement, cost effic...

This Position reports to: Delivery Manager-Tax Operations Roles and Responsibilities: The individual will be responsible for overseeing end-to-end compliance for both Indirect and Direct Taxes for multiple countries. This role will be reported directly to the Tax Operations Delivery Manager. Seeking a detail-oriented and proactive Tax Operations Specialist / Sr. Specialist to support the accurate and timely execution of tax-related processes across our organization. This role involves managing tax documentation, ensuring compliance with regulatory requirements, supporting tax reporting, and collaborating with internal and external stakeholders to streamline operations. Tax Documentation & Co...

We are looking for an Associate Content Editor to join our Clinical Studies team in Hyderabad . This is an amazing opportunity to work on Cortellis Clinical Trial Intelligence and Cortellis Drug Discovery Intelligence. The team consists of 20 people. We have a great skill set in Clinical and we would love to speak with you if you have skills in Clinical/Drugs As an Associate Content Editor in Clinical team, you will be responsible for actively seeking out information about Clinical Studies, analyze, cross reference, and update all new or previously updated information in the clinical records from various sources, which includes scientific meetings, conferences, trial registries, press releas...

About The Role Skill required: Pharmacovigilance Services - Pharmacovigilance & Drug Safety Surveillance Designation: Pharmacovigilance Services Associate Qualifications: Bachelor of Pharmacy Years of Experience: 1 to 3 years 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 enabling them to i...

About The Role Skill required: Pharmacovigilance Services - Pharmacovigilance & Drug Safety Surveillance Designation: Pharmacovigilance Services Associate Qualifications: Bachelor of Pharmacy Years of Experience: 1 to 3 years 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 enabling them to i...

About The Role Skill required: Pharmacovigilance Services - Pharmacovigilance & Drug Safety Surveillance Designation: Pharmacovigilance Services Associate Qualifications: Bachelor of Pharmacy Years of Experience: 1 to 3 years 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 enabling them to i...

About The Role Skill required: Pharmacovigilance Services - Pharmacovigilance & Drug Safety Surveillance Designation: Pharmacovigilance Services Associate Qualifications: Bachelor of Pharmacy Years of Experience: 1 to 3 years 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 enabling them to i...

About The Role Skill required: Pharmacovigilance Services - Pharmacovigilance & Drug Safety Surveillance Designation: Pharmacovigilance Services Associate Qualifications: Bachelor of Pharmacy Years of Experience: 1 to 3 years 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 enabling them to i...

About The Role Skill required: Pharmacovigilance Services - Pharmacovigilance & Drug Safety Surveillance Designation: Pharmacovigilance Services Associate Qualifications: Bachelor of Pharmacy Years of Experience: 1 to 3 years 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 enabling them to i...