Average salary: Rs237,500 /yearly
More statsSearch Results: 54 vacancies
...Job Description
Skill required: Pharmacovigilance Operations - Safety Writing
Designation: Pharmacovigilance Services Associate
Qualifications: Master of Pharmacy
Years of Experience: 1 to 3 years
About Accenture
Accenture is a global professional services...
...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...
...products.
Cooperate with other teams within the Medical Scientific Unit and other relevant groups within and outside of Teva Pharmacovigilance.
Quality control of literature reviews performed within signal detection process.
Perform all assigned tasks in line with...
...people to make a difference with.
How you’ll spend your day
Core member of the safety team and is responsible for performing pharmacovigilance activities within the North American PV unit, in partnership with the Drug Safety Specialists/Pharmacovigilance Safety...
...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...
...experience in case processing
The PV Officer will be working as part of a project team, performing, and supporting contracted pharmacovigilance activities on behalf of PrimeVigilance
PV Officers are expected to reach and maintain a high level of performance within 3...
...medical background - healthcare related degree (chemistry, biology, biotechnology, veterinary science) and demonstrated experience in Pharmacovigilance case processing and QCing responsibilities
ARGUS/Aris G experience preferred
Time and issue management, delegation,...
...We are PrimeVigilance (part of Ergomed PLC), a specialised mid-size pharmacovigilance service provider initially established in 2008. We are proud to have achieved global organic growth year after year, with staff based across Europe, North America and Asia all covering...
...Preferred: 0-1 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...
...systematic errors, and potential lack of compliance or fraud across trials.
The Position: (Note: This is not a role within Pharmacovigilance)
The Key Responsibilities in this position will be to perform a Medical Review of all trial subjects of all assigned...
...regulatory interactions with health authorities, including preparing meeting requests, packages, and taking meeting minutes.
Pharmacovigilance documentation like Drug Safety Update Reports (DSUR), Periodic Safety Update Reports (PSUR), Risk Management Plan (RMP), renewals...
...Job Description
Our Clinical Research and Pharmacovigilance team push the boundaries of global healthcare through research and innovation. Through clinical trials and surveillance, we ensure the safety and efficacy of our existing and pipeline products to produce safe,...
...health authorities and policymakers to shape future regulatory frameworks. Our team also focuses on product safety through safety pharmacovigilance, ensuring medicines are safe to use. We collect, analyze, and report safety data, and continuously monitor for new safety...
...Clinical Research Manager, Clinical Operations Manager, Medical Managers/Advisers; Medical Information team / specialists; affiliate pharmacovigilance / drug safety personnel
Marketing and Sales (including district sales manager, and national sale managers) for assigned...
...in product development and/or management, including at least 2 years in agile product development processes.
A background in Pharmacovigilance domain is a must and should have good understanding on E2B submission regulations.
The ability to understand customers' needs...
...Clinical Practice (GCP)/Good Manufacturing Practice (GMP) requirements.
Qualifications
Post graduate MD / MBBS with relevant Pharmacovigilance experience preferable.
Documented scientific experience, preferably from the pharmaceutical industry (0 to 1 plus years of...
...documents.
• Review and confirm completeness of documentation for the change request and seek approval.
What are we looking for? •Pharmacovigilance & Drug Safety Surveillance - PV, ICSR, Auditing experience must
•Internal Audit Quality Assurance
•Operational Audit &...
...clinical trial and/or marketed product projects. Performs day-to-day safety writing and related activities within a highly regulated pharmacovigilance environment, driven by strict timelines. Activities include but are not limited to delivery of low complexity safety writing...
...health authorities and policymakers to shape future regulatory frameworks. Our team also focuses on product safety through safety pharmacovigilance, ensuring medicines are safe to use. We collect, analyze, and report safety data, and continuously monitor for new safety...
...Lead System Consultant/Specialist (Pharmacovigilance / Drug Safety):
Exp: 5+
Location: Whitefield Bangalore.
Notice period: Immediate joiner
Skills:Argus or ArisG or Argus Safety databases
5+ years of overall experience in Pharmacovigilance / Drugs Safety...
