Pharmacovigilance Responsibilities- Monitoring and documenting adverse events and product complaints. Collaborating with cross-functional teams to ensure compliance with safety regulations. Preparing and submitting safety reports to health authorities. Contributing to the development of pharmacovigilance processes and procedures. Staying up-to-date with evolving pharmacovigilance guidelines and best practices Requirements And Skills- Bachelor’s degree in pharmacy, life sciences, or a related field. Strong understanding of pharmacovigilance regulations and guidelines. Excellent attention to detail and analytical skills. Effective communication and teamwork abilities. Proficiency in pharmacovigilance software and databases. Job Types: Full-time, Permanent, Fresher Pay: ₹19,191.63 - ₹48,236.01 per month Benefits: Health insurance Paid sick time Provident Fund Schedule: Day shift Supplemental Pay: Performance bonus Work Location: In person

Key Responsibilities Client interaction:- Understand customer needs, answer basic queries, and explain offerings clearly. Follow-ups & appointment setting:- Follow up with warm leads and schedule meetings or demos for the senior sales team. Data entry & reporting:- Maintain accurate call records in CRM or Excel and report daily/weekly progress. About Company: Here at Refined Reports Data, we take pride in our champion customer support team. Ensuring customer satisfaction is of utmost importance to us, so feel free to ask us anything, anytime. You can also schedule a free-of-cost consultation regarding your needs with one of our professionals, and also get a quote ready at the earliest. Show more Show less

Responsibilities: Monitor clinical trials to ensure adherence to protocols and regulations. Conduct site visits to verify data accuracy and compliance. Assist in patient recruitment and ensure informed consent procedures. Maintain trial documentation and report findings to stakeholders. Ensure proper handling and storage of investigational drugs. Collaborate with investigators, sponsors, and regulatory authorities. Key Skills: Attention to Detail: Ensuring accuracy in trial data and documentation. Regulatory Knowledge: Understanding of GCP, FDA, and ICH guidelines. Communication Skills: Effective interaction with research teams and sponsors. Problem-Solving: Addressing challenges in trial execution. Project Management: Coordinating multiple aspects of clinical studies. Job Type: Full-time Pay: ₹25,000.00 - ₹40,000.00 per month Benefits: Health insurance Provident Fund Schedule: Day shift Work Location: In person

Skills & Qualifications:  Bachelor of Science (or higher) in Biological Sciences, Pharmacology, Toxicology, Chemistry or related Health Sciences  Graduate Certificate in Pharmaceutical Regulatory Affairs  Must have a minimum of four years of experience filing regulatory submissions with Health Canada  Must have strong technical knowledge of CMC requirements and is able to critically analyze scientific data  Strong interpersonal skills and ability to foster strong working relationships with key stakeholders (internally and externally) and representatives from Health Canada  Strong working knowledge of Canadian Food and Drugs Act and Food and Drug Regulations, GMPs, ICH Guidelines and Health Canada Policies and Guidelines  Knowledge of the Medical Devices Regulations is an asset  Ability to prioritize workload to ensure all deadlines are met  Experience with publishing eCTD submissions is an asset  Ability to work independently with minimal supervision  Excellent organization, written and oral communication skills  Ability to effectively manage multiple projects in a fast-pace, results oriented environment  Strong commitment to quality, accuracy and detail  Ability to work well under pressure in a team based environment  Strong problem solving/analytical ability and issue resolution skills Drug Regulatory Affairs Specialist Responsibilities & Duties Develop and implement regulatory strategies to bring drugs to market in compliance with relevant laws and regulations. Conduct regulatory research and provide guidance on regulatory issues and requirements. Prepare and submit applications and regulatory submissions, such as INDs, NDAs, and BLAs. Communicate with regulatory agencies and respond to inquiries. Manage projects and timelines to ensure timely submission of regulatory documents. Work with cross-functional teams to ensure regulatory compliance throughout the product development process. Stay informed of regulatory changes and trends in the industry. Job Types: Permanent, Fresher Pay: ₹25,217.75 - ₹45,679.31 per month Benefits: Health insurance Paid sick time Provident Fund Schedule: Day shift Monday to Friday Supplemental Pay: Performance bonus Yearly bonus Work Location: In person