684 Meddra Jobs - Page 18

Job Overview Assist with the overall Clinical Safety and/or PSS operations associated with products including the entire adverse events process: which may include safety data collected from clinical trials and/or post marketing setting (i.e., unsolicited reports). Manage and process expeditable adverse events to the required standard and submit them to the client and the regulatory agencies (if required) within the agreed/stated timelines. Responsible for providing this service to clients either as a support function to the client project groups or as stand- alone business. Responsible to provide all clients, both internal and external, with the appropriate quality of service in a safe and c...

Skill required: Pharmacovigilance Operations - Pharmacovigilance & Drug Safety Surveillance Designation: Pharmacovigilance Services New Associate Qualifications: BSc/Bachelor of Pharmacy Years of Experience: 0 to 1 years Language - Ability: English(International) - Proficient 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. ...

We are looking for a skilled and dedicated Safety & Pharmacovigilance Specialist to join our team. This role is responsible for the collection, processing, and reporting of adverse event data, ensuring compliance with global regulations and company standards. The ideal candidate will have hands-on experience in pharmacovigilance and a strong understanding of safety reporting requirements to contribute to patient safety. Roles & Responsibilities Case Processing: Perform end-to-end management of Individual Case Safety Reports (ICSRs) , including data entry, coding of adverse events using MedDRA , and drug coding using WHO-DD . Ensure timely and accurate processing of adverse event reports from...

You will be working as a Clinical Data Coder 1 with a focus on MedDRA and WHODD coding. With 2-5 years of work experience, the role is based in Bangalore and requires office-based work. Your key skills will include expertise in MedDRA, WHODD, clinical data coding, and clinical coding. As a Clinical Data Coder, you will provide essential data management support to the Data Management team to meet sponsor and company requirements effectively. You will be responsible for Clinical Data Management and/or Coding activities, potentially leading as a Lead Coder or Data Operations Coordinator for specific tasks on mega trials. Your main responsibilities will include managing coding activities and pro...

As a Clinical Coding Specialist at Bengaluru Luxor North Tower, your primary responsibility will be to generate and maintain sets of medical and pharmacy codes for use in defining conditions, events, and treatments in studies using healthcare data. You will be required to drive stakeholder engagement by identifying coding needs for upcoming studies and providing expert consultation on code set selection. Additionally, you will maintain a coding library platform, support the re-use of defined code sets, and collaborate on automation in the code list generation process. Your role will also involve conducting effective literature reviews, documenting and archiving code lists, updating data dict...

As a Medical Reviewer, you will be responsible for reviewing Periodic Adverse Drug Experience Reports (PADERs) and periodic safety update reports (PSURs/PBRERs) in compliance with drug safety regulations and ICH guidelines Your role involves utilizing medical judgment to analyze adverse reports, resolving queries, and supporting global new product development (NPD) project teams and Product Life Cycle Management (PLCM) activities Primary Responsibilities: Medical review of PADERs and PSURs/PBRERs ensuring compliance with regulations and guidelines. Maintain awareness of safety issues on Apotex products through ongoing monitoring and literature review. Prepare responses to complex safety quer...

key Responsibilities Data Coding: Execute clinical medical data coding tasks for assigned projects, including activities during study start-up , maintenance , and completion stages. Career Development: Collaborate with management to enhance career growth , interpersonal skills , and meet competency standards . Collaboration: Partner with the Coding team and Lead Data Reviewer to provide project-specific coding updates and implement solutions to coding-related issues. Documentation Review: Review the Data Management Plan (DMP) and Study-Specific Dictionary Coding Conventions to ensure accuracy and alignment with coding standards. Quality Assurance: Support the setup , maintenance , and closur...

Key Responsibilities Case Management and Reporting Support the Pharmacovigilance team in collecting, tracking, and processing Adverse Events (AEs) from all sources with accuracy and efficiency. Independently triage AEs to determine reportability in compliance with regulatory guidelines and clinical assessment standards. Code AEs using MedDRA and WHODRUG , applying clinical judgment to ensure correct categorization. Conduct quality control checks on case data to ensure accuracy, consistency, and completeness in safety databases and regulatory reporting forms (e.g., MedWatch, CIOMS I). Regulatory Compliance and Documentation Ensure timely submission of expedited case reports to regulatory auth...

You will be responsible for providing support for medical safety management within the Patient Safety & Pharmacovigilance department. This includes conducting medical review and assessments of Individual Case Safety Reports (ICSR), aggregate reports, co-authoring safety documents, and assisting in providing safety input to regulatory and clinical documents, as well as ad-hoc Health Authority queries. Your role will involve creating quality deliverables within agreed timeframes and maintaining a high standard of accuracy in compliance with patient safety business rules, standard operating procedures, and global and local regulatory requirements. Additionally, you will be supporting in definin...

We're Hiring: Junior Pharmacovigilance Specialist Location: Pune | Full-Time | Entry-Level / 01 Year Experience Are you a Life Science or Pharmacy graduate looking to kickstart your career in Pharmacovigilance Join our growing team and play a key role in ensuring drug safety and patient well-being through adverse event reporting and regulatory compliance, ???? Role Highlights ?? Analyze & process adverse event reports ?? Prepare regulatory safety submissions ?? Follow GCP, GDP, ICH & MedDRA coding standards ?? Collaborate with project managers and team leads ?? Ensure data accuracy and audit readiness ???? What Were Looking For ??? B Pharm / M Pharm Graduates ???? Freshers ???? Familiarity w...

Looking for a motivated individual to join our team as a Trainee Medical Reviewer in Bengaluru. The ideal candidate should have 0-1 years of experience. Roles and Responsibility Conduct thorough medical reviews of patient records and reports to ensure accuracy and compliance with regulatory requirements. Collaborate with cross-functional teams to identify and resolve issues related to medical review. Develop and maintain expertise in medical terminology, regulations, and guidelines. Provide high-quality support to internal stakeholders through effective communication and documentation. Stay updated with changes in regulations and guidelines affecting medical review processes. Participate in ...

As a Clinical Data Coder 1 specializing in MedDRA and WHODD, with 2-5 years of work experience, your primary responsibility will be to provide comprehensive data management expertise to the Data Management (DM) team for meeting sponsor and company needs. You will be involved in performing Clinical Data Management and/or Coding activities, taking on leadership roles such as Lead Coder or Data Operations Coordinator (DOC) for specific CDM tasks, or leading coding tasks on mega trials. In this role, you will independently manage coding activities and projects throughout the full study life-cycle, ensuring high quality and timely delivery with minimal guidance. Your responsibilities will include...

Hiring | Full Stack .NET Developer Location: Hyderabad / Remote Contract Position Share your resume with Current CTC, Expected CTC & Location to: [your email here] Job Title: Full Stack Developer (.NET) Experience: 5+ Years Work Mode: Remote (Hyderabad preferred) Contract Duration: [Specify duration or ""Long-term/Extendable""] We are looking for a seasoned Full Stack Developer with extensive experience in .NET technologies, RESTful APIs, and Windows Services. This role requires a sharp problem-solver who can work independently, translate business needs into technical execution, and deliver high-performance applications. Key Responsibilities: Develop scalable applications using .NET (C#) wit...

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 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 ...

About The Role Skill required: Com.Bkg- Commercial Real Estate - Real Estate Due Diligence Designation: Banking Advisory Senior Analyst Qualifications: BCom Years of Experience: 5 to 8 years Language - Ability: English(Domestic) - Intermediate 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 Wha...

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 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 ...

We are looking for a highly skilled and experienced Pharmacist to join our team at MAX Hospital in Noida. The ideal candidate will have 3 to 8 years of experience in the pharmaceutical industry, with a strong background in pharmacy practice. Roles and Responsibility Dispense medications to patients and provide counseling on their proper use. Manage inventory and maintain accurate records of prescriptions and dispensing activities. Collaborate with healthcare professionals to develop and implement medication therapy plans. Conduct patient assessments and monitor their response to medication therapy. Develop and implement pharmacy protocols and procedures. Participate in quality improvement in...

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 ...

About The Role Skill required: Com.Bkg- Commercial Real Estate - Real Estate Due Diligence Designation: Banking Advisory Associate Qualifications: Any Graduation Years of Experience: 1 to 3 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 We help clients address quality a...

The Infection Control Nurse at Manipal Hospitals will be responsible for monitoring and preventing infections within the healthcare facility. This role involves developing and implementing infection control policies, protocols, and practices to ensure the safety of patients, staff, and visitors. The nurse will conduct regular training sessions for healthcare personnel to promote awareness of infection control measures. Additionally, the Infection Control Nurse will collect and analyze data related to infection rates, investigate outbreaks, and report findings to the healthcare team and relevant authorities. Collaborating with multidisciplinary teams will be crucial for achieving the organiza...

Job Title : Pharmacovigilance Specialist Location : Bangalore / Hyderabad Experience : Minimum 4 Years in PV ICSR Job Summary We are seeking a skilled and detail-oriented Pharmacovigilance (PV) Specialist with hands-on experience in Individual Case Safety Reports (ICSR) . The ideal candidate will be responsible for end-to-end case processing and ensuring compliance with global PV regulations and internal SOPs. Key Responsibilities : Perform case intake, triage, data entry, quality review, and submission of ICSRs. Evaluate and code adverse event reports using MedDRA and WHO-DD coding. Ensure timely reporting of adverse events to regulatory authorities and clients. Maintain compliance with pha...

Job Title : Pharmacovigilance Specialist Location : Bangalore / Hyderabad Experience : Minimum 2 Years in PV ICSR Job Summary We are seeking a skilled and detail-oriented Pharmacovigilance (PV) Specialist with hands-on experience in Individual Case Safety Reports (ICSR) . The ideal candidate will be responsible for end-to-end case processing and ensuring compliance with global PV regulations and internal SOPs. Key Responsibilities : Perform case intake, triage, data entry, quality review, and submission of ICSRs. Evaluate and code adverse event reports using MedDRA and WHO-DD coding. Ensure timely reporting of adverse events to regulatory authorities and clients. Maintain compliance with pha...

Role & responsibilities The responsibilities of the role include processing Individual Case Safety Reports (ICSRs) and conducting literature screening activities. The candidate will be responsible for reviewing and assessing the validity of literature abstracts and articles, with further processing into the safety database as required. Additionally, the role involves maintaining the Extended Eudravigilance Medical Product Dictionary (XEVMPD) and performing EVWEB updates, including revisions to the Summary of Product Characteristics (SPC/SmPC) and Patient Information Leaflets (PILs). The candidate will also perform comparative reviews of SmPC and PIL documents against reference products. A ke...

Role & responsibilities We are seeking a Pharmacovigilance Associate with 2 to 3 years of experience in the pharmaceutical industry. The ideal candidate should have hands-on experience in processing Individual Case Safety Reports (ICSRs) and performing literature screening to identify safety information. This includes assessing validity of literature abstracts/articles for database entry. The role also involves maintaining XEVMPD, performing EVWEB updates, revising SmPCs, PILs, and preparing Risk Management Plans (RMPs). Monitoring safety updates/signals and ensuring SOP & regulatory compliance is essential. Preferred candidate profile Eudravigilance, XEVMPD Maintenance, EVWEB Updates, SmPC ...

ProductLife Group is looking for Medical Reviewers, having 3-4 years of experience with MBBS/MD degree. Responsibilities: We are looking for a medical reviewer proficient in post-marketing drug safety. Post-Marketing (Pharmacovigilance) Medical review of the ICSRs (Spontaneous, literature, clinical studies) Support in seriousness assessment, Initial Triage Support in causality, medical assessment, benefit-risk evaluation of the medicinal product. perform additional review of cases to ensure competency. Participate in audits and inspections as required Ensure understanding of client needs, conventions and ensure expectations are met and exceeded Training and mentoring other team members on go...