Senior Pharmacovigilance Coordinator, Case Processing
2 days ago
For the past 20 years, ProPharma has improved the health and wellness of patients by providing advice and expertise that empowers biotech, med device, and pharmaceutical organizations of all sizes to confidently advance scientific breakthroughs and introduce new therapies. As the world’s largest RCO (Research Consulting Organization), ProPharma partners with its clients through an advise-build-operate model across the complete product lifecycle. With deep domain expertise in regulatory sciences, clinical research solutions, quality & compliance, pharmacovigilance, medical information, and R&D technology, ProPharma offers an end-to-end suite of fully customizable consulting solutions that de-risk and accelerate our partners’ most high-profile drug and device programs. Job Summary: The Senior Pharmacovigilance (PV) Coordinator, Case Processing assists PV Coordinator staff with entry of cases in the safety database. The Senior PV Coordinator oversees assigned mailboxes for client communications and assists with triaging questions. The Senior PV Coordinator maintains distinctive quality and commitment as the operating philosophy in carrying out all processes and continually seeks out ways to enhance customer service experience both internally and externally. The Senior PV Coordinator will be professional, diligent and liaise with Senior members on the team on any issues. The expectation is to lead by example and ensure quality standards are upheld. Essential Functions: Manage assigned mailboxes, including inbox triage of client communication, inbound reports, and internal case processing communications. Perform Duplicate searches and complete initial book-in as required. Screen and redact the source documents for PHI as per company procedures. Facilitate literature related activities as needed. Initial triage of regulatory authority database searches. Send draft reports to clients for review as needed. Enter basic data into safety database as required such as identifiable patient, report, suspect drug, and adverse event. As applicable perform full data entry into safety databased with proper experience and training. Help oversee team workload and client deliverables to make sure that daily/weekly goals are hit by the collective intake team as needed. Other duties as assigned. Necessary Skills and Abilities: Strong verbal, written and interpersonal communication skills. Proficient computer knowledge and computer keyboarding skills. Strong organization and prioritization skills, with strong attention to detail. Ability to work independently and within in interdisciplinary a team. Educational Requirements: Post-secondary education. Experience Requirements: Required: one year of related work experience. Preferred: one year of industry experience. We celebrate our differences and strive to create a workplace where each person can be their authentic self. We are committed to diversity, equity, and inclusion. Employees are encouraged to unleash their innovative, collaborative, and entrepreneurial spirits. With a holistic approach as an Equal Opportunity Employer, we provide a safe space where all employees feel empowered to succeed. ***ProPharma Group does not accept unsolicited resumes from recruiters/third parties. Please, no phone calls or emails to anyone regarding this posting.***
-
Team Leader
9 hours ago
Bengaluru, India Elanco Full timeJob Description At Elanco (NYSE: ELAN) it all starts with animals! As a global leader in animal health, we are dedicated to innovation and delivering products and services to prevent and treat disease in farm animals and pets. At Elanco, we are driven by our vision of Food and Companionship Enriching Life and our purpose all to Go Beyond for Animals,...
-
India ProPharma Group Full timeFor the past 20 years, ProPharma has improved the health and wellness of patients by providing advice and expertise that empowers biotech, med device, and pharmaceutical organizations of all sizes to confidently advance scientific breakthroughs and introduce new therapies. ProPharma partners with its clients through an advise-build-operate model across the...
-
Senior Medical Safety Advisor
2 weeks ago
India IQVIA Full timeRole: Senior Medical Safety Advisor Work Experience: 5+ Years. Clinical Experience: 3+ Years. Pharmacovigilance/PV Experience : 2+ Years Work location: PAN India Work Mode: Home Based Must Have Skills: Pharmacovigilance, ICSR. Job Overview The objective of this position is to provide medical expertise in the evaluation of safety data from a variety of...
-
Senior Medical Safety Advisor
2 days ago
India IQVIA Full timeJob Description Role: Senior Medical Safety Advisor Work Experience: 5+ Years. Clinical Experience: 3+ Years. Pharmacovigilance/PV Experience: 2+ Years Work location: PAN India Work Mode: Home Based Must Have Skills: Pharmacovigilance, ICSR. Job Overview The objective of this position is to provide medical expertise in the evaluation of safety data from a...
-
Noida, India Clarivate Full timeJob Description The Associate pharmacovigilance specialist performs pharmacovigilance services such as biomedical literature monitoring and assessing for adverse events reporting, indexing, and abstracting by using broad knowledge of scientific terms and medical terminology, drugs and therapeutic areas, and pharmacovigilance regulations. About You -...
-
Senior Safety Database Specialist
7 days ago
Chandigarh, , India YD Talent Solutions Full time ₹ 12,00,000 - ₹ 24,00,000 per yearSenior Safety Database Specialist - Chandigarh, India Company Overview Our Client is a contract research organization offering Pharmacovigilance, Regulatory, Evidence Evaluation and Technology Solutions, which are phase dependent. These verticals cover planning, launch and lifecycle management of Pharmaceutical, Consumer products and Medical devices. We are...
-
Pharmacovigilance Associate
3 weeks ago
India Novo Tech Full timeJob Description JOB DESCRIPTION About the role The Drug Safety Associate is responsible for complete and accurate case processing of adverse event reports following company standard operating procedures, internal business practices and regulatory guidance documents, to ensure compliance with worldwide safety regulations Responsibilities: - Preparation of a...
-
Senior Safety Physician
7 days ago
India - Remote Praxis Precision Medicines Full time ₹ 34,85,000 - ₹ 42,00,000 per yearLocation: Remote - IndiaThis is a remote position based in India, with flexibility for occasional travel as determined by business needs. Due to system limitations, the role may appear as "United States" on some job platforms—please disregard this; we're actively seeking talent in India.The OpportunityWe are seeking a Senior Safety Physician in India...
-
Case Coordinator
1 week ago
New Delhi, , India Red Earth Migration Full time ₹ 2,50,000 - ₹ 5,00,000 per yearDocumentation Reviewing & Follow -ups Responsive & Reminders mails to clients Looking For appropriate subclass for clients'Visa filling Arrange, Review & upload of documentsRequirementsClient Assessment2. Document Checklist and Application Process Guidance3. Documentation Review and Preparation4. Visa Application Preparation5. Liaison with Authorities6....
-
Analyst - R&D
1 week ago
All India Elanco Full time ₹ 6,00,000 - ₹ 12,00,000 per yearRole Overview: At Elanco, as an Analyst in R&D, you will be responsible for managing adverse event reports, ensuring data accuracy, and maintaining compliance with global pharmacovigilance regulations and timelines. Your role will involve data entry, seriousness assessment, causality assessment, and ensuring the completeness and quality of cases for...
