328 Endocrinology Jobs - Page 13

Our global activities are growing rapidly, and we are currently seeking a full-time, office-based Clinical Database Programmer to join our Biometrics team. This position will work in a team to accomplish tasks and projects that are instrumental to the company’s success. If you want an exciting career where you use your previous expertise and can develop and grow your career even further, then this is the opportunity for you. Responsibilities Develop, program, validate and maintain clinical trial databases according to company standards; Maintain and contribute to company library of standard CDASH compliant CRFs ; and Act as primary contact to the data management team for assigned studies, supplying all necessary technical support, and ensuring quality of the programming and adherence to company standards. Qualifications Bachelor’s degree/Advanced degree in Life Sciences or Computer Science or equivalent; Min 3 years of Rave study build experience in a similar position in Pharma/Healthcare sector; Custom function (C# Programming) experience is preferred; Certified Medidata Rave Study Builders preferred; Excellent verbal and written communication skills; and Meticulous attention to detail. Medpace Overview Medpace is a full-service clinical contract research organization (CRO). We provide Phase I-IV clinical development services to the biotechnology, pharmaceutical and medical device industries. Our mission is to accelerate the global development of safe and effective medical therapeutics through its scientific and disciplined approach. We leverage local regulatory and therapeutic expertise across all major areas including oncology, cardiology, metabolic disease, endocrinology, central nervous system, anti-viral and anti-infective. Headquartered in Cincinnati, Ohio, employing more than 5,000 people across 40+ countries. Why Medpace? People. Purpose. Passion. Make a Difference Tomorrow. Join Us Today. The work we’ve done over the past 30+ years has positively impacted the lives of countless patients and families who face hundreds of diseases across all key therapeutic areas. The work we do today will improve the lives of people living with illness and disease in the future. Medpace Perks Flexible work environment Competitive compensation and benefits package Competitive PTO packages Structured career paths with opportunities for professional growth Company-sponsored employee appreciation events Employee health and wellness initiatives Awards Recognized by Forbes as one of America's Most Successful Midsize Companies in 2021, 2022, 2023 and 2024 Continually recognized with CRO Leadership Awards from Life Science Leader magazine based on expertise, quality, capabilities, reliability, and compatibility What To Expect Next A Medpace team member will review your qualifications and, if interested, you will be contacted with details for next steps. EO/AA Employer M/F/Disability/Vets Show more Show less

We are currently seeking a full-time, remote-based Senior Study Start up Submissions Coordinator to join our Clinical Operations team in India, Delhi. Our culture is of expertise, and we empower our teams to employ their unique talents and experience to take an assertive approach to research, problem solving, and ultimately supporting our business partners. At Medpace, our employees embody our values and our approach to serving our clients. They work hard, understand our high expectations, and rise to the challenge. In return they are rewarded with interesting projects, career advancement, and recognition and exposure to our international footprint. These are just a few reasons why talented individuals join the Medpace team. Responsibilities To perform close follow up of Clinical Trials submitted to Drugs Controller General of India (DCGI), Face to face visits expected Facilitate meetings with DCGI, support consultation processes when needed Efficiently manage and successfully execute all aspects of local and Regional APAC start-up; Independently interact with Sponsor, sites, Institutional Review Boards (IRBs)/Ethics Committees (ECs) and regulatory agencies (minimum CDSCO and DCGI) Perform quality checks on submission documents and site essential documents; Prepare and approve informed consent forms; Review pertinent regulations to develop proactive solutions to start-up issues and challenges; and Present during bid defenses, general capabilities meetings, and audits. Qualifications Bachelor’s degree and more than 8 years of regulatory submissions experience in clinical research, preferably with a CRO. Experience may include CRA or project management experience; Strong Local experience mandatory for RSC level, Local and Regional APAC experience mandatory for RSM level Strong oral and written communication skills. Hands-on experience preparing, reviewing, and submitting regulatory documentation to EC and RA; including formulating responses to queries Medpace Overview Medpace is a full-service clinical contract research organization (CRO). We provide Phase I-IV clinical development services to the biotechnology, pharmaceutical and medical device industries. Our mission is to accelerate the global development of safe and effective medical therapeutics through its scientific and disciplined approach. We leverage local regulatory and therapeutic expertise across all major areas including oncology, cardiology, metabolic disease, endocrinology, central nervous system, anti-viral and anti-infective. Headquartered in Cincinnati, Ohio, employing more than 5,000 people across 40+ countries. Why Medpace? People. Purpose. Passion. Make a Difference Tomorrow. Join Us Today. The work we’ve done over the past 30+ years has positively impacted the lives of countless patients and families who face hundreds of diseases across all key therapeutic areas. The work we do today will improve the lives of people living with illness and disease in the future. Medpace Perks Flexible work environment Competitive compensation and benefits package Competitive PTO packages Structured career paths with opportunities for professional growth Company-sponsored employee appreciation events Employee health and wellness initiatives Awards Recognized by Forbes as one of America's Most Successful Midsize Companies in 2021, 2022, 2023 and 2024 Continually recognized with CRO Leadership Awards from Life Science Leader magazine based on expertise, quality, capabilities, reliability, and compatibility What To Expect Next A Medpace team member will review your qualifications and, if interested, you will be contacted with details for next steps. EO/AA Employer M/F/Disability/Vets Show more Show less

We are currently seeking a full-time, remote-based Study Start up Submissions Manager to join our Clinical Operations team in India, Delhi. Our culture is of expertise, and we empower our teams to employ their unique talents and experience to take an assertive approach to research, problem solving, and ultimately supporting our business partners. At Medpace, our employees embody our values and our approach to serving our clients. They work hard, understand our high expectations, and rise to the challenge. In return they are rewarded with interesting projects, career advancement, and recognition and exposure to our international footprint. These are just a few reasons why talented individuals join the Medpace team. Responsibilities To perform close follow up of Clinical Trials submitted to Drugs Controller General of India (DCGI), Face to face visits expected Facilitate meetings with DCGI, support consultation processes when needed Efficiently manage and successfully execute all aspects of local and Regional APAC start-up; Independently interact with Sponsor, sites, Institutional Review Boards (IRBs)/Ethics Committees (ECs) and regulatory agencies (minimum CDSCO and DCGI) Perform quality checks on submission documents and site essential documents; Prepare and approve informed consent forms; Review pertinent regulations to develop proactive solutions to start-up issues and challenges; and Present during bid defenses, general capabilities meetings, and audits. Qualifications Bachelor’s degree and more than 8 years of regulatory submissions experience in clinical research, preferably with a CRO. Experience may include CRA or project management experience; Strong Local experience mandatory for RSC level, Local and Regional APAC experience mandatory for RSM level Strong oral and written communication skills. Hands-on experience preparing, reviewing, and submitting regulatory documentation to EC and RA; including formulating responses to queries Medpace Overview Medpace is a full-service clinical contract research organization (CRO). We provide Phase I-IV clinical development services to the biotechnology, pharmaceutical and medical device industries. Our mission is to accelerate the global development of safe and effective medical therapeutics through its scientific and disciplined approach. We leverage local regulatory and therapeutic expertise across all major areas including oncology, cardiology, metabolic disease, endocrinology, central nervous system, anti-viral and anti-infective. Headquartered in Cincinnati, Ohio, employing more than 5,000 people across 40+ countries. Why Medpace? People. Purpose. Passion. Make a Difference Tomorrow. Join Us Today. The work we’ve done over the past 30+ years has positively impacted the lives of countless patients and families who face hundreds of diseases across all key therapeutic areas. The work we do today will improve the lives of people living with illness and disease in the future. Medpace Perks Flexible work environment Competitive compensation and benefits package Competitive PTO packages Structured career paths with opportunities for professional growth Company-sponsored employee appreciation events Employee health and wellness initiatives Awards Recognized by Forbes as one of America's Most Successful Midsize Companies in 2021, 2022, 2023 and 2024 Continually recognized with CRO Leadership Awards from Life Science Leader magazine based on expertise, quality, capabilities, reliability, and compatibility What To Expect Next A Medpace team member will review your qualifications and, if interested, you will be contacted with details for next steps. EO/AA Employer M/F/Disability/Vets Show more Show less

Consultant Endocrinologist - Agartala (Multi-Speciality Hospital) Experience: 1-6 Years Qualification: DM/DNB Budget : 5 LPM Share CV at manoj@intendminds.com Call me : 7349718665 WhatsApp Directly with me : wa.me/917349718665

Azurity Pharmaceuticals is a privately held, specialty pharmaceutical company that focuses on innovative products that meet the needs of underserved patients. As an industry leader in providing unique, accessible, and high-quality medications, Azurity leverages its integrated capabilities and vast partner network to continually expand its broad commercial product portfolio and robust late-stage pipeline. The company’s patient-centric products span the cardiovascular, neurology, endocrinology, gastro-intestinal, institutional, and orphan markets, and have benefited millions of patients. For more information, visit www.azurity.com. Azurity Pharmaceuticals is proud to be an inclusive workplace and an Equal Opportunity Employer. Azurity's success is attributable to our incredibly talented, dedicated team that focuses on benefiting the lives of patients by bringing the best science and commitment to quality into everything that we do. We seek highly motivated individuals with the dedication, integrity, and creative spirit needed to thrive in our organization. Brief Team/department Description Our Digital team at Azurity is building new capabilities utilizing cutting-edge Salesforce systems. We are looking for a dynamic, change inspired, Individual self-driven hands-on Team Member. The Senior Offshore Salesforce Developer – Life Sciences plays a key role in designing, developing, and optimizing Salesforce solutions for Azurity Pharma. This role focuses on customizing and enhancing Salesforce to support HCP/HCO engagement, medical affairs, field rep automation, regulatory compliance, and Commercial Operations. As a technical expert, this individual will work closely with onshore teams, architects, and business analysts to deliver scalable, secure, and high-performance CRM solutions. The ideal candidate has deep expertise in Apex, Lightning Web Components (LWC), integrations, and automation while ensuring compliance with HIPAA, GDPR, and FDA regulations. Principle Responsibilities Salesforce Life Sciences/Sales Cloud Development & Customization Develop and customize Life Sciences functionalities, including HCP/HCO engagement, KOL management, field medical interactions, and compliance tracking. Build custom objects, Apex triggers, Lightning Web Components (LWC), Visualforce pages, and declarative automation (Flows & Process Builder) to enhance business processes. Implement advanced workflow automation for medical science liaisons (MSLs), sales reps, and regulatory teams. Configure call planning, sample management, consent tracking, and territory management for pharma field teams. Integration & Data Management Develop integrations with third-party pharma applications (IQVIA, MDM platforms, sales engagement tools). Work with Salesforce APIs (REST, SOAP, Bulk API) and middleware platforms (MuleSoft, Informatica, Boomi) for seamless data exchange. Optimize data security, access controls, and compliance adherence (HIPAA, GDPR, FDA regulations). Performance Optimization & Security Ensure Salesforce scalability and performance optimization, implementing best practices for SOQL, Apex, and Lightning Components. Enforce role-based security, permission sets, and audit trails to maintain compliance with healthcare and life sciences regulations. Conduct code reviews and performance testing to ensure a robust and stable CRM platform. Collaboration & Agile Development Work closely with onshore architects, business analysts, and product owners to translate business needs into technical solutions. Participate in scrum meetings, sprint planning, and UAT support in an Agile development environment. Provide technical documentation, deployment support, and knowledge transfer to stakeholders. Continuous Improvement & Best Practices Stay up to date with Salesforce releases, new features, and industry trends to recommend improvements. Adhere to Salesforce DevOps best practices, using tools like Gearset, Copado, or Jenkins for CI/CD automation. Mentor junior offshore developers and contribute to a culture of innovation and technical excellence. Preferred Skills And Experience 5+ years of Salesforce development experience, with a strong focus on Sales Cloud, Veeva CRM, and Health Cloud. Strong expertise in Apex, Lightning Web Components (LWC), Visualforce, SOQL, and REST APIs. Experience with Salesforce integrations (IQVIA, Snowflake, MDM) Strong understanding of HCP engagement, MSL workflows, patient support, and regulatory compliance (HIPAA, GDPR, FDA, Sunshine Act). Hands-on experience with Salesforce DevOps tools (Gearset, Copado, Jenkins) for release management. Ability to work in an offshore-onshore collaboration model, supporting multiple time zones. Salesforce Platform Developer I & II, Sales Cloud certifications required. Strong analytical, communication, and problem-solving skills in a remote, global team setup By applying for this role, you confirm that you are mentally and physically capable of fulfilling the job responsibilities detailed in the job description without any restrictions. If you have any concerns or even the slightest disability that may affect your ability to perform the job, please inform HR in advance. Show more Show less

Our corporate activities are growing rapidly, and we are currently seeking a full-time, office-based Clinical Data Coder to join our Clinical Coding & Support team in Mumbai, India. This position will work on a team to accomplish tasks and projects that are instrumental to the company’s success. If you want an exciting career where you use your previous coding, pharmacy, or nursing expertise and can develop and grow your career even further, then this is the opportunity for you! Responsibilities Perform accurate coding of medical terms and medications utilizing industry-wide standards as well as company standards; Coordinate the assignment of appropriate dictionaries for meeting study requirements; and Develop and maintain coding guidelines Qualifications Bachelor Degree in Nursing, or more advanced clinical degree; Experience with using MedDRA and WHO Drug dictionaries; and Experience working with clinical trials or within the pharmaceutical environment is preferred. Medpace Overview Medpace is a full-service clinical contract research organization (CRO). We provide Phase I-IV clinical development services to the biotechnology, pharmaceutical and medical device industries. Our mission is to accelerate the global development of safe and effective medical therapeutics through its scientific and disciplined approach. We leverage local regulatory and therapeutic expertise across all major areas including oncology, cardiology, metabolic disease, endocrinology, central nervous system, anti-viral and anti-infective. Headquartered in Cincinnati, Ohio, employing more than 5,000 people across 40+ countries. Why Medpace? People. Purpose. Passion. Make a Difference Tomorrow. Join Us Today. The work we’ve done over the past 30+ years has positively impacted the lives of countless patients and families who face hundreds of diseases across all key therapeutic areas. The work we do today will improve the lives of people living with illness and disease in the future. Medpace Perks Flexible work environment Competitive compensation and benefits package Competitive PTO packages Structured career paths with opportunities for professional growth Company-sponsored employee appreciation events Employee health and wellness initiatives Awards Recognized by Forbes as one of America's Most Successful Midsize Companies in 2021, 2022, 2023 and 2024 Continually recognized with CRO Leadership Awards from Life Science Leader magazine based on expertise, quality, capabilities, reliability, and compatibility What To Expect Next A Medpace team member will review your qualifications and, if interested, you will be contacted with details for next steps. EO/AA Employer M/F/Disability/Vets Show more Show less

Medpace is growing rapidly, and we are currently seeking full-time, Junior Software QA Test Engineers (Validation Engineer) to join our growing Information Technology (IT) team in Mumbai office. Responsibilities Work closely with developers and end users throughout the software life cycle to ensure that applications meet the needs of the users; Perform testing using a variety of test methodologies, including manual, exploratory, and automated testing; Create and maintain test cases, test plans, and other documentation for projects; Participate in constructive peer review of test cases; Identify and report software defects and inconsistencies; Review, analyze, and supplement requirement specifications, and ensure 100% test coverage; and Help facilitate execution of acceptance test scripts by end users Qualifications Bachelor’s degree in Computeer Science, Information Systems or related field; Experience writing and executing manual testing for complex software applications; experience in automated testing is a plus! Experience communicating and working within cross-departmental teams consisting of software developers, department leads, and end users; Excellent computer skills; analytical, written, and oral communication skills; and Experience in the regulated healthcare industry is a plus. Medpace Overview Medpace is a full-service clinical contract research organization (CRO). We provide Phase I-IV clinical development services to the biotechnology, pharmaceutical and medical device industries. Our mission is to accelerate the global development of safe and effective medical therapeutics through its scientific and disciplined approach. We leverage local regulatory and therapeutic expertise across all major areas including oncology, cardiology, metabolic disease, endocrinology, central nervous system, anti-viral and anti-infective. Headquartered in Cincinnati, Ohio, employing more than 5,000 people across almost 40 countries. Why Medpace? People. Purpose. Passion. Make a Difference Tomorrow. Join Us Today. The work we’ve done over the past 30+ years has positively impacted the lives of countless patients and families who face hundreds of diseases across all key therapeutic areas. The work we do today will improve the lives of people living with illness and disease in the future. Medpace Perks Flexible work environment Competitive compensation and benefits package Competitive PTO packages Structured career paths with opportunities for professional growth Company-sponsored employee appreciation events Employee health and wellness initiatives Awards Recognized by Forbes as one of America's Most Successful Midsize Companies in 2021, 2022, 2023 and 2024 Continually recognized with CRO Leadership Awards from Life Science Leader magazine based on expertise, quality, capabilities, reliability, and compatibility What To Expect Next A Medpace team member will review your qualifications and, if interested, you will be contacted with details for next steps. EO/AA Employer M/F/Disability/Vets Show more Show less

Your Role at Cureocity As a Cureocity Doctor, you won’t just treat—you’ll decode health. You’ll work at the cutting edge of medicine, collaborating with our dieticians, trainers, and data tools to deliver outcomes that are evidence-based, personalized, and transformative. You will: Conduct root-cause consultations, exploring metabolic, hormonal, and lifestyle contributors to disease and dysfunction Work with clients managing chronic illnesses like diabetes, PCOS, thyroid disorders, and cardiovascular risk Lead clients in disease prevention and performance optimization, including muscle gain/loss, fat reduction, and healthy aging—through scientific and measurable methods Collaborate with dieticians and fitness trainers to design, monitor, and refine multi-disciplinary care plans Recommend and interpret diagnostics including blood markers, genetic/epigenetic panels, CGM, and wearable data Participate in AI-assisted progress tracking, dashboards, and data-supported clinical decisions Contribute to internal case reviews, protocol building, and research-backed care models --- What We’re Looking For MBBS (freshers and experienced welcome) Interest in preventive medicine, genetics, metabolic health, and human performance Comfort with scientific research, clinical data, and AI-enabled tools Collaborative mindset with strong communication skills Willingness to learn and grow within a multi-disciplinary, tech-enabled health ecosystem Bonus if you have exposure to family medicine, endocrinology, sports medicine, or functional health approaches --- Work Mode & Timing Location: Onsite, Cureocity Hub, Ernakulam Shift-based schedule: 8 hours per day, 3 days/week Morning Shift: 6 AM to 2 PM Afternoon Shift: 1 PM to 9 PM Structured client appointments, continuous learning, and team integration --- Perks & Growth Path Hands-on training in genetics, biohacking, metabolic optimization, and health-tech Collaborate with expert teams in nutrition, fitness, psychology, and AI modeling Involvement in podcasts, content development, and clinical research Opportunity to build your role into leadership, innovation, or system design Job Types: Full-time, Permanent Pay: ₹14,465.93 - ₹92,152.30 per month Work Location: In person

Azurity Pharmaceuticals is a privately held, specialty pharmaceutical company that focuses on innovative products that meet the needs of underserved patients. As an industry leader in providing unique, accessible, and high-quality medications, Azurity leverages its integrated capabilities and vast partner network to continually expand its broad commercial product portfolio and robust late-stage pipeline. The company’s patient-centric products span the cardiovascular, neurology, endocrinology, gastro-intestinal, institutional, and orphan markets, and have benefited millions of patients. For more information, visit www.azurity.com. Azurity Pharmaceuticals is proud to be an inclusive workplace and an Equal Opportunity Employer. Azurity's success is attributable to our incredibly talented, dedicated team that focuses on benefiting the lives of patients by bringing the best science and commitment to quality into everything that we do. We seek highly motivated individuals with the dedication, integrity, and creative spirit needed to thrive in our organization. Brief Team/department Description Seeking a Supply Chain Manager to oversee procurement, inventory management, and supplier coordination, ensuring efficiency and cost control. Ideal candidates will have strong analytical skills, experience in logistics, and a proven track record in optimizing supply chain operations. Principle Responsibilities This should specifically outline, in bullet form, the responsibilities of the job: Evaluate market demand, inventory status and prepare demand forecast for commercial products Prepare supply plan and issuing supply forecast and PO to suppliers Material planning and managing procurement / supply of components to CMOs like API Planning and managing pre-launch activities for products under approval Managing supplier relationships and supply agreements Budgeting for commercial products, approval of invoices Supporting BD/Alliance teams for COGS, supply agreements Periodic review of demand, pricing, supply status with Commercial & Marketing team Manage supply of commercial products to private label partners Qualifications And Education Requirements This section should include relevant qualifications and education requirements. 10+ years of experience as a supply management professional Master’s in pharmacy is preferred Bachelor’s in pharmacy is required By applying for this role, you confirm that you are mentally and physically capable of fulfilling the job responsibilities detailed in the job description without any restrictions. If you have any concerns or even the slightest disability that may affect your ability to perform the job, please inform HR in advance. Show more Show less

We require doctors for Medical Colleges & Hospitals PAN India Qualification: MD/MS, DNB, (All Department) Position: Consultant, SR, AP, Associate Professor, Professor Department: Clinical & Non Clinical Mansi Call/WhatsApp: 7986969416 weps.hrworld@gmail.com

We require doctors for Medical Colleges & Hospitals PAN India Qualification: MD/MS, DNB, (All Department) Position: Consultant, SR, AP, Associate Professor, Professor Department: Clinical & Non Clinical Tanu Call/WhatsApp: 7015609544 weps.careers@gmail.com

We require doctors for Medical Colleges & Hospitals PAN India Qualification: MD/MS, DNB, (All Department) Position: Consultant, SR, AP, Associate Professor, Professor Department: Clinical & Non Clinical Mamta Call/WhatsApp: 8708568683 weps.placement@gmail.com

We require doctors for Medical Colleges & Hospitals PAN India Qualification: MD/MS, DNB, (All Department) Position: Consultant, SR, AP, Associate Professor, Professor Department: Clinical & Non Clinical Sheetal Call/WhatsApp: 7814536255 weps.recruit@gmail.com

We require doctors for Medical Colleges & Hospitals PAN India Qualification: MD/MS, DNB, (All Department) Position: Consultant, SR, AP, Associate Professor, Professor Department: Clinical & Non Clinical Priyanka Call/WhatsApp: 90410 65797 weps.services@gmail.com

Pathologist Required at Bareilly UP Salary 2.5 Lakhs + Accommodation Lakhimpur UP Salary 1.5 to 1.75 Lakhs + Accommodation Required Candidate profile Doctor couple can be adjusted in their respective branch Or We can also help you to find out suitable job as per your preferred location

Dear All, Hiring for Endocrinology Consultant with a leading corporate hospital in Central India.DM/DNB freshers can also apply. Interested candidates can share their CV at panwar.sumit@huntnscouts.com for detailed discussion. Regards Sumit Panwar

Urologist Required at Amritsar / Gurdaspur Punjab Salary 5 to 6 Lakhs + Accommodation Bathinda Punjab Salary 5 to 6 Lakhs + Share Bharatpur Rajasthan Salary 5 to 6 Lakhs Azamgarh UP Salary 6 Lakhs + Required Candidate profile Veraval Gujarat Salary 6 Lakhs + Accommodation

We require doctors for Medical Colleges & Hospitals PAN India Qualification: MD/MS, DNB, (All Department) Position: Consultant, SR, AP, Associate Professor, Professor Department: Clinical & Non Clinical Priyanka Call/WhatsApp: 90410 65797 weps.services@gmail.com

We require doctors for Medical Colleges & Hospitals PAN India Qualification: MD/MS, DNB, (All Department) Position: Consultant, SR, AP, Associate Professor, Professor Department: Clinical & Non Clinical Mamta Call/WhatsApp: 8708568683 weps.placement@gmail.com

Cardiologist Required at Chandigarh Tricity Salary 5 to 6 Lakhs + Share Tohana Haryana Salary 8 Lakhs + Bharatpur Rajasthan Salary 8 Lakhs Jabalpur Madhya Pradesh Salary 9 to 10 Lakhs + Accommodation Veraval Gujarat Salary 10 Lakhs + Required Candidate profile Goalpara Assam Salary 10 Lakhs + Accommodation Rohtak Haryana Salary 8 Lakhs + Accommodation Lucknow UP Salary 6 to 7 Lakhs Bathinda Punjab Salary 6 to 8 Lakhs + Accommodation

Medical Oncologist Required at Bathinda Punjab Salary 6 Lakhs Rohtak Haryana Salary 5 to 6 Lakhs Chandigarh Part time (1.5 Hour) Salary 1 Lakh Required Candidate profile Surgical Oncologist Required at Lucknow UP Salary 5 to 6 Lakhs

General & Laparoscopic Surgeon Required at Gadchiroli Maharashtra Peripheral Location Salary 3.5 Lakhs + Accommodation + Food Charkhi Dadri Haryana Salary 3.5 Lakhs + Accommodation Saharanpur UP Salary 3.5 Lakhs + Accommodation Required Candidate profile Doctor couple can be adjusted in their respective branch

Urologist Required at Bharatpur Rajasthan Salary 5 to 6 Lakhs Azamgarh UP Salary 6 Lakhs + Veraval Gujarat Salary 6 Lakhs + Accommodation Gurdaspur and Batala Punjab Salary 5 to 6 Lakhs + Accommodation Bathinda Punjab Salary 5 to 6 Lakhs+

Key aspects of an MD in General Medicine: In-depth medical training: MDs in General Medicine receive advanced training in diagnosing and treating various medical conditions, including cardiovascular, respiratory, gastrointestinal, and infectious diseases. Patient-centered care: They are trained to provide holistic care, managing chronic diseases, and ensuring patient well-being. Clinical expertise: They develop strong clinical judgment to treat patients in both outpatient and inpatient settings. Broad scope of practice: General Medicine doctors are the backbone of clinical practice, managing a wide range of conditions. Diverse career opportunities: This specialization offers opportunities to work in hospitals, clinics, and research institutions. Collaboration with other specialists: MDs in General Medicine often collaborate with other healthcare professionals to provide comprehensive patient care. Focus on adult care: While general physicians provide care for all ages, MDs in General Medicine specifically focus on adult patients, often managing more complex medical conditions. MD Specializations:While MD in General Medicine is a broad specialization, MDs can further specialize in various sub-specialties, including: Internal Medicine: Focuses on the diagnosis and treatment of adult non-surgical diseases. Cardiology: Deals with the diagnosis and treatment of heart disease. Pulmonology: Focuses on the respiratory system. Gastroenterology: Focuses on the digestive system. Endocrinology: Focuses on hormone disorders. Other specializations: Numerous other sub-specialties are available, such as Anesthesiology, Dermatology, Psychiatry, Neurology, and more. Job Types: Full-time, Permanent Pay: ₹60,312.40 - ₹182,476.65 per month Work Location: In person Expected Start Date: 25/05/2025

A gastroenterologist is a medical specialist who diagnoses and treats diseases of the digestive system, including the stomach, intestines, liver, and pancreas. They perform various procedures like endoscopies, colonoscopies, and liver biopsies,