581 Clinical Operations Jobs - Page 7

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 ...

Collaborate with cross-functional teams to ensure successful clinical trial execution. Provide medical expertise and guidance on clinical trial protocols and procedures. Develop and maintain relationships with key stakeholders, including investigators, sponsors, and regulatory agencies. Conduct site feasibility assessments and provide recommendations for study locations. Ensure compliance with regulatory requirements and company policies. Participate in protocol development and review processes. Job Requirements Minimum 3-5 years of experience in clinical trials or a related field. Strong knowledge of clinical trial regulations, guidelines, and best practices. Excellent communication and int...

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...

Develop and implement effective medical monitoring strategies for clinical trials. Collaborate with cross-functional teams to ensure compliance with regulatory requirements. Conduct thorough reviews of medical data to identify trends and potential issues. Provide expert guidance on medical aspects of clinical development projects. Ensure timely reporting of adverse events and other critical information. Participate in quality control activities to maintain high standards of data accuracy. Job Requirements Strong understanding of clinical development principles and practices. Excellent analytical and problem-solving skills, with attention to detail. Effective communication and interpersonal s...

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 Good Clinical Practice (GCP) principles and reg...

Develop and implement effective medical monitoring strategies for clinical trials. Collaborate with cross-functional teams to ensure compliance with regulatory requirements. Conduct thorough reviews of medical data to identify trends and potential issues. Provide expert guidance on medical matters related to clinical development. Ensure timely reporting of adverse events and other safety concerns. Participate in quality control activities to maintain high standards of medical practice. Job Requirements Strong knowledge of clinical development principles and practices. Excellent analytical and problem-solving skills. Ability to work effectively in a fast-paced environment. Effective communica...

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 communication and problem-...

Roles and Responsibility 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 data-related issues and discrepancies. Job Requirements Strong knowledge of clinical data management principles and practices. Experience with Veeva EDC is highly desirable. ...

As a Senior Manager, Clinical Scientist at Bristol Myers Squibb, you will be responsible for designing and executing assigned clinical trial activities. You will work closely with clinical team members within the assigned project to execute activities associated with the conduct, and may even serve as a Clinical Trial Lead for one or more trials. Your responsibilities will include collaborating and liaising with external partners, seeking out and enacting best practices, providing regular and timely updates to management, developing Protocol and ICF documents, conducting literature reviews, and submitting clinical documents to TMF. Additionally, you will develop site and CRA training materia...

As the Lead Clinical Operations at a Digital Health Company based in Mumbai, your role will involve overseeing and managing the clinical operations of the cardiac rehabilitation program. You will be responsible for developing and implementing clinical protocols and guidelines in line with best practices to ensure high-quality patient care and adherence to clinical standards. Your key responsibilities will include: - Leading, mentoring, and training a multidisciplinary team of health professionals, including Dieticians, Care Managers, and Mental Wellness experts. - Conducting regular performance reviews and providing continuous professional development opportunities for the team. - Fostering ...

Role Overview: As a Project Training Coordinator at Covance in Bangalore, India, your primary responsibility will be to facilitate the creation, revision, and inactivation of project training requirements in the LMS. You will provide regular updates to project leaders and coordinators, monitor and track compliance of study teams to training requirements, send notifications to delinquent team members, and escalate repeated delinquent cases to project leads. Your role will also involve assigning and removing role-based curricula to staff members, ensuring the accuracy and quality of assignments and curricula, administering updates to the LMS, running ad hoc reports, performing reconciliations,...

Roles and Responsibility Collaborate with cross-functional teams to ensure successful clinical trial execution. Provide medical expertise and guidance on clinical trial protocols, procedures, and study designs. Develop and maintain relationships with key stakeholders, including investigators, sponsors, and regulatory agencies. Conduct site feasibility assessments and provide recommendations for study locations. Ensure compliance with regulatory requirements and company policies. Participate in protocol development and review meetings with internal and external stakeholders. Job Requirements Strong knowledge of clinical trials, including design, conduct, and reporting. Excellent communication...

Roles and Responsibility Collaborate with cross-functional teams to ensure successful clinical trial execution. Provide medical expertise and guidance on clinical trial protocols, procedures, and study designs. Develop and maintain relationships with key stakeholders, including investigators, sponsors, and regulatory agencies. Conduct site feasibility assessments and provide recommendations for study locations. Ensure compliance with regulatory requirements and company policies. Participate in protocol development and review processes. Job Requirements Minimum 4 years of experience in clinical trials or a related field. Strong knowledge of clinical trial principles, practices, and regulation...

Roles and Responsibility Collaborate with cross-functional teams to ensure successful clinical trial execution. Provide medical expertise and guidance on clinical trial protocols, procedures, and study designs. Develop and maintain relationships with key stakeholders, including investigators, sponsors, and regulatory agencies. Conduct site feasibility assessments and provide recommendations for study locations. Ensure compliance with regulatory requirements and company policies. Participate in protocol development and review processes. Job Requirements Minimum 2 years of experience in clinical trials or a related field. Strong knowledge of clinical trial principles, practices, and regulation...

We are looking for a skilled Clinical Data Manager to join our team at Gratitude India Manpower Consultants Pvt. Ltd., located in the IT Service & Consulting industry. The ideal candidate will have 1-5 years of experience and a strong background in clinical data management. Roles and Responsibility 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, guidelines, and best practices. Provide training and support to staff on data management systems. Identify an...

We are looking for a highly skilled and experienced Clinical Data Reconciliation Specialist to join our team at Gratitude India Manpower Consultants Pvt. Ltd., an IT Service & Consulting company based in [location to be specified]. The ideal candidate will have 4-6 years of experience in clinical data reconciliation. Roles and Responsibility Manage and oversee the clinical data reconciliation process to ensure accuracy and quality. Develop and implement effective data reconciliation strategies to meet project requirements. Collaborate with cross-functional teams to identify and resolve data discrepancies. Analyze and report on data reconciliation results, identifying trends and areas for imp...

We are looking for a highly skilled and experienced Clinical Data Reconciliation Specialist to join our team at Gratitude India Manpower Consultants Pvt. Ltd., an IT Service & Consulting company based in [location to be specified]. The ideal candidate will have 3-4 years of experience in clinical data reconciliation. Roles and Responsibility Manage and oversee the clinical data reconciliation process to ensure accuracy and quality. Develop and implement effective data reconciliation strategies to meet project requirements. Collaborate with cross-functional teams to identify and resolve data discrepancies. Analyze and report on data reconciliation results, identifying trends and areas for imp...

We are looking for a highly skilled and experienced Clinical Data Reconciliation Specialist to join our team at Gratitude India Manpower Consultants Pvt. Ltd., an IT Service & Consulting company based in [location to be specified]. The ideal candidate will have 5-10 years of experience in clinical data reconciliation. Roles and Responsibility Manage and oversee the clinical data reconciliation process to ensure accuracy and quality. Develop and implement effective data reconciliation strategies and procedures. Collaborate with cross-functional teams to identify and resolve data discrepancies. Analyze and interpret complex data sets to identify trends and patterns. Develop and maintain docume...

We are looking for a skilled Clinical Data Manager with expertise in Veeva EDC to join our team at Gratitude India Manpower Consultants Pvt. Ltd. The ideal candidate will have a strong background in the IT Service & Consulting industry and 2-7 years of experience. Roles and Responsibility 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 and resolve data-related issues. Conduct regular audits to ensure adherence to data management standards. Provide training and support to staff on data manageme...

We are looking for a highly skilled Regulatory Medical Writer with 1 to 6 years of experience to join our team in Mumbai. The ideal candidate will have a strong background in regulatory affairs and medical writing, with excellent communication and analytical skills. Roles and Responsibility Develop high-quality regulatory documents, including clinical study reports, marketing authorizations, and other related materials. Collaborate with cross-functional teams, including regulatory affairs, product development, and clinical operations. Conduct thorough reviews of regulatory documents to ensure accuracy, completeness, and compliance with regulatory requirements. Stay up-to-date with changing r...

We are looking for a skilled Clinical Data Manager with expertise in Veeva EDC to join our team at Gratitude India Manpower Consultants Pvt. Ltd. The ideal candidate will have a strong background in clinical data management and experience working with IT Service & Consulting companies. Roles and Responsibility Manage and oversee the development, implementation, and maintenance of clinical databases using Veeva EDC. Ensure data quality, integrity, and compliance with regulatory requirements. Collaborate with cross-functional teams to identify and prioritize data management needs. Develop and implement data management plans and procedures. Conduct regular audits and reviews of data management ...

We are looking for a skilled Clinical Data Manager with expertise in Veeva EDC to join our team at Gratitude India Manpower Consultants Pvt. Ltd. The ideal candidate will have a strong background in clinical data management and experience working with IT Service & Consulting companies. Roles and Responsibility Manage and oversee the development, implementation, and maintenance of clinical databases using Veeva EDC. Ensure data quality, integrity, and compliance with regulatory requirements. Collaborate with cross-functional teams to ensure seamless integration of clinical data into larger systems. Develop and implement data management plans, procedures, and standards. Conduct regular audits ...

Roles and Responsibility Monitor medical enquiries and respond to customer inquiries professionally. Provide excellent customer service and ensure high customer satisfaction. Collaborate with internal teams to resolve customer complaints and concerns. Develop and maintain strong relationships with customers and stakeholders. Analyze customer feedback and suggest improvements to processes and procedures. Ensure compliance with company policies and procedures. Job Requirements Strong communication and interpersonal skills are essential. Ability to work in a fast-paced environment and meet deadlines is required. Excellent problem-solving and analytical skills are necessary. Strong attention to ...

Roles and Responsibility Manage and oversee the collection, review, and reporting of clinical trial data. Develop and implement effective data management plans and procedures. Collaborate with cross-functional teams to ensure compliance with regulatory requirements. Conduct quality control checks on data accuracy and integrity. Provide training and support to staff members on data management best practices. Ensure timely delivery of high-quality data products to stakeholders. Job Requirements Strong knowledge of Good Clinical Practice (GCP) principles and regulations. Experience with clinical trial databases and data management systems. Excellent analytical and problem-solving skills with at...