clinical application support specialist

Global Mission Support Services LLC

<p>The Internal Medicine Specialist will provide comprehensive medical care for adult patients, including diagnosis, treatment, and management of a wide range of complex medical conditions. Preference will be given to candidates with subspecialty experience or training in Oncology or Cardiology. The specialist will play a key role in strengthening Nauru&rsquo;s internal medicine services, supporting clinical governance, and mentoring local healthcare professionals.</p><p>Key Responsibilities:</p><p>Provide specialist-level inpatient and outpatient care in internal medicine.</p><p>Diagnose and manage acute and chronic medical conditions.</p><p>Lead multidisciplinary case discussions and participate in ward rounds.</p><p>Develop and implement evidence-based treatment protocols and clinical guidelines.</p><p>Support early detection, screening, and management programs for chronic diseases and cancer.</p><p>Provide training, supervision, and mentorship to junior doctors, nurses, and allied health staff.</p><p>Collaborate with visiting specialists, referral hospitals, and regional health networks.</p><p>Participate in on-call duties as required.</p><p>Contribute to clinical audits, research, and quality improvement initiatives.</p><p>Qualifications &amp; Experience:</p><p>Medical degree (MD, MBBS, or equivalent) from a recognized institution.</p><p>Postgraduate qualification and board certification in Internal Medicine.</p><p>Additional training or clinical experience in Cardiology or Oncology preferred.</p><p>Current registration and license to practice medicine.</p><p>Minimum of 5 years post-specialization experience in hospital or clinical settings.</p><p>Strong diagnostic and problem-solving skills.</p><p>Excellent communication and leadership abilities.</p><p>Experience working in resource-limited or remote environments is an advantage.</p><p>Contract &amp; Benefits:</p><p>Competitive salary (commensurate with experience and qualifications).</p><p>Accommodation and food will be provided.</p><p>Round-trip airfare and relocation assistance.</p><p>30days paid Annual leave and professional development opportunities.</p><p>Supportive working environment within the Nauru health system.</p><p>Job Types: Full-time, Contract<br/>Contract length: 12 months</p><p>Application Question(s):</p><ul><li>Are you willing to relocate to Nauru Island once you got selected?</li><li>Do you have a valid Registration or license to work as an internal medicine specialist ?</li><li>Do you have experience in Oncology or Cardiology department as an internal medicine specialist?</li></ul>

INTERNAL MEDICINE SPECIALIST -NAURU DEPLOYMENT

King's College Hospital London

<p>  Join Our Team at King s: Clinical Nurse Specialist   Endometriosis</p>
<p>  Location: King s College Hospital London   Dubai</p>
<p>  Employment Type: Full-Time</p>
<p>King s College Hospital London   Dubai is committed to delivering the highest standards of patient care, reflecting the excellence and legacy of our London counterpart. We are now seeking a highly motivated and compassionate Clinical Nurse Specialist (CNS) in Endometriosis to join our leading Women s Health team.</p>
<p>This is a unique opportunity to make a meaningful difference in the lives of women with complex pelvic pain and endometriosis, while working in a multidisciplinary, patient-centred environment grounded in UK clinical best practices.</p>Role Overview:<br><p>As a Clinical Nurse Specialist   Endometriosis, you will:</p>
<ul>
 <li>Lead on the delivery of evidence-based, specialist nursing care for women with endometriosis and chronic pelvic pain.</li>
 <li>Provide expert clinical support, education, and counselling to patients throughout their treatment journey.</li>
 <li>Act as a key liaison between patients and the wider multidisciplinary team   including gynaecologists, pain specialists, fertility consultants, dietitians, and physiotherapists.</li>
 <li>Support nurse-led clinics, contribute to patient education initiatives, and help shape our specialist care pathways.</li>
 <li>Drive continuous service improvement and uphold the highest standards of clinical practice.</li>
</ul>Qualifications &amp; Requirements:<br><ul>
 <li>DHA-licensed or eligible Registered Nurse.</li>
 <li>Minimum 5 years at least as RN and 2 years in CNS role with endometriosis</li>
 <li>Postgraduate qualification or demonstrable expertise in endometriosis care (preferred).</li>
 <li>A confident, autonomous practitioner with exceptional communication and coordination skills.</li>
 <li>Passionate about delivering holistic, patient-focused care that empowers women.</li>
</ul>

Clinical Nurse Specialist Endometriosis

ICON plc

<div>Site Specialist II, Study Start Up<div></div><div>
ICON plc is a world-leading healthcare intelligence and clinical research organization. We&rsquo;re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development</div><div></div><div>
We are currently seeking a Site Specialist II (Study Start Up Associate II) to join our diverse and dynamic team. As a Site Specialist II at ICON, you will play a pivotal role in leading the initiation of clinical trials, ensuring compliance with regulatory requirements, and contributing to the advancement of innovative treatments and therapies.</div><div></div><div>
What you will be doing</div><ul><li><div>
Leading the preparation and submission of regulatory documents, including clinical trial applications, ethics committee submissions, and regulatory agency communications.</div></li></ul><ul><li><div>
Coordinating and liaising with internal and external stakeholders to obtain necessary approvals and authorizations for study initiation.</div></li></ul><ul><li><div>
Managing and maintaining comprehensive and accurate records of regulatory submissions, approvals, and correspondence</div></li></ul><ul><li><div>
Providing guidance and support to study teams on regulatory requirements and best practices for study start-up activities.</div></li></ul><ul><li><div>
Participating in process improvement initiatives to streamline study start-up processes and enhance efficiency.</div></li></ul><div></div><div>
Your profile</div><ul><li><div>
Bachelor's degree in life sciences or a related field.</div></li></ul><ul><li><div>
Minimum of 2 years of experience in clinical research or regulatory affairs, with specific experience in study start-up activities.</div></li></ul><ul><li><div>
Strong understanding of regulatory requirements and guidelines for clinical trials, including ICH-GCP and local regulatory requirements.</div></li></ul><ul><li><div>
Excellent organizational and project management skills, with the ability to prioritize and manage multiple tasks simultaneously.</div></li></ul><ul><li><div>
Excellent communication and interpersonal skills, with the ability to collaborate effectively with cross-functional teams.</div></li></ul><div></div><div>
What ICON can offer you:</div><div></div><div><div><div><div><div>
Our success depends on the quality of our people. That&rsquo;s why we&rsquo;ve made it a priority to build a diverse culture that rewards high performance and nurtures talent.</div><div></div><div>
In addition to your competitive salary, ICON offers a range of additional benefits. Our benefits are designed to be competitive within each country and are focused on well-being and work life balance opportunities for you and your family.</div><div></div><div>
Our benefits examples include:</div><ul><li><div>
Various annual leave entitlements</div></li><li><div>
A range of health insurance offerings to suit you and your family&rsquo;s needs.</div></li><li><div>
Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead.</div></li><li><div>
Global Employee Assistance Programme, TELUS Health, offering 24-hour access to a global network of over 80,000 independent specialised professionals who are there to support you and your family&rsquo;s well-being.</div></li><li><div>
Life assurance</div></li><li><div>
Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidised travel passes, health assessments, among others.</div></li></ul></div></div></div></div><div></div><div>
Visit our <div>careers site</div> to read more about the benefits ICON offers.</div><div></div><div>
At ICON, inclusion &amp; belonging are fundamental to our culture and values. We&rsquo;re dedicated to providing an inclusive and accessible environment for all candidates. ICON is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.</div><div></div><div><div><div><div><div>
If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know</div><div></div><div><div>
Interested in the role, but unsure if you meet all of the requirements? We would encourage you to apply regardless &ndash; there&rsquo;s every chance you&rsquo;re exactly what we&rsquo;re looking for here at ICON whether it is for this or other roles.</div></div></div></div></div></div></div><div></div>

Site Specialist II, Study Start Up

Carilion Clinic

<div><h2 class="jobSectionHeader"><b>Employment Status:
</b></h2>Full time
<h2 class="jobSectionHeader"><b>Shift:
</b></h2>Day (United States of America)
<h2 class="jobSectionHeader"><b>Facility:
</b></h2>213 S Jefferson St - Roanoke
<h2 class="jobSectionHeader"><b>Requisition Number:
</b></h2>R155647 Regulatory Affairs Specialist &ndash; Cardiology, Department of Medicine Clinical Research Unit (Open)&amp;#xa;&amp;#xa;
<h1 class="jobSectionHeader"><b>How You&rsquo;ll Help Transform Healthcare:
</b></h1>Please title the posting: Regulatory Affairs Specialist &ndash; Cardiology, Department of Medicine Clinical Research Unit
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Description text:
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The Regulatory Affairs Specialist will support clinical trials in the Department of Cardiology at Carilion Clinic. Under the supervision of the Department of Medicine Clinical Research Unit, this position is charged with maintaining compliance with study protocols, institutional policy, and federal regulations. Basic responsibilities include preparation of informed consent documents and IRB applications, regulatory submission and maintenance, assistance with monitoring visits, and participation in quality management of research studies. In collaboration with other research support staff, this position will support research investigators/physicians with guidance on research processes and enable successful collaborations with research sponsors. Direct experience with clinical research coordination or clinical trials desired but not required.&amp;#xa;&amp;#xa;<br>
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This is Carilion Clinic ...<br>
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An organization where innovation happens, collaboration is expected and ideas are valued. A not-for-profit, mission-driven health system built on progress and partnerships. A courageous team that is always learning, never discouraged and forever curious.<br>
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Headquartered in Roanoke, Va., you will find a robust system of award winning hospitals, Level 1 and 3 trauma centers, Level 3 NICU, Institute of Orthopedics and Neurosciences, multi-specialty physician practices, and The Virginia Tech Carilion School of Medicine and Research Institute.<br>
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Carilion is where you can make your own path, make new discoveries and, most importantly, make a difference. Here, in a place where the air is clean, people are kind and life is good. Make your tomorrow with us.
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<h1 class="jobSectionHeader"><b>What We Require:<br>
</b></h1><p><br>
<b>Education: </b>Bachelors degree required.
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<b>Experience: </b>Preferred - 1 year in healthcare or research or experience working with an IRB.
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<b>Licensure, certification, and/or registration: </b>clinical research certification through SoCRA or ACRP is required as soon as eligibility requirements are met.
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<b>Other Minimum Qualifications: </b>Knowledge of medical terminology desired. Must be competent in word processing and spreadsheets. Knowledgeable about data base management systems. Must have effective interpersonal and problem-solving skills. Must be self-directed and excel in attention to detail. Must use good judgment with regard to priorities and deadlines. Candidates must have excellent writing skills in order to generate reports, forms, correspondence.
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<p></p><p><b>Recruiter:
</b></p>HAYLEY OHL
<p><b>Recruiter Email:
</b></p>hcfield@carilionclinic.org
<p></p><p><b>For more information, contact the HR Service Center at 1-800-599-2537.
</b></p><p></p><p>Carilion Clinic is an Equal Opportunity Employer: We provide equal employment opportunities to all employees and applicants without regard to race, color, religion, sex, national origin, age (40 or older), disability, genetic information, or veterans status. Carilion is a Drug-Free Workplace. For more information or for individuals with disabilities needing special assistance with our online application process contact Carilion HR Service Center at 800-599-2537, 8:00 a.m. to 4:30 p.m., Monday through Friday.
</p><p></p><p>For more information on E-Verify: https://www.carilionclinic.org/eoe-e-verify-and-right-work-policies
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<h2 class="jobSectionHeader"><b>Benefits, Pay and Well-being </b><b>at Carilion Clinic
</b></h2><p></p><p>Carilion understands the importance of prioritizing your well-being to help you develop and thrive. T hat&rsquo;s why we offer a well-rounded benefits package, and many perks and well-being resources to help you live a happy, healthy life &ndash; at work and when you&rsquo;re away.<br>
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When you make your tomorrow with us, we&rsquo;ll enhance your potential to realize the best in yourself. Below are benefits available to you when you join Carilion:
</p><p></p><ul><li>Comprehensive Medical, Dental, &amp; Vision Benefits
</li><li>Employer Funded Pension Plan, vested after five years (Voluntary 403B)
</li><li>Paid Time Off (accrued from day one)
</li><li>Onsite fitness studios and discounts to our Carilion Wellness centers
</li><li>Access to our health and wellness app, Virgin Pulse
</li><li>Discounts on childcare
</li><li>Continued education and training</li></ul></div>

Regulatory Affairs Specialist – Cardiology, Department of Medicine Clinical Research Unit

Life Medical Equipment LLC

<p><b>Job Title:</b></p><p>1. Product Specialist &ndash; Cardiology<br/>2. Product Specialist - Ortho Department<br/><b>Location:</b> Oman</p><p>We are seeking a skilled and motivated <b>Product Specialist</b> to support our <b>Cardiology and Orthopedic</b> product portfolios in Oman. The successful candidate will serve as the primary link between healthcare providers, and internal departments, ensuring effective product promotion, clinical support, and customer satisfaction across hospitals and medical centers in Oman.</p><p><b>Key Responsibilities:</b></p><ul><li>Provide in-depth product knowledge and clinical support during surgical procedures.</li><li>Assist physicians and operating room staff in the correct usage of products.</li><li>Train hospital staff on product features, handling, and maintenance.</li><li>Support sales team in identifying and developing business opportunities in cardiology and orthopaedic departments across private and government healthcare institutions.</li><li>Conduct product presentations, trials, and workshops for physicians and procurement teams.</li><li>Assist in tender submissions, product evaluations, and regulatory documentation.</li><li>Develop strong relationships with key opinion leaders (KOLs), surgeons, cardiologists, and biomedical engineers.</li><li>Act as the first point of contact for customer feedback and technical issues.</li><li>Ensure timely follow-up with clients and deliver high-quality after-sales service.</li><li>Deliver product training for internal sales teams and external stakeholders.</li><li>Coordinate with global or regional teams for product updates, marketing materials, and training resources.</li><li>Submit regular reports to management on sales performance, competitor activity, and market trends.</li></ul><p><b>Requirements:</b></p><ul><li>Bachelor&rsquo;s degree in Biomedical Engineering, or a related field.</li><li>1-2 years of experience in a product specialist, clinical support, or sales role within the medical device or healthcare industry in Oman.</li><li>Strong understanding of cardiology and orthopedic procedures.</li></ul><p>Job Type: Full-time</p><p>Pay: RO750.000 - RO900.000 per month</p>

Product Specialist

Global Clinical Cura

<p><b>Position Title: Application Specialist &ndash; BioMedical Devices</b></p><p><b>Location:</b> Sector F, DHA Phase 1, Islamabad</p><p><b>Department:</b> Customer Support Department</p><p><b>Bachelor&rsquo;s degree:</b> MLT, Microbiology, Chemistry, Life Sciences, or a related fields.</p><p><b>Key Responsibilities:</b></p><ul><li><b>Key Responsibilities:</b></li><li>Possess a comprehensive understanding of medical equipment and devices.</li><li>Identify, approach, and secure new business opportunities across hospitals, diagnostic laboratories, and clinics.</li><li>Demonstrate experience in laboratory disciplines such as chemistry, immunoassay, and microbiology.</li><li>Be prepared for fieldwork, including outstation travel for product installation, troubleshooting, and support.</li><li>Formulate and execute strategies to achieve assigned sales goals and enhance the organization&rsquo;s market footprint.</li><li>Handle the complete sales process&mdash;from lead identification and client engagement to negotiation and final deal closure.</li><li>Establish and nurture long-term professional relationships with physicians, biomedical engineers, and procurement departments.</li><li>Perform consistent follow-ups to ensure customer satisfaction and identify opportunities for cross-selling and upselling.</li><li>Generate accurate sales forecasts, detailed reports, and performance summaries for management evaluation.</li><li>Conduct live product demonstrations, clinical presentations, and hands-on training sessions for medical professionals.</li><li>Deliver both technical and clinical assistance during installations, product trials, and post-sales services.</li><li>Work closely with technical and service departments to ensure seamless product deployment and top-quality performance.</li><li>Share market insights and feedback with product and marketing teams to refine offerings and design targeted campaigns.</li><li>Keep meticulous records of all sales activities, client communications, and customer feedback.</li><li>Ensure timely submission of reports, documentation, and updates as required by management.</li><li>Preferred: Previous experience in the sales or application support of medical devices or diagnostic instruments.</li><li>Exhibit excellent communication, negotiation, and presentation capabilities.</li><li>Possess sound technical knowledge of medical equipment and its clinical usage.</li><li>Demonstrate the ability to function both independently and within cross-functional teams.</li><li>Be open to frequent travel for client meetings, training sessions, and product demonstrations.</li><li>Show self-motivation, enthusiasm for healthcare technology, and a customer-first attitude.</li><li>Maintain a proactive, problem-solving approach with a focus on delivering value to clients.</li></ul><p>Job Type: Full-time</p><p>Pay: Rs65,000.00 - Rs85,000.00 per month</p><p>Experience:</p><ul><li>Diagnostic Industry: 2 years (Preferred)</li></ul><p>Work Location: In person</p>

Application Specialist (BioMedical Devices Company)

Danaher Life Sciences

Clinical Application Specialist - Chemistry / Immunoassay - Madina Based <p>Beckman Coulter Diagnostics, a Danaher Corporation operating company, develops, manufactures, and markets innovative solutions that simplify, automate, and advance complex biomedical testing. Our diagnostic systems are trusted in hospitals and critical care settings worldwide, providing physicians with vital information to diagnose disease, guide treatment decisions, and monitor patient health. In the life sciences, our research instruments empower scientists to investigate the underlying causes of disease and explore potential new therapies and drugs.</p> <p>As part of Danaher-a global science and technology leader-Beckman Coulter is driven by a shared purpose: Helping Realize Life's Potential. We offer a broad portfolio of competitive benefits designed to support associates and their families, from comprehensive healthcare coverage to paid time off, enabling a fulfilling life beyond work.</p> Position Overview <p>We are seeking a passionate, clinically skilled, and commercially driven professional to assess and address customer needs, providing pre- and post-sales technical expertise, application support, and workflow optimization. This role involves designing tailored solutions, delivering product demonstrations, and facilitating customer training-both onsite and at industry events-to ensure optimal use of Beckman Coulter solutions in line with manufacturer specifications.</p> Responsibilities <ul> <li>Build and sustain strong, long-term relationships with end users in the assigned territory by understanding and meeting their needs.</li> <li>Expand the adoption of Beckman Coulter's test menu and product portfolio.</li> <li>Identify and implement technical solutions aligned with customer requirements and product specifications.</li> <li>Diagnose and resolve technical issues related to parameters, calibration, and quality control.</li> <li>Deliver product training to end users and provide clinical support to sales and service teams.</li> <li>Represent Beckman Coulter at internal and external meetings, trade shows, and seminars.</li> <li>Support customers with External Quality Control programs (e.g., RIQAS).</li> <li>Contribute clinical expertise to project execution and respond to field safety notifications in collaboration with the regulatory team.</li> <li>Work closely with Service, Commercial, and Marketing teams to introduce new tests to the market.</li> </ul> Qualifications & Experience <ul> <li>Bachelor's degree in Science, Biochemistry, or Medical Laboratory Sciences.</li> <li>Proven diagnostic and laboratory experience.</li> <li>Strong clinical and commercial acumen.</li> <li>Fluent in English and Arabic.</li> <li>Excellent relationship-building skills with stakeholders including end-users, purchasing agents, and distributors.</li> <li>In-depth knowledge of the Saudi Arabian diagnostics market.</li> <li>High agility and flexibility, with the ability to travel extensively.</li> </ul> <p>For more information, visit .</p><img src="https://www.jobg8.com/Tracking.aspx?FQXNT6u9OH0nJsN0LeC0cF0atY8Li3OMl" width="0" height="0" />

Clinical Application Specialist - Chemistry / Immunoassay - Madina Based

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