1999 Clinical Trials Jobs - Page 15

About The Role Skill required: Com.Bkg- Commercial Real Estate - Real Estate Due Diligence Designation: Banking Advisory Associate Qualifications: BCom/MCom/Master of Business Administration Years of Experience: 1 to 3 years What would you do? We help clients address quality and productivity issues, keep pace with customer expectations, navigate regulatory and operational pressures and ensure business sustainability by transforming their banking operations into an agile, resilient operating model.The Corporate banking /Wholesale banking team is responsible for helping clients and organizations processes trade finance transactions by providing superior service delivery to trade customers whil...

Role & responsibilities Collaborate with clinical and research teams to design clinical trials, including statistical analysis plans and sample size calculations. Perform statistical analyses of clinical trial data using appropriate statistical methods and software. Prepare statistical reports, summaries, and contribute to the writing of regulatory submissions, manuscripts, and presentations. Ensure the accuracy and integrity of data through comprehensive reviews and validation of datasets. Provide guidance to CDM in preparation of CRF designing and identification of critical data points and data validation. Work closely with Global Medical Affairs biostatisticians to identify statistical an...

Position overview: We are seeking a highly motivated healthcare graduate passionate about infectious diseases and public health as a Management Trainee. In this role, you will work closely with the Medial affairs team to support the development, implementation and evaluation of clinical initiatives, antimicrobial stewardship interventions, and other digital initiatives. This role is ideal for recent graduates in medicine, pharmacy, or life sciences with a strong interest in clinical strategy, infectious diseases, or public health. Responsibilities: Assist in planning and executing Orchid AMS clinical initiatives, including pilot programs, training workshops, and collaborative interventions. ...

Location: Hyderabad We are searching for a dynamic and experienced Business Analyst with a strong background in Generative AI and a deep understanding of the life sciences domain. You will be pivotal in bridging the gap between advanced AI technologies and their practical application in pharmaceutical research, development, and clinical operations. As a strategic thinker, you will be responsible for analyzing complex business needs, utilizing Generative AI to derive actionable insights, and supporting the implementation of AI-driven solutions. **About the Role** **Major Accountabilities** **Domain Expertise:** - Apply in-depth knowledge of life sciences, including drug discovery, development...

As a Clinical Data Manager I at Avance Clinical, you will be responsible for performing activities associated with the Data Cleaning activities of Clinical trials to ensure that the trials are conducted in accordance with the protocol, company Standard Operating Procedures (SOPs), ICH GCP guidelines, and other applicable regulatory requirements. Your core responsibilities will include autonomously developing study-related documents or plans, leading the Data management team as the Lead CDM, raising data queries in the EDC, ensuring accurate and timely filing as per SOP requirements, maintaining effective communication across the study team, participating in study-specific or vendor audits, a...

Imaging Endpoints (IE) is an Imaging Technology and Imaging Clinical Research Organization (iCRO) passionately focused on the vision to Connect Imaging to the CureTM. Everything is aligned with this singular purpose, advancing imaging science, technology, and services to bring curative technologies to humankind. The organization has been instrumental in supporting impactful new drug approvals in oncology and is seeking talented individuals globally to assist in customizing each clinical trial's imaging for optimal efficacy. Imaging Endpoints, headquartered in Scottsdale, Arizona, with offices in various global locations, is affiliated with HonorHealth and Scottsdale Medical Imaging Limited (...

The Senior Biostatistician plays a pivotal role in the research and development of clinical projects by applying statistical methods and providing insights through data analysis. This position requires expertise in R programming and a deep understanding of statistical techniques such as Analysis of Variance (ANOVA) and Analysis of Covariance (ANCOVA). The Senior Biostatistician will not only collaborate with various teams to ensure compliance with regulatory standards but also contribute to the development of statistical analysis plans and the interpretation of results. Given the importance of accurate statistical evaluations in clinical trials, this role is critical to the decision-making p...

Job Summary: The Officer - Onco Solid Oral will be responsible for supporting clinical development activities related to solid tumor oncology therapies, specifically focusing on oral drug formulations. This role involves coordinating clinical trials, liaising with cross-functional teams, ensuring regulatory compliance, and contributing to project timelines and deliverables. Key Responsibilities: Assist in planning and execution of clinical trials for oral oncology products targeting solid tumors. Coordinate with clinical research organizations (CROs), investigators, and internal teams. Monitor trial progress, ensure adherence to protocols, and manage documentation. Support regulatory submiss...

Responsible for planning, programming strategy, coordination, oversight, and execution of team activities following J&J IM and industry standards for one or more clinical trials or projects. Designs and develops programs in support of complex clinical data analysis and reporting activities. Supports submission activities including but not limited to creation, verification, and delivery of CDISC compliant and/or non-standard data packages and reviewer s guides. Provides technical and project-specific guidance to team members, ensuring high-quality, efficiency and on-time deliverables in compliance with departmental processes and procedures. Ensures use of latest standards and deployment of cu...

Job Purpose: Were seeking an experienced Principal Investigator (PI) to lead BA/BE clinical trials at our site in Noida. The PI will ensure studies are conducted ethically, maintaining subject safety, data integrity, and full compliance with study protocols and regulatory guidelines. Key Responsibilities: Lead and supervise BA/BE studies per protocol, ICH-GCP, and regulatory standards. Conduct medical assessments, manage subject eligibility, and oversee adverse event reporting. Ensure informed consent is transparent, ethical, and patient-friendly. Provide immediate medical care during emergencies and ensure proper documentation. Ensure accurate data capture and completeness of source documen...

About The Team In this role, you will be part of the Global Distribution Management team, with responsibility to support all efforts to enhance the team's effectiveness by driving and improving operational processes You would be required to coordinate our efforts and actions across teams, keeping constant customer and broker focus with particular emphasis on improving the features on the CRM application, managing data quality within the application, setting up processes for manual data operations and supporting other operational activities, About The Role Analyze and test both new and existing features in internal CRM digital applications, Develop and maintain reports & trackers to monitor p...

At Saleshandy, we help businesses scale outbound sales with automation, personalisation, and precision Were a fast-growing, bootstrapped SaaS company trusted by 4,000+ customers globally Onboarding is our first shot at delight ? and we dont take that lightly, Were looking for an Onboarding Specialist who can turn new users into power users ? fast, This isnt a hand-holding role Its about educating, enabling, and empowering customers to get real value from Day 1, If youve owned onboarding journeys, improved time-to-value, or helped drive early adoption ? lets talk, ??? What Youll Own First 30 Days Run fast-paced, value-driven onboarding calls Setup ? Activation ? First win, Personalised Journe...

"Role Assistant Store Manager PURPOSE & IMPACT ON ORGANIZATION: Be aware of store sales and KPI targets, as well as individual performance targets, take ownership over them and effectively use all available store resources to meet or exceed them Identify sales and KPI improvement opportunities and communicate suggestions to store management to address them and drive commercial success Be a role model for customer service and meeting or exceeding customersexpectations Share your customer service experience and train selected team members to fine tune their service skills Be a resource for Retail Professionals in dealing with complex customer service situations Be a Brand Ambassador, consisten...

Join our innovative Digital Physiology team supporting the Respiratory business unit, where you ll play a key role in validating and assuring the quality of software used in respiratory clinical studies. As a Software Quality Engineer , you ll take ownership of the testing lifecycle from reviewing and approving Computer System Validation (CSV) packages to executing test strategies that meet regulatory and clinical standards. This hands-on role offers the opportunity to work on impactful projects that directly support patient outcomes, while collaborating with global teams in a fast-paced, agile environment. What We Offer Competitive compensation + shift allowances Attractive benefits (securi...

Play a key role in advancing clinical research with Clario s Clinical Adjudication team in India. Are you meticulous, analytical, and driven by purposeAs a Project Support Analyst , you ll be at the heart of clinical trial adjudication ensuring that source data is accurately processed, translated, and reviewed in line with GxP standards and study-specific protocols. Your work will directly support the integrity of clinical outcomes, helping global studies meet regulatory and scientific benchmarks. If you re fluent in English, quick to learn new tools, and thrive in a collaborative, detail-focused environment, we invite you to join our mission to improve lives through smarter clinical evidenc...

Remote monitoring of Hydrogen electrolyzer throughout India and across different locations. Safe startup & safe shutdown of the hydrogen electrolyzer based on the customer requirements and involve in diagnostic assistance. Proactively Monitor the operational data obtained through our server and applications. Respond quickly to the call center and ticketing systems in support of customer needs. Assess customer and regional monitoring protocols to support compliant data processing. Alarm server monitoring. Develop several analytics to closely monitor the health and performance of the electrolyser. Prepare the Daily Production Report (DPR) and send it across for the budgeting. Prepare operation...

You should have experience in building reporting and analytics solutions, along with knowledge of clinical trials. It is important to be flexible to work in shifts, with the base location being Bangalore. The shift timing will be from 11.30 am to 8.30 pm. In terms of education qualification, a Bachelors degree in Statistics, Biostatistics, Mathematics, Computer Science, Information Technology, or a related field is required. The domain expertise should be in Pharmaceutical, Biotech, CRO, or Regulatory. The work location specified is Koramangala, Bangalore.,

The Centralized Monitoring Lead position requires a minimum of 4 plus years of experience in Clinical Research Associate (CRA) and Clinical trials monitoring. The work location can be in Bangalore, Thane, Pune, Ahmedabad, Kochi, or Hyderabad, and the work mode is Hybrid/Office Based with a shift from 2.00 pm to 11.00 pm. The key skills required for this role include Onsite/Remote/Risk Based Monitoring, Clinical Research, and Clinical Trials. As the Centralized Monitoring Lead, you will provide leadership to the centralized monitoring team in collaboration with project and clinical leads and other functional teams. Your primary responsibility will be to ensure the successful delivery of proje...

Are you seeking a rewarding career in Project Management within the Clinical Research industry Join Clario's Medical Imaging team in Bengaluru, India, and become a part of a legacy with over 30 years of expertise. Clario specializes in offering seamless, secure, and compliant medical imaging solutions that enhance clinical trials. At Clario, we have set ambitious goals and have a clear vision for the future. This is your opportunity to be a part of our journey as a Clinical Project Manager. What we offer: - Competitive compensation - Attractive benefits including security, flexibility, support, and well-being - Engaging employee programs - Technology for hybrid working and great onsite facil...

About The Role Skill required: Clinical Data Services - Clinical Reports Management Designation: Clinical Data Svs Associate Qualifications: BE/BTech Years of Experience: 1 to 3 years About Accenture Combining unmatched experience and specialized skills across more than 40 industries, we offer Strategy and Consulting, Technology and Operations services, and Accenture Song all powered by the worlds largest network of Advanced Technology and Intelligent Operations centers. Our 699,000 people deliver on the promise of technology and human ingenuity every day, serving clients in more than 120 countries. Visit us at www.accenture.com What would you do You will be aligned with our Life Sciences R&...

Skill required: Clinical Data Services - Clinical Reports Management Designation: Clinical Data Svs Specialist Qualifications: BE/BTech/MCA Years of Experience: 7 to 11 years About Accenture Combining unmatched experience and specialized skills across more than 40 industries, we offer Strategy and Consulting, Technology and Operations services, and Accenture Song all powered by the worlds largest network of Advanced Technology and Intelligent Operations centers. Our 699,000 people deliver on the promise of technology and human ingenuity every day, serving clients in more than 120 countries. Visit us at www.accenture.com What would you do You will be aligned with our Life Sciences R&D vertica...

Project Name: - Assessment of Emicizumb (low Dose) in hemphilia patients Pl Dr. Rucha Patil, Scientist D. Name of the Post :- Project Technical Support-II No.of Vacancy :- 01 Emoluments :- 20,000/- om + 30% HRA Essential Qualification :- 12th in Science + Diploma (MLT/DMT or equivalent) + five years experience in relevant subject. Three years Graduate degree in relvant subject/ field + two years experience in relevant subject. Desirable Qualification :- Pipetting skills, phlebotomy, molecular techiques, experience in clinical trial studies, data handing, and handling large data sets. Age limit :- The Upper age limit is 35 years. Location :- ICMR- NIIH, Mumbai Duration :- Till February, 2026 ...

Job Overview Principal Data Manager position is to oversee data operations tasks for a team of data managers from study start-up to database lock, to produce a clean and analyzable database. Essential Functions Serve as Data Team Lead (DTL) on a program of 6-10 global clinical trials or 40+ increasingly complex central laboratory studies Provide leadership to CDM team. Manage CDM customer relationship for CDM project team to include leading (with minimal guidance) CDM customer negotiations on complex timeline, budgetary and other issues. Provide marketing capabilities presentations and business development presentations. . Or serve as Data Operations Coordinator (DOC) for one or three global...

Principal Data Manager position is to oversee data operations tasks for a team of data maagers from study start-up to database lock, to produce a clean and analyzable database. Essential Functions Serve as Data Team Lead (DTL) on a program of 6-10 global clinical trials or 40+ increasingly complex central laboratory studies Provide leadership to CDM team. Manage CDM customer relationship for CDM project team to include leading (with minimal guidance) CDM customer negotiations on complex timeline, budgetary and other issues. Provide marketing capabilities presentations and business development presentations. . Or serve as Data Operations Coordinator (DOC) for one or three global clinical tria...

IP Strategy & Risk Management Conduct comprehensive patent landscape and whitespace analyses across global markets (India, US, EU, China, Brazil, Japan, etc.) to identify IP barriers and opportunities. Draft, file, and prosecute patent applications (including formulation, process, and use patents) to strengthen the company s IP portfolio. Perform Freedom to Operate (FTO) analysis to assess risk and enable informed product development and commercialization decisions. Predict potential blocking patents and assess the probability of patent grant or litigation risks. 2 . Portfolio & Lifecycle Intelligence Monitor competitor activities, brand pipelines, patent expiry timelines, and ongoing clinic...