scientist immunology

Anvia Therapeutics

<div>
 
 
 Job Title: Scientist II- Immunology
 
 
 
 
 Location: NYC
 
 
 
 
 About Us:
 
 
 
 Anvia Therapeutics is a dynamic and innovative biotech company dedicated to developing small molecule inhibitors targeted at treating inflammatory and autoimmune diseases. We foster a collaborative environment where scientific excellence and creativity drive our mission to develop impactful medicines.
 
 
 
 
 
 
 Job Summary
 
 
 
 We are seeking a highly motivated immunology Scientist to drive hypothesis-driven in vitro immunology research in a fast-paced and innovative drug discovery environment. The successful candidate will design, develop, and execute complex cellular assay systems, including primary human immune cells, patient-derived samples, and disease-relevant cell lines to support immune pharmacology and mechanism-of-action (MoA) studies across inflammatory disease programs such as IBD, rheumatoid arthritis, and dermal inflammation.
 
 
 
 
 
 
 Key Responsibilities
 
 
 <ul>
 <li>
 Design and execute hypothesis-driven cellular assays to support immune pharmacology, target validation, and MoA studies.
 </li>
 <li>
 Develop, optimize, and validate complex in vitro assay systems using primary immune cells, patient-derived samples, and disease-relevant or engineered cell lines.
 </li>
 <li>
 Perform functional immune assays including cell activation, proliferation, cytokine production, signaling, and cytotoxicity, using both primary and cell-line&ndash;based systems.
 </li>
 <li>
 Contribute to immune pharmacology assessments, including compound potency, pathway modulation, selectivity, and translational relevance.
 </li>
 <li>
 Apply a strong mechanistic understanding of immune and inflammatory signaling pathways to guide assay design and data interpretation.
 </li>
 <li>
 Utilize flow cytometry, ELISA/MSD/other cytokine/chemokine profiling techniques, protein- and signaling-based assays, and related techniques to generate high-quality, reproducible data.
 </li>
 <li>
 Analyze, interpret, and clearly communicate experimental results to project and leadership teams.
 </li>
 <li>
 Troubleshoot and refine experimental systems to improve robustness, scalability, and biological relevance.
 </li>
 <li>
 Maintain accurate experimental records using electronic laboratory notebooks.
 </li>
 <li>
 Collaborate closely with lead discovery, chemistry, translational, and external partners to advance program milestones.
 </li>
 <li>
 Stay current with emerging immunology technologies and incorporate innovative methodologies where appropriate.
 </li>
 </ul>
 
 
 
 
 
 Required Qualifications
 
 
 <ul>
 <li>
 PhD in Immunology, Biology, Biotechnology, Molecular Biology, or a related field with 2+ years of relevant experience.
 </li>
 <li>
 Hands-on experience developing and executing complex cellular assays using primary immune cells, patient-derived samples, and cell line&ndash;based systems.
 </li>
 <li>
 Experience working with functional immune readouts, including flow cytometry&ndash;based phenotyping and signaling assays, and cytokine measurement (ELISA/MSD/other).
 </li>
 <li>
 Demonstrated expertise in protein-level analysis of signaling pathways, including Western blotting and related biochemical techniques used to assess pathway activation, inhibition, and mechanism of action.
 </li>
 <li>
 Strong understanding of cell signaling pathways relevant to immune and inflammatory biology.
 </li>
 <li>
 Proven ability to independently design experiments, troubleshoot assays, and manage multiple priorities.
 </li>
 <li>
 Proficiency with data analysis and visualization tools (e.g., GraphPad Prism, FlowJo, Excel).
 </li>
 <li>
 Excellent written and verbal communication skills.
 </li>
 </ul>
 
 
 
 
 
 Preferred Qualifications
 
 
 <ul>
 <li>
 Experience supporting immune pharmacology and MoA characterization in early drug discovery.
 </li>
 <li>
 Background in inflammatory or autoimmune disease biology (IBD, RA, dermatology preferred).
 </li>
 <li>
 Familiarity with assay validation, quantitative potency assessment and translational biomarker analysis/ identification.
 </li>
 <li>
 Experience working in a fast-paced, innovative biotech environment.
 </li>
 </ul>
 
 
 
 
 Why Join Us?
 
 <ul>
 <li>
 Be part of a passionate team making a difference in biotech innovation.
 </li>
 <li>
 Collaborative and dynamic work environment.
 </li>
 <li>
 Hands-on experience with state-of-the-art technologies.
 </li>
 <li>
 Opportunities for professional development and advancement.
 </li>
 <li>
 Competitive compensation and benefits.
 </li>
 </ul>
 
 
 
 
 The salary range for this position is $115,000-$150,000 per year. The actual compensation offered will be based on factors such as relevant experience, education, and skills. In addition to base salary, we offer a comprehensive benefits package, including health insurance, paid time off, and retirement plan options.
 
 
 
 
 
 Anvia Therapeutics is an equal opportunity employer. We do not discriminate against any employee or applicant for employment because of race, creed (religion), color, national origin, sex (including gender identity and sexual orientation), age, disability, marital status, citizenship status, military status, genetic information, or any other characteristic protected by federal, state, or local law.
 
 
 
 
 
 Our employment decisions are based on merit, qualifications, and business needs. We are committed to providing a work environment free from discrimination, harassment, and retaliation, and we undertake affirmative action efforts to promote equal opportunity for all employees and applicants.
 
 
 
 
</div>

Scientist II, Immunology

Cyber Security Academy Southampton

<div>
 Interview Date: in the week commencing 26 January 2026
 
 
 
 Project Summary
 
 
 
 An exciting opportunity is available to join the laboratories of Dr Salah Mansour and Dr Ali Roghanian at the University of Southampton. We are seeking a collaborative and motivated postdoctoral scientist to work on our Blood Cancer UK-funded programme developing next-generation, off-the-shelf immunotherapies for acute myeloid leukaemia (AML).
 
 
 This three-year project will harness cytotoxic invariant Natural Killer T (iNKT) cells for precision targeting of AML, an aggressive leukaemia with poor survival outcomes. Building on strong preliminary data, it combines mechanistic and translational immunology with bespoke
 
 in vivo
 
 models to define and exploit therapeutically relevant subsets. The Research Fellow will lead studies on cytotoxic T cell mechanisms, oversee preclinical validation, and advance CAR-iNKT platforms optimised for AML immunotherapy.
 
 
 The role bridges basic and translational research and suits a creative scientist with interests in tumour immunology, T cell engineering, and immunotherapy. You will join a multidisciplinary team spanning immunology, and bioinformatics, with access to advanced flow cytometry, 10X Genomics,
 
 in vivo
 
 imaging platforms.
 
 
 
 Key Responsibilities
 
 
 
 <ul>
 <li>
 To work within the Mansour and Roghanian labs, and with collaborators at Southampton and beyond.
 </li>
 <li>
 To design, conduct, and analyse in vitro and in vivo immunology experiments.
 </li>
 <li>
 To lead the optimisation and functional assessment of human T cells and CAR T cells.
 </li>
 <li>
 To liaise and coordinate between project collaborators and core facilities.
 </li>
 <li>
 To record analyses accurately and present results at group meetings, national, and international conferences.
 </li>
 <li>
 To contribute to dissemination of findings through publications and grant applications.
 </li>
 <li>
 To supervise and support junior researchers and students.
 </li>
 <li>
 Any other duties appropriate to the scope and grade of the post.
 
 
 </li>
 </ul>
 Postdoctoral Fellows are expected to lead their own projects, collaborate on others, and guide PhD and Master&rsquo;s students.
 
 
 
 Essential Qualifications, Experience And Competencies
 
 
 
 <ul>
 <li>
 PhD (or near completion) in human T cell immunology, cancer biology, or a related discipline.
 </li>
 <li>
 Strong practical experience with core immunological assays (e.g. FACS, ELISA, T cell assays).
 </li>
 <li>
 Proven competence in the design and execution of experiments using mouse models of cancer.
 </li>
 <li>
 Ability to manage projects to timelines, supervise junior staff, and work both independently and collaboratively.
 </li>
 <li>
 Excellent communication and presentation skills, including at conferences.
 
 
 </li>
 </ul>
 
 Desirable
 
 
 
 <ul>
 <li>
 Experience with single-cell or bulk sequencing (e.g. 10X Genomics, RNA-seq).
 </li>
 <li>
 Familiarity with bioinformatics pipelines and large dataset interpretation.
 </li>
 <li>
 Experience in engineering human T cells, viral transduction, or related approaches.
 </li>
 <li>
 Home Office Personal Licence.
 
 
 </li>
 </ul>
 
 About Us
 
 
 
 The University of Southampton offers a strong environment for translational immunology. Clinical and Experimental Sciences (CES) is a hub for infection and immunology, while the Centre for Cancer Immunology (CCI) is the UK&rsquo;s first dedicated cancer immunology centre. Together, they unite expertise in T cell biology, multiomics, immunotherapy, preclinical modelling, and clinical translation, supported by an embedded Clinical Trials Unit and close links with NHS and industry partners.
 
 
 
 Working At The University Of Southampton
 
 
 
 Check out the staff benefits and why you should join us at The University of Southampton!
 
 
 
 Applicants Should Provide
 
 
 
 <ul>
 <li>
 A CV
 </li>
 <li>
 A cover letter outlining suitability for the role
 </li>
 <li>
 Contact details for at least two recent referees
 
 
 </li>
 </ul>
 Email details to a friend
 
 
 Apply Online
 
 
 
 Further Details
 
 
 
 <ul>
 <li>
 Job Description and Person Specification
 
 
 </li>
 </ul>
 As a university we aim to create an environment where everyone can thrive and are proactive in fostering a culture of inclusion, respect and equality of opportunity. We believe that we can only truly meet our objectives if we are reflective of society, so we are passionate about creating a working environment in which you are free to bring your whole self to work. With a generous holiday allowance as well as additional university closure days we are committed to supporting our staff and students and open to a flexible working approach.
 
 
 Apply by 11.59 pm GMT on the closing date. For assistance contact Recruitment on +44(0)2380 592750 or recruitment@soton.ac.uk quoting the job number.
 
 
 
 Share
 
 
 
 View All Vacancies
</div>

Research Fellow in Cancer Immunotherapy

Syngene International Limited

<div>
 Date: 2 Dec 2025
 
 
 Location:
 
 
 Bangalore, KA, IN, 560099
 
 
 Division: Discovery Services
 
 
 
 Job Title: In Vivo PK scientist
 
 
 
 
 Job Location: Bengaluru
 
 
 
 About Syngene : Syngene (www.syngeneintl.com) is an innovation-led contract research, development and manufacturing organization offering integrated scientific services from early discovery to commercial supply.
 
 
 
 At Syngene, safety is at the heart of everything we do personally and professionally. Syngene has placed safety at par with business performance with shared responsibility and accountability, including following safety guidelines, procedures and SOPs, in letter and spirit
 
 
 
 
 Mandatory expectation for all roles as per Syngene safety guidelines
 
 
 
 <ul>
 <li>
 Overall adherence to safe practices and procedures of oneself and the teams aligned
 </li>
 <li>
 Contributing to development of procedures, practices and systems that ensures safe operations and compliance to company&rsquo;s integrity &amp; quality standards
 </li>
 <li>
 Driving a corporate culture that promotes environment, health, and safety (EHS) mindset and operational discipline at the workplace at all times.
 </li>
 <li>
 Ensuring safety of self, teams and lab/plant by adhering to safety protocols and following environment, health, and safety (EHS) requirements at all times in the workplace.
 </li>
 <li>
 Ensure all assigned mandatory trainings related to data integrity, health, and safety measures are completed on time by all members of the team including self
 </li>
 <li>
 Compliance to Syngene&rsquo; s quality standards at all times
 </li>
 <li>
 Hold self and their teams accountable for the achievement of safety goals
 </li>
 <li>
 Govern and Review safety metrics from time to time
 
 
 </li>
 </ul>
 
 Core Purpose of the Role:
 
 Conduct of
 
 in vivo
 
 pharmacokinetics study in rodents
 
 
 
 Education:
 
 M. Pharm /PHD (Pharmacology &amp; Toxicology) with an expert in conducting the studies in an industry setting
 
 
 
 Role Accountabilities
 
 
 
 <ul>
 <li>
 Conduct of pharmacokinetic studies in rodents.
 </li>
 <li>
 Documenting the lab notebooks online and compound management.
 </li>
 <li>
 Ability to adapt to the dynamic team environment.
 </li>
 <li>
 Possess the knowledge and exposure to environment, health, and safety (EHS) practices
 </li>
 <li>
 Follow environment, health, and safety (EHS) requirements at all times in the workplace ensuring individual and lab/plant safety
 </li>
 <li>
 Ensure environment, health, and safety (EHS) measures are imparted via training and adhered within the team.
 
 
 </li>
 </ul>
 
 Syngene Values
 
 
 
 All employees will consistently demonstrate alignment with our core values
 
 
 <ul>
 <li>
 Excellence
 </li>
 <li>
 Integrity
 </li>
 <li>
 Professionalism
 
 
 </li>
 </ul>
 
 Skills And Capabilities
 
 
 
 <ul>
 <li>
 Well versed with surgical procedures like cannulation of jugular, femoral, portal vein in rats. Chronic bile duct cannulations in rat and various animal models used for in vivo pharmacokinetics studies.
 </li>
 <li>
 Collection of different vital organs during tissue distribution studies in rodents
 </li>
 <li>
 Pharmacokinetic data analysis using Phoenix WinNonlin and other data analysis tool.
 </li>
 <li>
 Collection of various biological fluids like cerebrospinal fluid, bile, urine, synovial fluid lavage during PK and tissue distribution studies in rodents.
 </li>
 <li>
 Should have preliminary understanding about formulations to be used for pharmacokinetics, efficacy and toxicity studies.
 </li>
 <li>
 Knowledge about regulatory guidelines followed for drug metabolism and pharmacokinetics is desirable.
 
 
 </li>
 </ul>
 
 Behavioral Skills
 
 
 
 <ul>
 <li>
 Ready to take new challenges, committed to work and timelines
 </li>
 <li>
 Should have learning attitude, enthusiastic and hard working
 </li>
 <li>
 Good in communication skills
 </li>
 <li>
 Good work ethics.
 </li>
 <li>
 Good interpersonal skills, and the ability to work effectively in a team environment.
 </li>
 <li>
 Ability to work with co&hyphen;workers professionally.
 </li>
 <li>
 General ability to thrive in a growing infrastructure and culture and also think out of box approach when troubleshooting and problem solving.
 
 
 </li>
 </ul>
 
 Equal Opportunity Employer
 
 
 
 <ul>
 <li>
 It is the policy of Syngene to provide equal employment opportunity (EEO) to all persons regardless of age, color, national origin, citizenship status, physical or mental disability, race, religion, creed, gender, sex, sexual orientation, gender identity and/or expression, genetic information, marital status, status with regard to public assistance, veteran status, or any other characteristic protected by applicable legislation or local law. In addition, Syngene will provide reasonable accommodations for qualified individuals with disabilities.
 </li>
 </ul>
</div>

Invivo PK Scientist

HEOR Scientist - Pneumococcal Vaccines Location: RemoteContract Type: TemporaryRate: £650-800 per day approx. (Umbrella) SRG are supporting a leading global pharmaceutical company with their search for an HEOR Scientist supporting Pneumococcal Vaccines. This will be an initial 9 month contract and the role is predominantly remote based. Reporting to the Global RWE & Health Outcomes Research Lead, you'll play a key role in designing and delivering impactful real-world evidence (RWE) studies that inform strategic decisions and support global market access. Key Responsibilities <ul> <li>Design and execute multiple RWE studies, managing timelines, deliverables, and budgets.</li><li>Ensure quality and compliance across study documentation including protocols, analysis plans, and publications.</li><li>Translate strategic evidence needs into innovative study concepts and protocols.</li><li>Advise internal and external stakeholders on scientific design and data sources.</li><li>Build strong cross-functional relationships across medical, market access, and commercial teams.</li><li>Engage with external thought leaders to ensure robust and credible research approaches.</li></ul> Requirements & Experience <ul> <li>MSc or equivalent in health economics, epidemiology, pharmacy, or life sciences.</li><li>1-3 years' experience in the pharmaceutical industry, ideally within a multinational setting.</li><li>Proven ability to manage projects and budgets in a matrix environment.</li><li>Experience with RWE study designs and HTA/reimbursement evidence generation.</li><li>Experience with Pneumococcal Vaccines would be a major advantage - Vaccines in general or Immunology also useful experience</li><li>Strong communication skills to translate complex data for diverse audiences.</li><li>Knowledge of global healthcare systems and payer decision-making processes.</li></ul> Preferred: PhD/PharmD, launch experience, and direct payer engagement. To Apply If you are interested and want to find out more about this role, please click to apply or contact Theo Charles to discuss further. Carbon60, Lorien & SRG - The Impellam Group STEM Portfolio are acting as an Employment Business in relation to this vacancy.

HEOR Scientist - Vaccines

Novartis

<div><div><h3 class="jobSectionHeader">Summary
</h3><div>An exciting opportunity to join our Medical Team. As MSL, your roles will be to lead scientific engagement with their Medical Experts, implement clinical and educational strategies and respond to unsolicited medical enquiries. 
#LI-Onsite</div>
</div><div><h3 class="jobSectionHeader">About the Role
</h3><div>Major accountabilities:<ul><li>
Contributes to mapping / profiling of KOL/decision makers in line with segmentation</li><li>
Liaise and provide up-to-date medical support to relevant external groups to facilitate inclusion of products in medical guidelines, and support pricing and health-economic discussions</li><li>
Provide and discuss scientific information and data to healthcare professionals to ensure quality and accuracy of medical and scientific information on new treatment options including Novartis products and selected areas of therapeutic interest</li><li>
Collaborate with Novartis colleagues to actively support medical and scientific meetings by collecting and interpreting insights /presentations/ results, and evaluating impact of competitive information to share internally and externally as post-meeting deliverables</li><li>
Provide medical support and training (i.e. disease state and product) to Novartis colleagues.</li><li>
Contributes to the identification of appropriate clinical investigators and facilitates placement into Novartis sponsored clinical trials.</li><li>
Support the investigational sites as needed , as part of a cross-functional team with GDD and others as appropriate</li></ul> 
Requirements:<ul><li>
Strong and Sustainable performance track record.</li><li>
Previous experience as MSL is preferred</li><li>
Relevant Therapeutic Area experience is preferred</li><li>
Strong demonstration of cross functional collaboration.</li><li>
Demonstrated ability to develop and foster peer-to-peer, credible relationships with health care professionals.</li><li>
Previous experience in the respective Therapeutic Area is preferred.</li><li>
Externally focused with proven exceptional external customer focus and building strong relationship with KOLs.</li><li>
Sound knowledge of the Healthcare System and of the research procedures as well as the ICH guidelines, GCP and other ethical guidelines relevant to the pharmaceutical industry.</li><li>
Ability to synthesize recent scientific information, analyze them within strategic and regulatory settings.</li><li>
MD, PharmD, Pharmacist, PHD and other life sciences with solid medical/technical background and proven competencies influencing skills, clinical research insight, business, and market knowledge.</li><li>
Externally focused with proven exceptional external customer focus and building strong relationship with KOLs.</li><li>
Sound knowledge of the Healthcare System and of the research procedures as well as the ICH guidelines, GCP and other ethical guidelines relevant to the pharmaceutical industry</li><li>
Ability to synthesize recent scientific information, analyze them within strategic and regulatory settings.</li><li>
Gulf experience in preferred.</li></ul> 
Skills Desired
Medical expertise, Communication, Compliance, Conflict Management, Cross-Functional Work, Customer Insights, Ethics, Healthcare Industry, Influencing Skills, Negotiation, Technical Skills</div> 

</div><div><div>Why Novartis: Helping people with disease and their families takes more than innovative science. It takes a community of smart, passionate people like you. Collaborating, supporting and inspiring each other. Combining to achieve breakthroughs that change patients&rsquo; lives. Ready to create a brighter future together? https://www.novartis.com/about/strategy/people-and-culture
Benefits and Rewards: Read our handbook to learn about all the ways we&rsquo;ll help you thrive personally and professionally: https://www.novartis.com/careers/benefits-rewards</div></div></div>
 <div><div>Division
<div>International
</div></div><div>Business Unit
<div>Development
</div></div><div>Location
<div>Utd.Arab Emir.
</div></div><div>Site
<div>Dubai
</div></div><div>Company / Legal Entity
<div>AE01 (FCRS = AE001) Novartis Middle East FZE (Representative Office)
</div></div><div>Functional Area
<div>Research &amp; Development
</div></div><div>Job Type
<div>Full time
</div></div><div>Employment Type
<div>Regular
</div></div><div>Shift Work
<div>No
</div></div><div></div><div>Novartis is committed to building an outstanding, inclusive work environment and diverse teams' representative of the patients and communities we serve.</div></div>

MSL Immunology Gulf

Johns Hopkins Health System

<div>The Johns Hopkins Hospital is a world-renowned leader in patient care, serving the greater Baltimore community and patients from all across the globe. 
Our friendly and knowledgeable staff teams provide support throughout our many specialty departments and centers, from primary visits to emergency care.

What Awaits You?
<ul>
<li>Career growth and development</li>
<li>Tuition Assistance
</li><li>Diverse and collaborative working environment</li>
<li>Affordable and comprehensive benefits package</li>
</ul>
Location: Johns Hopkins Hospital Baltimore, MD- Core Lab

Nights-11pm-7:30am

Weekend Rotations Required

***Will Consider Clinical Laboratory Scientist I, II or III***

Position Summary:
<ul>
<li>Demonstrating an advanced level of laboratory experience, the Clinical Lab Scientist 3 (Medical Technologist or Medical Lab Scientist) reports to Pathology Lab Manager, Supervisor or Lead (or assigned Charge). Performs a variety of both routine and complex clinical laboratory tests and records and reports results following standard operating procedures, policies and regulatory guidelines. These require a professional level of knowledge to properly execute and analyze results, especially where results are abnormal or atypical.</li>
<li>Supports needs of the laboratory including both pre-analytical and analytical areas as assigned.</li>
<li>Provides training of both new hires, current colleagues, students, residents/fellow, and others assigned in the laboratory. Sets up and maintains equipment; monitors quality control standards.</li>
<li>Assigned tasks in bringing online new testing and programs, validation, QA, and research support.
</li><li>Responsible for resolving problems, provides expertise in operating equipment or testing protocols, as well as the workflow of specimens.
</li><li>Where assigned reviews lab requisitions and collects pertinent clinical and medical chart data.</li>
<li>May perform data entry, pre-analytical set up, routine clerical and service duties as required.</li>
<li>May support the laboratory inventory/ordering, and back-up to other tasks as assigned.</li>
<li>The CLS3 may serve as &ldquo;charge&rdquo; in the absence of Lead, Supervisor, or Manager and are appointed to committees and project teams as needed. The CLS 3 may also be assigned to perform competency testing of others.</li>
</ul>
Minimum Qualifications:

Education:
<ul>
<li>BS degree in Medical Lab Sciences, Medical Technology, or Clinical Lab Science related field, required.
</li><li>May consider BS degree in Biology, Chemistry, Microbiology or categorical related field where education included clinical laboratory internship/clinical rotations and degree/experience with an approved Med Tech certification.</li>
<li>Work requires formal education/coursework in biology, chemistry, hematology, immunology, cytogenetics and/or microbiology meeting regulatory requirements for testing.</li>
</ul>
Work Experience:
<ul>
<li>Minimum 2 years of direct clinical laboratory experience is required.</li>
</ul>
Required Licensure, Certification, On-going Training:
<ul>
<li>For this level, verified certification as a Medical Technologist (MT, MLS) from ASCP or other department approved agency is required and must be maintained at all times by employee.</li>
</ul>
Important Notices:

***Authorization to Work in the United States: Applicants who require sponsorship now or in the future will not be considered for this position.

Salary Range: Minimum 24.54/hour - Maximum 52.69/hour. Compensation will be commensurate with equity and experience for roles of similar scope and responsibility. In cases where the range is displayed as a $0 amount, salary discussions will occur during candidate screening calls, before any subsequent compensation discussion is held between the candidate and any hiring authority.

We are committed to creating a welcoming and inclusive environment, where we embrace and celebrate our differences, where all employees feel valued, contribute to our mission of serving the community, and engage in equitable healthcare delivery and workforce practices.

Johns Hopkins Health System and its affiliates are drug-free workplace employers.</div>

Clinical Laboratory Scientist III (Medical Technologist)-Core Lab

Good Samaritan Hospital

<div>Hourly Wage Estimate: $52.00 - $72.00 / hour 
Learn more about the benefits offered for this job. 
The estimate displayed represents the typical wage range of candidates hired. Factors that may be used to determine your actual salary may include your specific skills, how many years of experience you have and comparison to other employees already in this role. The typical candidate is hired below midpoint of the range.<h5 class="jobSectionHeader">
Introduction</h5>
Do you have the PRN career opportunities as a Clinical Lab Scientist II PRN you want with your current employer? We have an exciting opportunity for you to join Good Samaritan Hospital which is part of the nation's leading provider of healthcare services, HCA Healthcare.<h5 class="jobSectionHeader">
Benefits</h5>
Good Samaritan Hospital, offers a total rewards package that supports the health, life, career and retirement of our colleagues. The available plans and programs include:<ul><li>
Comprehensive medical coverage that covers many common services at no cost or for a low copay. Plans include prescription drug and behavioral health coverage as well as telemedicine services and free AirMed medical transportation. 
</li><li>
Additional options for dental and vision benefits, life and disability coverage, flexible spending accounts, supplemental health protection plans (accident, critical illness, hospital indemnity), auto and home insurance, identity theft protection, legal counseling, long-term care coverage, moving assistance, pet insurance and more. 
</li><li>
Fertility and family building benefits through Progyny 
</li><li>
Free counseling services and resources for emotional, physical and financial wellbeing 
</li><li>
Family support, including adoption assistance, child and elder care resources and consumer discounts</li><li>
401(k) Plan with a 100% match on 3% to 9% of pay (based on years of service)</li><li>
Employee Stock Purchase Plan 
</li><li>
Retirement readiness and rollover services and preferred banking partnerships 
</li><li>
Education assistance (tuition, student loan, certification support, dependent scholarships) 
</li><li>
Colleague recognition program 
</li><li>
Time Away From Work Program (paid time off, paid family leave, long- and short-term disability coverage and leaves of absence)</li></ul> 
Learn more about Employee Benefits
Note: Eligibility for benefits may vary by location. 
Our teams are a committed, caring group of colleagues. Do you want to work as a Clinical Lab Scientist II PRN where your passion for creating positive patient interactions is valued? If you are dedicated to caring for the well-being of others, this could be your next opportunity. We want your knowledge and expertise!<h5 class="jobSectionHeader">
Job Summary and Qualifications</h5>
Our Clinical Lab Scientists (level II) perform clinical testing in one or more of the following areas: blood bank, chemistry, serology, hematology, urinalysis, coagulation, special chemistry, microbiology and manual tests.Our team is amazing, we consider ourselves a family who work hard to support each other and we are looking for someone who feels patient care is as meaningful as we do. If that is you, come be a part of what makes us great and apply today!<ul><li>
You will perform automated, semi-automated and manual procedures in the fields of bacteriology, parasitology, hematology, coagulation, serology, chemistry, urinalysis, immunology, and immunohematology. According to established procedures and policies</li><li>
You will perform preventative maintenance on laboratory instrumentation, interpret results as to their accuracy, acceptability and critical limits and organizes work to meet established deadlines and record all data obtained</li><li>
You will work actively and be cooperative with nursing and other hospital staff to ensure timely patient care as well as assist with regulatory compliance</li><li>
You will be responsible for training lab personnel and are expected to perform in-charge assignment in the absence of a manager</li></ul>
<h6 class="jobSectionHeader">What qualifications you will need:</h6><ul><li>
Current Clinical Laboratory Scientist license per CA State Board required</li><li>
Bachelor&rsquo;s Degree in Medical Technology or equivalent from an accredited college or university required</li><li>
Minimum five years experience as a Clinical Laboratory Scientist required</li></ul>
Good Samaritan Hospital has been serving Silicon Valley since 1965, giving patient's access to highly-trained physicians and advanced technology. Our 470+ bed facility is a recognized leader in advanced cardiology services and provides a full array of diagnostic and interventional coronary peripheral services. Other specialized programs include echocardiography, Vascular Sonograph and EKG services. Good Samaritan is a Joint Commission Accredited comprehensive stroke center. We are also one of 3 hospitals in the US to receive a 5th consecutive Outstanding Achievement Award from the American College of Surgeon&rsquo;s Commission on Cancer. Among these accomplishments, our facility is a Bay Area Parent Magazine Hall of Fame recipient for &ldquo;Best Place to Have a Baby&rdquo;, complete with a CCS certified Level III neonatal ICU with pediatric surgery specialization.
HCA Healthcare has been recognized as one of the World&rsquo;s Most Ethical Companies&reg; by the Ethisphere Institute more than ten times. In recent years, HCA Healthcare spent an estimated $3.7 billion in cost for the delivery of charitable care, uninsured discounts, and other uncompensated expenses. 
 
&quot;Bricks and mortar do not make a hospital. People do.&quot;- Dr. Thomas Frist, Sr. 
HCA Healthcare Co-Founder
If you are looking for an opportunity that provides satisfaction and personal growth, we encourage you to apply for our Clinical Lab Scientist II PRN opening. We review all applications. Qualified candidates will be contacted for interviews. Unlock the possibilities and apply today!
We are an equal opportunity employer. We do not discriminate on the basis of race, religion, color, national origin, gender, sexual orientation, age, marital status, veteran status, or disability status</div>

Clinical Lab Scientist II PRN

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