Managing the MD's calendar, correspondence, travel, and meetings. Key responsibilities include drafting documents and presentations, liaising with internal and external stakeholders, maintaining confidentiality, and assisting with various administrative tasks to ensure the smooth operation of the MD's office. Google sheet updating. Key Responsibilities: Calendar and Meeting Management: Schedule and coordinate meetings, manage the MD's complex calendar, and arrange meeting rooms and logistics. Correspondence and Communication: Handle and screen incoming and outgoing calls, emails, and other correspondence, acting as a key point of contact. Document Preparation: Prepare, edit, and format documents, reports, presentations, and other correspondence. Travel Arrangements: Organize travel logistics, including flights, accommodation, and detailed itineraries. Stakeholder Liaison: Serve as a liaison between the MD and internal departments, clients, and other external stakeholders. Administrative Support: Provide comprehensive administrative support and assist with various tasks to ensure efficient operations. Information Management: Manage and maintain confidential information with integrity and discretion. Job Types: Full-time, Permanent Pay: ₹11,095.72 - ₹45,493.09 per month Benefits: Cell phone reimbursement Health insurance Paid sick time Language: English (Preferred) Work Location: In person
Managing the MD's calendar, correspondence, travel, and meetings. Key responsibilities include drafting documents and presentations, liaising with internal and external stakeholders, maintaining confidentiality, and assisting with various administrative tasks to ensure the smooth operation of the MD's office. Google sheet updating. Key Responsibilities: Calendar and Meeting Management: Schedule and coordinate meetings, manage the MD's complex calendar, and arrange meeting rooms and logistics. Correspondence and Communication: Handle and screen incoming and outgoing calls, emails, and other correspondence, acting as a key point of contact. Document Preparation: Prepare, edit, and format documents, reports, presentations, and other correspondence. Travel Arrangements: Organize travel logistics, including flights, accommodation, and detailed itineraries. Stakeholder Liaison: Serve as a liaison between the MD and internal departments, clients, and other external stakeholders. Administrative Support: Provide comprehensive administrative support and assist with various tasks to ensure efficient operations. Information Management: Manage and maintain confidential information with integrity and discretion. Job Types: Full-time, Permanent Pay: ₹11,095.72 - ₹45,493.09 per month Benefits: Cell phone reimbursement Health insurance Paid sick time Language: English (Preferred) Work Location: In person
Ensuring Compliance:Guaranteeing that drug development, manufacturing, and marketing align with national and international regulatory guidelines and industry standards. Regulatory Submissions:Preparing, reviewing, and submitting comprehensive dossiers and applications (e.g., New Drug Applications (NDAs), Investigational New Drugs (INDs)) to regulatory agencies like the FDA or EMA. Documentation Management:Overseeing the creation and maintenance of critical documents, including clinical trial protocols, product labels, and promotional materials. Liaising with Regulatory Agencies:Serving as the primary point of contact and communication between the company and health authorities, addressing concerns and facilitating approvals. Interpreting Regulations:Providing expert guidance on the interpretation and application of evolving regulations and guidelines to internal project teams and management. Labeling and Advertising Review:Ensuring that drug labels, package inserts, and marketing materials are accurate, compliant, and provide necessary information on use, dosage, and side effects. Clinical Trial Support:Collaborating with clinical research teams to ensure that clinical trials are conducted according to Good Clinical Practice (GCP) and meet regulatory requirements. Post-Market Surveillance:Assisting with ongoing compliance activities, such as submitting periodic safety update reports (PSURs) and managing post-marketing surveillance data. Skills and Qualifications Analytical Skills:Ability to interpret complex regulations and scientific data. Communication Skills:Clear and effective communication to liaise with various departments, senior management, and regulatory agencies. Attention to Detail:Meticulousness in preparing precise and compliant documentation. Knowledge of Guidelines:Understanding of key regulatory guidelines, such as Good Manufacturing Practice (GMP), Good Clinical Practice (GCP), and Common Technical Job Types: Full-time, Permanent Pay: ₹25,000.00 - ₹35,000.00 per month Benefits: Food provided Health insurance Paid time off Work Location: In person
Ensuring Compliance:Guaranteeing that drug development, manufacturing, and marketing align with national and international regulatory guidelines and industry standards. Regulatory Submissions:Preparing, reviewing, and submitting comprehensive dossiers and applications (e.g., New Drug Applications (NDAs), Investigational New Drugs (INDs)) to regulatory agencies like the FDA or EMA. Documentation Management:Overseeing the creation and maintenance of critical documents, including clinical trial protocols, product labels, and promotional materials. Liaising with Regulatory Agencies:Serving as the primary point of contact and communication between the company and health authorities, addressing concerns and facilitating approvals. Interpreting Regulations:Providing expert guidance on the interpretation and application of evolving regulations and guidelines to internal project teams and management. Labeling and Advertising Review:Ensuring that drug labels, package inserts, and marketing materials are accurate, compliant, and provide necessary information on use, dosage, and side effects. Clinical Trial Support:Collaborating with clinical research teams to ensure that clinical trials are conducted according to Good Clinical Practice (GCP) and meet regulatory requirements. Post-Market Surveillance:Assisting with ongoing compliance activities, such as submitting periodic safety update reports (PSURs) and managing post-marketing surveillance data. Skills and Qualifications Analytical Skills:Ability to interpret complex regulations and scientific data. Communication Skills:Clear and effective communication to liaise with various departments, senior management, and regulatory agencies. Attention to Detail:Meticulousness in preparing precise and compliant documentation. Knowledge of Guidelines:Understanding of key regulatory guidelines, such as Good Manufacturing Practice (GMP), Good Clinical Practice (GCP), and Common Technical Job Types: Full-time, Permanent Pay: ₹25,000.00 - ₹35,000.00 per month Benefits: Food provided Health insurance Paid time off Work Location: In person