clinical cytopathologist

Britt Medical Search

Health Center is seeking a BC/BE Pathologist to join its team. Employing experienced phlebotomists, ASCP-certified clinical lab scientists and technicians, and board-certified pathologists, the lab processes more than 500,000 clinical specimens and 10,000 surgical and cytology specimens each year. The laboratory is a vital part of the hospital and patient care, and an important part of the community. To that end, the laboratory sponsors an active educational outreach program including visits by lab personnel to local schools, job-shadowing programs, phlebotomy instruction with Lake Land College, participation in the hospital s high school Health Occupation classes, and a Science Lab program to provide schools in our region with tools and resources promoting interactive and hands-on learning in the classroom. This is an employed position with a progressive and financially secure Health System. Find your work/life balance with a family-centered community. Join a strong team of employed physicians who offer a direct source for referrals and specialties. The culture is one you'll not find elsewhere with employee accountability and pride in our organization. You have to see this for yourself! Practice Opportunity Details: Competitive base salary with bonus potential Paid malpractice CME Relocation assistance Strong pension plan Health, vision, dental, life and disability coverage 33 vacation days flexible call schedule Community, Facility and Organization: The Health Center provides a full range of acute-care, general services and home health services to approximately 357,000 residents of Coles and the surroundings 12 counties. The Health Center's active and consulting medical staff includes nearly 200 providers representing multiple specialties. A strong employed physician base means built-in referrals and excellent collaboration on patient care. In a recent survey, we ranked in the 95th percentile in employee engagement and in the 91st percentile in physician satisfaction. We've got something special here and our culture is at the heart of it all. Most employees enjoy a commute of less than 15 minutes which makes a great work/life balance. The cities offer a small town feel while offering larger city amenities such as shopping, family activities, cultural activities and leisure. Mattoon-Charleston is home to Eastern Illinois University, Lake Land Community College and Fox Ridge State Park. We also boast the first ever Jimmy John's store, THE Burger King, Lender's Bagels factory and several famous EIU alumni. With safe communities, outdoor activities, community events and easy access to metro areas this is a great place to raise a family. APPLY NOW or TEXT Job & email address to 636 - 628 - 2412. Search all of our provider opportunities at: brittmedical DOT com<img src="https://www.jobg8.com/Tracking.aspx?3GSCoU9cNcYHE8y8CJXOlDrpaqiVh1iBm" width="0" height="0" />

Physician / Pathology / Illinois / Permanent / Pathologist opening south of Champaign, IL Job

Health Center is seeking a BC/BE Pathologist to join its team. Employing experienced phlebotomists, ASCP-certified clinical lab scientists and technicians, and board-certified pathologists, the lab processes more than 500,000 clinical specimens and 10,000 surgical and cytology specimens each year. The laboratory is a vital part of the hospital and patient care, and an important part of the community. To that end, the laboratory sponsors an active educational outreach program including visits by lab personnel to local schools, job-shadowing programs, phlebotomy instruction with Lake Land College, participation in the hospital s high school Health Occupation classes, and a Science Lab program to provide schools in our region with tools and resources promoting interactive and hands-on learning in the classroom. This is an employed position with a progressive and financially secure Health System. Find your work/life balance with a family-centered community. Join a strong team of employed physicians who offer a direct source for referrals and specialties. The culture is one you'll not find elsewhere with employee accountability and pride in our organization. You have to see this for yourself! Practice Opportunity Details: <ul> <li> Competitive base salary with bonus potential </li> <li> Paid malpractice </li> <li> CME </li> <li> Relocation assistance </li> <li> Strong pension plan </li> <li> Health, vision, dental, life and disability coverage </li> <li> 33 vacation days </li> <li> flexible call schedule </li> </ul> Community, Facility and Organization: The Health Center provides a full range of acute-care, general services and home health services to approximately 357,000 residents of Coles and the surroundings 12 counties. The Health Center's active and consulting medical staff includes nearly 200 providers representing multiple specialties. A strong employed physician base means built-in referrals and excellent collaboration on patient care. In a recent survey, we ranked in the 95th percentile in employee engagement and in the 91st percentile in physician satisfaction. We've got something special here and our culture is at the heart of it all. Most employees enjoy a commute of less than 15 minutes which makes a great work/life balance. The cities offer a small town feel while offering larger city amenities such as shopping, family activities, cultural activities and leisure. Mattoon-Charleston is home to Eastern Illinois University, Lake Land Community College and Fox Ridge State Park. We also boast the first ever Jimmy John's store, THE Burger King, Lender's Bagels factory and several famous EIU alumni. With safe communities, outdoor activities, community events and easy access to metro areas this is a great place to raise a family. APPLY NOW or TEXT Job & email address to 636 - 628 - 2412. Search all of our provider opportunities at: brittmedical DOT com <img src="https://www.jobg8.com/Tracking.aspx?YN6DMgfvrzBkRu1N%2fu5OZ0lCIY7DEq5qf" width="0" height="0" />

Seeking a BC/BE General Pathologist to join our health center north of Syracuse, NY. AP/CP Pathologist; Certified or eligible for certificate of qualifications in all areas of Anatomic and Clinical Pathology. Must be comfortable with sign-out in all areas of pathology including limited hematopathology cases <ul> <li> Hospital employed full-time position joining two BC seasoned and well respected Pathologists </li> <li> Our full service laboratory dedicated to serving the dynamic needs of healthcare providers. </li> <li> Staffed with 60 employees, including medical technologists, medical laboratory technicians, laboratory assistants, histotechnicians, cytotechnologists and other support staff </li> <li> Services are operational 24 hours a day to include weekends and holidays; over 1,000 tests are performed daily </li> <li> Accredited by the New York State Department of Health, The Joint Commission on Accreditation of Healthcare Organizations and the American Association of Blood Banks </li> <li> Walker Center for Cancer Care, a state-of-the-art facility completed in 2017, is affiliated with Roswell Park Comprehensive Cancer Center in Buffalo, NY. Roswell Park actively participates in our multidisciplinary tumor board, which convenes twice monthly to review and coordinate patient care </li> </ul> Compensation & Benefits: <ul> <li> Annual Base Salary $431,932 </li> <li> Signing Bonus $50,000 </li> <li> Annual Educational Loan Repayment $20,000 </li> <li> Relocation Reimbursement $15,000 </li> </ul> The Community: Northern New York offers safe and attractive neighborhoods, quiet rural areas, affordable housing, light traffic, first-rate school systems and a gorgeous landscape, all combined with easy accessibility to major metropolitan areas. We are a half hour from the Canadian border. International Airport is just 15-minutes away. Take a boat tour of the Thousand Islands with a visit to Boldt Castle, owned by George C. Boldt, proprietor of the Waldorf-Astoria Hotel in New York City. Boating, swimming, scuba diving and fishing are popular pursuits throughout the Thousand Islands. We have four YMCA fitness centers in the area with endless recreational activities for kids and adults - including indoor swimming! Our local ski area is a gathering spot during the winter for family and friends offering ski/snowboarding lessons for all ages. At the foot of the Adirondacks, the Tug Hill Region gets as much as 300 inches of snow annually and is the perfect place for skiers, snowboarders, snowmobilers, and snow lovers of all ages. APPLY NOW or TEXT Job and email address to 636 - 628 - 2412. Search all of our provider opportunities here: brittmedical DOT com <img src="https://www.jobg8.com/Tracking.aspx?lMNKBtJ7lGy%2fD7AF2lmqq5qDtwbIwta%2bw" width="0" height="0" />

Physician / Pathology / New York / Permanent / Pathologist opening north of Syracuse, NY - $50K sign-on! Job

Midmark Corporation

<div>JOB SUMMARY:
The Clinical Solutions Advisor serves as Midmark&acirc;&euro;&trade;s senior, field-facing clinical authority for escalated customer needs and a clinical expert partner to cross-functional teams throughout the product lifecycle. Reporting to the Chief Medical Officer, the Clinical Solutions Advisor blends real-world clinical expertise with strong customer engagement, collaboration, and communication skills to strengthen product performance, elevate clinical credibility, improve customer satisfaction, and assist continuous improvement efforts. The role balances direct customer interactions with internal project contributions and periodic thought-leadership content, while traveling extensively as business needs arise. 
ESSENTIAL/PRIMARY DUTIES:
<ul><li>Lead Tier-2 clinical support operations, ensuring timely resolution of escalated customer issues, and maintaining excellence in clinical performance and satisfaction.
</li><li>Engage strategically with customers, sales teams, and clinical education (virtual and onsite) to assess, troubleshoot, and resolve clinical challenges in real time.
</li><li>Analyze and communicate findings from field engagements, recommending corrective actions and continuous improvement initiatives to Clinical Affairs, Q&amp;R, and Product Development leadership.
</li><li>Collaborate with Sales leadership to provide clinical expertise during pre-sales activities, clarifying clinical workflows, use cases, and solution value.
</li><li>Serve as the primary clinical advisor throughout solution development, influencing design, and commercialization strategies to align with user needs and clinical realities.
</li><li>Define and advocate for clinical requirements including workflow integration, ergonomics, usability, and key quality standards that enhance product effectiveness.
</li><li>Provide clinical oversight and input to verification, validation, usability studies, and evidence or claims development, ensuring alignment with regulatory and quality objectives.
</li><li>Engage and manage relationships with external clinical experts to gather insights that inform innovation, design decisions, and market readiness.
</li><li>Advance Midmark&acirc;&euro;&trade;s clinical thought leadership through authored content, presentations, and active representation at industry events and customer forums.
</li><li>Mentor and empower internal teams, elevating clinical knowledge, cross-functional collaboration, and field readiness to strengthen Midmark&acirc;&euro;&trade;s clinical excellence. 
</li></ul>SECONDARY DUTIES:
<ul><li>N/A 
</li></ul>EDUCATION and/or EXPERIENCE:
Registered Nurse (RN) with a BSN (MSN or Advanced Practice Degree preferred; MBA a plus) and possess 5+ years of clinical experience, ideally in emergency, acute, perioperative, or primary care settings, or an equivalent combination of education and experience. They are knowledgeable in medical devices, clinical workflows, ergonomics, and human factors, with excellent presentation and technical writing abilities. 
COMPETENCY and/or SKILL:
<ul><li>Deep understanding of clinical practice, patient care processes, and healthcare environments.
</li><li>Proven ability to build trust, manage relationships, and address complex clinical and operational concerns.
</li><li>Demonstrates strong customer-facing and problem-solving skills, with proven ability in conflict management, complaint resolution, and effective communication across diverse audiences.
</li><li>Familiar with medical technologies, clinical workflows, ergonomics, and human factors.
</li><li>Clear, confident communicator with strong presentation, facilitation, and technical writing skills.
</li><li>Translates clinical insights into product strategy, design requirements, and measurable business value.
</li><li>Excels in cross-functional collaboration to align clinical, commercial, and technical objectives.
</li><li>Experience authoring clinical content (e.g., blogs, white papers) and representing the organization in professional forums.
</li><li>Thrives in dynamic environments, adjusting priorities and supporting short-notice travel, and field demands.
</li><li>Dedicated to developing internal clinical knowledge and enhancing team capability and performance. 
</li></ul>SUPERVISORY RESPONSIBILITIES:
<ul><li>None</li></ul></div> <div></div>

Clinical Solutions Advisor

Gadgeon Medical Systems Pvt Ltd.

About Webcardio Webcardio is a leading provider of innovative cardiac monitoring solutions, offering Doctors and patients real-time, remote cardiac diagnostics through advanced wearable ECG technology. Our mission is to improve cardiac care delivery using AI driven insights and seamless technology.Role OverviewThe Medical Affairs Manager will lead and oversee clinical and medical activities, ensuring high-quality, compliant, and evidence-based clinical research and communication. The role involves managing clinical studies, regulatory compliance, cross-functional collaboration, and scientific communication to support product development, marketing, and sales initiatives.Key Responsibilities:1. Clinical Study Management<ul><li>Design, plan, and manage clinical trials, including Real-World Evidence (RWE) studies.</li><li>Ensure adherence to Good Clinical Practices (GCP) and ethical guidelines.</li><li>Collaborate with investigators, Key Opinion Leaders (KOLs), and research sites.</li><li>Collect, analyse, and interpret post-marketing clinical data.</li><li>Conduct retrospective analyses of WebCardio data.</li><li>Lead prospective clinical trials, including protocol design, medical writing, and data analysis to ensure smooth execution.</li></ul>2. Regulatory &amp; Compliance Oversight<ul><li>Ensure compliance with regulatory requirements (e.g., CDSCO) and internal standards.</li><li>Prepare clinical documentation for regulatory submissions and approvals.</li><li>Monitor evolving clinical and regulatory standards to ensure ongoing compliance.</li></ul>3. Cross-Functional Collaboration<ul><li>Partner with marketing, sales, and other functions to provide clinical insights that enhance strategy and product development.</li><li>Support sales teams in addressing clinical objections with evidence-based information.</li><li>Collaborate with KOLs to gather insights for ongoing and future projects.</li><li>Travel as required to support studies and stakeholder engagement.</li></ul>4. Scientific &amp; Medical Communication<ul><li>Prepare clinical study reports, white papers, and publications.</li><li>Present clinical data at conferences, webinars, and to internal and external stakeholders.</li><li>Provide scientific training to KOLs, speakers, and the sales team as required.</li></ul>Qualifications &amp; Experience:<ul><li>Degree in Medicine, Pharmacy, or Life Sciences (MBBS,PHD,PharmD, or equivalent).</li><li>Proven experience in clinical study management, medical affairs, or regulatory roles in healthcare/medical device/biotech sectors.</li><li>Strong knowledge of GCP, clinical research methodology, and regulatory requirements.</li><li>Excellent communication, collaboration, and analytical skills.</li><li>Place of work- Delhi/NCR (WFH)</li><li>Min 3+ Years of experience</li><li>Travel- 25% of time and depends on study requirements.</li></ul>Job Types: Full-time, PermanentPay: &#8377;800,000.00 - &#8377;1,200,000.00 per yearApplication Question(s):<ul><li>Current CTC</li><li>Expected CTC</li></ul>Education:<ul><li>Bachelor's (Required)</li></ul>Experience:<ul><li>clinical study management: 2 years (Required)</li></ul>Location:<ul><li>Delhi, Delhi (Required)</li></ul>Willingness to travel:<ul><li>25% (Required)</li></ul>Work Location: Remote

Medical Affairs Manager

IQVIA

<div>Job Overview
 
Perform daily administrative activities, in conjunction with the Clinical Research Associates and Regulatory and Start-Up teams, to ensure a complete and accurate Trial Master File delivery.
 
 
Essential Functions
 
&bull; Assist Clinical Research Associates (CRAs) and Regulatory and Start-Up (RSU) team with accurately updating and maintaining clinical documents and systems (e.g., Trial Master File (TMF)) that track site compliance and performance within project timelines.
 
&bull; Assist the clinical team with the preparation, handling, distribution, filing, and archiving of clinical documentation and reports according to the scope of work and standard operating procedures.
 
&bull; Assist with periodic review of study files for completeness.
 
&bull; Assist CRAs and RSU with preparation, handling and distribution of Clinical Trial Supplies and maintenance of tracking information. Coordinate the tracking and management of Case Report Forms (CRFs), queries and clinical data flow.
 
&bull; Act as a central contact for the clinical team for designated project communications, correspondence and associated documentation.
 
&bull; May accompany CRAs on site visits to assist with clinical monitoring duties upon completion of required training.
 
&bull; May collaborate with the clinical team on the preparation, handling, distribution, filing, and archiving of clinical documentation and reports according to the scope of work and standard operating procedures.
 
 
Qualifications
 
&bull; High School Diploma or equivalent Req
 
&bull; At least 1 year experience as CTA with Finance responsibilities
&bull; Experience in contracts, payments, budgeting, invoicing
&bull; Equivalent combination of education, training and experience.
 
&bull; Minimum one year clinical research experience strongly preferred.
 
&bull; Computer skills including working knowledge of Microsoft Word, Excel and PowerPoint.
 
&bull; Written and verbal communication skills including good command of Greek and English language.
 
&bull; Effective time management and organizational skills.
 
&bull; Ability to establish and maintain effective working relationships with coworkers, managers, and clients.
 
&bull; Basic knowledge of applicable clinical research regulatory requirement, i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines as provided in company training.
 
&bull; Knowledge of applicable protocol requirements as provided in company training.
IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide . Learn more at https://jobs.iqvia.com</div>

Clinical Trials Assistant with Finance Responsibilities Sponsor-dedicated

Jupiter Life Science Consulting

<div>
 Clinical Research Scientist
 
 
 The Clinical Research Scientist will be responsible for the development of post-market clinical research strategies of orthopedic devices to support global regulatory and post-market surveillance requirements.
 
 
 
 About Red Nucleus
 
 
 
 Our purpose is advancing knowledge to improve lives. We succeed by being the premier provider of strategic learning and development, scientific advisory services (commercial, market access, medical affairs), and medical communications solutions for the life sciences industry. Our global team is composed of nearly 1,000 full-time employees whose commitment to creativity, quality, and on-time delivery is unrivaled in our space.
 
 
 At Red Nucleus, we believe in providing a rich working environment that pushes us to innovate in ways that engages our employees to be their best selves. Our culture is about meaningful work, a true sense of community, and fun. We love to celebrate our people and we are proud to have been Internationally recognized as a &ldquo;Great Place to Work".
 
 
 
 Responsibilities Include
 
 
 
 <ul>
 <li>
 Work closely with cross-functional teams (Clinical, Medical, Regulatory, R&amp;D, Marketing) to develop post market clinical evidence generation strategies that consider evidence needs for EU Medical Device Regulations (EU MDR). Facilitate clinical evidence reviews with cross functional team to align clinical evidence strategies, document / track decisions and risks, and write PMCF Plans.
 </li>
 <li>
 Develop and write high quality Post-market Clinical Follow-up (PMCF) plans and reports with minimal supervision. Support development and drafting of clinical study protocols, registry plans, epidemiology studies, informed consents, investigator brochures, and other study materials where needed.
 </li>
 <li>
 Review summaries of clinical evidence and PMCF strategies in other areas of the Technical Documentation for accuracy and completeness. This includes the Clinical Evaluation Plan, Clinical Evaluation Report (CEP), Post Market Surveillance Plan and Periodic Safety Update Report (PSUR).
 </li>
 <li>
 Where required, foster relationships with surgeons, hospitals and research teams to gain input into study design, evaluate study feasibility, and identify sites for study execution or data collection. Develop strong collaborative relationships with the study core team and others to ensure study progress for assigned projects and that issues are identified and communicated to leaders.
 </li>
 <li>
 Partner with the Contracts and Payments team to ensure timely execution of all study agreements and corresponding payments for achieved milestones and deliverables.
 </li>
 <li>
 Support clinical scientific discussions with internal stakeholders within Clinical, Medical, Regulatory, R&amp;D and Marketing to drive support of the clinical and regulatory strategy, communicate evidence needs.
 </li>
 <li>
 Contribute to appropriate interpretation and dissemination of all evidence generated, including abstracts, manuscripts, and Clinical Study Reports (CSR), epidemiology study results and clinical literature.
 </li>
 <li>
 Develop a strong understanding of the orthopedic device product portfolio and business needs for clinical evidence to meet regulatory requirements.
 
 
 </li>
 </ul>
 
 Qualifications
 
 
 
 <ul>
 <li>
 A Master&rsquo;s degree in Biological Science or related discipline, with a minimum of 4 years&rsquo; experience in the medical device industry or healthcare field is required
 </li>
 <li>
 Advanced technical writing skills is required, with demonstrated experience in writing PMCF plans / reports strongly preferred.
 </li>
 <li>
 Clinical expertise in the medical device sector
 </li>
 <li>
 Proven experience in conducting clinical studies, registries particularly in the field of orthopaedics
 </li>
 <li>
 Strong project management skills required, with demonstrable track record of success managing multiple projects simultaneously with minimal supervision.
 </li>
 <li>
 Excellent communication skills, including effective interaction with healthcare professionals (HCPs), hospital staff etc.
 
 
 </li>
 </ul>
</div>

Clinical Research Scientist (Device, Ortho)

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5242 clinical cytopathologist jobs NEAR_ME

Physician / Pathology / Illinois / Permanent / Pathologist opening south of Champaign, IL Job

Physician / Pathology / Illinois / Permanent / Pathologist opening south of Champaign, IL Job

Physician / Pathology / New York / Permanent / Pathologist opening north of Syracuse, NY - $50K sign-on! Job

Clinical Solutions Advisor

Medical Affairs Manager

Clinical Trials Assistant with Finance Responsibilities Sponsor-dedicated

Clinical Research Scientist (Device, Ortho)