Average salary: Rs289,716 /yearly
More stats ...solutions drive job opportunities and satisfaction for all stakeholders.
Role Description
This is a full-time on-site role for a Pharmacovigilance Trainer. The Pharmacovigilance Trainer will be responsible for developing and delivering training programs on pharmacovigilance...
Technoledge
Noida
1 day ago
...complete product lifecycle. With deep domain expertise in regulatory sciences, clinical research solutions, quality compliance, pharmacovigilance, medical information, and RD technology, ProPharma offers an end-to-end suite of fully customizable consulting solutions that de...
...Pharmacovigilance Associate Responsibilities:
Process and manage adverse event reports: This includes reviewing AE reports from healthcare professionals, patients, and other sources. They need to assess the seriousness of the event and determine whether it needs to be...
...Job Description
• Is the Single Point of Contact (SPOC) for the contracted Pharmacovigilance activities and assists Project Manager for project operation oversight.
• Provide oversight and direction of all Pharmacovigilance services/ activities throughout the duration...
...Job Description
Skill required: Pharmacovigilance Services - Pharmacovigilance & Drug Safety Surveillance
Designation: Pharmacovigilance Services Specialist
Qualifications: MBBS
Years of Experience: 7 to 11 years
Language - Ability: English - Proficient...
...serve as the main point of contact for the customer for the life-cycle of assigned stand alone projects and programs, and the main pharmacovigilance point of contact for assigned full-service projects
• Develops, implements, and monitors profitability, objectives, metrics of...
...and accurately.
• Serve as Functional Lead on case processing or medical information projects as assigned; coordinates teams of Pharmacovigilance associates on project level and serves as the Pharmacovigilance point of contact for project teams.
• Effectively maintains...
Remote job
...Pharmacovigilance Associate- Freshers
Essential Duties and Responsibilities
Collect and evaluate adverse event reports from various sources, including healthcare professionals, patients, and drug company representatives
Assess the severity and causality of adverse...
...Job Description
Skill required: Pharmacovigilance Operations - Pharmacovigilance & Drug Safety Surveillance
Designation: Pharmacovigilance Services New Associate
Qualifications: Bachelor of Pharmacy/Master of Pharmacy
Years of Experience: 0 to 1 years
Language...
...accuracy will improve health outcomes that people and communities depend on – now and in the future.
Our detailed, goal-oriented Pharmacovigilance colleagues manage the safety profile of new drugs in clinical trials, oversee case-processing activities through all phases of...
Remote job
...named Vantive) remains subject to the satisfaction of customary conditions.
This position is a member of Global Patient Safety – Pharmacovigilance Compliance and Safety Operations -PV Technology and Systems support team. This position is a Team Lead position and is...
...Responsibilities for pharmacovigilance scientist
- Act as core member for assigned products
- Ensure timely, quality reports/safety analyses related to core deliverables with oversight as appropriate
- Provide complete PVRM product life-cycle support for assigned product...
...Position : MICC Executive (Pharmacovigilance)
Experience : 0-3 Years
Qualification : M. Pharm /B. Pharm/ B.sc/ M.sc
Location : Gota Ahmedabad
Salary - Up to 4 Lacs
JD:
- Receive and process assigned voicemails
- Update the Voicemail Tracker
- Receive information...
...submissions, clinical trials, marketing authorization applications (MAA), chemistry manufacturing and controls (CMC), CMC variations, pharmacovigilance projects, and regulatory strategy, among others, and we would love to speak with you if you have any of the skills or expertise...
...changes on authority website, communicate to global team and accordingly initiate the artwork revision.
To assist superior for Pharmacovigilance related activities
Be a proactive member of the Regulatory team to ensure Baxter's continuing compliance with FDA and other...
Rs 6 - 8 lakhs p.a.
...firm in the Pharmaceutical & Life Sciences sector, trusted for its expertise and commitment. Specializing in Regulatory Affairs, Pharmacovigilance, and GxP Compliance, we offer tailored solutions through our unique Commit-Collaborate-Carry Model, aimed at enhancing patient...
Rs 8 - 9 lakhs p.a.
...Company Overview:
Pharmazone is a leading Consulting company specializing in Regulatory Affairs, Pharmacovigilance, and GxP Compliance solutions for global clients. With a strong legacy of trust, we strive to improve patients' lives through our unique Commit-Collaborate...
...in the pharmaceutical industry.
Familiarity with digital health, competitive intelligence, disease understanding, statistics, pharmacovigilance, non-clinical and clinical pharmacology.
Knowledge of patient access, real-world evidence, and proficiency in written and...
...Preferred: 01 year work experience in job areas such as: o Clinical trial coordinator at site
Clinical data management
Pharmacovigilance
Records management
Key Personal Attributes:
Highly personable nature that fosters teamwork
Excellent communication skills...
...Preferred: 01 year work experience in job areas such as: o Clinical trial coordinator at site
Clinical data management
Pharmacovigilance
Records management
Key Personal Attributes:
Highly personable nature that fosters teamwork
Excellent communication skills...
...personnel: Clinical Research Managers, Clinical Operations Managers, Medical Advisors; Medical Information team / specialists; EPD Pharmacovigilance / drug safety personnel
•Marketing department across therapeutic area
• Sales organization of the geographic area of...
...experience in areas such as Clinical Data Review,
relevant experience in Clinical Data Management,
relevant experience in Pharmacovigilance
relevant experience in Clinical Project Management.
Please use the below link for job application and quicker response....
...subject/patient’s safety and clinical data integrity at an investigator/physician site such as protocol deviation/violations and pharmacovigilance issues.
• Immediately communicates/escalates serious issues to the project team and with guidance develops action plans....
...publication in peer-reviewed journals on original research and review article.
Work in Clinical Trials, Regulatory Affairs, Pharmacovigilance etc.
Involves coordination with R&D, QA department, CROs for submission of dossiers for product registration.
Participates...
...take complete ownership of requirement gathering, workshop, design, development, and product implementation cycles by providing Pharmacovigilance domain, Oracle products & services and solution skills in an individual as well as team capacity.
Key technical areas include...
...and in the future.
Purpose:
Subject matter expert of day-to-day application configuration and maintenance activities of the Pharmacovigilance (PV) Safety database Oracle Argus, ensuring that performed tasks comply with SOPs and policies, industry standards, and...
...and ensures timely close out w/ all proper documentation in Astellas systems.
Actively collect as well as guide PS to collect pharmacovigilance information such as adverse events (“AE”), special situations
KOL Relationship Management
Engage with potential...
...partners to implement cross-functional processes, technologies, solutions, and services, supporting innovation in technology enabled Pharmacovigilance Operations to continuously improve PS&PV organizational performance. Accountable for implementation and continuous improvement...
...ethnicities. We recognize this is our strength and celebrate it.
Key words: Aggregate Report Physician, MD, Medical Doctor, MBS, Pharmacovigilance, PV, GVP, Signal Management, Risk Management, Aggregate Report, PBRER, Clinical Research, CRO, Contract Research Organisation,...
...and understanding of business management principles.
Knowledge of R&D value chain, digital health, competitive intelligence, pharmacovigilance, clinical pharmacology, market access, and real-world evidence generation preferred.
About the Department
The RA Labelling...