Healthcare roles for doctors & students

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

Title: Sr. 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

This is sirisha arora, AM-HR, from Kolors Designation : Consultant - Doctor Required qualification : MBBS with Cosmetology experience or freshers also consider. Kolors Skin Care Treatments Clinic Offers Skin Treatment Fairness and Pimple Treatment, Dry and Oily Skins. Anti Ageing Treatment, Deep Scar Removal, Laser Hair Removal, Skin Polishing, Mole And Wart Removal, Under Eye Dark Circles, Wrinkle Treatment, Acne Treatment, Dark Spot Treatment Details : salary + incentives 9hrs shift we will take 2yrs commitment …but whenever u want to leave u nee dot give prior notice 2months incentive percentage is 4% in all injectable U will get minimum 20k + as incentives No week off in weekends U can take any one day week off from Monday to Friday… Job Types: Full-time, Permanent Pay: ₹40,000.00 - ₹60,000.00 per month Benefits: Health insurance Provident Fund Schedule: Day shift Evening shift Morning shift Supplemental Pay: Overtime pay Performance bonus Education: Bachelor's (Preferred) License/Certification: MBBS (Required) 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 hr@gaudiumivfcentre.com 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

Job description BDS, BAMS, MBBS. Medical officer for Gynaec and IVF hospital. Initiates the medical record by creating and processing the patient care record folder. Patient counseling/ doubt clearing/ coordinating and Gathering patient demographic and personal information. Maintain quality and accurate records by following hospital procedures. Ensures medical records are assembled in standard order and are accurate and complete. Ensure patient charts, paperwork and reports are completed in an accurate and timely manner. Communicate with Medical Staff, health care team members and patient departments. When required ward manage/support. Keeps health care providers informed by communicating availability or unavailability of the record. Maintains continuity of work operations by documenting and communicating actions, irregularities, and continuing needs. Maintains patient confidence by keeping patient records information confidential. Enhances medical records and hospital reputation by accepting ownership for accomplishing new and different requests; exploring opportunities to add value to job accomplishments. Job Types: Full-time, Permanent Pay: ₹25,000.00 - ₹40,000.00 per month Schedule: Day shift Morning shift Education: Diploma (Preferred) Experience: total work: 1 year (Preferred) Job Types: Full-time, Permanent Pay: ₹25,000.00 - ₹40,000.00 per month Education: Bachelor's (Preferred) Experience: total work: 1 year (Required)

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

JD - Teleconsultation Role Job Title: Teleconsultation Doctor – Prescription Validation Job Type: Full time/Part-Time Working Hours: 3:00 PM to 1:00 AM Shift Duration: 5 hours (Part time) - Break : 25minutes 9 hours (Full time) - Break : 50 minutes Job Role: As a Teleconsultation Doctor at MyRx, you will be responsible for prescription validation and conducting proper teleconsultations to ensure accurate and safe medical guidance for patients. Key Responsibilities: Prescription Validation. Review prescriptions received as orders. Accept the order and initiate a call through the system. Verify prescribed medicines with the patient. Approve the order after validation. Requirements: MBBS & MBBS Valid and registered medical license in India. Prior experience in teleconsultation (preferred). Strong communication and patient-handling skills. Job Types: Full-time, Part-time Pay: ₹20,000.00 - ₹40,000.00 per month Expected hours: 35 – 63 per week Benefits: Work from home Schedule: Day shift Evening shift Fixed shift Morning shift Rotational shift Weekend availability Supplemental Pay: Overtime pay Performance bonus Application Question(s): Do you have Medical council license? Experience: Teleconsultation: 1 year (Preferred) Work Location: Remote Application Deadline: 20/07/2025 Expected Start Date: 16/07/2025

Job Title: ICU Resident Medical Officer (RMO) Location: Aastha Hospital L-2/50 New Mahavir Nagar Opp. Kangra Niketan Outer Ring Road New Delhi-110018 Department: Intensive Care Unit (ICU) Reports To: Medical Director/ Medical Superintendent Job Summary: We are seeking a dedicated and skilled ICU Resident Medical Officer (RMO) to join our dynamic Intensive Care Unit team. The ideal candidate, preferably male, will be responsible for providing high-quality medical care to critically ill patients, assisting in the management of complex clinical conditions, and working collaboratively with a multidisciplinary team. Key Responsibilities: Patient Care: Provide comprehensive medical care to patients in the ICU, including assessment, diagnosis, and treatment planning. Monitoring: Continuously monitor patients' vital signs, laboratory results, and response to treatment; adjust care plans as necessary. Collaboration: Work closely with consultants, nursing staff, and other healthcare professionals to ensure integrated patient care. Documentation: Maintain accurate and timely medical records, including histories, physical examinations, and progress notes. Emergency Response: Participate in emergency procedures and interventions as required, and assist in resuscitation efforts. Education: Participate in the training and education of junior medical staff, interns, and medical students. Research: Engage in clinical research and quality improvement initiatives within the ICU setting. Compliance: Adhere to hospital policies, procedures, and standards of care. Qualifications: Education: MBBS or equivalent medical degree; completion of internship. Experience: Previous experience in an ICU setting is preferred but not mandatory. Licensure: Current medical license to practice in [Insert State/Country]. Certification: Basic Life Support (BLS) and Advanced Cardiovascular Life Support (ACLS) certifications required. Skills and Abilities: Strong clinical assessment and diagnostic skills. Excellent communication and interpersonal skills. Ability to work under pressure in a fast-paced environment. Team-oriented with a collaborative approach to patient care. Commitment to continuous learning and professional development. Note: This position is open to male candidates Job Type: Full-time Pay: From ₹40,000.00 per month Schedule: Rotational shift Work Location: In person

Role and Responsibilities ● To provide in-person clinical consultation and teleconsultation at a primary health centre based in Sahakar Nagar, Bangalore. ● Carry out the diagnosis, treatment based on standard management protocols and guidelines, counselling and also referral, where and when necessary. ● Evaluate patients and provide appropriate medical treatment for various illnesses and injuries. ● Explain procedures or prescribed treatments to patients. ● Maintain confidentiality and impartiality at all times. ● Collect record and maintain sensitive patient information such as examination results, medical history and reports. ● Keep up-to-date with medical developments, treatment and medication. ● Document all patient evaluations, treatments, medications and transactions according to company policies and procedures ● Besides physical consultation , communicate with patients through Online mode (i.e. e-consultations on voice/video/chat) ● Help in organizing Health Camps at community and corporate level whenever required. Job Types: Full-time, Permanent Pay: ₹60,000.00 - ₹80,000.00 per month Benefits: Health insurance Leave encashment Paid sick time Provident Fund Application Question(s): Is your MBBS from India? Are you planning NEET this year? Or are you planning PLAB/USMLE? How many years of experience you have post internship? Do you speak Kannada? The shift timings are from 9.30 am to 1 pm and 4 pm to 8.30 pm. You are required to do both the shifts. Are you OK with the shifts? Are you staying close to Sahakar Nagar.( within 5-6 km) or willing to relocate to Sahakar Nagar? 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