ad - doctor operations & clinical protocols (mbbs) Jobs in Bangalore Jobs In Mangaluru

ad - doctor operations & clinical protocols (mbbs)

medical officer Jobs in Bangalore Jobs In Mangaluru

medical officer

neurosurgery doctor Jobs in Bangalore Jobs In Mangaluru

neurosurgery doctor

radiologist doctor Jobs in Bangalore Jobs In Mangaluru

radiologist doctor

anesthesia doctor

VSH Hospital

<div>
 Clinical Services 5 Years of Experience Salary: ₹1000000.00 LPA Qualification: MBBS MD Posted on December 26, 2025
 
 
 
 Job Summary
 
 
 
 An Anesthesia Doctor (Anesthesiologist) job description involves assessing patients pre-op, developing anesthesia plans, administering drugs (general/regional), monitoring vitals (HR, BP, O2) during procedures, managing complications/emergencies, providing post-op pain relief, and collaborating with surgical teams for safe patient recovery, requiring MD/DO, board certification, excellent decision-making, and strong communication skills.
 
 
 Intrested can share profiles to
 
 hr@vshhospital.com or whats app to 7022660333
 
 
 
 
 Responsibilities
 
 
 
 Key Responsibilities
 
 
 <ul>
 <li>
 Patient Assessment: Review medical history, conduct physical exams, and analyze lab results to determine anesthesia risk.
 </li>
 <li>
 Anesthesia Planning: Create tailored plans for various procedures (surgery, labor, critical care).
 </li>
 <li>
 Administration: Administer general, regional anesthesia, sedation, and analgesics.
 </li>
 <li>
 Monitoring: Continuously track vital signs (heart rate, blood pressure, oxygen) and adjust anesthesia levels.
 </li>
 <li>
 Airway Management: Perform intubation, ventilation, and extubation.
 </li>
 <li>
 Emergency Response: Handle adverse reactions, complications, and cardiac events (e.g., defibrillation).
 </li>
 <li>
 Post-Op Care: Manage pain and ensure safe recovery from anesthesia.
 </li>
 <li>
 Collaboration: Work with surgeons, nurses, and other staff.
 </li>
 <li>
 Documentation: Maintain accurate patient records and procedure details.
 </li>
 <li>
 Supervision: Oversee nurse anesthetists and technical staff.
 
 
 </li>
 </ul>
 Skill Required
 
 
 
 Essential Qualifications &amp; Skills
 
 
 
 <ul>
 <li>
 Education: Doctor of Medicine (MD) or Doctor of Osteopathic Medicine (DO).
 </li>
 <li>
 Certification: Board-certified in Anesthesiology.
 </li>
 <li>
 Licensure: Valid medical license.
 </li>
 <li>
 Skills: Strong problem-solving, critical thinking, manual dexterity, focus, stamina, and compassionate communication.
 
 
 </li>
 </ul>
 Key Qualities
 
 
 <ul>
 <li>
 Detail-oriented, meticulous, calm under pressure, empathetic, and a good team player.
 </li>
 </ul>
</div>

Anesthesia Doctor

2070 Health

<div>
 
 
 About The Company
 
 
 
 
 Elevate Now is India's first medical weight-loss company, transforming how people approach weight management through science-based, doctor-led programs. We combine modern medical interventions, personalized nutrition, and dedicated health coaching to deliver sustainable results &mdash; not just short-term weight loss. Our mission is to help individuals improve their health, confidence, and long-term well-being through evidence-based, compassionate care.
 
 
 
 
 About The Role
 
 
 
 
 We are looking for a clinically strong, research-driven leader to design all medical protocols, frameworks, and doctor-facing systems. This role is ideal for someone deeply scientific, detail-oriented, and experienced in obesity care, GLP, and evidence-based clinical operations.
 
 
 
 
 Requirements
 
 
 
 
 
 Key Responsibilities
 
 
 
 
 Clinical Strategy, Training &amp; Protocol Design
 
 
 
 <ul>
 <li>
 Design, standardise, and optimise treatment protocols, clinical workflows, and patient care journeys
 </li>
 <li>
 Build structured doctor training content, onboarding modules, and upskilling frameworks
 </li>
 <li>
 Ensure all protocols follow ethical guidelines, GLP principles, and regulatory standards
 
 
 </li>
 </ul>
 
 Doctor Network Leadership
 
 
 
 <ul>
 <li>
 Lead doctor hiring strategy, competency framework, and selection standards
 </li>
 <li>
 Build and nurture a strong network of in-house and consultant doctors
 </li>
 <li>
 Mentor, coach, and support doctors on clinical quality and patient management
 
 
 </li>
 </ul>
 
 Quality, Compliance &amp; Collaboration
 
 
 
 <ul>
 <li>
 Oversee clinical governance, medical accuracy, and quality benchmarks
 </li>
 <li>
 Work cross-functionally with product, tech, ops, and leadership to integrate clinical excellence
 </li>
 <li>
 Track patient outcomes, treatment efficacy, and feedback to refine protocols
 
 
 </li>
 </ul>
 
 
 Requirements
 
 
 
 
 <ul>
 <li>
 MBBS required (MD preferred)
 </li>
 <li>
 Strong knowledge of obesity medicine, nutrition, weight management, and supplements
 </li>
 <li>
 6-10 years in clinical operations, medical advisory, or digital health
 </li>
 <li>
 Strong scientific temperament, analytical mindset, excellent communication
 </li>
 <li>
 Bangalore-based, comfortable in a fast-paced hybrid startup culture
 
 
 </li>
 </ul>
 
 
 Benefits
 
 
 
 
 <ul>
 <li>
 Top Benefit: You work with Super-Smart people
 </li>
 <li>
 Industry competitive salary
 </li>
 </ul>
</div>

AD - Doctor Operations & Clinical Protocols (MBBS)

<div>
 Medical Services 5 Years of Experience Salary: ₹1000000.00 LPA Qualification: MD Posted on December 27, 2025
 
 
 
 Job Summary
 
 
 
 A radiologist's job involves using medical imaging (X-ray, CT, MRI, Ultrasound) to diagnose and treat diseases, requiring analysis of scans, writing detailed reports for other doctors, and communicating findings, sometimes performing image-guided procedures like biopsies, ensuring patient safety, and staying updated on technology. They're medical doctors who interpret visual data to identify issues like fractures, tumors, or heart conditions, guiding patient care plans
 
 
 Interested can share resume to
 
 hr@vshhospital.com or whats app 7022660333
 
 
 
 
 Responsibilities
 
 
 
 Key Responsibilities
 
 
 <ul>
 <li>
 Interpret Medical Images: Analyze various imaging modalities (X-rays, CT, MRI, ultrasound) to diagnose and monitor diseases.
 </li>
 <li>
 Collaborate with Healthcare Professionals: Work closely with referring physicians and other medical staff to discuss findings and determine appropriate treatment plans.
 </li>
 <li>
 Perform Interventional Procedures: Conduct image-guided procedures such as biopsies, drainages, and injections when necessary.
 </li>
 <li>
 Ensure Patient Safety: Follow radiation safety protocols and ensure that imaging equipment is functioning correctly to protect patients and staff.
 </li>
 <li>
 Maintain Accurate Records: Document findings and maintain patient records in compliance with healthcare regulations.
 </li>
 <li>
 Stay Updated: Keep abreast of advancements in radiology and imaging technology to provide the best patient care possible.
 
 
 </li>
 </ul>
 Skill Required
 
 
 
 Required Skills And Qualifications
 
 
 
 <ul>
 <li>
 Medical Degree: Must have a Doctor of Medicine (MD) or Doctor of Osteopathic Medicine (DO) degree, with specialized training in radiology.
 </li>
 <li>
 Licensure: Must be licensed to practice medicine in the relevant jurisdiction and board-certified in radiology.
 </li>
 <li>
 Analytical Skills: Strong ability to interpret complex medical images and make accurate diagnoses.
 </li>
 <li>
 Communication Skills: Excellent verbal and written communication skills to convey findings to patients and healthcare teams effectively.
 </li>
 <li>
 Attention to Detail: High level of precision in analyzing images and documenting results.
 </li>
 </ul>
</div>

Radiologist Doctor

Emmes Group

<div>
 JOB_DESCRIPTION.SHARE.HTML
 
 
 CAROUSEL_PARAGRAPH
 
 
 JOB_DESCRIPTION.SHARE.HTML
 
 
 <ul>
 <li>
 Bengaluru, India
 </li>
 <li>
 Medical &amp; Safety
 </li>
 <li>
 Yes
 </li>
 <li>
 Regular Full-Time
 </li>
 <li>
 2748
 
 
 </li>
 </ul>
 Emmes Global
 
 
 mail_outline
 
 
 Get future jobs matching this search
 
 
 or
 
 
 
 Overview
 
 
 
 Job Description
 
 
 
 Job Posting Title
 
 
 
 
 India Bengaluru - hybrid
 
 
 
 Emmes Group: Building a better future for us all.
 
 
 Emmes Group is transforming the future of clinical research, bringing the promise of new medical discovery closer within reach for patients. Emmes Group was founded as Emmes more than 47 years ago, becoming one of the primary clinical research providers to the US government before expanding into public-private partnerships and commercial biopharma. Emmes has built industry leading capabilities in cell and gene therapy, vaccines and infectious diseases, ophthalmology, rare diseases, and neuroscience.
 
 
 We believe the work we do will have a direct impact on patients&rsquo; lives and act accordingly. We strive to build a collaborative culture at the intersection of being a performance and people driven company. We&rsquo;re looking for talented professionals eager to help advance clinical research as we work to embed innovation into the fabric of our company. If you share our motivations and passion in research, come join us!
 
 
 
 Primary Purpose
 
 
 
 The Medical Officer has functional responsibility for medical monitoring of clinical trials, medical reviewing of activities and for broad spectrum of internal and external medical consulting, including, but not limited to, advising related to protocol development, preparation of medical strategy for feasibility studies, involvement in bid preparation and bid defense meetings, delivery of medical trainings for relevant stakeholders, professional engagement with external clinical experts, etc.
 
 
 
 Responsibilities
 
 
 
 <ul>
 <li>
 Works directly with the Head of Pharmacovigilance and Medical Monitoring, in managing both corporate and project-related activities. Cooperates directly with Safety Monitors, Project Leadership, Data Managers and other relevant functional groups.
 </li>
 <li>
 </li>
 <li>
 At the project level, will function in the role of a Medical Monitor leading the clinical trial monitoring of safety and efficacy data for the assigned protocols in scope of the contract with the client and in compliance with relevant SOP and/or other relevant study specific documents.
 </li>
 <li>
 Provides safety oversight throughout the lifecycle of the clinical study including evaluation, assessment, and monitoring of safety events and protocol deviations.
 </li>
 <ul>
 <li>
 Cooperates with Safety Monitors to implement safety management activities and achieve study project objectives.
 </li>
 <li>
 Evaluates adverse events, serious adverse events (SAE) including expedited reporting, as well as other protocol defined safety events.
 </li>
 <li>
 Reviews SAE narratives and other safety reports.
 </li>
 <li>
 Reviews IND/IDE safety reports (MedWatch safety reports, FDA Form 3500A), Council for International Organizations of Medical Sciences (CIOMS) safety reports, Development Safety Update Reports (DSUR), and other aggregate reports as applicable.
 </li>
 <li>
 Reviews and approves Medical Dictionary for Regulatory Activities (MedDRA) and WHO Drug coding.
 </li>
 <li>
 Reviews the FDA MedWatch Alerts, safety communications and/or other communications from other relevant Regulatory Authorities and recommends action for implementation by study teams, as applicable.
 </li>
 </ul>
 <li>
 Provides medical input during development of protocol and associated documents &ndash; in scope agreed with the client, primarily focusing on the safety aspect of the clinical development.
 </li>
 <ul>
 <li>
 Advises study sponsor and study team on protocol development, inclusion/exclusion criteria, eligibility questions, protocol study design and halting rules, etc.
 </li>
 <li>
 Per agreement with client ensures the medical and scientific quality of safety sections of documents such as clinical trial protocols, investigator&rsquo;s brochure, informed consent document, patient diaries, and case report forms.
 </li>
 <li>
 Works directly with project-level staff to develop appropriate study documents and project plans (e.g., Safety Monitoring Plan, Medical Monitoring Plan, Communication Plan, and Training Plan).
 </li>
 <li>
 Supports preparation of safety section of clinical trial reports such as annual reports and clinical study reports.
 </li>
 </ul>
 <li>
 Engages with safety oversight committees (SOC) and consults with sponsors, investigators, and pharmaceutical partners, as appropriate.
 </li>
 <ul>
 <li>
 Participates in safety oversight committee meetings (DSMB/DMC/SMC); answers questions about safety monitoring and related procedures (e.g., review of halting rules).
 </li>
 <li>
 Reviews SOC Charter, safety reports, and meeting minutes.
 </li>
 <li>
 Participates in sponsor meetings and investigator training meetings.
 </li>
 <li>
 Participates in regulatory (FDA or other) meetings and scientific review meetings.
 </li>
 <li>
 Interacts with pharmaceutical companies and other study partners.
 </li>
 </ul>
 <li>
 Cooperates with business development teams as medical expert, participates in bid preparation and bid presentations.
 </li>
 <li>
 Acts as the internal medical consultant in broad spectrum of activities, e.g., prepares medical strategy for the feasibility activities and proposal of country mix, ensures relevant medical training for the assigned project staff, engages with identified external consultants to gain information from clinical practice, etc.
 </li>
 <li>
 If contracted with client and if relevant to level of own medical expertise, Medical Officer provides broad spectrum of medical consultancy services, including medical review of relevant documents and/or data (e.g., clinical study specific documents, clinical study report, training materials, scientific communication or communication materials with medical content, etc.).
 </li>
 <li>
 Participates in corporate process improvement and corporate quality assurance activities through Internal Quality Audit Team (IQAT) processes, SOP development, participation in internal and external audits, and professional development activities.
 </li>
 <li>
 Other corporate activities include annual SOP reviews, participation in corporate safety meetings/activities, and other relevant corporate activities.
 
 </li>
 </ul>
 
 Qualifications
 
 
 
 <ul>
 <li>
 Medical Doctor (MD, MBBS, MBBCh, or other equivalent) degree is required.
 </li>
 <li>
 2 years of working experience, preferably a combination of clinical practice and experience in the area of pharmaceutical medicine (i.e., clinical research, pharmacovigilance, medical affairs, regulatory etc.).
 </li>
 <li>
 Demonstrated clinical medicine expertise through practice experience preferred.
 </li>
 <li>
 Excellent clinical judgement and ability to communicate complex clinical issues in a scientifically sound and understandable way.
 </li>
 <li>
 Experience working with regulatory submissions.
 </li>
 <li>
 Expertise in safety and/or medical monitoring and serious adverse event reporting preferred.
 </li>
 <li>
 Demonstrated experience with or training in clinical trial data collection.
 </li>
 <li>
 Ability to work as a team member and function on a cross-functional team.
 </li>
 <li>
 Ability to direct activities and encourage positive team-based culture.
 </li>
 <li>
 Capacity to provide leadership and creativity in the work environment.
 </li>
 <li>
 Excellent verbal and written communication skills.
 
 
 </li>
 </ul>
 
 CONNECT WITH US!
 
 
 
 
 Follow us on Twitter - @EmmesCRO
 
 
 
 
 Find us on LinkedIn - Emmes
 
 
 
</div>

Medical Officer

Dexcom Deutschland GmbH

<div>
 singlePosition
 
 
 View All Jobs
 
 
 APAC Clinical Science Liaison (CSL) &ndash; India
 
 
 Bengaluru, India
 
 
 Find out how well you match with this job
 
 
 Job ID
 
 
 JR115542
 
 
 
 The Company
 
 
 
 Dexcom Corporation (NASDAQ DXCM) is a pioneer and global leader in continuous glucose monitoring (CGM). Dexcom began as a small company with a big dream: To forever change how diabetes is managed. To unlock information and insights that drive better health outcomes. Here we are 25 years later, having pioneered an industry. And we're just getting started. We are broadening our vision beyond diabetes to empower people to take control of health. That means personalized, actionable insights aimed at solving important health challenges. To continue what we've started: Improving human health.
 
 
 We are driven by thousands of ambitious, passionate people worldwide who are willing to fight like warriors to earn the trust of our customers by listening, serving with integrity, thinking big, and being dependable. We've already changed millions of lives and we're ready to change millions more. Our future ambition is to become a leading consumer health technology company while continuing to develop solutions for serious health conditions. We'll get there by constantly reinventing unique biosensing-technology experiences. Though we've come a long way from our small company days, our dreams are bigger than ever. The opportunity to improve health on a global scale stands before us.
 
 
 
 Meet The Team
 
 
 
 Become a key member of the Dexcom APAC team, driving excellence in clinical education and sales training in India. As the Clinical Science Liaison lead, you will report directly to the APAC CSL Manager, work in close partnership with country leaders, distributor networks, and collaborate with the global matrix of the commercial organization.
 
 
 You will help shape clinical messaging, deliver impactful education programs, and foster partnerships with healthcare professionals, diabetes societies, and industry leaders. You will also play a vital role in designing, localizing, and delivering training programs that support product launches, distributor enablement, and ongoing development initiatives in India.
 
 
 Your work will directly influence the adoption of CGM as a standard of care, supporting patients and healthcare providers across the region.
 
 
 
 Where You Come In
 
 
 
 As the APAC CSL Lead in India you will:
 
 
 <ul>
 <li>
 Lead Clinical Education &amp; Advocacy: Develop and deliver clinical education programs for patients, clinicians, and diabetes societies. Promote emerging clinical trial data, expanded indications, and strategic publications through presentations and forums.
 </li>
 <li>
 Collaborate Across Functions: Work closely with Medical/Clinical Affairs, Marketing, R&amp;D, Regulatory, Quality, Customer Support, and Field Sales to meet customer needs and drive product knowledge.
 </li>
 <li>
 Act as Regional Expert: Serve as a speaker and subject matter expert at local, regional, and international congresses, providing technical and clinical insights on CGM.
 </li>
 <li>
 Drive Initiatives: Lead KOL development, identify CGM advocates, and facilitate partnerships to advance CGM as standard of care.
 </li>
 <li>
 Support Distributors: Responsible for clinical education and product sales training of distributors. You will:
 </li>
 <li>
 Serve as the trusted advisor and liaison in development and execution of HCP events and training, including the development and approval of content, sourcing and liaising with international and local speakers.
 </li>
 <li>
 Deliver comprehensive training programs both vitually and in-person, ensuring alignment with India business objectives.
 </li>
 <li>
 Support launches and key regional projects by designing, localising and executing tailored training plans that accelerate adoption and performance. In doing so, you collaborate with cross-functional teams, including but not limited to global sales training, marketing, clinical, customer operations, tech support, and regulatory groups, as well as external partners.
 </li>
 <li>
 Collaborate closely with the manager and regional stakeholders to assess training needs, update curriculum, and implement best practices across markets.
 </li>
 <li>
 Drive the development and maintenance of training resources, including leveraging Learning Management Systems (LMS) for ongoing learning initiatives.
 </li>
 <li>
 Act as a trusted advisor to distributor partners, providing coaching and feedback to enhance sales effectiveness and market penetration.
 
 
 </li>
 </ul>
 
 What Makes You Successful
 
 
 
 <ul>
 <li>
 Clinical Expertise: Licensed Medical Doctor (MD), Dietitian (RD/LD), Registered Nurse (RN), or relevant clinical degree required. MD with specialist diabetes experience or Certified Diabetes Educator preferred. Minimum 4 years&rsquo; experience in diabetes education and treatment, with at least 2 years focused on CGM.
 </li>
 <li>
 Technical Knowledge: Familiarity with advanced diabetes technologies, including CGM, and emerging diabetes therapeutics.
 </li>
 <li>
 Language Skills: Fluent in both English and native language and possess excellent verbal and written communication skills. Additional language proficiency in Southeast Asian markets is an advantage.
 </li>
 <li>
 Professional Experience: Typically requires a bachelor&rsquo;s degree and 10+ years of related experience, or a graduate degree with 6+ years.
 </li>
 <li>
 Travel &amp; Flexibility: Willingness to travel (up to 50%), especially during high-volume cycles, and adapt to diverse environments and stakeholder needs.
 </li>
 <li>
 Expertise in training, with a solid understanding of territory management, healthcare markets and distributor dynamics. Proven experience in designing and delivering training programs for diverse audiences. Skilled in virtual and in-person facilitation, with proficiency in tools and technology that enhance training delivery.
 </li>
 <li>
 Highly organized and adaptable; thrive in a remote, fast-paced environment, managing multiple priorities effectively.
 </li>
 <li>
 Excellent project management, problem-solving, and interpersonal skills, with the ability to influence and engage stakeholders across cultures.
 </li>
 <li>
 Judgment &amp; Independence: Ability to work independently, exercise sound judgment, and develop innovative approaches to unique challenges.
 
 
 </li>
 </ul>
 
 Experience And Education
 
 
 
 <ul>
 <li>
 Typically requires a bachelor&rsquo;s degree with 10+ years of clinical experience
 </li>
 <li>
 Experience and proven success in sales training and program design, ideally within healthcare or medical device sectors.
 </li>
 <li>
 Experience working on regional strategy or partnership initiatives is strongly preferred.
 </li>
 <li>
 Previous experience in diabetes-related medical device sales with a proven track record of success.
 </li>
 <li>
 Nice to have: 2&ndash;5 years of previous management or lead experience with familiarity with global brand and distributor frameworks
 
 
 </li>
 </ul>
 
 Ready to make a difference in diabetes care across India and the Asia-Pacific? Join us and help lead the way in clinical education, advocacy, and innovation.
 
 
 
 
 What You&rsquo;ll Get
 
 
 
 <ul>
 <li>
 A front row seat to life changing CGM technology. Learn about our brave #dexcomwarriors community.
 </li>
 <li>
 A full and comprehensive benefits program.
 </li>
 <li>
 Growth opportunities on a global scale.
 </li>
 <li>
 Access to career development through in-house learning programs and/or qualified tuition reimbursement.
 </li>
 <li>
 An exciting and innovative, industry-leading organization committed to our employees, customers, and the communities we serve.
 
 
 </li>
 </ul>
 
 To all Staffing and Recruiting Agencies: Our Careers Site is only for individuals seeking a job at Dexcom. Only authorized staffing and recruiting agencies may use this site or to submit profiles, applications or resumes on specific requisitions. Dexcom does not accept unsolicited resumes or applications from agencies. Please do not forward resumes to the Talent Acquisition team, Dexcom employees or any other company location. Dexcom is not responsible for any fees related to unsolicited resumes/applications.
 
 
 
 Similar jobs
 
 
 <ul>
 <li>
 Sr Medical Affairs Specialist
 
 
 </li>
 </ul>
 Remote - Saudi Arabia
 
 
 Remote
 
 
 Posted 24 days ago
 
 
 <ul>
 <li>
 Sr Medical Affairs Specialist - Regulatory Writing and Scientific Communications
 
 
 </li>
 </ul>
 San Diego, California
 
 
 Remote
 
 
 Posted 23 days ago
 
 
 <ul>
 <li>
 Sr. Regulatory Affairs Specialist
 
 
 </li>
 </ul>
 Bengaluru, India
 
 
 Hybrid
 
 
 Posted 3 days ago
 
 
 <ul>
 <li>
 Staff Clinical Safety Monitor
 
 
 </li>
 </ul>
 Manila, Philippines
 
 
 Hybrid
 
 
 Posted 3 months ago
 
 
 <ul>
 <li>
 Senior Regulatory Affairs Specialist
 
 
 </li>
 </ul>
 San Diego, California
 
 
 Remote
 
 
 Posted 22 days ago
 
 
 <ul>
 <li>
 Senior Director, India Country Lead
 
 
 </li>
 </ul>
 Bengaluru, India
 
 
 Company Priority
 
 
 Hybrid
 
 
 Posted a month ago
 
 
 <ul>
 <li>
 India - Information Technology
 
 
 </li>
 </ul>
 Bengaluru, India
 
 
 Posted 3 months ago
 
 
 <ul>
 <li>
 Sr Manager Regulatory Affairs
 
 
 </li>
 </ul>
 San Diego, California
 
 
 Hybrid
 
 
 Posted 22 days ago
 
 
 <ul>
 <li>
 Intern I - Clinical Affairs
 
 
 </li>
 </ul>
 San Diego, California
 
 
 Posted 23 days ago
 
 
 <ul>
 <li>
 Marketing Lead
 
 
 </li>
 </ul>
 Bengaluru, India
 
 
 Posted 3 days ago
</div>

APAC Clinical Science Liaison (CSL) – India

Explore 5+ Anesthesia doctor in Bangalore Jobs In Mangaluru this January. Find roles across top companies and apply now to boost your career.

5 anesthesia doctor jobs IN Bangalore Jobs In Mangaluru

Anesthesia Doctor

AD - Doctor Operations & Clinical Protocols (MBBS)

Radiologist Doctor

Medical Officer

APAC Clinical Science Liaison (CSL) – India