610 Case Processing Jobs - Page 7

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...

Our Product Support team for MedTech Insights is looking for Healthcare & Research Data Analyst. Join this small, collaborative group responsible for the quality control of market research reports and other product lines. The Product Support team works closely with our market research analyst group and other internal departments to produce high-quality deliverables. Talented analysts will experience numerous exciting opportunities during their tenure at Clarivate, including learning about growing and dynamic medical markets across the globe, working on a variety of Clarivate product lines, and interacting with different teams across the company. Its a wonderful opportunity for a strong criti...

The person is responsible for responding to and resolving customer problems via calls, emails and remote access for Aptean products. The support focuses on in-depth problem analysis of Aptean products and their integration into enterprise-wide mixed environments. Isolate and provide resolution to customer issues or qualify them for further assistance from R&D or other functions. Responsible for problem tracking, diagnosis, replication, troubleshooting and resolution. Should be able to work independently, showing empathy and sense of urgency to escalate customer issues and collaborate to provide timely resolution. Should adhere to department performance goals and production standards. Should ...

Quality Assurance based in Waghodia, Vadodara. The ideal candidate brings 3-10 Years and a strong record of GMP/cGMP compliance within regulated pharma, chemicals or biotech environments. Key responsibilities include ownership of day-to-day operations, documentation integrity, SOP creation/review, deviation/OOS handling, CAPA and change control management, audit readiness, cross-functional coordination with Production, QC, Engineering and Supply Chain, and proactive risk assessment to protect product quality and patient safety. The role requires hands-on problem solving, stakeholder communication, coaching junior staff, and contribution to continuous improvement (5S/Lean/Kaizen). Strengthen ...

Quality Control based in Waghodia, Vadodara The ideal candidate brings 4-7 Years and a strong record of GMP/cGMP compliance within regulated pharma, chemicals or biotech environments Key responsibilities include ownership of day-to-day operations, documentation integrity, SOP creation/review, deviation/OOS handling, CAPA and change control management, audit readiness, cross-functional coordination with Production, QC, Engineering and Supply Chain, and proactive risk assessment to protect product quality and patient safety The role requires hands-on problem solving, stakeholder communication, coaching junior staff, and contribution to continuous improvement (5S/Lean/Kaizen) Additional info: R...

We are looking for a dedicated and compassionate Nursing professional to join our team in the Healthcare industry. The ideal candidate will have a strong background in nursing and a passion for delivering high-quality patient care. Roles and Responsibility Provide exceptional nursing care to patients, including assessing, planning, implementing, and evaluating individualized care plans. Collaborate with interdisciplinary teams to develop and implement comprehensive care strategies that meet patient needs. Administer medications, perform medical procedures, and maintain accurate patient records. Educate patients and their families on healthy habits, disease prevention, and management of chron...

Role Overview: As a Data Entry and Case Processing Representative, your main responsibility is to represent clients on various projects by performing data entry and case processing of forms. You will manage day-to-day activities of patient and healthcare provider support requests through multiple communication channels such as fax, chat, and email. Your role involves performing intake of cases, capturing all relevant information in the Case Management system, ensuring timely and accurate processing of requests, and transcribing information into client databases accurately. Additionally, you will escalate complex cases when necessary and maintain excellent quality standards for all client pro...

Project Role : Business Process Architect Project Role Description : Analyze and design new business processes to create the documentation that guides the implementation of new processes and technologies. Partner with the business to define product requirements and use cases to meet process and functional requirements. Participate in user and task analysis to represent business needs. Must have skills : SAP PP Production Planning & Control Discrete Industries Good to have skills : NAMinimum 12 year(s) of experience is required Educational Qualification : 15 years full time education Summary :As a Business Process Architect, you will analyze and design new business processes to create the doc...

Case Management QA Vendor Sr Associate What you will do Support interactions with business partners (license partners) and vendors for all case intake and processing activities. Vendor oversight of all case intake and processing activities and case quality including analysis and reporting of trends in quality measures. Ensure vendor compliance with approved processes and training requirements. Submission of all individual case safety reports to FDA/EMA, business partners (license partners), and vendors. Act as US/EU local safety office and FDA/EMA point of contact for safety reporting. Provide audit & external inspection support. Assist in assuring quality of Individual Case Safety Report (I...

Reports To: Global Systematic Literature Review Team Lead Position Summary The Global Systematic Literature Review (SLR) Senior Associate provides expertise in designing, executing, and managing literature review services within Amgens Global HEOR function. The SLR Senior Associate will collaborate closely with team lead and Global HEOR Product Leads to align with HEOR product strategy. This role supports global access to Amgen's therapies through the generation of high-quality, evidence-based outputs across the product lifecycle. Key Responsibilities Refine literature review questions in alignment with team lead and prepare research protocols. Design literature searches for electronic datab...

What you will do The Global HEOR Systematic Literature Review (SLR) Leader oversees the development and delivery of systematic literature review activities within Amgens Global HEOR function. This operational and managerial role includes supervision of a team of Global HEOR SLR Analysts, ensuring high-quality, timely, and scientifically robust literature review outputs. The Global HEOR SLR Leader will align closely with Global HEOR TA Heads in support of global market access and value demonstration for Amgens products across their lifecycle. Lead, mentor, and handle a team of Global HEOR SLR Analysts, fostering a high-performance culture. Oversee the design, execution, and quality control of...

What you will do Support interactions with business partners (license partners) and vendors for all case intake and processing activities. Vendor oversight of all case intake and processing activities and case quality including analysis and reporting of trends in quality measures. Ensure vendor compliance with approved processes and training requirements. Submission of all individual case safety reports to FDA/EMA, business partners (license partners), and vendors. Act as US/EU local safety office and FDA/EMA point of contact for safety reporting. Provide audit & external inspection support. Assist in assuring quality of Individual Case Safety Report (ICSR) processing globally for clinical t...

What you will do In this vital role you will Prepare and oversee the preparation of regulatory submission documents that comply with global regulatory standards Write or oversee the writing of clinical study reports and Investigator Brochures for products in all phases of clinical development (phase 1 through 4) Write CTD sections including the Summary of Clinical Efficacy, Summary of Clinical Safety, Summary of Clinical Pharmacology, Summary of Biopharmaceutics, Clinical Overview, Table of All Studies, briefing documents, and safety documents, across therapeutic areas and for biosimilars (mandate) Write other regulatory submission documents (eg, RTQs, PIP, white papers, breakthrough therapy...

Role Description: The Scientific Communications MLR Technical Reviewer is responsible for checking all medical content for data and scientific accuracy, and reference appropriateness for materials submitted through the Medical, Legal, and Regulatory (MLR) process. This role ensures that all content adheres to Amgens scientific and compliance standards, while supporting timely review and approval of assets that inform and engage healthcare providers, patients, and internal stakeholders. Working closely with the US Scientific Communications MLR Reviewer, the Technical Reviewer brings scientific expertise, attention to detail, and compliance awareness to evaluate the submissions. This role cont...

Medcare Hospitals Medical Centres is looking for Registered Nurse - Nursing to join our dynamic team and embark on a rewarding career journey. Supervise nursing staff in a hospital or clinical settings. Oversee patient care, make management and budgetary decisions, set work schedules, coordinate meetings, and make personnel decisions. Recruit and train nurses and other health care professionals and maintain a facilitys records. Work with staff to apply emerging nursing theories to care delivery. Also implement state and federal regulatory guidelines for patient safety and educate staff about any changes in the laws and how they impact care delivery. Disclaimer: This job description has been ...

Medcare Hospitals Medical Centres is looking for Charge Nurse - Nursing Services to join our dynamic team and embark on a rewarding career journey. Supervise nursing staff in a hospital or clinical settings. Oversee patient care, make management and budgetary decisions, set work schedules, coordinate meetings, and make personnel decisions. Recruit and train nurses and other health care professionals and maintain a facilitys records. Work with staff to apply emerging nursing theories to care delivery. Also implement state and federal regulatory guidelines for patient safety and educate staff about any changes in the laws and how they impact care delivery. Disclaimer : This job description has...

Medcare Hospitals Medical Centres is looking for Senior Registered Nurse - Nursing Services to join our dynamic team and embark on a rewarding career journey. Supervise nursing staff in a hospital or clinical settings. Oversee patient care, make management and budgetary decisions, set work schedules, coordinate meetings, and make personnel decisions. Recruit and train nurses and other health care professionals and maintain a facilitys records. Work with staff to apply emerging nursing theories to care delivery. Also implement state and federal regulatory guidelines for patient safety and educate staff about any changes in the laws and how they impact care delivery. Disclaimer: This job descr...

Employment Type: Full time, Regular, Hybrid work arrangement Roles and Responsibilities Primary Duties Ready to work in 24/7 shift timings. Excellent communication (written and oral) and interpersonal skills Monitor security systems and networks for suspicious activity. Validating alert triggered by security information and event management (SIEM) tools. Triage events and investigate to identify security incidents. Investigate security incidents and determine their severity. Contribute to incident response, maintaining relevant communication and information in emails, ticket summaries, analysis and reporting. Escalate security incidents to the next level for further investigation. Make recom...

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...

Support Associate Director ESP Engagements for the setup of new global ESPs. Support Associate Director ESP Engagements with contract setup & management. Support ESP account management including but not limited to GDDB account, Citrix account, maintenance of dashboard & data etc. Collaborate and support PS&PV QA in QMS implementation for outsourced activities. Support ESP Engagements team for the implementation of ESP governance and oversight of the outsourced activities. Support oversight of process improvement and innovation initiatives at ESPs. Act as Point of Contact (POC) for ESP IT issues. Supports ESP Engagements team to supervise compliance and quality of ESPs performing activities o...

Assist the Principal Investigator in fieldwork, data collection, and analysis. Draft, refine, and administer research tools such as questionnaires and interview schedules. Conduct literature review and support preparation of research reports. Coordinate with participants, stakeholders, and institutions relevant to the project. Assist in documentation, progress reports, and dissemination of project findings.

Job Details Performing triage and review for initial validity assessment of cases including spontaneous, health authority, Clinical Trial and literature cases. Responsible for quality management, workload management, compliance management and document management for the assigned PV projects Evaluation of the need for expedited reporting to Health Authorities / partners of a client concerned, including reporting timelines Preparation of standard reporting forms (e.g., CIOMS I / MedWatch Forms and XML Preparation and sending of follow up requests Submission of ICSRs to Health Authorities and partners of a client Acts as line manager of assigned staff Manages project coordination and resource a...

Role Overview: As a Medical Safety Expert, your primary role will be to provide medical safety expertise to Sponsors of drugs, devices, and combination products during the post-marketing period. You will be responsible for undertaking the primary medical review of cases, updating and documenting case data, and assuming complete responsibility for assigned deliverables while maintaining quality, compliance, and productivity standards. Additionally, you will provide training and guidance to the case processing team on medical aspects of case processing. Key Responsibilities: - Undertake primary medical review of cases including assessment for seriousness, listedness/labeling, causality, advers...

Skill required: Pharmacovigilance Services - Pharmacovigilance & Drug Safety Surveillance Designation: Delivery Lead Manager Qualifications: MD Years of Experience: 13 to 18 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 converging around the patie...

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...