610 Case Processing Jobs - Page 8

Skill required: Pharmacovigilance Services - Pharmacovigilance & Drug Safety Surveillance Designation: Pharmacovigilance Services New Associate Qualifications: Bachelor of Pharmacy,BSc. Nursing,Bachelor of Physiotheraphy Years of Experience: 1 to 2 year 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.accentu...

Immediate Openings on Business Consultant _ Gurgaon_Contract Skill: Business Consultant Notice Period: Immediate . Employment Type: Contract Working Mode : Hybrid Job Description Top 3 skills which is mandatory Aris, BPM, Functional and Technical Setup and ongoing maintenance and oversight of the ARIS architecture & libraries Design and develop the reporting capabilities on ARIS to meet the requirements of the Group Configuration of ARIS system for the Process Mapping team ensuring it remains fit for purpose for the Group`s requirements. Develop detailed understanding of ARIS standard setup and functionality Responsibility for the day-to-day administration of ARIS including user set up, lice...

About The Role Skill required: Pharmacovigilance Operations - Pharmacovigilance & Drug Safety Surveillance Designation: Pharmacovigilance Services Associate Qualifications: 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 li...

Our Team: Sanofi Business Operations (SBO) is an internal Sanofi resource organization setup to centralize processes and activities to support Specialty Care, Vaccines, General Medicines, CHC, CMO, and R&D, Data & Digital functions SBO strives to be a strategic and functional partner for tactical deliveries to Medical, HEVA, and Commercial organizations in Sanofi, Globally Main responsibilities: The overall purpose and main responsibilities are listed below: Responsible for project management support to the scientific writer ensuring the end-to-end effective project delivery of the designated publication/medical education deliverable across all phases Initiate and amend submission based on c...

Main responsibilities: The overall purpose and main responsibilities are listed below: Responsible for project management support to the scientific writer ensuring the end-to-end effective project delivery of the designated publication/medical education deliverable across all phases. Initiate and amend submission based on comments (as required). Support the writer with internal and external stakeholder communication. Track the delivery of activities (including managing issues and risks) and support follow up. Support required submission, compliance/ approval activities, and ensure compliance with publication processes and end-to-end publication management tools (e.g., iEnvision - previously,...

Assist Data Management Study Lead in maintenance of eCRF, Data Validation Specifications, and Study Specific Procedures. Manage clinical and third-party data reconciliation based on edit specifications and data review plans. Tracks and communicates status of study and task metrics to clinical data scientist, project team, and functional management. Address data related questions and recommend potential solutions. Identify root cause to systematically resolve data issues. Your profile Bachelors degree in a relevant field, such as Life Sciences or Healthcare. Intermediate kNwledge of clinical data management within the pharmaceutical or biotechNlogy industry. Familiarity with data management s...

Contribute to the creation and maintenance of risk management plans & provides support for the effective implementation of Additional Risk Minimisation measures. Safety mailbox and communications management. Support Aggregate Report related activities. Maintenance of PV Awareness and other related Training content. Implementation of Pharmacovigilance Agreements. Individual Case Safety Report (ICSR) related activities, including literature screening, and submissions to local Health Authorities and Ethics Committees. Safety Data Quality activities e. g. PV System Master File maintenance, deviations/CAPA management, other quality control and oversight activities. Compilation of PV-related docum...

Roles and Responsibility Coordinate and manage regulatory submissions, ensuring compliance with relevant laws and regulations. Develop and implement effective submission strategies to achieve business objectives. Collaborate with cross-functional teams to ensure timely and accurate submissions. Conduct thorough reviews of submissions to identify areas for improvement. Maintain accurate records of submissions and follow up on pending submissions. Stay updated with changes in regulatory requirements and guidelines. Job Requirements Strong knowledge of regulatory submissions and compliance. Excellent communication and project management skills. Ability to work in a fast-paced environment and me...

Roles and Responsibility Publish regulatory submissions on time, ensuring accuracy and compliance with relevant regulations. Collaborate with cross-functional teams to prepare and review regulatory documents. Develop and maintain relationships with regulatory authorities and stakeholders. Stay updated with changes in regulatory requirements and implement necessary updates. Ensure all regulatory submissions meet required standards and quality criteria. Coordinate with internal teams to gather information and support for regulatory submissions. Job Requirements Strong knowledge of regulatory requirements and guidelines. Excellent communication and interpersonal skills. Ability to work independ...

Roles and Responsibility Conduct thorough medical reviews of patient data to ensure accuracy and compliance with regulatory requirements. Collaborate with cross-functional teams to identify and resolve issues related to medical review. Develop and implement effective strategies to improve medical review processes and outcomes. Provide expert guidance on medical review best practices to junior team members. Stay up-to-date with changing regulations and guidelines related to medical review. Participate in quality improvement initiatives to enhance medical review efficiency and effectiveness. Job Requirements Strong knowledge of medical terminology and regulatory requirements. Excellent analyti...

Roles and Responsibility Conduct thorough medical reviews of device-related documents, including clinical trial protocols and study reports. Collaborate with cross-functional teams to ensure compliance with regulatory requirements and industry standards. Develop and maintain expertise in medical devices and equipment, staying up-to-date on new technologies and trends. Provide guidance and support to junior staff members on medical review processes and procedures. Participate in quality improvement initiatives to enhance the efficiency and effectiveness of medical review activities. Communicate complex technical information effectively to non-technical stakeholders through written reports and...

Roles and Responsibility Collaborate with cross-functional teams to develop and implement clinical research studies. Provide medical expertise and guidance on study design, methodology, and statistical analysis. Develop and maintain relationships with key stakeholders, including investigators, sponsors, and regulatory agencies. Conduct thorough reviews of study protocols, informed consent forms, and other study-related documents. Ensure compliance with regulatory requirements and company policies. Participate in ongoing quality improvement initiatives to enhance study delivery. Job Requirements Strong understanding of clinical research principles, regulations, and guidelines. Excellent commu...

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 data quality and integrity. Analyze and resolve complex data-related issues and discrepancies. Ensure compliance with regulatory requirements and industry standards. Provide training and support to junior staff members on data management best practices. Job Requirements Strong knowledge of clinical data management principles and practices. Experience with data analysis and reporting tools such as SAS or R. Excellent problem-solving skills and attention to detail. Ability to work effect...

Skill required: Pharmacovigilance Services - Safety Writing Designation: Pharmacovigilance Services Sr Analyst Qualifications: Bachelor of Pharmacy Years of Experience: 5 to 8 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 ...

About The Role Skill required: Pharmacovigilance Services - Pharmacovigilance & Drug Safety Surveillance Designation: Pharmacovigilance Services Specialist Qualifications: MBBS Years of Experience: 7 to 11 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 outcome...

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...

Conduct thorough medical reviews of devices and their associated documentation. Collaborate with cross-functional teams to ensure compliance with regulatory requirements. Develop and maintain expertise in medical terminology and device regulations. Provide guidance on medical aspects of device development and implementation. Stay updated with changing trends and developments in medical technology. Participate in quality improvement initiatives to enhance review processes. Job Requirements Strong understanding of medical terminology and device regulations. Excellent analytical and problem-solving skills. Ability to work effectively in a team environment. Effective communication and interperso...

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...

Collaborate with cross-functional teams to develop and implement clinical research studies. Provide medical advisory services to clients on clinical trial design, methodology, and statistical analysis. Develop and maintain relationships with key stakeholders, including investigators, sponsors, and regulatory agencies. Conduct site feasibility assessments and coordinate with investigators to ensure successful study execution. Review and approve clinical protocols, informed consent forms, and other study-related documents. Stay up-to-date with industry trends and developments in clinical research. Job Requirements Minimum 2 years of experience in clinical research or a related field. Strong kn...

Develop and implement aggregate reporting solutions to meet business requirements. Collaborate with cross-functional teams to identify and prioritize reporting needs. Design and maintain complex reports using various reporting tools and technologies. Analyze data to identify trends and patterns, providing insights to stakeholders. Ensure data accuracy and integrity in all reports and dashboards. Provide training and support to end-users on reporting tools and technologies. Job Requirements Strong understanding of aggregate reporting principles and methodologies. Proficiency in designing and developing complex reports using various reporting tools and technologies. Excellent analytical and pr...

Conduct thorough analysis of clinical trial data to identify potential safety concerns. Develop and implement effective safety protocols to mitigate risks associated with medical devices. Collaborate with cross-functional teams to ensure compliance with regulatory requirements. Perform risk assessments and provide recommendations for improving patient safety. Monitor and report adverse events related to medical devices. Stay updated with changing regulations and guidelines related to clinical safety. Job Requirements Strong understanding of clinical trials, safety protocols, and regulatory requirements. Experience working with medical devices and their applications. Excellent analytical and ...

Manage and analyze aggregate reporting data to provide insights and recommendations. Develop and implement effective reporting strategies to meet business needs. Collaborate with cross-functional teams to ensure accurate and timely reporting. Identify and resolve issues related to reporting data quality and integrity. Develop and maintain complex reports using various reporting tools and technologies. Provide expert guidance on reporting best practices and standards. Job Requirements Strong understanding of aggregate reporting principles and methodologies. Proficiency in analyzing large datasets and providing actionable insights. Excellent communication and interpersonal skills, with the abi...

Manage and analyze aggregate reporting data to provide insights and recommendations. Develop and implement effective reporting strategies to meet business needs. Collaborate with cross-functional teams to ensure accurate and timely reporting. Identify and mitigate risks associated with reporting processes. Develop and maintain relationships with stakeholders to ensure effective communication. Stay up-to-date with industry trends and best practices in aggregate reporting. Job Requirements Strong understanding of aggregate reporting principles and methodologies. Experience with data analysis and interpretation to inform business decisions. Excellent communication and interpersonal skills. Abil...

Roles and Responsibility Collaborate with cross-functional teams to ensure successful clinical trial execution. Provide medical expertise and guidance on clinical trial protocols and procedures. Conduct site feasibility assessments and coordinate with investigators. Develop and maintain relationships with key stakeholders, including sponsors and regulatory agencies. Ensure compliance with regulatory requirements and company policies. Participate in risk assessment and mitigation strategies for clinical trials. Job Requirements Strong knowledge of clinical trial regulations and guidelines. Excellent communication and interpersonal skills. Ability to work effectively in a fast-paced environmen...