Safety Associate

The primary duty of a Drug Safety Associate involves the ongoing monitoring and evaluation of adverse effects and safety concerns associated with drugs and medical products following market approval. As a Drug Safety Associate, your responsibilities will include monitoring, assessing, and reporting adverse events related to pharmaceutical products. You will...

Responsibilities: - Receive and process adverse event reports from various sources, including healthcare professionals, consumers, and clinical trials. - Conduct initial assessment of reported adverse events to determine seriousness, expectedness, and causality. - Enter adverse event data into safety databases accurately and in a timely manner, ensuring...

**Experience: 3-5 years** The role of a Site Safety Officer is crucial in ensuring the well-being of workers and the compliance of the workplace with safety regulations.. **Salary - RS 22000/- to RS 25000/- per month** Person should know risk analysis, PPE inspection, JSA, TBT, method statemet, incident investigation and statutory laws about EHS. He must...

Minimum 1 year of experience in safety scientific writing/PSUR/PBRER/Aggregate report/Signal Provide medical, safety input and review of all required safety reports, such as- but not limited to -Periodic Safety Update Reports (PSURs)/ Periodic Benefit Risk Assessment Reports (PBRERs)/Periodic Adverse Drug Experience Reports (PADERS), Risk Management Plans...

Job Purpose: The Solutions Support Consultant, Safety Services works in partnership with the Solutions and Account Management Associate Director(s) and Director(s) and operational and commercial teams to optimize new business awards though the development of creative, cost-effective and high-quality competitive strategies and business solutions which...

Job Purpose: The Solutions Support Consultant, Safety Services works in partnership with the Solutions and Account Management Associate Director(s) and Director(s) and operational and commercial teams to optimize new business awards though the development of creative, cost-effective and high-quality competitive strategies and business solutions which...

**Job Summary**: The Pharmacovigilance Associate plays a key role in monitoring and ensuring the safety of pharmaceutical products throughout their lifecycle. Working within a multidisciplinary team, the associate is responsible for the collection, assessment, and reporting of adverse events and safety information associated with medicinal products. This...

(India) **About Us** Kateric is a strategic partner for biopharmaceutical companies that consistently delivers superior quality regulatory documents through excellence, experience, and intelligent execution. Kateric’s resources are located across multiple time zones in the United States, as well as in India, the EU and Canada, and also have experience...

We are looking for experienced candidates for the position of Senior Drug Safety Physician with minimum 2 Years of ICSR experience.Location - Chandigarh/Mohali/Hyderabad/ Homebased Job Purpose:Provide medical review, analysis and guidance during the case handling and reporting cycle of Adverse Event and Adverse Reaction reports received for investigational...

We are looking for experienced candidates for the position of Senior Drug Safety Physician with minimum 2 Years of ICSR experience.Location - Chandigarh/Mohali/Hyderabad/ Homebased Job Purpose:Provide medical review, analysis and guidance during the case handling and reporting cycle of Adverse Event and Adverse Reaction reports received for investigational...

We are looking to recruit a Junior Pharmacovigilance Associate reporting to the Pharmacovigilance Manager **What will you be doing?** As the Junior Pharmacovigilance Associate, you will be responsible for a variety of different tasks including: - Play an active role within the Pharmacovigilance Team, accountable for monitoring and managing all aspects of...

Job Description Summary The Associate Product Manager Clinical Trial Supply Logistics & Safety Services is a strategic Business Professional who takes proactivity & ownership on innovations led or supported by Clinical Trial Supply Logistics and/or Safety Services assuring alignment across Parexel SBUs. The role will follow the Product Lifecycle Management...

**Regulatory Affairs Associate** - Around 2 to 4 years of relevant experience in handling of pre and post approval life cycle management of drug products (small molecules as well as biologics) in various markets. - Contribute to preparation (including authoring where relevant) and delivery of simple, and with experience, increasingly more complex regulatory...

Regulatory Affairs Associate Around 2 to 4 years of relevant experience in handling of pre and post approval life cycle management of drug products (small molecules as well as biologics) in various markets. Contribute to preparation (including authoring where relevant) and delivery of simple, and with experience, increasingly more complex regulatory...

**Who we are**: For 25 years, we’ve been leaders in the baby safety (Levana) and DIY security space (Defender), creating ground - breaking consumer electronics that bring peace of mind to millions of people all over the world. We sell directly through our brand websites, Amazon, and through our retail partners like Costco and Walmart. **How You’ll Make...

Key accountability in this role will be to oversee the technical elements of the region, people leadership, customer service, process efficiency, health and safety, and financial management functions of the bases within the region. **PeopleCert** is looking for an exceptional and talented individual to join our team as **Procurement Associate**. **As a...

Senior Regulatory Affairs AssociateAround 4-8 years of relevant experience in handling of pre and post approval life cycle management of drug products (small molecules as well as biologics) in various markets.Good understanding of regulatory framework, including regional trends, for various types of applications and proceduresContribute to preparation...

Premier Research is looking for a Site Start Up Associate 1 to join the SSU Team in India. You will help biotech, medtech, and specialty pharma companies transform life-changing ideas and breakthrough science into new medicines, devices, and diagnostics. What we do is profoundly connected to saving and improving lives, and we recognize our team members are...

Senior Regulatory Affairs AssociateAround 4-8 years of relevant experience in handling of pre and post approval life cycle management of drug products (Biologics) in various markets.Good understanding of regulatory framework, including regional trends, for various types of applications and proceduresContribute to preparation (including authoring where...

**Responsibilities**: - Supervise daily store operations to achieve sales goals and maximize profitability. - Train and develop sales associates to provide superior customer service and product knowledge. - Ensure compliance with company policies and procedures, including inventory management, cash handling, and safety protocols. - Implement effective...