260 Crf Jobs - Page 3

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...

About The Role Skill required: Clinical Data Services - Clinical Reports Management Designation: Clinical data SVS Analyst Qualifications: Any Graduation,BE,MCA Years of Experience: 3-5 Yrs 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 improve outcomes by converging around...

About The Role Skill required: Clinical Data Operations - Clinical Database Testing Designation: Clinical Data Svs Analyst Qualifications: Master Degree in Life Sciences Years of Experience: 3 to 5 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 ...

Desired Candidate Profile: 6+ years of experience in clinical research, with at least 2 years in a leadership role. Strong understanding of clinical trial methodology and regulatory landscape (DCGI, ICH-GCP, etc.) Experience in managing multi-site studies in India and/or global trials. Excellent communication, organizational, and project management skills. Ability to lead cross-functional teams and manage multiple priorities. Proficient in CTMS, EDC systems, and MS Office tools. Job Description We are seeking an experienced and motivated Clinical Trials Team Lead to oversee and manage clinical research projects across various phases. The ideal candidate will lead a team of clinical research ...

As an expectation a fitting candidate must have/be: Ability to analyze business problem and cut through the data challenges. Ability to churn the raw corpus and develop a data/ML model to provide business analytics (not just EDA), machine learning based document processing and information retrieval Quick to develop the POCs and transform it to high scale production ready code. Experience in extracting data through complex unstructured documents using NLP based technologies. Good to have : Document analysis using Image processing/computer vision and geometric deep learning Technology Stack: Python as a primary programming language. Conceptual understanding of classic ML/DL Algorithms like Reg...

We are looking for a highly skilled and experienced Kids Den Associate to join our team. The ideal candidate will have excellent communication skills, be able to work well under pressure, and have a passion for working with children. Roles and Responsibility Develop and implement engaging activities for kids in the den. Create a welcoming and inclusive environment for all kids. Collaborate with other staff members to achieve common goals. Maintain accurate records of kids' progress and development. Provide individualized support and guidance to kids as needed. Participate in ongoing training and professional development to stay current on best practices. Job Requirements Proven experience wo...

You will be joining Allucent, a company dedicated to aiding small-medium biopharmaceutical companies in efficiently navigating the complex world of clinical trials to bring life-changing therapies to patients worldwide. As a TMF Specialist at Allucent, your main responsibility will involve coordinating the indexing of documents within the Trial Master File. You will be in charge of ensuring the quality of documents filed in the TMF and completing the approval step for documents. Key Responsibilities: - Review documents to ensure compliance with Good Document Practices and ALCOA+ standards. - Confirm the categorization of documents according to the DIA reference model and Allucent TMF Index. ...

Ensure the integrity of data and that the study is conducted in compliance with approved protocol, GCP, applicable regulations, and internal SOPs Prepare and maintain documents related to clinical trials. Generate data entry queries and test clinical applications for numerous clinical trials. Analyze clinical trials data and prepared reports for Data Coordinator and Sponsor. Serve as liaison between Data Management and other departments in Clinical application developments. Manage clinical research data for the new and ongoing electronic clinical trials. Conduct UAT Testing and validate software application processes for the management of clinical trials. Assist with the creation of data man...

Role Overview: As a Senior Clinical Programmer at Syneos Health, you will play a crucial role in accelerating customer success by translating clinical, medical affairs, and commercial insights into outcomes. You will be part of a team that puts the customer and patient at the center of everything they do, aiming to simplify and streamline work processes for enhanced collaboration and innovation. Your contributions will be pivotal in helping customers achieve their goals and ultimately changing lives. Key Responsibilities: - Utilize primary development tools such as Medidata, Rave, Oracle OC/RDC, Oracle Inform, and SAS to design, write, validate, and maintain software in adherence to specific...

Role & responsibilities : Supports development of specifications for technical data management processes and systems Contribute to the Request for Proposal (RFP) and Request for Information (RFI) process. Prepares input for and participates in proposal bid defense meetings where appropriate Acts as Subject Matter Experts (SME) for designated systems/databases used by Data Management (DM) Supports DM to ensure processes in relation to systems/databases are consistent and that best practices are maintained globally. Can consult with internal functional teams and sponsors as a SME Assists with developing, monitoring and enforcing productivity, quality standards and efficiencies, input into the ...

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...

Skill required: Clinical Data Services - Clinical eTMF Management Designation: Clinical Data Svs Associate Qualifications: BTech/Bachelor of Pharmacy/Master 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 improve outcomes by conv...

Skill required: Clinical Data Services - Clinical Data Management Designation: Clinical Data Svs Associate Qualifications: BTech/Bachelor of Pharmacy/Master 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 improve outcomes by conv...

Skill required: Clinical Data Services - Clinical Data Management Designation: Clinical Data Svs Sr Analyst Qualifications: Bachelor of Pharmacy/Master of Pharmacy Years of Experience: 5 to 8 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 improve outcomes by convergin...

Roles and Responsibility Conduct thorough reviews of clinical trial data to ensure accuracy, completeness, and compliance with regulatory requirements. Collaborate with cross-functional teams to identify and resolve data discrepancies and issues. Develop and maintain detailed reports of findings and recommendations for data improvements. Participate in developing and implementing process improvements to enhance data quality and efficiency. Provide training and support to junior staff members on data review procedures and best practices. Stay up-to-date with changing regulations and guidelines related to clinical data management. Job Requirements Strong understanding of clinical data manageme...

Roles and Responsibility Collaborate with cross-functional teams to develop and implement clinical trial protocols. Provide medical expertise and guidance on clinical research studies, including protocol development and review. Conduct site feasibility assessments and coordinate with investigators to ensure successful study execution. Develop and maintain relationships with key stakeholders, including sponsors, investigators, and regulatory agencies. Stay updated with changing regulations and guidelines governing clinical research, ensuring compliance and adherence to best practices. Participate in quality assurance activities to ensure high-quality deliverables. Job Requirements Strong unde...

Roles and Responsibility Manage and maintain accurate and up-to-date clinical trial data. Develop and implement effective data management plans and procedures. Collaborate with cross-functional teams to ensure compliance with regulatory requirements. Analyze and interpret complex data sets to inform business decisions. Develop and maintain reports and dashboards to track key performance indicators. Ensure data quality and integrity by implementing robust validation and verification processes. Job Requirements Strong knowledge of clinical data management principles and practices. Experience with data analysis and interpretation tools and techniques. Excellent communication and collaboration s...

We are looking for a skilled SDN Controller with 17+ years of experience to join our team in Bangalore. The ideal candidate will have expertise in OSS, SDN domain controller, TMF eTOM Framework, and Telecom Standards. Roles and Responsibility Manage service assurance, fulfillment, and inventory for seamless operations. Implement SDN domain controllers to optimize network performance. Develop and maintain TMF eTOM frameworks to ensure compliance with telecom standards. Collaborate with stakeholders to achieve business objectives. Analyze data to identify areas for improvement and implement changes. Ensure effective communication with internal teams and external partners. Job Requirements Stro...

Description Sr CDA (Data Acquisition Specialist-Non-CRF) Syneos Healthis a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success We translate unique clinical, medical affairs and commercial insights into outcomes to address modern market realities Our Clinical Development model brings the customer and the patient to the center of everything that we do We are continuously looking for ways to simplify and streamline our work to not only make Syneos Health easier to work with, but to make us easier to work for Whether you join us in a Functional Service Provider partnership or a Full-Service environment, youll collaborate with passionate problem ...

Manage and oversee clinical study 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 and resolve data-related issues. Conduct regular audits to ensure adherence to data management standards. Provide training and support to junior staff members on data management best practices. Ensure timely delivery of high-quality results while maintaining attention to detail. Job Requirements Strong understanding of clinical trial conduct, including GCP guidelines and regulatory requirements. Experience with data management systems, such...

Manage and resolve discrepancies in clinical trial data. Develop and implement effective data reconciliation processes. Collaborate with cross-functional teams to ensure accurate and timely resolution of data issues. Analyze and report on data trends and patterns to identify areas for improvement. Ensure compliance with regulatory requirements and industry standards. Provide training and support to junior team members on data reconciliation best practices. Job Requirements Strong understanding of clinical trial data management principles and practices. Experience with data reconciliation tools and technologies. Excellent analytical and problem-solving skills. Ability to work effectively in a...

Manage and oversee the development, implementation, and maintenance of clinical databases. Ensure data quality, accuracy, and compliance with regulatory requirements. Collaborate with cross-functional teams to design and implement data-driven solutions. Develop and maintain data standards, policies, and procedures. Provide training and support to staff on data management systems. Identify and mitigate risks associated with data management. Job Requirements Strong knowledge of clinical data management principles and practices. Experience with clinical trial conduct and regulatory requirements. Excellent communication and interpersonal skills. Ability to work effectively in a fast-paced enviro...

Develop and maintain complex statistical models and databases for clinical trial data. Design and implement data visualization tools to effectively communicate insights to stakeholders. Collaborate with cross-functional teams to identify business needs and develop solutions. Analyze large datasets to extract meaningful trends and patterns. Develop and maintain technical documentation of data systems and processes. Provide training and support to junior team members on R and SAS programming best practices. Job Requirements Strong proficiency in R and SAS programming languages. Experience working with clinical trial data and statistical modeling techniques. Excellent analytical and problem-sol...

Manage and oversee the development and implementation of clinical data management systems. Ensure compliance with regulatory requirements and industry standards for clinical data management. Collaborate with cross-functional teams to identify and prioritize project requirements. Develop and maintain data quality control processes to ensure accuracy and integrity of clinical data. Provide training and support to staff on clinical data management systems and procedures. Analyze and resolve complex technical issues related to clinical data management. Job Requirements Strong knowledge of clinical data management principles and practices. Experience with Veeva EDC is highly desirable. Excellent ...

Develop and maintain complex statistical models and databases for clinical trial data. Design and implement data visualization tools to effectively communicate insights to stakeholders. Collaborate with cross-functional teams to identify business needs and develop solutions. Conduct thorough data quality checks and ensure compliance with regulatory requirements. Provide expert-level support for data-related queries and issues. Stay up-to-date with industry trends and emerging technologies in clinical data analysis. Job Requirements Strong proficiency in R and SAS programming languages. Experience working with large datasets and complex statistical models. Excellent problem-solving skills and...