clinical science consultant

Dexcom

<div>
 
 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.
 
</div>

APAC Clinical Science Liaison (CSL) – India

<div>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.
<div><div>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 , yo u will report directly to the APAC C SL Manager , work in close partnership with country leaders, distributor networks , and collaborate with the global matrix of the commercial organization .
</div><div>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.
</div><div>Your work will directly influence the adoption of CGM as a standard of care, supporting patients and healthcare providers across the region. 
</div><div>Where You Come In :
</div><div>As the APAC CSL Lead in India you will:
</div><div><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></ul></div><div><ul><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></ul></div><div><ul><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></ul></div><div><ul><li>Drive Initiatives: Lead KOL development, identify CGM advocates, and facilitate partnerships to advance CGM as standard of care.
</li></ul></div><div><ul><li>Support Distributors : Responsible for clinical education and product sales training of distributors. You will:
</li></ul></div><div><ul><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></ul></div><div><ul><li>D eliver comprehensive training programs both v i tually and in-person, ensuring alignment with India business objectives .
</li></ul></div><div><ul><li>Support launches and key regional projects by designing , localising and executing tailored training plans that accelerate adoption and performance. In doing so, you collaborat e 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></ul></div><div><ul><li>Collaborate closely with the manager and regional stakeholders to assess training needs, update curricul um , and implement best practices across markets.
</li></ul></div><div><ul><li>Drive the development and maintenance of training resources, including leveraging Learning Management Systems (LMS) for ongoing learning initiatives.
</li></ul></div><div><ul><li>A ct as a trusted advisor to distributo r partners, providing coaching and feedback to enhance sales effectiveness and market penetration. 
</li></ul></div><div>What Makes You Successful:
</div></div><div><div><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 C ertified Diabetes Educator preferred. Minimum 4 years&rsquo; experience in diabetes education and treatment, with at least 2 years focused on CGM.
</li></ul></div><div><ul><li>Technical Knowledge: Familiarity with advanced diabetes technologies , including CGM, and emerging diabetes therapeutics.
</li></ul></div><div><ul><li>Language Skills: Fluent i n both English and native language and possess excellent verbal and written communication skills . Additional language proficiency in Southeast Asian markets is an advantage.
</li></ul></div><div><ul><li>Professional Experience: Typically requires a bachelor&rsquo;s degree and 1 0 + years of related experience, or a graduate degree with 6+ years.
</li></ul></div><div><ul><li>Travel &amp; Flexibility: Willingness to travel ( up to 50%), especially during high-volume cycles, and adapt to diverse environments and stakeholder needs.
</li></ul></div><div><ul><li>Expertise in training , with a solid understanding of territory management, healthcare markets and distributor dynamics. P roven 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></ul></div><div><ul><li>H ighly organized and adaptable ; thrive in a remote, fast-paced environme nt, mana ging multiple priorities effectively.
</li></ul></div><div><ul><li>Excellent project management , problem-solving, and interpersonal skills, with the ability to influence and engage stakeholders across cultures.
</li></ul></div><div><ul><li>Judgment &amp; Independence: Ability to work independently, exercise sound judgment, and develop innovative approaches to unique challenges. 
</li></ul></div><div>Experience and Education :
</div><div><ul><li>Typically requires a bachelor&rsquo;s degree with 10+ years of clinical experience
</li></ul></div><div><ul><li>Experience and proven success in sales training and program design, ideally within healthcare or medical device sectors.
</li></ul></div><div><ul><li>Experience working on regional strategy or partnership initiatives is strongly preferred.
</li></ul></div><div><ul><li>Previous experience in diabetes-related medical device sales with a proven track record of success.
</li></ul></div><div><ul><li>Nice to have: 2&ndash;5 years of previous management or lead experience with f amiliarity with global brand and distributor framework s 
</li></ul></div><div>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. 
</div><div>What you&rsquo;ll get:
</div><div><ul><li>A front row seat to life changing CGM technology. Learn about our brave #dexcomwarriors community .
</li></ul></div><div><ul><li>A full and comprehensive benefits program.
</li></ul></div><div><ul><li>Growth opportunities on a global scale.
</li></ul></div><div><ul><li>Access to career development through in-house learning programs and/or qualified tuition reimbursement.
</li></ul></div><div><ul><li>An exciting and innovative, industry-leading organization committed to our employees, customers, and the communities we serve.
</li></ul></div></div>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.</div>

Bristol Myers Squibb

<div>
 
 Working with Us
 
 
 
 Challenging. Meaningful. Life-changing. Those aren't words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms the lives of patients, and the careers of those who do it. You'll get the chance to grow and thrive through opportunities uncommon in scale and scope, alongside high-achieving teams. Take your career farther than you thought possible.
 
 
 Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment. We offer a wide variety of competitive benefits, services and programs that provide our employees with the resources to pursue their goals, both at work and in their personal lives. Read more: careers.bms.com/working-with-us .
 
 
 The Clinical Scientist function provides scientific expertise necessary to design and deliver clinical studies and programs.
 
 
 <ul>
 <li>
 Will be responsible for design and execution of assigned clinical trial activities and work closely with clinical team members within the assigned project to execute activities associated with the conduct
 </li>
 <li>
 May serve as Clinical Trial Lead for one or more trials
 </li>
 <li>
 May lead or support trial level activities for one or more trials with the necessary supervision
 </li>
 <li>
 May co-lead study team meetings in partnership with GDO protocol manager and collaborate with cross-functional study team members
 </li>
 <li>
 Collaborate and liaise with external partners (e.g., KOLs)
 </li>
 <li>
 Seek out and enact best practices with instruction
 </li>
 <li>
 Provide regular and timely updates to manager/management as requested
 </li>
 <li>
 Develop Protocol and ICF documents / amendments and present these to governance committee and development team meetings as required
 </li>
 <li>
 Conduct literature review
 </li>
 <li>
 Submit clinical documents to TMF
 </li>
 <li>
 Develop site and CRA training materials and present these at SIVs and Investigator meetings
 </li>
 <li>
 Review clinical narratives
 </li>
 <li>
 Monitor clinical data for specific trends
 </li>
 <li>
 Develop Data Review Plan in collaboration with Data Management
 </li>
 <li>
 Ensure CRF design adequately supports data collection in alignment with the protocol in collaboration with Data Management/Programming
 </li>
 <li>
 Submit clinical contributions to clinical study reports (CSRs) and clinical portions of Regulatory Documents (e.g., IB, DSUR, PSUR, Orphan Annual Reports, HA, EC, IRB responses and contribute to regulatory submission.)
 </li>
 <li>
 Degree in Life Sciences (MD, PhD, Pharm D, MS, RN or other scientific field preferred). Appropriate for new entrance to pharma (post fellowship/ new to industry)
 </li>
 <li>
 Basic knowledge of GCP/ICH, drug development process, study design, statistics, clinical operations
 </li>
 <li>
 Ability to understand assigned protocol(s) and their requirements
 </li>
 <li>
 Basic knowledge skills to support program-specific data review and trend identification
 </li>
 <li>
 Intermediate medical writing skills and medical terminology
 </li>
 <li>
 Basic planning/project management skills (develop short range plans that are realistic and effective)
 </li>
 <li>
 Detail-oriented with commitment to quality
 </li>
 <li>
 Basic knowledge of disease area, compound, current clinical landscape
 </li>
 <li>
 Basic knowledge of the establishment and operation of data monitoring committees, dose review teams, and independent response adjudication committees
 </li>
 <li>
 Intermediate critical thinking and problem-solving skills
 </li>
 <li>
 Adaptable / flexible (willing and able to adjust to multiple demands and shifting priorities; ability to meet day-to-day challenges with confidence and professionalism)
 </li>
 <li>
 Intermediate skills in Microsoft Word/Excel/PowerPoint and data review tools (e.g., Pt Profiles, report generating tools)
 
 
 </li>
 </ul>
 Domestic and International travel may be required.
 
 
 
 Compensation
 
 
 
 Brisbane, CA and Cambridge, MA $173,390-$210,110
 
 
 New Jersey $150,770 - $182,701
 
 
 San Diego, CA and Seattle, WA $165,850-$200,974
 
 
 If you come across a role that intrigues you but doesn't perfectly line up with your resume, we encourage you to apply anyway. You could be one step away from work that will transform your life and career.
 
 
 
 Compensation Overview
 
 
 
 The starting compensation range(s) for this role are listed above for a full-time employee (FTE) basis. Additional incentive cash and stock opportunities (based on eligibility) may be available. The starting pay rate takes into account characteristics of the job, such as required skills, where the job is performed, the employee's work schedule, job-related knowledge, and experience. Final, individual compensation will be decided based on demonstrated experience.
 
 
 Eligibility for specific benefits listed on our careers site may vary based on the job and location. For more on benefits, please visit https://careers.bms.com/life-at-bms/.
 
 
 
 Benefits
 
 
 
 Benefit offerings are subject to the terms and conditions of the applicable plans in effect at the time and may require enrollment. Our benefits include:
 
 
 <ul>
 <li>
 Health Coverage: Medical, pharmacy, dental, and vision care.
 </li>
 <li>
 Wellbeing Support: Programs such as BMS Well-Being Account, BMS Living Life Better, and Employee Assistance Programs (EAP).
 </li>
 <li>
 Financial Well-being and Protection: 401(k) plan, short- and long-term disability, life insurance, accident insurance, supplemental health insurance, business travel protection, personal liability protection, identity theft benefit, legal support, and survivor support.
 
 
 </li>
 </ul>
 
 Work-life benefits include:
 
 
 
 Paid Time Off
 
 
 <ul>
 <li>
 US Exempt Employees: flexible time off (unlimited, with manager approval, 11 paid national holidays (not applicable to employees in Phoenix, AZ, Puerto Rico or Rayzebio employees)
 </li>
 <li>
 Phoenix, AZ, Puerto Rico and Rayzebio Exempt, Non-Exempt, Hourly Employees: 160 hours annual paid vacation for new hires with manager approval, 11 national holidays, and 3 optional holidays
 
 
 </li>
 </ul>
 Based on eligibility*, additional time off for employees may include unlimited paid sick time, up to 2 paid volunteer days per year, summer hours flexibility, leaves of absence for medical, personal, parental, caregiver, bereavement, and military needs and an annual Global Shutdown between Christmas and New Years Day.
 
 
 All global employees full and part-time who are actively employed at and paid directly by BMS at the end of the calendar year are eligible to take advantage of the Global Shutdown.
 
 
 <ul>
 <li>
 Eligibility Disclosure: T he summer hours program is for United States (U.S.) office-based employees due to the unique nature of their work. Summer hours are generally not available for field sales and manufacturing operations and may also be limited for the capability centers. Employees in remote-by-design or lab-based roles may be eligible for summer hours, depending on the nature of their work, and should discuss eligibility with their manager. Employees covered under a collective bargaining agreement should consult that document to determine if they are eligible. Contractors, leased workers and other service providers are not eligible to participate in the program.
 
 
 </li>
 </ul>
 
 Uniquely Interesting Work, Life-changing Careers
 
 
 
 With a single vision as inspiring as Transforming patients' lives through science&trade; , every BMS employee plays an integral role in work that goes far beyond ordinary. Each of us is empowered to apply our individual talents and unique perspectives in a supportive culture, promoting global participation in clinical trials, while our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues.
 
 
 
 On-site Protocol
 
 
 
 
 Responsibilities
 
 
 
 BMS has an occupancy structure that determines where an employee is required to conduct their work. This structure includes site-essential, site-by-design, field-based and remote-by-design jobs. The occupancy type that you are assigned is determined by the nature and responsibilities of your role:
 
 
 Site-essential roles require 100% of shifts onsite at your assigned facility. Site-by-design roles may be eligible for a hybrid work model with at least 50% onsite at your assigned facility. For these roles, onsite presence is considered an essential job function and is critical to collaboration, innovation, productivity, and a positive Company culture. For field-based and remote-by-design roles the ability to physically travel to visit customers, patients or business partners and to attend meetings on behalf of BMS as directed is an essential job function.
 
 
 
 Supporting People With Disabilities
 
 
 
 BMS is dedicated to ensuring that people with disabilities can excel through a transparent recruitment process, reasonable workplace accommodations/adjustments and ongoing support in their roles. Applicants can request a reasonable workplace accommodation/adjustment prior to accepting a job offer. If you require reasonable accommodations/adjustments in completing this application, or in any part of the recruitment process, direct your inquiries to adastaffingsupport@bms.com . Visit careers.bms.com/ eeo -accessibility to access our complete Equal Employment Opportunity statement.
 
 
 
 Candidate Rights
 
 
 
 BMS will consider for employment qualified applicants with arrest and conviction records, pursuant to applicable laws in your area.
 
 
 If you live in or expect to work from Los Angeles County if hired for this position, please visit this page for important additional information: https://careers.bms.com/california-residents/
 
 
 
 Data Protection
 
 
 
 We will never request payments, financial information, or social security numbers during our application or recruitment process. Learn more about protecting yourself at https://careers.bms.com/fraud-protection .
 
 
 Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations.
 
 
 If you believe that the job posting is missing information required by local law or incorrect in any way, please contact BMS at TAEnablement@bms.com . Please provide the Job Title and Requisition number so we can review. Communications related to your application should not be sent to this email and you will not receive a response. Inquiries related to the status of your application should be directed to Chat with Ripley.
 
 
 R1598007 : Clinical Scientist, Early Development
 
 
</div>

Clinical Scientist, Early Development

health7careers

Overview We are looking for an experienced pathologist to be responsible for performing tests laboratory work and pathological research. Your duties will include analyzing bodily fluids and tissue samples to study diagnose and treat disease. You will work in various medical settings and carry-out research and patient tests in order to assist fellow medical professionals in their diagnoses.To be successful as a pathologist you must have an inquiring mind extensive medical knowledge of diseases in your specialty and remain current in all research and testing methods. Responsibilities <ul><li>Performing specimen analysis by using laboratory tools and equipment in order to study samples and perform tests to accurately analyse bodily fluids and tissue specimens.</li><li>Looking for abnormalities in samples that evidence disease and conveying this information to the relevant medical practitioner.</li><li>Using checklists medical software and retesting to get thorough and precise results.</li><li>Suggesting potential treatment options.</li><li>Writing pathology reports detailing specimens tested results of tests and the final diagnosis.</li><li>Undertaking research to improve identification and testing methods and finding innovative ways to treat disease.</li><li>Staying up to date with developments in the fields of pathology and medical practice.</li></ul> Requirements <ul><li>Proven work experience as a Pathologist or similar role</li><li>Valid and active medical license</li><li>Experience using lab testing equipment such as microscopes and flow cytometers</li><li>Exceptional analytical and research skills</li><li>Strong oral and written communication skills</li><li>Relevant training and / or specialization degree as a Pathologist</li><li>Bachelors of medicine degree</li></ul> Key Skills Mac Os, Helpdesk, Fitness, E Learning, AC Maintenance, Arabic Employment Type Full Time Experience years Vacancy 1

Clinical Pathologist Consultant

Ankura Hospital for Women & Children AS Rao Nagar

Roles &amp; Responsibilities:<ul><li>Ensure that well prepared nutritious food is served in the hospital. Develop diet chart appropriate as per medical needs.</li><li>To meet patients and gather information on their dietary habits on admission and discharge.</li><li>Get familiarized with the cause of hospitalization and medical history of the patient.</li><li>To educate the patient on the dietary requirements as per his / her condition or as per orders of Consultant / Doctor.</li><li>Identifying nutrition problems and assessing the nutritional status of patients in a clinical setting.</li><li>Developing diet plans and counseling patients on special diet modifications.</li><li>Follow Departmental Protocols / Procedures.</li></ul>Qualification:<ul><li>Degree in nutritional science with minimum 2 years experience in hospital.</li><li>Ability to converse in local language, Hindi and English</li><li>Work Location: Kompally</li></ul>Interested Candidates can your updated resume to hrkompally@ankurahospital.comFor further details contact HR: 8977524838Job Types: Full-time, PermanentPay: ₹25,000.00 - ₹30,000.00 per monthBenefits:<ul><li>Health insurance</li><li>Paid sick time</li><li>Provident Fund</li></ul>Work Location: In person

Clinical Dietitian

THE AGILE RECRUITMENT AGENCY

Nuclear Medicine Consultant &ndash; Hyderabad (Full-Time)We are hiring a qualified Nuclear Medicine Consultant for reputed healthcare facilities located in Punjagutta and Himayatnagar, Hyderabad. This opportunity is ideal for specialists seeking strong clinical exposure and professional growth in diagnostic and therapeutic nuclear medicine services.Job Details<ul><li>Position: Nuclear Medicine Consultant</li><li>Locations:</li><li>Punjagutta, Hyderabad</li><li>Himayatnagar, Hyderabad</li><li>Experience Required: 0&ndash;3 years</li><li>Salary: ₹2,00,000 &ndash; ₹5,00,000 per month</li><li>Job Type: Full-time</li></ul>Job DescriptionThe Nuclear Medicine Consultant will be responsible for performing, interpreting, and reporting nuclear medicine diagnostic studies and providing high-quality patient care. The role involves close coordination with referring physicians and adherence to radiation safety protocols.Key Responsibilities<ul><li>Perform and interpret nuclear medicine procedures including PET-CT, SPECT, and other radionuclide imaging studies</li><li>Prepare accurate diagnostic reports and clinical interpretations</li><li>Ensure compliance with radiation safety and regulatory standards</li><li>Coordinate with technologists, physicists, and clinical teams</li><li>Participate in quality assurance and departmental audits</li><li>Provide patient counselling related to nuclear medicine procedures</li></ul>Required Qualifications<ul><li>MD / DNB in Nuclear Medicine</li><li>Valid medical council registration</li><li>0&ndash;3 years of post-qualification experience</li><li>Strong diagnostic and reporting skills</li></ul>Skills &amp; Competencies<ul><li>Knowledge of nuclear imaging protocols</li><li>Attention to detail and clinical accuracy</li><li>Good communication and patient interaction skills</li><li>Ability to work independently and as part of a multidisciplinary team</li></ul>How to ApplyInterested candidates may apply by contacting our recruitment team:Nuclear Medicine Consultant jobs Hyderabad, Nuclear Medicine doctor vacancy, PET CT specialist jobs, Nuclear Medicine careers India, Hyderabad doctor jobs.Job Type: Full-timePay: ₹200,000.00 - ₹300,000.00 per monthWork Location: In person

Nuclear Medicine Consultant – Hyderabad (Full-Time)

Woodston Personnel Ltd.

<div>Woodston Personnel are seeking a highly qualified and experienced Consultant in Pediatric Emergency Medicine to join our client&rsquo;s hospital in Saudi Arabia. The Consultant will provide expert clinical leadership and high-quality care to children and adolescents presenting to the Emergency Department. The postholder will oversee the assessment, stabilization, and management of acute and life-threatening illnesses and injuries in paediatric patients, ensuring safe, efficient, and compassionate service delivery. The consultant will also contribute to education, service development, and clinical governance within the department.
Main Duties and Responsibilities<ul><li>
Provide specialist clinical assessment, diagnosis, and management of infants, children, and adolescents presenting to the emergency department.</li><li>
Lead the resuscitation and stabilization of critically ill or injured paediatric patients.</li><li>
Ensure timely and appropriate investigations, interventions, and referrals in accordance with current evidence-based guidelines.</li><li>
Collaborate closely with multidisciplinary teams, including paediatricians, surgeons, anaesthetists, and intensive care specialists.</li><li>
Supervise and support junior doctors, nurses, and allied health professionals in managing paediatric emergency cases.</li><li>
Provide on-call and out-of-hours cover for the paediatric emergency department as required.</li><li>
Maintain meticulous documentation and ensure compliance with safeguarding procedures for children.</li><li>
Provide clinical leadership in the delivery and continuous improvement of paediatric emergency services.</li><li>
Contribute to the development and implementation of clinical protocols, pathways, and policies.</li><li>
Participate in strategic planning for departmental growth and integration with other paediatric and emergency services.</li><li>
Lead and support quality improvement initiatives aimed at optimizing patient safety and outcomes.</li><li>
Serve as a role model for professionalism, clinical excellence, and compassionate care.</li><li>
Teach and mentor medical students, residents, nursing staff, and allied professionals in paediatric emergency care.</li><li>
Participate in simulation-based training and clinical skills development programs.</li><li>
Support continuing professional development (CPD) activities and encourage staff participation in learning opportunities.Contribute to regional or national educational programs in Paediatric Emergency Medicine.</li><li>
Participate in and, where possible, lead clinical research, audits, and service evaluations.</li><li>
Promote evidence-based practice and contribute to publications or presentations in the field.</li></ul><ul><li>
Implement findings from audits and research into clinical practice.</li><li>
Ensure adherence to hospital policies, clinical governance frameworks, and child protection regulations.</li><li>
Participate in risk management, incident review, and morbidity and mortality meetings.</li><li>
Contribute to departmental performance reviews, workforce planning, and rota management.</li><li>
Maintain registration, appraisals, and revalidation with the relevant professional body.</li></ul>
Full time contracts with excellent renumeration and benefits available
Please apply with your CV to register your interest in this role. 
MBBS or equivalent medical qualification
US Board/ FRCS - Irish, UK, Canadian, New Zealand or Australian/ Diploma d'Etudes Specialises (DES)/ CIS French Board/ Fachart &amp; Sub- Board/ Fellowship / Board / Fellowship / Sweden / Belgium / Finland / Spain
Must have at least 3-5 years of post-consultant or senior specialist experience
Eligible for consultant licensure with the Saudi Commission for Health Specialties (SCFHS)</div>

Consultant in Pediatric Emergency

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