location_0_addressRegionName

location_0_addressCountryName

OFFSITE

UNKNOWN

ADAPTED_NOW

Laboratory Technician

ACTIVE

<h1>JOB DESCRIPTION</h1><h2>Summary</h2>Under the supervision of the laboratory supervisor the Microbiology Lab Technician provides support tasks in a fast-paced laboratory setting. This is a safety sensitive position as defined by state and federal laws that will require working with hazardous materials and/or handling medicine. As a "safety sensitive" classification, you will be subject to drug and alcohol testing, including random testing. Marijuana is one of the substances included in the drug panel screening. Possession of a medical marijuana license will not excuse you from the testing process, or the consequences of testing positive for marijuana. <h2>Classification  </h2>Non-exempt <h2>Category  </h2>Non-management<h2>Reports to </h2>Microbiology Supervisor<h2>Essential Functions</h2><ol><li>Media preparation </li><li>Glassware cleaning </li><li>Inventory / ordering </li><li>Lab cleaning and sanitization </li><li>Autoclaving various reagents and supplies </li><li>Assist laboratory personnel in daily activities to maintain high scientific quality and compliance with SOPs, protocols, and safety standards </li><li>Ability to wear, maintain, and properly use appropriate safety equipment, including, but not limited to eye protection, gloves, full face respirator, and lab coat.</li><li>Adherence to all ARL Bio Pharma safety standards, policies, procedures, and protocols</li></ol><h2>Competencies</h2><ol><li>Communication Proficiency. </li><li>Problem Solving/Analysis. </li><li>Collaboration Skills. </li></ol><h2>Supervisory Responsibility</h2>This position has no supervisory responsibilities. <h2>Work Environment</h2>This job operates in a laboratory environment.  Attendance at the office is required. While performing the duties of the job the employee is frequently exposed to various microorganisms and may be exposed to toxic or hazardous chemicals.  The employee will be required to wear all appropriate safety equipment including but not limited to eye protection, gloves, full face respirator and lab coat.  This role routinely uses standard office equipment such as computers, phones, photocopiers, filing cabinets and fax machines. <h2></h2><h2>Physical Demands</h2>The role requires standing for prolonged periods of time; dexterity in fingers and hands to perform complex and precise manipulations; ability to walk and stoop; ability to lift and move up to 50 pounds; see in the normal visual range including the ability to distinguish colors and shades and hear in the normal audio range with or without correction. <h2>Position Type/Expected Hours of Work</h2>This is a full-time position. Days and hours of work are TBD.<h2>Travel</h2>No travel is required for this position. <h2> Required Education and Experience</h2><ol><li>High School diploma with 2+ years working experience OR </li><li>Associate degree in Microbiology or related science field OR </li><li>Bachelor’s degree in Microbiology or related science field </li></ol><h2>Preferred Education and Experience</h2><ol><li>A minimum of an associate degree in Microbiology or related science field. </li></ol><h2>AAP/EEO Statement</h2>ARL Bio Pharma, Inc.  provides equal employment opportunity to all individuals regardless of their race, color, creed, religion, gender, age, sexual orientation, gender identity, national origin, disability, veteran status, genetics or any other characteristic protected by state, federal, or local law.  ARL Bio Pharma, Inc. expressly prohibits any form of workplace harassment based on race, color, creed, religion, gender, age, sexual orientation, gender identity, national origin, disability, veteran status, genetics or any other characteristic protected by state, federal, or local law.  Improper interference with the ability of ARL Bio Pharma, Inc.  employees to perform their job duties may result in discipline up to and including discharge. Further, the company takes affirmative action to ensure that applicants and employees are treated without regard to any of these characteristics. <h2></h2><h2>Other Duties</h2>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.

ARL Bio Pharma

Laboratory Technician - Microbiology Lab

monster

ONSITE

FULL_TIME

YEAR

Research Associate

Axbio Inc., a well funded silicon valley based startup developing fast molecular In-Vitro diagnostic technology, is seeking a highly motivated research associate or senior research associate to make significant contributions to our molecular biology pipeline. The successful candidate will work independently in a fast-paced and a results-focused group, will be provided with learning opportunity in a multi-disciplinary environment. Responsibilities:<ul><li>Initiate and execute protocols.</li><li>Work closely with senior scientist on various projects.</li><li>Report results in the biology team.</li></ul>Requirements:<ul><li>At least B.S. in Molecular Biology, Cell Biology, Biochemistry or related discipline.</li><li>Extensive experience and skills in molecular biology, such as enzymatic assays and PCR or primer extension-based experiments.</li><li>Knowledge and hand-on experience on protein expression, purification (AKTA experience is a plus), and characterization (such as PAGE and western blots).</li><li>Decent problem-solving skills and data analysis skills.</li><li>Ability to work in a collaborative and dynamic environment.</li><li>Flexibility, and the capability and willingness to perform a wide range of duties.</li><li>3 or more years of research experience in industry or academia.</li></ul>Axbio is an equal opportunity employer

Axbio, Inc.

(Senior) Research Associate– Molecular Biology

INTEGRATED

Unclassified Occupations

https://www.youtube.com/watch?v=aV0cEhLLbi4

job summary: As the world's largest staffing and recruitment agency in the world, we can commit to find you the perfect role that gives you the opportunity to learn and grow in the life sciences arena. Utilizing a recruiter for your job search gives you access to a large network of top employers as well as detailed information about hundreds of positions. We supply prestigious life sciences and biopharma companies with job seekers like you to achieve their business goals. If you're looking for a position where you can serve as an asset to your company while making a difference in others' lives, we have the ideal position for you!   location: Cambridge, Massachusetts job type: Contract salary: $20.05 - 23.59 per hour work hours: 9 to 5 education: Bachelors   responsibilities: The Early Development Department is seeking a motivated research associate to join our team to support the Sample Management group in the receiving and storage of nonclinical samples. We are seeking a highly organized individual that is able to work quickly and efficiently in a fast-paced laboratory setting. This Sample Management Associate must collaborate on a team and coordinate tasks with various stakeholders to ensure deadlines are met.<ul><li>Support daily laboratory operation</li><li>Maintain database of samples used for nonclinical and clinical samples ensuring accurate and prompt distribution of samples</li><li>Assist analysts in procuring nonclinical and clinical samples and reference materials utilizing a LIMS system</li><li>Support preparation of nonclinical tissue samples (i.e. weighing, grinding, and lysis) to extract target siRNA for downstream analysis</li><li>Maintain inventory of common laboratory consumables used for Sample Management</li><li>Manage the overall inventory of nonclinical and clinical samples and reference materials</li><li>Support electronic organization and filing of documents such as study protocols, reports, amendments, and deviations and associated sample management documents</li><li>Maintain protocols and forms for receipt, storage, and disposition of nonclinical and clinical samples and reference materials</li><li>Perform all receipt, storage, and disposition of nonclinical and clinical samples and reference materials utilizing a LIMS system</li><li>Maintain a high level of organization and great attention to detail</li><li>Complete assignments in a timely and clearly documented manner</li><li>Handle tasks quickly and efficiently in a fast-paced work environment</li><li>Understand company goals and relationship of individual goals to specific projects</li><li>Operate in a team-based environment</li><li>Communicate openly and directly with lab group in order to provide sufficient solutions that will work for all team members</li><li>Utilize feedback to improve performance and efficiency</li></ul>  qualifications: <ul><li>Minimal requirement of Bachelor's Degree (in scientific discipline preferred</li><li>1-3 years experience in a laboratory setting preferred</li><li>Experience with LIMS applications is preferred</li><li>Exceptional interpersonal skills and the ability to function in a high capacity within a fast-paced team environment</li><li>Excellent attention to detail, organizational skills, eagerness to learn, and the ability to follow written and verbal instruction.</li><li>Working knowledge of standard Microsoft Office applications including Excel, Outlook, PowerPoint, and Word.</li><li>Ability to lift ~50 lbs and work on feet for long periods of time.</li></ul>  skills: Laboratory Information Management Systems (LIMS), Sample Testing Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status.

Randstad was founded in 1960 by Frits Goldschmeding. We've never let go of his passion or the values that he established. By staying true to those fundamentals, we've expanded to represent more than 90 percent of the HR services market.We provide outsourcing, staffing, consulting and workforce solutions within the areas of engineering, accounting and finance, healthcare, human resources, IT, legal, life sciences, manufacturing and logistics, office and administration and sales and marketing. We can’t wait to tell you all about it.Our mission is to be a world leader in matching demand for, and supply of, labor and HR services. We believe in the value of work as a unifying force that shapes society for the better. We live by the core values established early in our company's history: to know, serve and trust, striving for perfection and simultaneous promotion of all interests.

Randstad US

Sample Management Associate I

Randstad Life Sciences

Clinical Research Associate

Based remotely, and reporting to the Director, Clinical Trials, the Site Manager/Clinical Research Associate (SM/CRA) is responsible for all site management and monitoring activities for Company’s clinical trials. As a SM/CRA, you are expected to oversee and manage the progress of the investigator sites to ensure the trials are conducted, recorded, and reported in accordance with the protocol, Company standard operating procedures (SOPs), ICH-GCP, and all applicable local and federal regulatory requirements.JOB RESPONSIBILITIES<ul><li>Responsible for assigned sites at the time of study start-up activities as to provide support with IRB and/or IBC submissions, preparation and assembly of study documents and study materials.</li><li>Perform all tasks associated with the preparation, conduct (remote and on-site) and follow-up of investigational site monitoring visits (selection, initiation, interim monitoring, and close-out) ensuring regulatory, ICH-GCP and protocol compliance</li><li>Serve as main point of contact for assigned sites</li><li>Manage and oversee site level activities, including site performance with enrollment, data entry/cleaning, protocol adherence, regulatory requirements, timely safety reporting</li><li>Ensure action items are addressed in a timely manner as per the Monitoring Plan</li><li>Identify and assist with the review of protocol deviations and data listings to ensure reliable quality data are obtained</li><li>Identify and manage or escalate trial related issues as appropriate</li><li>Provide trial training/re-training (i.e., protocol, system, process, etc.) to site staff</li><li>Maintain investigational site files within the study’s Trial Master File</li><li>Assist with preparation and conduct of investigator meetings, project team meetings and other study trainings as required.</li><li>Actively participate in applicable trial, department, company and/or vendor meetings</li><li>Review trial documents, forms, and plans</li><li>Provide training and mentoring to other CRAs</li><li>Perform other duties as assigned by the Director of Clinical Trials</li></ul> QUALIFICATIONS<ul><li>B.S./B.A. in nursing, biology, or a related life sciences discipline required</li><li>1-2 years of site management experience in a CRA role with a pharmaceutical/biotech company required</li><li>In-depth knowledge of clinical trial processes and activities as well as current regulatory and ICH-GCP guidelines</li><li>Ability to work independently and prioritize tasks and activities</li><li>Ability to interact with all levels of staff to coordinate and execute study activities both internally and externally</li><li>Strong organizational skills</li><li>Excellent written and verbal communication and presentation skills</li><li>Proficiency with Microsoft Office applications (Word, Excel, PowerPoint) required</li><li>Preferred 2+ years monitoring experience</li><li>Prior oncology experience preferred</li><li>Prior experience with CTMS, EMR, EDC, eTMF, IRS preferred</li><li>Must be able to travel up to 75% of the time domestically (fly and/or drive)</li><li>Proven ability to work effectively in a home-based/remote environment</li><li>Must have valid driver’s license</li></ul>

Clinical Dynamix, Inc.

Remote Clinical Research Associate

Top Echelon

401K

Life Insurance

Medical, Dental and Vision

https://www.youtube.com/watch?v=LuxOkFo--yU

<div class="job-detail-jobdescription">Molecular Technologist Opening in Waltham, MA!Apex Systems combines with parent company On Assignment to make it the 2nd largest IT staffing agency in the country.Apex has an opportunity for a Molecular Technologist role in Waltham, MA. This is a 1 year contract to hire position and the pay rate is flexible depending on experience. Here are the details:                        For applicants who are interested in this opportunity; please send a Word resume to Rachel Buzzotta, Technical Recruiter, at rbuzzotta@apexsystems.com.Position:  Molecular Technologist Apex Job ID:  1182793 Location: Waltham, MA Rate: Negotiable Duration: 1 year contract to hirePosition Description:Position Description:We are looking for a candidate with experience working with nucleic acids in a CLIA environment. This is a great opportunity for you to get your foot in the door at a growing biotech company!Responsibilities: Testing Personnel:<ul><li>Responsible for specimen processing, test performance, and for reporting test results.	<ul><li>Performs only those high complexity tests that are authorized by the Laboratory Director and require a degree of skill commensurate with the individual’s education, training or experience, and technical abilities.</li></ul></li></ul>Each individual performing high complexity testing must<ol><li>Follow the laboratory’s procedure for specimen handling and processing, test analyses, reporting and maintain records of patient test results</li><li>Adhere to the laboratory’s quality control policies, document all quality control activities, instrument and procedural calibrations and maintenance performed.</li><li>Follow the laboratory’s established policies and procedures whenever test systems are not within the laboratory’s established acceptable levels of performance.</li><li>Be capable of identifying problems that may adversely affect test performance or reporting of test results and either must correct the problems or immediately notify the General Supervisor, Technical Supervisor, Clinical Consultant, or Laboratory Director.</li><li>Document all corrective actions taken when test systems deviate from the laboratory’s established performance specifications</li><li>Except as specified in the qualifications, perform high complexity testing only under the onsite direct supervision of a General Supervisor qualified.</li></ol>Required Skills:<ul><li>Bachelor's degree in biological or clinical laboratory sciences</li><li>1-3 years of experience in a molecular biology laboratory</li><li>Experience with a Laboratory Information Management system (LIMS)</li><li>Experience with PCR, RT-PCR, Nucleic Acid, DNA/ RNA extraction, assays.</li></ul>Desired Skills (not required but candidate will have exposure to these skills in this role):1. CLIA experienceAdditional Requirements:**IF THIS APPLIES TO THE JOB** Candidates must be US citizens able to obtain and/or maintain a Department of Defense security clearance as a condition of employmentAdditional Benefits:For this opportunity, you will also be eligible for benefits through Apex for the contract period, 401K, medical/health benefits options, a W2 hourly rate, weekly pay, and direct deposit!Perks:EEO EmployerApex is an Equal Employment Opportunity/Affirmative Action Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, age, sexual orientation, gender identity, national origin, disability, protected veteran status, or any other characteristic protected by law. Apex will consider qualified applicants with criminal histories in a manner consistent with the requirements of applicable law. If you have visited our website in search of information on employment opportunities or to apply for a position, and you require an accommodation in using our website for a search or application, please contact our Employee Services Department at employeeservices@apexsystemsinc.com or 844-463-6178.EEO EmployerApex Systems is an equal opportunity employer. We do not discriminate or allow discrimination on the basis of race, color, religion, creed, sex (including pregnancy, childbirth, breastfeeding, or related medical conditions), age, sexual orientation, gender identity, national origin, ancestry, citizenship, genetic information, registered domestic partner status, marital status, disability, status as a crime victim, protected veteran status, political affiliation, union membership, or any other characteristic protected by law. Apex will consider qualified applicants with criminal histories in a manner consistent with the requirements of applicable law. If you have visited our website in search of information on employment opportunities or to apply for a position, and you require an accommodation in using our website for a search or application, please contact our Employee Services Department at mailTo:employeeservices@apexsystemsinc.com or 844-463-6178.</div>

Apex Systems, a segment of ASGN Inc. (NYSE: ASGN), is a technology services business that delivers emerging technology solutions to bring our clients digital visions to life. Apex has presence in over 70 markets across US, Canada and Mexico. Our consultants work with all types of companies throughout all industries, including more than 300 of the Fortune 500 companies. Are you an innovator with high standards who wants to help shape the world? We want you! Learn more about how to find your purpose with Apex, visit www.apexsystems.com.
Apex Systems is an equal opportunity employer. We do not discriminate or allow discrimination on the basis of race, color, religion, creed, sex (including pregnancy, childbirth, breastfeeding, or related medical conditions), age, sexual orientation, gender identity, national origin, ancestry, citizenship, genetic information, registered domestic partner status, marital status, disability, status as a crime victim, protected veteran status, political affiliation, union membership, or any other characteristic protected by law. Apex will consider qualified applicants with criminal histories in a manner consistent with the requirements of applicable law. If you have visited our website in search of information on employment opportunities or to apply for a position, and you require an accommodation in using our website for a search or application, please contact our Employee Services Department at <a>employeeservices@apexsystems.com</a> or 844-463-6178.

Apex Systems

Molecular Technologist

By clicking the Apply button, I understand that my employment application process with Takeda will commence and that the information I provide in my application will be processed in line with Takedas<a href="https://urldefense.proofpoint.com/v2/url?u=https-3A__www.takedajobs.com_privacynotice&d=DwMFAg&c=eIGjsITfXP_y-DLLX0uEHXJvU8nOHrUK8IrwNKOtkVU&r=R7Z8seTzCwqpIAi7APe73INoZm9-sxCdHQKjwfWPCQs&m=dHDH9k7lo2jkh-wOGxeg4p4mAfV8Vr_FCuR60MDlbTo&s=Tj67ufwJLuB1vZlHjecELumJYbWpaHHiC9kI2nnRDKU&e=" rel="nofollow noopener noreferrer" target="_blank">Privacy Notice</a>and <a href="https://urldefense.proofpoint.com/v2/url?u=https-3A__www.takeda.com_terms-2Dof-2Duse_&d=DwMFAg&c=eIGjsITfXP_y-DLLX0uEHXJvU8nOHrUK8IrwNKOtkVU&r=R7Z8seTzCwqpIAi7APe73INoZm9-sxCdHQKjwfWPCQs&m=dHDH9k7lo2jkh-wOGxeg4p4mAfV8Vr_FCuR60MDlbTo&s=_CIJE9CeroUy1ZLHeCKCoxM1jCAPZSz9Vq5yEGoRCGg&e=" rel="nofollow noopener noreferrer" target="_blank">Terms of Use</a>. I further attest that all information I submit in my employment application is true to the best of my knowledge.<h2>Job Description</h2>Are you looking for a patient-focused, innovation-driven company that will inspire you and empower you to shine? Join us as a Senior Research Associate, Analytical Development - Cell Therapy in our Cambridge, MA office.At Takeda, we are transforming the pharmaceutical industry through our R&D-driven market leadership and being a values-led company. To do this, we empower our people to realize their potential through life-changing work. Certified as a Global Top Employer, we offer stimulating careers, encourage innovation, and strive for excellence in everything we do. We foster an inclusive, collaborative workplace, in which our global teams are united by an unwavering commitment to deliver Better Health and a Brighter Future to people around the world.Here, you will be a vital contributor to our inspiring, bold mission.As a member of the analytical development team, you will have the opportunity to contribute in multiple development programs. As a Senior Research Associate working on the Analytical Development team, you will be empowered to develop, validate and transfer analytical methods to rapidly advance Takeda`s portfolio.POSITION OBJECTIVES:Responsible for executing basic/routine experiments under limited supervision. This position also plans basic experiments and experiments and performs specialized/complex experiments with assistance from supervisor as appropriate.POSITION ACCOUNTABILITIES:                                        <ul><li>Perform testing of samples as per established test method as part of method validation/transfer</li><li>Contributes to technical documents such as test methods, reports, protocols, and internal presentations</li><li>Contributes significantly in a small team of scientists towards the optimization, qualification and technical transfer of analytical methods in a compliance-based environment in a timely manner to meet program timelines</li><li>Identifies and communicates routine technical problems within scope of responsibility </li><li>Contribute significantly to project team and local initiatives as appropriate</li><li>Makes and understands basic experimental decisions within scope of responsibility.</li><li>Contribute to technical transfer of experimental data/procedures to vendors as appropriate</li><li>Documents personal experimental results accurately and completely in laboratory notebook.</li><li>Coordinates departmentally as well as cross functionally with peers on project work as appropriate.  </li></ul>EDUCATION, EXPERIENCE, BEHAVIOURAL COMPETENCIES AND SKILLS:  Education and Experience:Required:<ul><li>Bachelors in chemistry, biology, pharmacy, engineering or related pharmaceutical science; 2-5 years relevant industry experience</li><li>Masters degree in chemistry, biology, pharmacy, engineering or related pharmaceutical science; 0-5 years relevant industry experience</li></ul>Knowledge and Skills:<ul><li>Knowledge in immunology and/or immune oncology.</li><li>Experiences in immune cell handling, including cell isolation, culture and transduction.</li><li>Experiences in cellular characterization assays, including flow cytometry-based, ELISA, qPCR and other cell based assays.</li><li>Experiences with assay validation and tech transfer.</li><li>Teamwork  Ability to work well in a highly cross-functional team environment</li><li>Communication - Able to expresses ones self clearly and concisely within team; documents issues and/or concerns concisely with colleagues ; timely and effectively communicates issues to supervisor; technical writing skills to support contributing to internal technical documents</li><li>Organization   Exercises good time management and prioritization skills and is able to successfully manage multiple tasks simultaneously </li></ul>TRAVEL REQUIREMENTS:<ul><li>May require approximately 5% travel.</li></ul>WHAT TAKEDA CAN OFFER YOU:<ul><li>401(k) with company match and Annual Retirement Contribution Plan</li><li>Tuition reimbursement</li><li>Company match of charitable contributions</li><li>Health & Wellness programs including onsite flu shots and health screenings</li><li>Generous time off for vacation and the option to purchase additional vacation days</li><li>Community Outreach Programs</li></ul>Empowering Our People to ShineDiscover more at takedajobs.comNo Phone Calls or Recruiters Please.#LI-KD1This job posting excludes CO applicants.EEO StatementTakeda is proud in its commitment to creating a diverse workforce and providing equal employment opportunities to all employees and applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, gender expression, parental status, national origin, age, disability, citizenship status, genetic information or characteristics, marital status, status as a Vietnam era veteran, special disabled veteran, or other protected veteran in accordance with applicable federal, state and local laws, and any other characteristic protected by law.<h2>Locations</h2>Boston, MA<h2>Worker Type</h2>Employee<h2>Worker Sub-Type</h2>Regular<h2>Time Type</h2>Full time

Takeda Pharmaceutical

Senior Research Associate, Analytical Development - Cell Therapy

Capital Markets Placement_feed

Laboratory Assistant

-Collects, processes and stores patient samples as per protocol and safety guidelines. -Performs patient testing within specified timelines. -Maintains a clean, safe work environment. -Maintains the equipment, ensuring that calibration and maintenance are completed within appropriate time frames. Schedule for this part-time Lab Assistant position is as follows (subject to variation) Monday 8:00a – 11:30aTuesday 8:00a – 10:30aWednesday 8:00a – 10:30aThursday 8:00a – 10:30aFriday 8:00a – 10:30aSaturday 8:00a – 11:30a COVID-19 Vaccine required.Why Work at The Iowa Clinic?At The Iowa Clinic, our physicians and employees are our most valued resource and the differentiator in the service and care we provide. We exemplify our Star Values of Service Excellence, Teamwork, Accountability, Respect and Stewardship which enables a work environment where each individual can contribute and excel. The Iowa Clinic values the diversity and unique skills and talents of each individual and strives to create a workplace that supports and develops its people. The Iowa Clinic is locally owned by doctors living and working in our communities. That means decisions about patient care are determined by you and your physician, not someone else. We are proud that our 250+ healthcare providers consistently rank top in quality and outcomes as recognized by Iowa’s largest health insurer. PI146577469

The Iowa Clinic

Lab Assistant (Part-Time)

JobTarget

Description <div>Is trained to perform processing blood and other body fluids, sendouts, and other tests as required. Obtains blood samples from the correct patient, ensuring that the blood is properly drawn and labeled following established procedures to assure the proper specimen for the requested testing. Is trained to become competent at venipunctures and skin punctures. May register and interview patients, obtaining accurate demographic and financial information. May be required to verify medical necessity for all Medicare patients.</div>

In 1999, two historic Catholic charities became one, forming CHRISTUS Health and creating a unique purpose in the modern health care market - to take better care of people. To extend the healing ministry of Jesus Christ, the mission that the Sisters of Charity Health Care system and Incarnate Word Health system shared for more than a century, is now also the mission of CHRISTUS Health. Ranked among the top 10 Catholic health systems in the United States by size, the CHRISTUS Health system includes more than 40 hospitals and facilities in seven U.S. states, Chile and six states in Mexico, with assets of more than $4.6 billion. Whether seeking care in Alexandria Louisiana, or Coahuila, Mexico, patients discover that the healing spirit is alive at CHRISTUS Health.

CHRISTUS Health

Lab Assistant FT/40HRS

Employee Referral Program

Maternity/Paternity Paid Leave

Paid sick days

Vacation/paid time off

Our client in Elmwood is seeking several Lab Assistants for a specimen management opportunity. Data entry skills are required for this job and the ideal candidate would have open availability. This a contract opportunity that offers the possibility of going permanent. - Hourly pay rate: $15.00 hourly - Various shifts available: 3:00 AM - 11:30 AM / 3:00 PM - 11:00 PM / 7:00 PM - 3:30 AM. Responsibilities: - Receive, organize and process patient specimens. - Management of specimens to include order entry, registration, triaging, specimen labeling & centrifugation. - Preparing referrals to outside laboratories and storing specimens properly. - Communicate and collaborate with technical staff to promote quality and cost-effective patient care. Working hours: 3:00 PM - 11:00 PM Skills: - Windows based PC friendly - Data entry - Able to work in a team setting - Address problems proactively Education: High School Experience: 0-1 years Qualifications: - Previous typing experience with ability to type 35 WPM - High school diploma - Some college, science or computer education preferred - Knowledge of laboratory terminology or previous exposure to medical field and/or data processing - Louisiana State Laboratory Assistant license preferred Please apply online and a recruiter will reach out to you in 24-48 hours to discuss your application. If you have any questions or would prefer to forward your resume directly feel free to do so: 504-455-6565, spherionneworleans@spherion.com. Let's get to work! Spherion has helped thousands of people just like you find work happiness! Our experienced staff will listen carefully to your employment needs and then work diligently to match your skills and qualifications to the right job and company. No one works harder for you than Spherion. EEO Employer: Race, Religion, Color, National Origin, Citizenship, Sex, Sexual Orientation, Gender Identity, Age, Disability, Ancestry, Veteran Status, Genetic Information, Service in the Uniformed Services or any other classification protected by law.

<h4>WE'RE SPHERION. OUR VISION IS TO DRIVE CAREERS, GROW BUSINESSES, AND BETTER THE COMMUNITIES WE CALL HOME.</h4>
 
<h4>We're a national recruiting and staffing enterprise that blends the resources of a global HR company with the local insights of our independent franchise owners. A pioneer in the staffing industry, we’ve been providing companies with the workforce solutions they need for over 75 years, while helping people find jobs and build careers where they can thrive.</h4>

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