3474 Clinical Trials Jobs - Page 27

Conduct thorough medical reviews of device-related documents to ensure compliance with regulatory requirements. Collaborate with cross-functional teams to identify and resolve issues related to device safety and efficacy. Required Candidate profile Strong understanding of medical devices, including their design, development, and testing. Excellent analytical and problem-solving skills, with attention to detail

Manage and oversee clinical data management activities, ensuring compliance with regulatory requirements. Develop and implement effective data management plans to ensure data quality and integrity. Collaborate with cross-functional teams to identify Required Candidate profile Strong knowledge of clinical data management principles and practices. Experience with data management systems and software applications. Excellent analytical and problem-solving skills

Develop and implement statistical analysis plans for clinical trials. Conduct statistical programming activities, including data management, reporting, and visualization. Collaborate with cross-functional teams to ensure timely Required Candidate profile Strong knowledge of biostatistics and statistical programming principles. Excellent analytical, problem-solving, and communication skills. Ability to work independently and as part of a team.

Conduct thorough reviews of ECRF data to ensure accuracy and compliance with regulatory requirements. Identify and report any discrepancies or issues found during data review. Collaborate with cross-functional teams to resolve data-related issues. Required Candidate profile Strong understanding of ECRF data management principles and practices. Excellent analytical and problem-solving skills, with attention to detail.

Design, develop, and implement clinical SAS programs for data management and analysis. Develop and maintain complex SQL databases for data storage and retrieval. Collaborate with cross-functional teams to identify business requirements Required Candidate profile Strong proficiency in SAS programming language, including Base SAS, Enterprise Guide, and Macros. Experience with SQL database management systems, including design, development, and maintenance.

Develop high-quality medical content for various platforms, including reports and presentations.Conduct thorough research on medical topics and stay updated with the latest developments.Edit and proofread content for clarity, grammar, Required Candidate profile Strong understanding of medical terminology and concepts. Excellent writing and communication skills. Ability to work independently and as part of a team.Strong analytical and problem-solving skills.

Develop high-quality aggregate reports on medical data, including patient safety and efficacy.Conduct thorough analysis of medical records to identify trends and patterns.Collaborate with cross-functional teams to ensure accurate Required Candidate profile Minimum 2 years of experience in medical writing, preferably in Pharmacovigilance. Strong knowledge of medical terminology, regulations, and industry standards. Excellent writing, communication,

Conduct clinical trials to ensure compliance with regulatory requirements and company protocols.Collaborate with cross-functional teams to design, implement, and monitor study protocols. Provide medical guidance and support to trial participants. Required Candidate profile Strong knowledge of clinical trial principles, practices, and regulations. Excellent communication and interpersonal skills are required for effective collaboration with patients, families

Develop and implement statistical analysis plans for clinical trials. Conduct statistical reviews of case report forms, annotated CRFs, database structures, and study-related documentation. Required Candidate profile Strong knowledge of statistical concepts, techniques, and tools. Experience in the employment firm or recruitment industry is preferred. Excellent communication and interpersonal skills.

Conduct clinical trials to ensure compliance with regulatory requirements and company protocols. Collaborate with cross-functional teams to design, implement, and monitor study procedures. Required Candidate profile Strong understanding of clinical trial principles, regulations, Excellent communication, interpersonal, and problem-solving skills. Ability to work independently and as part of a team.

Design, develop, and maintain SAS programs for clinical trial data management and analysis. Collaborate with cross-functional teams to ensure timely delivery of high-quality results. Develop and implement data validation Required Candidate profile Strong knowledge of SAS programming language and its application in clinical trial data management and analysis. Experience working with clinical trial databases and data management systems.

Publish regulatory submissions to relevant authorities, ensuring compliance with required standards. Coordinate with cross-functional teams to ensure timely submission of regulatory documents. Required Candidate profile Strong understanding of regulatory requirements and guidelines. Excellent communication and coordination skills. Ability to work independently and as part of a team.

5 years into Veeva Vault Promomats, clinical trial processes, workflows, application support in GxP regulated environments. 4 years into Vault Admin Console, security configuration, ServiceNow, Jira & validation (CSV or CSA).

Role Overview: As a Clinical Research Coordinator at Concept Clinical Service in Surat, your primary responsibility will be to coordinate clinical trials effectively. You will play a crucial role in obtaining informed consent from participants, ensuring adherence to study protocols, managing research documentation, and maintaining regulatory compliance. Your daily tasks will involve patient recruitment, data collection, monitoring activities, and facilitating communication within the study team and investigators. Key Responsibilities: - Coordinate clinical trials efficiently - Obtain informed consent from study participants - Adhere to study protocols and ensure compliance with regulatory re...

As an Associate Medical Expert in TCO (Translational Clinical Oncology) at Novartis Healthcare Private Limited, your role involves serving as the medical leader for assigned global, roll-over, and long-term follow-up studies, as well as studies in the close-out phase. Additionally, you may provide medical support for specific aspects of a global TCO study under the guidance of a Clinical Program Leader (CPL) and/or Medical Expert. TCO is a department within the Biomedical Research division responsible for conducting early-phase clinical studies in cancer patients, bridging the gap between drug discovery and late-phase clinical development to deliver innovative oncology medicines. Key Respons...

Job Purpose Bajaj Finance Ltd. As part of its Payments strategy wants to enter into the space of QR Acquiring. The QR Acquiring Area Manager will be required to build the business grounds up for his/her defined territory, by hiring and putting the entire team in place, and then managing the execution of the QR deployment, transactions & GMV. Culture Anchor:Work Hard - Consistently puts in effort. plans and tracks daily progress to achieve targetsExecute with Rigor - Takes responsibility for meeting targets with focus and effortOwn It - Maintains honesty and fairness in all interactions in line with organizations policiesAct with Integrity Duties and Responsibilities FOS Management:- Recruit,...

Job Purpose Bajaj Finance Ltd. As part of its Payments strategy wants to enter into the space of QR Acquiring. The QR Acquiring Area Manager will be required to build the business grounds up for his/her defined territory, by hiring and putting the entire team in place, and then managing the execution of the QR deployment, transactions & GMV. Culture Anchor:Work Hard - Consistently puts in effort. plans and tracks daily progress to achieve targetsExecute with Rigor - Takes responsibility for meeting targets with focus and effortOwn It - Maintains honesty and fairness in all interactions in line with organizations policiesAct with Integrity Duties and Responsibilities FOS Management:- Recruit,...

Technical/Functional Responsibilities: Utilizes project management skills and competencies to deliver a collaborative and efficient high performing Established Brands team. Develops and maintains an integrated program/project timeline in approved system(s) with a clear focus and understanding for critical path accountability and delivery of the brand strategy, including but not limited to activities that ensure: Ongoing commercial supply and regulatory compliance Brand optimization (e. g. , markets, stock keeping units [SKU] rationalization) Completion of post approval commitments/requirements, or response to health authority information requests, and completion of any remaining marketing au...

MDM Strategy & Leadership Develop and execute the enterprise MDM strategy, aligning with business objectives and IT roadmap. Lead the design, implementation, and optimization of Informatica Master Data Services solutions. Establish and enforce data governance policies, standards, and best practices for master data domains (e. g. , customer, product, vendor, employee). Informatica MDM Implementation & Management Oversee the configuration, deployment, and maintenance of Informatica MDM solutions. Manage data modeling, data integration, data quality, and workflow processes within Informatica. Collaborate with Informatica support and vendor teams to resolve technical issues and optimize platform...

Be a contributing member of Global Clinical Study Delivery s Leadership Team to include effective partnering and collaboration with fellow LT members as well as key stakeholders. Be accountable to set a strategy and vision for: Leadership and management of Senior Global Study Managers and Global Study Management Line Managers, driving effective line management practices across the group and locations. Engagement of Senior Global Study Managers and Global Study Management Line Managers in business improvement/process optimization efforts aligned to key acceleration and innovation targets. Continual Embedding and strengthening of the Study Team Operating Model (STOM) within the GSM team Senior...

Job Purpose Bajaj Finance Ltd. As part of its Payments strategy wants to enter into the space of QR Acquiring. The QR Acquiring Area Manager will be required to build the business grounds up for his/her defined territory, by hiring and putting the entire team in place, and then managing the execution of the QR deployment, transactions & GMV. Duties and Responsibilities FOS Management: - Recruit, train and motivate the team - Manage the FOS productivity Distribution development: -Acquire merchant - Drive QR deployment, SB deployment and POS/EDC Deployment -Build distribution for the business (business development). -Initiating and developing relationships with key decision makers in the relat...

Job Purpose Bajaj Finance Ltd. As part of its Payments strategy wants to enter into the space of QR Acquiring. The QR Acquiring Area Manager will be required to build the business grounds up for his/her defined territory, by hiring and putting the entire team in place, and then managing the execution of the QR deployment, transactions & GMV. Duties and Responsibilities FOS Management: - Recruit, train and motivate the team - Manage the FOS productivity Distribution development: -Acquire merchant - Drive QR deployment, SB deployment and POS/EDC Deployment -Build distribution for the business (business development). -Initiating and developing relationships with key decision makers in the relat...

Job Purpose Bajaj Finance Ltd. As part of its Payments strategy wants to enter into the space of QR Acquiring. The QR Acquiring Area Manager will be required to build the business grounds up for his/her defined territory, by hiring and putting the entire team in place, and then managing the execution of the QR deployment, transactions & GMV. Duties and Responsibilities FOS Management: - Recruit, train and motivate the team - Manage the FOS productivity Distribution development: -Acquire merchant - Drive QR deployment, SB deployment and POS/EDC Deployment -Build distribution for the business (business development). -Initiating and developing relationships with key decision makers in the relat...

We are looking for a highly skilled and experienced Biostatistician to join our team at Syngene International Limited, a leading player in the Pharmaceutical & Life Sciences industry. The ideal candidate will have a strong background in biostatistics and experience working with cross-functional teams. Roles and Responsibility Develop and implement statistical analysis plans for clinical trials. Conduct statistical reviews of case report forms, annotated CRFs, database structures, and study-related documentation. Collaborate with data management teams to ensure accurate and timely delivery of data. Provide statistical input into protocol development and review. Review and draft final producti...

We are looking for a skilled Medical Writer with 5-10 years of experience to join our team in Hyderabad. The ideal candidate will have excellent writing and editing skills, with the ability to create clear, concise, and engaging content. Roles and Responsibility Develop high-quality medical content, including articles, blogs, and other written materials. Conduct research and analyze complex scientific concepts to create accurate and informative content. Collaborate with cross-functional teams to ensure consistency and quality of content. Edit and proofread content for clarity, grammar, and punctuation. Stay up-to-date with industry trends and developments in medical science and technology. P...