clinical scientist

Alignerr

<div>
 <strong>
  About The Job
  <br/>
  <br/>
 </strong>
 At Alignerr, we partner with the world&rsquo;s leading AI research teams and labs to build and train cutting-edge AI models.
 <br/>
 <br/>
 We are seeking a Principal Clinical Scientist to bring senior-level expertise in clinical trial design and regulatory-grade data interpretation into AI-driven research workflows. In this role, you will help ensure that clinical data used to train and evaluate advanced AI systems meets the rigor, structure, and regulatory standards expected in real-world submissions.
 <br/>
 <br/>
 <strong>
  Organization
 </strong>
 : Alignerr
 <strong>
  Position
 </strong>
 : Principal Clinical Scientist
 <strong>
  Type
 </strong>
 : Hourly Contract
 <strong>
  Compensation
 </strong>
 : $40&ndash;$80 /hour
 <strong>
  Location
 </strong>
 : Remote
 <strong>
  Commitment
 </strong>
 : 10&ndash;40 hours/week
 <br/>
 <br/>
 <strong>
  What You&rsquo;ll Do
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   Design and review clinical trial protocols used to generate high-quality, regulator-ready datasets.
  </li>
  <li>
   Interpret and audit clinical trial results to ensure accuracy, consistency, and regulatory relevance.
  </li>
  <li>
   Evaluate AI-generated clinical analyses for scientific soundness and alignment with regulatory expectations.
  </li>
  <li>
   Provide expert feedback to improve how AI models reason about clinical trial data and outcomes.
   <br/>
   <br/>
  </li>
 </ul>
 <strong>
  What We&rsquo;re Looking For
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   Senior-level experience designing clinical trial protocols for regulatory submission.
  </li>
  <li>
   Deep expertise interpreting clinical data for agencies such as FDA, EMA, or equivalent.
  </li>
  <li>
   Strong background in clinical research methodology, biostatistics, or translational science.
   <br/>
   <br/>
  </li>
 </ul>
 <strong>
  Preferred
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   Prior experience with data annotation, data quality, or evaluation systems
   <br/>
   <br/>
  </li>
 </ul>
 <strong>
  Why Join Us
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   Competitive pay and flexible remote work.
  </li>
  <li>
   Work directly on frontier AI systems impacting clinical and biomedical research.
  </li>
  <li>
   Influence how AI understands and evaluates real-world clinical evidence.
  </li>
  <li>
   Freelance perks: autonomy, flexibility, and global collaboration.
  </li>
  <li>
   Potential for contract extension.
   <br/>
   <br/>
  </li>
 </ul>
 <strong>
  Application Process (Takes 15&ndash;20 min)
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   Submit your resume
  </li>
  <li>
   Complete a short screening
  </li>
  <li>
   Project matching and onboarding
   <br/>
   <br/>
  </li>
 </ul>
 <em>
  PS: Our team reviews applications daily. Please complete your AI interview and application steps to be considered for this opportunity.
 </em>
</div>


Principal Clinical Scientist

Calico Life Sciences

<div><h4 class="jobSectionHeader"><b>Who We Are:</b></h4>
<p>
Calico (Calico Life Sciences LLC) is an Alphabet-founded research and development company whose mission is to harness advanced technologies and model systems to increase our understanding of the biology that controls human aging. Calico will use that knowledge to devise interventions that enable people to lead longer and healthier lives. Calico&rsquo;s highly innovative technology labs, its commitment to curiosity-driven discovery science and, with academic and industry partners, its vibrant drug-development pipeline, together create an inspiring and exciting place to catalyze and enable medical breakthroughs.</p>
<p><b>
Position Description:</b></p>
<p>
The Associate Director, Clinical Scientist at Calico is responsible for the planning and execution of the translational and clinical development plans and protocols for several projects across therapeutic areas, related to Calico&rsquo;s mission to improve human healthspan by understanding aging and age-related diseases. The successful candidate will participate in and drive the development of clinical strategies for assigned program(s)/indication(s) and should be able to support novel and innovative clinical plans while ensuring a positive and collaborative team environment.</p>
<p><b>
Responsibilities:</b></p>
<ul>
<li>In coordination with the Head of Clinical Science and/or Medical Director(s), leads or represents the Clinical Science function in cross-functional project and study teams that develop and execute the clinical development plan to translate preclinical mechanistic data to humans for novel aging-related targets</li>
<li>Authors clinical sections of assigned protocols from Phase 0 through Phase 2, collaborating with other functions required for protocol development, including Research, Biomarkers, Clinical Operations, Regulatory Affairs, Clinical Pharmacology, Biometrics, Pharmacovigilance, Toxicology, and Medical Writing</li>
<li>Contributes to the design and execution of experimental medicine studies to demonstrate proof-of-mechanism of novel targets in aging and age-related diseases</li>
<li>Interfaces with academic investigators to assist in execution of Investigator initiated trials</li>
<li>Contributes to and/or reviews relevant study documents including Investigational Brochures, Clinical Study Reports, Statistical Analysis Plans, Operations/Technical Manuals, IND/CTAs, case report forms and data tables, listings and figures, CSRs</li>
<li>Trains CROs and study site personnel on assigned protocols and addresses protocol queries as they arise</li>
<li>Participates in the assessment of CROs and study vendors</li>
</ul>
<p><b>Position Requirements:</b></p>
<ul>
<li> BS/MS in a relevant scientific discipline with 8+ years or PhD/PharmD with 5+ years of experience in early clinical drug development in the biotech/pharmaceutical industry performing the responsibilities described above</li>
<li>Experience in early clinical trial methodology (Phase 0, Phase 1, Phase 2) and knowledge of drug development process and clinical deliverables from IND through clinical proof-of-concept</li>
<li>Excellent understanding of clinically relevant ICH GCP guidance, FDA and EMA regulations</li>
<li>Ability to perform role responsibilities largely independently</li>
<li>Proven leadership skills and ability to bring out the best in others on a cross-functional team</li>
<li>Able to provide effective leadership through influence across organizations on partnered programs</li>
<li>Detail-oriented mindset with excellent oral and written English communication skills</li>
<li>Must be willing to work onsite at least 4 days a week</li>
</ul>
<p>The estimated base salary range for this role is $238,000 - $245,000. Actual pay will be based on a number of factors including experience and qualifications. This position is also eligible for two annual cash bonuses.</p></div><p></p>

Associate Director, Clinical Scientist

Prime Healthcare Services

<div>Overview:
<p>
We are seeking a <b>Clinical </b><b>Laboratory</b><b> Scientist, </b>also referred to as a Medical Technologist (Med Tech) at Riverview Regional Medical Center a member of Prime Healthcare. The Clinical Lab Scientist (CLS) requires a blend of technical expertise, analytical skills, attention to detail, and the ability to work collaboratively within a healthcare team. They play an important role in the diagnostic process, contributing significantly to patient care and treatment.</p><p></p><p><i><br>
** If you have experience as a Medical Laboratory Scientist (MLS), Medical Technologist (MT), Medical Laboratory Technician (MLT) you are encouraged to apply for this position.</i></p><p></p><div><b><br>
Shift&rsquo;s Available: </b>10 hour shifts
</div><div><b>Employment Type:</b> Full Time</div><div><b>
Hours: </b>6:00am to 4:30pm, every other weekend and holiday. Every third month the shift is 8am-630pm, every other weekend and holiday.</div><div><b>
Location: </b>Riverview Regional Medical Center - Gadsden, AL</div><div></div><div><b><i><br>
Here are some of the benefits of working at Prime Healthcare:</i></b></div><ul><li>
Health, dental, and vision insurance options</li><li>
Paid vacation, sick time and holidays</li><li>
Bereavement leave, FMLA and other leave options</li><li>
Employer 401K options</li><li>
Tuition reimbursement options</li><li>
Life, disability, and other insurance options</li><li>
Many other amazing benefits</li></ul><br>
<div></div>
Responsibilities:
<div><b><i>
Essential Duties and Responsibilities (includes, but not limited to):</i></b></div><ul><li>
perform laboratory tests on blood, tissues, and other bodily fluids to aid in the diagnosis of diseases and conditions, this may include routine tests as well as specialized tests</li><li>
interpret lab test results and identify any abnormalities, ensure the accuracy and reliability of these results to assist doctors in making informed decisions about patient care</li><li>
implement and monitor quality control procedures to maintain high standards in laboratory testing, you may also calibrate and maintain laboratory instruments and equipment</li><li>
keep accurate and detailed records of all laboratory tests performed and their results, input data into our laboratory information systems</li><li>
ensure all laboratory operations comply with hospital policies, governmental regulations, and accreditation requirements</li></ul>
Qualifications:
<div><b>
Education and Work Experience</b></div><ul><li>
ASCP certification, or equivalent required</li><li>
One year hospital laboratory work experience preferred, but not required.</li><li>
bachelor's degree in chemical, physical, biological science, or Medical Laboratory Technology from an accredited institution, or other educational requirements as stated in CLIA (42 CFR 493.1489)</li><li>
Current and valid state license if the laboratory is located in a state where required</li></ul><div>
Full benefits at Prime Healthcare: https://www.primehealthcare.com/careers/benefits/</div><div></div><div><br>
#LI-AZ1</div><br>
<div></div>
Employment Status: Full Time Shift: Days Equal Employment Opportunity:
<div><div><div><div>
Company is an equal employment opportunity employer. Company prohibits discrimination against any applicant or employee based on race, color, sex, sexual orientation, gender identity, religion, national origin, age (subject to applicable law), disability, military status, genetic information or any other basis protected by applicable federal, state, or local laws. The Company also prohibits harassment of applicants or employees based on any of these protected categories. Know Your Rights: https://www.eeoc.gov/sites/default/files/2022-10/EEOC_KnowYourRights_screen_reader_10_20.pdf</div></div></div></div></div><div></div>

Clinical Laboratory Scientist

BayCare Health System

<p></p><div><div><h3 class="jobSectionHeader"><b>Join BayCare as a Clinical Laboratory Scientist I
 </b></h3><p><b>Location: </b>St. Joseph&rsquo;s Main &amp; Children&rsquo;s
 <br>
<b>Facility: </b>BayCare Health System, Chemistry &ndash; SJH
 <br>
<b>Shift: </b>Nights | 8:30 PM &ndash; 7:00 AM
 <br>
<b>Schedule: </b>Full-Time | Onsite
 <br>
<b>Weekend Work: </b>Every Other Weekend<br>
<br>
</p><p></p><h3 class="jobSectionHeader"><b>About BayCare
</b></h3><p>At BayCare, we are proud to be one of the largest employers in the Tampa Bay area. Our network includes 16 community-based hospitals, a long-term acute care facility, home health services, outpatient centers, and thousands of physicians. Supported by more than 30,000 team members, BayCare promotes a forward‑thinking philosophy built on trust, dignity, respect, responsibility, and clinical excellence.
</p><p></p><h3 class="jobSectionHeader"><b>Role Overview
</b></h3><p>As a <b>Clinical Laboratory Scientist I </b>, you will support high‑quality diagnostic services by performing and overseeing laboratory testing while ensuring compliance with established policies, procedures, and quality standards.
</p><p><b>Key responsibilities include:
</b></p><ul><li>Performing diagnostic testing and quality control procedures
</li><li>Preparing reagents and reporting results according to established policies and procedures
</li><li>Reviewing and overseeing moderate to high complexity laboratory testing
</li><li>Monitoring and maintaining laboratory computer applications
</li><li>Maintaining laboratory equipment and supply inventory
</li><li>Performing other duties as assigned
</li></ul><p></p><h3 class="jobSectionHeader"><b>Qualifications
</b></h3><h4 class="jobSectionHeader"><b>Education
</b></h4><p><b>Required:
</b></p><ul><li>Associate&rsquo;s degree in Medical Technology <b>OR </b>a related field
</li></ul><p><b>Preferred:
</b></p><ul><li>Bachelor&rsquo;s degree in a related field
</li></ul><h4 class="jobSectionHeader"><b>Experience
</b></h4><ul><li>Clinical laboratory experience required
</li><li>Minimum of four (4) months of Clinical Laboratory Scientist experience
</li></ul><h4 class="jobSectionHeader"><b>Licensure / Certification
</b></h4><p><b>Required:
</b></p><ul><li>State of Florida <b>Clinical Laboratory Technologist License
</b></li></ul><p></p><h3 class="jobSectionHeader"><b>What We Offer
</b></h3><p>BayCare provides a competitive total rewards package designed to support your career and well‑being, including:
</p><ul><li>Comprehensive Medical, Dental &amp; Vision Benefits
</li><li>Paid Time Off
</li><li>Tuition Assistance
</li><li>401(k) Match plus Annual Employer Contribution
</li><li>Wellness programs and community perks
</li></ul><p></p><h3 class="jobSectionHeader"><b>Take the Next Step
</b></h3><p>Bring your laboratory expertise to BayCare and help deliver accurate, timely diagnostic testing that supports exceptional patient care.
 </p><p><b>Apply today to join BayCare as a Clinical Laboratory Scientist I!
</b></p><p></p><p><i>BayCare is an Equal Opportunity Employer. Veterans and individuals with disabilities are encouraged to apply.</i></p></div></div><p></p>

Clinical Laboratory Scientist I

US Specialty Labs

<div><div><p><b>Essential Functions</b></p><p>
Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.</p><ul><li>
Ensure our facility is compliant to the appropriate guidelines</li><li>
Ensure organization is audit ready for CLIA/CAP/CMS</li><li>
Liaison with Clinical Laboratory Director and lead the charge with building our clinical testing group</li><li>
Identify and resolve problems that may adversely affect test outcomes and either correct the problem or report it immediately to Medical Director.</li><li>
Generate and archive reports for corrective action performed in laboratory, if necessary.</li><li>
Write and follow written SOPs as well as be able to identify and gap fill missing procedures, if necessary.</li><li>
Perform competency analysis for laboratory staff, including CLSs and MLTs.</li></ul><p><b>
Competencies</b></p><ul><li>
Current California Clinical Laboratory Scientist license</li><li>
Must have strong analytical and problem-solving skills</li><li>
Must be detail-oriented and comfortable with technology</li><li>
Must have good written and oral communication skills</li><li>
Working knowledge of handling potentially infectious human blood and body fluids</li><li>
Good pipetting skills and understanding of aseptic techniques</li><li>
Ability to work with automated and manual platforms</li><li>
Analytical judgment, problem solving skills, accuracy and strong attention to details</li><li>
High level of integrity and honesty in performing tests, documenting test results and maintaining patient, client, employee and laboratory business confidentiality</li><li>
Must have strong critical-thinking skills and the ability to prioritize workflow in a high-throughput laboratory environment.</li><li>
Proven track record with CLIA/CAP/CMS audit preparedness</li><li>
Mass spectroscopy experience is a big plus</li><li>
National Certification as MLS (ASCP) or MT (ASCP)</li></ul><p><b>
Work Environment</b></p><p>
This job operates in a professional office environment. This role routinely uses standard office equipment such as computers, phones, photocopiers, filing cabinets and fax machines.</p><p><b>
Physical Demands</b></p><p>
The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job.</p><p>
While performing the duties of this job, the employee is regularly required to talk or hear. The employee frequently is required to stand; walk; use hands to finger, handle or feel; and reach with hands and arms.</p><p><b>
Other Duties</b></p><p>
Please note this job description is not designed to cover or contain a comprehensive listing of activities, duties or responsibilities that are required of the employee for this job. Duties, responsibilities and activities may change at any time with or without notice.</p></div></div>

Clinical Lab Scientist

Pfizer

<div><div>The Clinical Development Scientist (Director) ensures scientific integrity and participant safety in clinical trials, designs and executes high-quality studies, maintains compliance, manages risks and emerging clinical issues, and supports interpretation and communication of clinical data. This role is the primary contact for internal and external stakeholders for clinical aspects the protocol, supports strategic development, and may provide matrix management.</div><div></div><div>
Job Responsibilities</div><ul><li><div>
Leadership</div><ul><li><div>
Autonomously and independently leads clinical execution of one or more studies of medium - high complexity and significant business impact. May be accountable for program level clinical deliverables.</div></li><li><div>
Contributes to continuous improvement / process enhancement activities and innovative approaches to maximize effectiveness of clinical trial execution.</div></li><li><div>
May provide matrix management support to one or more clinical colleagues.</div></li></ul></li><li><div>
Content Creation</div><ul><li><div>
Provides clinical input to support development of the protocol design document (PDD).</div></li><li><div>
Leads development of the protocol from the approved PDD and ensures efficient protocols which maximize operational efficiency, trial quality and participant / site engagement and which minimize the likelihood of amendments or quality issues. Partners with/supports the Global Development Lead in governance review and approval process.</div></li><li><div>
Leads development of protocol amendments, Protocol Administrative Change Letters, and Dear Investigator Letters.</div></li><li><div>
Authors and manages approval of Informed Consent Documents (ICDs) including responses to external stakeholder questions.</div></li></ul></li><li><div>
Clinical &amp; Safety Oversight</div><ul><li><div>
Provides clinical input to the development of data collection tools.</div></li><li><div>
Responsible for providing clinical input to statistical analysis plan (SAP), tables, listings, figures (TLFs) and blinded data review (BDR).</div></li><li><div>
Accountable for establishing Data Monitoring Committees (DMCs) and endpoint adjudication committees, including chartering, contracts, provision of relevant data and documentation of outcomes.</div></li><li><div>
Provides clinical input to development of the Integrated Quality Management Plan (IQMP). Review and approves final document.</div></li><li><div>
Inputs to, reviews and approves, Risk Management and Safety Review Plan. Ensures activities are conducted consistent with the approved plan and partners with key stakeholders (clinical operations, safety risk lead, etc.) to develop and implement any risk mitigations.</div></li><li><div>
Reviews and approves country selection, develops site selection criteria, and contributes to authoring and delivery of site training materials.</div></li><li><div>
Serves as the primary contact with external investigators and internal study team for questions relating to clinical aspects of protocol</div></li><li><div>
Reviews, reports and manages protocol deviations.</div></li><li><div>
Reviews patient level and cumulative data per the data review plan across one or more studies.</div></li><li><div>
Reviews safety data, serious adverse event (SAE) reports, targeted medical events (TMEs), designated medical events (DMEs) and ensures clinical documents (eg ICD) are updated as required.</div></li><li><div>
Tracks and reconciles SAEs across a study and leads presentation of data during Safety Review Team meetings.</div></li><li><div>
Ensures trial master file (TMF) compliance for clinical documents</div></li></ul></li><li><div>
Clinical Reporting</div><ul><li><div>
May contribute to clinical sections of regulatory filings (Pediatric Investigational Plan, Investigator Brochure (IB), IND/NDA Annual Reports, and Periodic Safety Update Reports and Regulatory authority responses) if required.</div></li><li><div>
May support responsible colleagues with the development of responses to regulatory queries and Clinical Trial Applications (CTAs)</div></li><li><div>
Inputs and reviews the Clinical Study Report including the review of narratives. Responsible for supporting disclosure of safety and efficacy data and trial conclusions. Contributes to primary publication of clinical trial results.</div></li><li><div>
Provides clinical support to the study team or clinical program in response to audits or inspections, including providing support as needed to audit/inspection</div></li></ul></li></ul><div></div><div>
BASIC QUALIFICATIONS</div><ul><li><div>
Advanced degree or professional certification in a health care related, scientific or technical discipline required</div></li></ul><ul><li><div>
Years of experience in biopharmaceutical industry in clinical research and development:</div><ul><li><div>
BA/BS with 8+ years of experience</div></li><li><div>
MBA/MS with 7+ years of experience</div></li><li><div>
PhD with 5+ years of experience</div></li></ul></li><li><div>
Clinical research experience in phase 3/pivotal space</div></li><li><div>
Extensive knowledge of clinical development, global and regional regulation, ICH/GCP, adverse event management</div></li><li><div>
Demonstrated clinical, administrative, and project management capabilities, as well as excellent verbal and written communication skills in English, in relating to individuals both inside and outside Pfizer</div></li><li><div>
Demonstrated experience establishing, managing, and training teams in clinical development</div></li><li><div>
Candidate demonstrates a breadth of diverse leadership experiences and capabilities including: the ability to influence and collaborate with peers, develop and coach others, oversee and guide the work of other colleagues to achieve meaningful outcomes and create business impact.</div></li></ul><div></div><div>
PREFERRED QUALIFICATIONS</div><ul><li><div>
Oncology experience highly preferred</div></li><li><div>
Demonstrates a passion for helping patients</div></li><li><div>
Proven analytical skills with the ability to work on large data sets</div></li><li><div>
Effective communication, presentation, and organizational skills to ensure coordinated and timely delivery</div></li><li><div>
Demonstrated scientific writing skills</div></li><li><div>
Has a global perspective and mindset; works well in a diverse team environment with colleagues from diverse cultures, backgrounds, and geographies both as a leader and a key contributor; works effectively with internal and external partners and investigators/medical professionals</div></li><li><div>
Has solid understanding of related disciplines, e.g., clinical operations, safety, biostatistics, regulatory, study management, pre-clinical, pharmacology, quality assurance</div></li><li><div>
Proficient with basic IT; efficiently using a computer and telecommunications (voice and video)</div></li><li><div>
Has the flexibility to adapt and navigate through an ever-changing work environment while maintaining integrity and quality in the work assigned</div></li><li><div>
Must have the relevant personality features and competencies supporting the responsibilities:</div><ul><li><div>
Demonstrates effective problem-solving, and agile decision-making in execution of clinical responsibilities</div></li><li><div>
Leverages knowledge and support from others related to overall objectives, strategy, critical issues, and policies</div></li><li><div>
Embraces evolving technologies and adopts best practices aimed at improving the efficiency and quality of clinical development</div></li><li><div>
Promotes team health and exemplifies Pfizer&rsquo;s leadership behaviors and actionable attitudes</div></li><li><div>
Has foresight and judgment in complex decisions:</div><ul><li><div>
Leverages a variety of communication tools and techniques to communicate results</div></li><li><div>
Builds partnerships across the company to achieve the needs of the program</div></li><li><div>
Collaborative problem solving (handles conflict constructively)</div></li><li><div>
Promotes innovation and takes appropriate risks to challenge the status quo to enhance the efficiency of current processes</div></li><li><div>
Ability to work proactively and independently, organize tasks, time and priorities of self and others</div></li></ul></li></ul></li></ul><div></div><div>
NON-STANDARD WORK SCHEDULE, TRAVEL OR ENVIRONMENT REQUIREMENTS</div><div></div><div>
Global travel may be required</div><div></div><div>
Work Location Assignment: This is a hybrid role requiring you to live within commuting distance and work on-site an average of 2.5 days per week.</div><br>
<div></div>
The annual base salary for this position ranges from $176,600.00 to $282,900.00. In addition, this position is eligible for participation in Pfizer&rsquo;s Global Performance Plan with a bonus target of 20.0% of the base salary and eligibility to participate in our share based long term incentive program. We offer comprehensive and generous benefits and programs to help our colleagues lead healthy lives and to support each of life&rsquo;s moments. Benefits offered include a 401(k) plan with Pfizer Matching Contributions and an additional Pfizer Retirement Savings Contribution, paid vacation, holiday and personal days, paid caregiver/parental and medical leave, and health benefits to include medical, prescription drug, dental and vision coverage. Learn more at Pfizer Candidate Site &ndash; U.S. Benefits | (uscandidates.mypfizerbenefits.com). Pfizer compensation structures and benefit packages are aligned based on the location of hire. The United States salary range provided does not apply to Tampa, FL or any location outside of the United States.<div></div><div>
Relocation assistance may be available based on business needs and/or eligibility.</div><div></div><div><div><div><div><div><div><div><div><div>
Sunshine Act</div><div>
Pfizer reports payments and other transfers of value to health care providers as required by federal and state transparency laws and implementing regulations. These laws and regulations require Pfizer to provide government agencies with information such as a health care provider&rsquo;s name, address and the type of payments or other value received, generally for public disclosure. Subject to further legal review and statutory or regulatory clarification, which Pfizer intends to pursue, reimbursement of recruiting expenses for licensed physicians may constitute a reportable transfer of value under the federal transparency law commonly known as the Sunshine Act. Therefore, if you are a licensed physician who incurs recruiting expenses as a result of interviewing with Pfizer that we pay or reimburse, your name, address and the amount of payments made currently will be reported to the government. If you have questions regarding this matter, please do not hesitate to contact your Talent Acquisition representative.</div></div></div></div></div></div></div></div></div><div></div><div>
EEO &amp; Employment Eligibility</div><div>
Pfizer is committed to equal opportunity in the terms and conditions of employment for all employees and job applicants without regard to race, color, religion, sex, sexual orientation, age, gender identity or gender expression, national origin, disability or veteran status. Pfizer also complies with all applicable national, state and local laws governing nondiscrimination in employment as well as work authorization and employment eligibility verification requirements of the Immigration and Nationality Act and IRCA. Pfizer is an E-Verify employer. This position requires permanent work authorization in the United States.</div><div></div><div>
Pfizer endeavors to make <div>www.pfizer.com/careers</div> accessible to all users. If you would like to contact us regarding the accessibility of our website or need assistance completing the application process and/or interviewing, please email <div>disabilityrecruitment@pfizer.com</div>. This is to be used solely for accommodation requests with respect to the accessibility of our website, online application process and/or interviewing. Requests for any other reason will not be returned.</div><div></div>
Medical</div><div></div>

Clinical Development Scientist, Director

SSM Health

<div><p><b>It's more than a career, it's a calling</b></p>
WI-SSM Health St. Mary's Hospital - Madison<p></p><div><div><div><div><div><div><div><p><b>
Worker Type:</b></p></div></div></div></div></div></div></div><p></p>
Regular<p></p><p><b>
Job Highlights:</b></p><p>
This is a full time evening shift Clinical Lab Scientist Lead position for Central Accessioning at St. Mary's Hospital in Madison. Apply today and make a difference where accuracy and leadership matters most.</p><p></p><p><b>
Work Schedule: </b>Monday-Friday, 2:00 PM - 10:30 PM; every third<br>
weekend rotation; 2-3 holidays per year</p><p></p><p><b>
Job Summary:</b></p>
Under general direction, supervises assignments within the laboratory and acts as a resource to the laboratory.<p></p><p><b>
Job Responsibilities and Requirements:</b></p><div>
PRIMARY RESPONSIBILITIES</div><div><div><div><div><ul><li>
Performs a full range of laboratory tests from simple blood tests to more complex tests.</li><li>
Interprets test reports and communicates findings to physicians.</li><li>
Escalates unusual, critical or abnormal results.</li><li>
Operates complex electronic equipment, computers and precision instruments.</li><li>
Maintains accuracy of equipment and reagents by performing established preventive maintenance procedures.</li><li>
Assists providers in choosing appropriate lab test.</li><li>
Performs and evaluates quality control procedures.</li><li>
Operates, maintains, calibrates and troubleshoots instruments.</li><li>
Assists with the proper storage of hazardous materials.</li><li>
Reviews current literature and attends meetings and seminars to keep informed of new developments in field.</li><li>
Assists in the proficiency testing program in the lab.</li><li><p>
Works in a constant state of alertness and safe manner.</p></li><li>
Performs other duties as assigned.</li></ul><p></p><p>
EDUCATION</p><ul><li>
Associate's degree or equivalent years of experience and education</li></ul><p></p><p>
EXPERIENCE</p><ul><li>
Two years' experience</li></ul><p></p><p>
PHYSICAL REQUIREMENTS</p><ul><li>
Frequent lifting/carrying and pushing/pulling objects weighing 0-25 lbs.</li><li>
Frequent sitting, standing, walking, reaching and repetitive foot/leg and hand/arm movements.</li><li>
Frequent use of vision and depth perception for distances near (20 inches or less) and far (20 feet or more) and to identify and distinguish colors.</li><li>
Frequent use of hearing and speech to share information through oral communication. Ability to hear alarms, malfunctioning machinery, etc.</li><li>
Frequent keyboard use/data entry.</li><li>
Occasional bending, stooping, kneeling, squatting, twisting and gripping.</li><li>
Occasional lifting/carrying and pushing/pulling objects weighing 25-50 lbs.</li><li>
Rare climbing.</li></ul><p></p><p><b>
REQUIRED PROFESSIONAL LICENSE AND/OR CERTIFICATIONS</b><br>
<br>
<b>State of Work Location: Illinois, Missouri, Oklahoma, Wisconsin</b></p><ul><li>
 Blood Bank Technologist (BB) (International Included) - American Society for Clinical Pathology (ASCP)</li><li><b>
 </b>Or</li><li>
 Chemistry Technologist (C) (International Included) - American Society for Clinical Pathology (ASCP)</li><li>
 Or</li><li>
 Clinical Chemist - California Department of Public Health</li><li>
 Or</li><li>
 Clinical Chemist Scientist - California Department of Public Health</li><li>
 Or</li><li>
 Clinical Hematologist Scientist - California Department of Public Health</li><li>
 Or</li><li>
 Clinical Laboratory Personnel - Florida Department of Health</li><li>
 Or</li><li>
 Clinical Laboratory Practitioners - West Virginia Department of Health</li><li>
 Or</li><li>
 Clinical Laboratory Scientist (CLS) - American Society for Clinical Pathology (ASCP)</li><li>
 Or</li><li>
 Clinical Laboratory Scientist (Generalist) - California Department of Public Health</li><li>
 Or</li><li>
 Clinical Laboratory Specialist - ND Board of Clinical Laboratory Practice</li><li>
 Or</li><li>
 Clinical Laboratory Specialist - State of Hawaii Department of Health</li><li>
 Or</li><li>
 Clinical Laboratory Technician (CLT) - American Society for Clinical Pathology (ASCP)</li><li>
 Or</li><li>
 Clinical Laboratory Technician - New York State Education Department</li><li>
 Or</li><li>
 Clinical Microbiologist - California Department of Public Health</li><li>
 Or</li><li>
 Clinical Microbiologist Scientist - California Department of Public Health</li><li>
 Or</li><li>
 CLS &ndash; Clinical Laboratory Scientist License - Montana Department of Labor &amp; Industry</li><li>
 Or</li><li>
 CLS &ndash; Clinical Laboratory Scientist - New York State Education Department</li><li>
 Or</li><li>
 CLS &ndash; Clinical Laboratory Specialist License - Montana Department of Labor &amp; Industry</li><li>
 Or</li><li>
 CLS &ndash; Clinical Laboratory Technician License - Montana Department of Labor &amp; Industry</li><li>
 Or</li><li>
 CLS - Generalist - Louisiana State Board of Medical Examiners</li><li>
 Or</li><li>
 CLS - Specialist - Louisiana State Board of Medical Examiners</li><li>
 Or</li><li>
 CLS - Technician - Louisiana State Board of Medical Examiners</li><li>
 Or</li><li>
 Cytogenetics Technologist (CG) (International Included) - American Society for Clinical Pathology (ASCP)</li><li>
 Or</li><li>
 Hematology Technologist (H) (International Included) - American Society for Clinical Pathology (ASCP)</li><li>
 Or</li><li>
 Laboratory Personnel - TN Department of Health</li><li>
 Or</li><li>
 Medical Laboratory Scientist (MLS) (International Included) - American Society for Clinical Pathology (ASCP)</li><li>
 Or</li><li>
 Medical Laboratory Technician (MLT)/Clinical Laboratory Technician (CLT) - ND Board of Clinical Laboratory Practice</li><li>
 Or</li><li>
 Medical Laboratory Technician (MLT) (International Included) - American Society for Clinical Pathology (ASCP)</li><li>
 Or</li><li>
 Medical Laboratory Technician (MLT) - American Association for Bioanalysts (AAB)</li><li>
 Or</li><li>
 Medical Laboratory Technician (MLT) - American Medical Technologists (AMT)</li><li>
 Or</li><li>
 Medical Laboratory Technician - California Department of Public Health</li><li>
 Or</li><li>
 Medical Laboratory Technician - State of Hawaii, Department of Health</li><li>
 Or</li><li>
 Medical Lab Personnel - Department of Health and Human Services Nevada Division of Public and Behavioral Health (DPBH)</li><li>
 Or</li><li>
 Medical Lab Scientist (MLS) - American Medical Technologists (AMT)</li><li>
 Or</li><li>
 Medical Technologist (MT)/Clinical Laboratory Scientist (CLS) - ND Board of Clinical Laboratory Practice</li><li>
 Or</li><li>
 Medical Technologist (MT) - American Association for Bioanalysts (AAB)</li><li>
 Or</li><li>
 Medical Technologist (MT) - American Medical Technologists (AMT)</li><li>
 Or</li><li>
 Medical Technologist (MT) - American Society for Clinical Pathology (ASCP)</li><li>
 Or</li><li>
 Medical Technologist - State of Hawaii, Department of Health</li><li>
 Or</li><li>
 Microbiology Technologist (M) (International Included) - American Society for Clinical Pathology (ASCP)</li><li>
 Or</li><li>
 Molecular Biology Technologist (MB) (International Included) - American Society for Clinical Pathology (ASCP)</li><li>
 Or</li><li>
 Specialist in Blood Banking (SBB) (International Included) - American Society for Clinical Pathology (ASCP)</li><li>
 Or</li><li>
 Specialist in Chemistry (SC) (International Included) - American Society for Clinical Pathology (ASCP)</li><li>
 Or</li><li>
 Specialist in Cytology (SCT) (International Included) - American Society for Clinical Pathology (ASCP)</li><li>
 Or</li><li>
 Specialist in Cytometry (SCYM) (International Included) - American Society for Clinical Pathology (ASCP)</li><li>
 Or</li><li>
 Specialist in Microbiology (SM) (International Included) - American Society for Clinical Pathology (ASCP)</li><li>
 Or</li><li>
 Specialist in Molecular Biology (SMB) (International Included) - American Society for Clinical Pathology (ASCP)</li></ul><p><br>
</p></div></div></div></div><p></p><p><b>Work Shift:</b></p>
Evening Shift (United States of America)<p></p><div><div><div><div><div><div><div><p><b>
Job Type:</b></p></div></div></div></div></div></div></div>
Employee<p></p><div><div><div><div><div><div><div><p><b>
Department:</b></p></div></div></div></div></div></div></div>
3406000007 Lab - Central Access<p></p><div><b>
Scheduled Weekly Hours:</b></div>
40<p></p><p><b>
Benefits:</b></p><p></p><p>
SSM Health values our exceptional employees by offering a comprehensive benefits package to fit their needs.</p><p></p><ul><li><p><b>
Paid Parental Leave</b><b>:</b> we offer eligible team members one week of paid parental leave for newborns or newly adopted children (pro-rated based on FTE).</p></li><li><p><b>
Flexible Payment Options:</b> our voluntary benefit offered through DailyPay offers eligible hourly team members instant access to their earned, unpaid base pay (fees may apply) before payday.</p></li><li><p><b>
Upfront Tuition Coverage</b>: we provide upfront tuition coverage through FlexPath Funded for eligible team members.</p></li></ul><p></p><p>
Explore All Benefits</p><p></p><p><i>
SSM Health is an equal opportunity employer. SSM Health does not discriminate on the basis of race, color, religion, national origin, age, disability, sex, sexual orientation, gender identity,</i><b><i> </i></b><i>pregnancy, veteran status</i><b><i>, </i></b><i>or any other characteristic protected by applicable law. </i>Click here to learn more.</p></div><p></p>

Clinical Lab Scientist Lead

Search 6439+ Clinical scientist jobs near you this March. New roles added regularly across leading industries. Apply today.