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Summary To write, support and manage projects to prepare high quality medical and scientific communications including, literature review, abstracts, posters, slide sets, Manuscripts (complex) for publication/ presentation at congresses or internal medical and/or clinical team. About the Role Location – Hyderabad #LI Hybrid Major Responsibilities: Prepares, literature review, abstracts, posters, and slide sets, and Manuscripts (complex) working from various data sources including clinical study reports, patient profiles, protocols etc. Performs quality control (QC) checking / proof reading of the above-mentioned deliverables to meet customer expectations. Manages multiple projects of up to two brands at any given time. Obtains feedback from customers and implements customer management tactics. Complies with and support group’s project management tool, standards, policies and initiatives. Follows Novartis specifications for documentation, specifically Novstyle, templates etc. Follows and tracks clinical trial milestones for assigned projects. Maintains records for all assigned projects including archiving. Maintains audit, SOP and training compliance. Train new joiners, fellow colleagues as and when required. Performs additional tasks as assigned. Minimum Requirements: Minimum Education - Science degree or equivalent, B.Sc./equivalent with 8 years Clinical Research (CR) experience, M.Sc./M.Pharm +6 years of clinical research (CR) experience. Desired – Doctoral Degree or Qualification in Medical Sciences (MBBS/MD/equivalent). PhD + 4 year of CR experience, MBBS/equivalent + 4 year of CR experience, MD +2 years of CR experience. Why Novartis: Our purpose is to reimagine medicine to improve and extend people’s lives and our vision is to become the most valued and trusted medicines company in the world. How can we achieve this? With our people. It is our associates that drive us each day to reach our ambitions. Be a part of this mission and join us! Learn more here: https://www.novartis.com/about/strategy/people-and-culture You’ll receive: You can find everything you need to know about our benefits and rewards in the Novartis Life Handbook. https://www.novartis.com/careers/benefits-rewards Commitment to Diversity and Inclusion: Novartis is committed to building an outstanding, inclusive work environment and diverse teams' representative of the patients and communities we serve. Join our Novartis Network: If this role is not suitable to your experience or career goals but you wish to stay connected to hear more about Novartis and our career opportunities, join the Novartis Network here: https://talentnetwork.novartis.com/network. Why Novartis: Helping people with disease and their families takes more than innovative science. It takes a community of smart, passionate people like you. Collaborating, supporting and inspiring each other. Combining to achieve breakthroughs that change patients’ lives. Ready to create a brighter future together? https://www.novartis.com/about/strategy/people-and-culture Join our Novartis Network: Not the right Novartis role for you? Sign up to our talent community to stay connected and learn about suitable career opportunities as soon as they come up: https://talentnetwork.novartis.com/network Benefits and Rewards: Read our handbook to learn about all the ways we’ll help you thrive personally and professionally: https://www.novartis.com/careers/benefits-rewards Division US Business Unit Universal Hierarchy Node Location India Site Hyderabad (Office) Company / Legal Entity IN10 (FCRS = IN010) Novartis Healthcare Private Limited Functional Area Research & Development Job Type Full time Employment Type Regular Shift Work No Accessibility and accommodation Novartis is committed to working with and providing reasonable accommodation to individuals with disabilities. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the recruitment process, or in order to perform the essential functions of a position, please send an e-mail to [email protected] and let us know the nature of your request and your contact information. Please include the job requisition number in your message. Novartis is committed to building an outstanding, inclusive work environment and diverse teams' representative of the patients and communities we serve.

Job Summary: The MBBS Cosmetology Doctor will provide expert medical and cosmetic services to clients at the wellness center, focusing on non-surgical aesthetic treatments. This role requires a licensed medical professional with specialized training or experience in cosmetology, who is dedicated to enhancing client confidence and wellness through personalized aesthetic services. Key Responsibilities: Client Consultation and Assessment: Conduct thorough consultations with clients to understand their aesthetic goals, assess medical history, and explain available cosmetic procedures. Recommend suitable treatments based on individual needs, ensuring alignment with the center's wellness philosophy. Cosmetic and Aesthetic Treatments: Perform a variety of non-surgical cosmetic procedures such as Botox, dermal fillers, laser treatments, chemical peels, and other skin rejuvenation therapies. Ensure all procedures are conducted safely, following medical protocols and regulatory standards. Monitor and manage post-treatment care and follow-up to ensure client satisfaction and treatment effectiveness. Health and Safety Compliance: Adhere strictly to health and safety protocols, ensuring a sterile environment and appropriate handling of medical equipment. Stay informed of the latest regulations and best practices in cosmetic medicine, ensuring compliance at all times. Patient Education and Counseling: Provide clients with detailed information on post-treatment care and any necessary lifestyle recommendations to maximize results. Address any client concerns, offering guidance on maintaining and enhancing their wellness and appearance. Documentation and Record Keeping: Maintain accurate, confidential medical records of all consultations, treatments, and follow-up notes. Ensure timely updates and documentation in the center’s electronic health records system. Continuous Learning and Development: Stay current with advancements in cosmetology and aesthetic medicine, including new techniques, products, and equipment. Participate in ongoing training and certifications as needed to enhance skills and provide the highest level of care. Qualifications: MBBS degree from a recognized medical institution. Certification or specialized training in cosmetology/aesthetic medicine is preferred. Valid medical license to practice in Chennai & Telangana 1+ years of experience in cosmetology, dermatology, or aesthetic medicine. Job Type: Full-time Pay: ₹60,000.00 - ₹90,000.00 per month Benefits: Health insurance Provident Fund Schedule: Day shift Work Location: In person

Medical Doctor – Sexual Health (Part-Time / On-Site) Company: Niche Agriculture and Pharmaceutical Limited Location: Rohini, New Delhi Job Type: Part-Time / Flexible Schedule (In-Clinic) Experience Required: Minimum 2 Years Job Description: Niche Agriculture and Pharmaceutical Limited is looking for experienced and qualified medical doctors to join our in-house clinical team at our facility located in Rohini, New Delhi. We are currently hiring for the following specialties: Sexual and Reproductive Health Specialist Ayurveda Doctor (BAMS/MD Ayurveda) These roles offer part-time and flexible scheduling options. Ideal for professionals who wish to contribute their expertise in a structured, supportive in-clinic environment while maintaining their independent practice or other engagements. Key Responsibilities: Conduct in-person consultations with patients at our Rohini clinic Diagnose, treat, and counsel patients as per medical standards Maintain accurate patient records and case notes Work collaboratively with our internal healthcare team when required Ensure high standards of care, privacy, and patient satisfaction Qualifications: MBBS, MD, BAMS, or equivalent in a relevant specialization Valid registration with MCI or State Medical Council Minimum 2 years of clinical experience Good communication and interpersonal skills Comfortable working in an offline, clinic-based setting Working Hours & Flexibility: Part-time, fixed hours or flexible shifts available Consulting hours can be adjusted based on mutual availability Opportunity to practice during peak hours or on specific weekdays What We Offer: Modern, well-equipped clinic in Rohini, New Delhi Patient management support and operational assistance A collaborative and ethical medical environment Consistent footfall of patients Flexible scheduling to suit part-time professionals Job Type: Full-time Pay: ₹10,000.00 - ₹60,000.00 per month Benefits: Commuter assistance Schedule: Day shift Ability to commute/relocate: Delhi, Delhi: Reliably commute or planning to relocate before starting work (Preferred) Language: English (Preferred) Work Location: In person Job Type: Full-time Pay: ₹10,000.00 - ₹60,000.00 per month Benefits: Cell phone reimbursement Schedule: Day shift Supplemental Pay: Performance bonus Experience: Clinical: 1 year (Required) Language: English (Required) License/Certification: MBBS, MD, BAMS, or equivalent in a relevant specialization (Preferred) Work Location: In person

Roles & Responsibilities \* Engage with potential customers via phone calls, providing information about NEET-PG/FMGE courses. \* Convert leads into sales and ensure smooth handover to the post-sales team. \* Manage and update customer information in our CRM or sales software. \* Collaborate with the sales manager for daily reporting and performance tracking. \* Assist in developing and executing strategies for user acquisition and sales growth. Qualifications: Requirements and skills- \* 1-2 years of experience in abroad counselling, preferably in MBBS , NEET courses \* Strong communication and interpersonal skills. \* Proficiency in CRM management or similar sales software. \* Ability to work independently and as part of a team. \* A proactive approach to problem-solving and customer engagement Thanks & Regards HR Team Job Type: Full-time Pay: ₹20,000.00 - ₹28,000.00 per month Benefits: Cell phone reimbursement Work Location: In person

Position: IVF Consultant/Specialty (Female) Job Description: Full time and permanent job Only Female candidates can apply Job Location, SRINAGAR Requirement: MBBS Any post graduate (MBBS, DGO) Handle OPD and Campaign Activity. Minimum 1-3 yrs experience. Please share your resume at [email protected] Job Types: Full-time, Permanent Pay: ₹900,000.00 - ₹2,000,000.00 per year Experience: total work: 2 years (Preferred) Work Location: In person

Title: Manager-Regulatory Medical Writing Date: Jul 14, 2025 Location: Gurgaon - R&D Company: Sun Pharmaceutical Industries Ltd Job Purpose Clinical Development department is one of the key departments at SPIL which handles, analyzes, and portrays scientific data and information. Providing authentic, objective, and accurate information to regulatory agencies, the scientific community, healthcare professionals, and patients in a consistent and timely fashion across the entire drug development cycle is fundamental to SPIL. The purpose of SPIL Medical Writer is to work with cross-functional, multidisciplinary teams to author, manage, and lead the development of documents intended for regulatory agencies and audiences (including but not limited to Protocols, Clinical Study Reports, Investigator Brochures, Briefing Documents, Submission Documents, Health Authority Regulatory responses, IND/NDA Applications and Marketing Authorization Applications). Key Roles and Responsibilities Preparation of the medical writing documents under the purview of Clinical Development department that may be required for domestic and international regulatory submissions across the globe. Effectively collect, and evaluate data, information, and inputs from multiple functions, sources to create a cohesive content strategy for writing projects Plan including organizing/preparing outlines, write, edit, review, co-ordinate, obtain approval, and complete the regulatory documents supporting Clinical Development Conduct effective document initiation meetings and comments resolution meeting(s) to ensure review team alignment and understanding Ensure data are presented in a clear, complete, accurate, and concise manner. Ensure key data, statements, and conclusions are consistent across related documents and that inferences/conclusions are integrated, accurate, and supported by appropriate data. Coordinate scientific reviews, collate reviewer’s comments, develop content of document as required based on internal/external inputs, and prepare final version. Ensure and coordinate quality checks for accuracy; perform quality checks of documents Perform peer review of documents Exhibit flexibility in working across multiple document types and therapeutic areas Influence or negotiate content of document and timelines, with cross functional teams to deliver optimum quality documents Escalate issues if any, to medical writing supervisors/HOD Anticipate and mitigate risks to delivery Maintain and enhance TA knowledge of SPIL portfolio Maintain and be abreast of medical writing regulatory guidelines / policies/ procedures Maintain and enhance scientific knowledge skills to align with audience needs and changes in technology and platforms Provide coaching to others by sharing technical information and providing guidance Maintain/ support metrics, tracking sheets, and training records as per the process requirements Complete required trainings within stipulated due dates Be audit compliant and audit ready per organizational needs Network with others (medical writing team and other functions) to identify and share best practices. Contribute to process improvements May build and manage relationships with vendors, if required. Qualification, Skill and Competencies Requirements Qualification: A doctoral or post-graduate degree in Life Science/Pharmacy disciplines or clinical degrees (MBBS/BDS/BAMS/BHMS, etc.) with minimum of 3 years of experience and good knowledge in regulatory medical writing, with proven and progressive leadership capabilities is required. Advanced degree (e.g., MD, PhD) is preferred… Skills and Competencies Good knowledge of scientific, statistical, and research principles and regulatory guidelines such as ICH requirements. Demonstrated written and/or communication skills. Demonstrated project management and decision-making skills. Demonstrated interpersonal skills to build relationships, act as change agent, and adapt to rapidly changing organizational & business challenges. Demonstrated innovative thinking to allow for optimal execution of clinical development strategies. Good knowledge of global regulations and pharma industry standards Job Duration Full Time Part time Job Location Mumbai/ Gurgaon, INDIA Reporting To Global Medical Writing Lead/ Head - Global Medical Writing

Dr requirement 8hrs duty 6days a week​ Experience-1.5yrs+ Job Type: Full-time Pay: ₹59,000.00 - ₹60,000.00 per month Education: Bachelor's (Preferred) Work Location: In person

Urgent requirement of Assistant Professor Pharmacology Positions- Senior resident/ Assistant Professor/ Associate Professor/ Professor Qualification- MBBS with MD Pharmacology Salary- Best in industry- Negotiable Accommodation- based on availability Job Type: Full-time Schedule: Day shift Work Location: In person

Qualification: MBBS Medical degree (MBBS or equivalent) Valid medical license to practice in the region Completed residency in a relevant medical field Previous experience in a hospital or clinical setting, preferably in emergency or night shifts Strong decision-making and problem-solving skills Excellent communication and interpersonal skills Ability to work independently and under pressure Skills Patient assessment Emergency response Treatment planning Medical documentation Medication prescribing Critical thinking Team coordination Communication Job Type: Full-time Schedule: Night shift Work Location: In person

Mukat Hospital is seeking experienced ICU nursing staff to join our dedicated healthcare team. Key Responsibilities: Monitor and manage critically ill patients admitted in the ICU under the guidance of the ICU In-Charge or Intensivist. Perform daily clinical rounds, assess patient condition, and implement treatment plans as per protocols. Respond promptly to medical emergencies in the ICU, initiate resuscitation procedures (CPR, intubation, defibrillation). Monitor vital signs, ventilator settings, invasive lines (CVP, arterial lines), and ensure proper patient care documentation. Administer prescribed medications, infusions, and manage blood products as per standard ICU protocols. Maintain clear communication with senior consultants, nursing staff, and patient attendants regarding patient progress. Ensure proper handover of critical information during shift changes. Follow infection control protocols and ICU care bundles. Assist in ICU procedures such as central line insertion, arterial cannulation, intubation, tracheostomy, etc., under supervision if required. Attend Code Blue situations within the hospital premises when on duty. Maintain updated patient records and ICU charts as per hospital norms. Qualification & Experience: MBBS/BAMS degree with valid registration from Medical Council. Preferably with ICU experience (minimum 1 year) or Critical Care certification. BLS/ACLS certification preferred. Job Type: Full-time Work Location: In person