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Weekend Clinical Molecular Technologist Jobs (NOW HIRING)

The molecular pathology technologist requires minimal oversight to complete assigned tasks ... for clinical analysis. * Molecular Pathology Testing: Performs and reports tests according to ...

Entering clinical patient data into the Laboratory Information Management system. Obtain 12 ... with molecular biology * BS/BA in medical technology, clinical laboratory science, chemical ...

The molecular pathology technologist requires minimal oversight to complete assigned tasks ... for clinical analysis. * Molecular Pathology Testing: Performs and reports tests according to ...

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Weekend Clinical Molecular Technologist information

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$27

$50

$70

How much do weekend clinical molecular technologist jobs pay per hour?

As of Sep 8, 2026, the average hourly pay for weekend clinical molecular technologist in the United States is $50.94, according to ZipRecruiter salary data. Most workers in this role earn between $32.93 and $67.31 per hour, depending on experience, location, and employer.

What is a weekend clinical molecular technologist?

Weekend Clinical Molecular Technologists are specialized laboratory professionals who work primarily on weekends to perform high-complexity molecular diagnostic tests. They analyze DNA, RNA, and other biomarkers to help diagnose diseases, monitor treatment, and guide patient care. These technologists operate cutting-edge equipment, ensure quality control, and maintain accurate records, often in hospital or reference lab settings. Their work is essential for providing timely and accurate results, particularly during off-hours when other staff may not be available.

What skills and qualifications are needed to thrive as a weekend clinical molecular technologist?

To thrive as a Weekend Clinical Molecular Technologist, you need a solid background in molecular biology, laboratory techniques, and a relevant bachelor’s degree, often accompanied by ASCP certification. Familiarity with PCR, next-generation sequencing platforms, laboratory information systems (LIS), and quality control protocols is essential. Attention to detail, strong problem-solving skills, and effective communication are vital soft skills for this role. These competencies ensure accurate diagnostic results, compliance with regulatory standards, and efficient collaboration during independent weekend shifts.

What unique challenges do weekend clinical molecular technologists face compared to weekday staff?

Weekend Clinical Molecular Technologists often work with reduced on-site staff and may handle a broader range of responsibilities, such as troubleshooting instruments or managing urgent cases independently. They are expected to maintain high-quality standards while working with limited immediate supervision and support. Effective communication with off-site supervisors and ensuring smooth handoffs for incoming weekday teams are key aspects of the role. This position is ideal for individuals who are comfortable with autonomy and can adapt to a dynamic environment.

What is the difference between Weekend Clinical Molecular Technologist vs Weekend Clinical Laboratory Technician?

AspectWeekend Clinical Molecular TechnologistWeekend Clinical Laboratory Technician
CredentialsTypically requires a Bachelor's degree in Molecular Biology, Genetics, or related field; certification such as ASCP is commonUsually requires an Associate's degree or relevant certification; less specialized
Work EnvironmentSpecialized molecular labs, working with DNA/RNA analysis and genetic testingGeneral clinical labs, performing routine tests on blood, urine, and other samples
Employer & IndustryHospitals, diagnostic labs, research institutionsHospitals, clinics, diagnostic laboratories
Search & Comparison IntentOften searched for comparison due to similar roles in clinical labs with different focus areas

The Weekend Clinical Molecular Technologist focuses on molecular testing techniques like DNA analysis, requiring specialized training and certifications. In contrast, the Weekend Clinical Laboratory Technician performs routine lab tests with broader responsibilities. Both roles work in clinical lab settings but differ in technical complexity and focus area.

What cities are hiring for Weekend Clinical Molecular Technologist jobs?

Cities with the most Weekend Clinical Molecular Technologist job openings:

What are the most commonly searched types of Clinical Molecular Technologist jobs?

The most popular types of Clinical Molecular Technologist jobs are:

What states have the most Weekend Clinical Molecular Technologist jobs?

States with the most job openings for Weekend Clinical Molecular Technologist jobs include:

What are popular job titles related to Weekend Clinical Molecular Technologist jobs?

For Weekend Clinical Molecular Technologist jobs, the most frequently searched job titles are:

$22/hr

Full-time

Medical, Retirement, PTO

Re-posted 8 days ago


Charles River Laboratories rating

8.3

Company rating: 8.3 out of 10

Based on 95 frontline employees who took The Breakroom Quiz

25th of 86 rated pharmaceutical


Job description

For 75 years, Charles River employees have worked together to assist in the discovery, development and safe manufacture of new drug therapies. When you join our family, you will have a significant impact on the health and well-being of people across the globe. Whether your background is in life sciences, finance, IT, sales or another area, your skills will play an important role in the work we perform. In return, we’ll help you build a career that you can feel passionate about.

Job Overview

We are seeking a Molecular Technologist I for our MALDI Lab located in Newark, DE.

The working hours for this role are Monday - Friday 10:00 am- 6:30 pm.

The Lab-Molecular Technologist will Process customer samples in the microbiology laboratory utilizing the various technology platforms including but not limited to bacterial 16S rDNA and fungal ITS2 sequencing, MALDI-TOF mass spectrometry and ribotyping. Ensure adherence to regulatory requirements and GMP compliance.

The following are responsibilities related to the Molecular Technologist I:

• Conduct accurate processing of customer samples in accordance with current SOPs.

• Receive, unpack, log, and subculture customer samples according to current SOPs.

• Aliquot and prepare reagents.

• Perform test streaks for isolation, PCR, sequencing, mass spectrometry of customer samples and other laboratory processes

• Perform continual maintenance, repair and cleaning of all laboratory equipment.

• Operate and maintain laser cutter.

• Provide backup for all laboratory functions when needed.

• Dispose of microbe cultures, chemicals and glass in proper waste containers.

• Collaborate with technical support to resolve discrepancies with customer samples.

• Comply with all aspects of laboratory safety, safety stations, safety manuals, safety SOP, and MSDS sheets.

• Suggest process improvements.

• Perform or support special projects in the lab when needed.

• Perform all other related duties as assigned. 

Qualifications

The following are minimum requirements related to the Molecular Technologist I position:

  • Bachelor’s Degree (B.A. /B.S.) or Associates Degree in Biology or related discipline required.
  • 0-2 years of experience in Laboratory setting (GMP Preferred)
  • Experience with Microbiology Culture Techniques (Understanding in Microbiology Agars, Microbiology Colony Morphology, Mixed Cultures or Mixed samples) is preferred
  • Must have ability to work in a fast paced and team-oriented work/lab environment.
  • Strong Attention to detail is required

The pay for this position is $22/hr. Please note that salaries vary within the range based on factors including, but not limited to, experience, skills, education, and location.

About Microbial Solutions
Our Microbial Solutions business group has a comprehensive portfolio of endotoxin testing, microbial detection and microbial identification products and services is unlike any other, and has been purposefully designed to meet the complex and ever-changing needs of the industry. We help clients to ensure product safety and quality with easy-to-use yet robust testing solutions that satisfy regulatory requirements, support critical decision making and improve operational efficiencies.


About Charles River
Charles River is an early-stage contract research organization (CRO). We have built upon our foundation of laboratory animal medicine and science to develop a diverse portfolio of discovery and safety assessment services, both Good Laboratory Practice (GLP) and non-GLP, to support clients from target identification through preclinical development. Charles River also provides a suite of products and services to support our clients’ clinical laboratory testing needs and manufacturing activities. Utilizing this broad portfolio of products and services enables our clients to create a more flexible drug development model, which reduces their costs, enhances their productivity and effectiveness to increase speed to market.

With over 20,000 employees within 110 facilities in 20 countries around the globe, we are strategically positioned to coordinate worldwide resources and apply multidisciplinary perspectives in resolving our client’s unique challenges. Our client base includes global pharmaceutical companies, biotechnology companies, government agencies and hospitals and academic institutions around the world. And in 2019, revenue increased to $2.62 billion.

At Charles River, we are passionate about our role in improving the quality of people’s lives. Our mission, our excellent science and our strong sense of purpose guide us in all that we do, and we approach each day with the knowledge that our work helps to improve the health and well-being of many across the globe. We have proudly supported the development of 80% of the drugs approved by the FDA in the last five years.

We’re committed to providing benefits that elevate your quality of life.  Based on your position these may include:  bonus/incentives based on performance, 401K, paid time off, stock purchase program, Health and wellness coverage, employee and family wellbeing support programs, and work life balance flexibility.

Equal Employment Opportunity
Charles River Laboratories is an Equal Opportunity Employer - all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, or national origin, veteran or disability status.

It is unlawful in some states (including Massachusetts) to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability.

If you are interested in applying to Charles River Laboratories and need special assistance or an accommodation due to a disability to complete any forms or to otherwise participate in the resume submission process, please contact a member of our Human Resources team by sending an e-mail message to crrecruitment_US@crl.com. This contact is for accommodation requests for individuals with disabilities only and cannot be used to inquire about the status of applications.

For more information, please visit www.criver.com.


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About Charles River

Sourced by ZipRecruiter

Charles River is an early-stage contract research organization (CRO). We have built upon our foundation of laboratory animal medicine and science to develop a diverse portfolio of discovery and safety assessment services, both Good Laboratory Practice (GLP) and non-GLP, to support clients from target identification through preclinical development. Charles River also provides a suite of products and services to support our clients' clinical laboratory testing needs and manufacturing activities. Utilizing this broad portfolio of products and services enables our clients to create a more flexible drug development model, which reduces their costs, enhances their productivity and effectiveness to increase speed to market. With over 20,000 employees within 110 facilities in 20 countries around the globe, we are strategically positioned to coordinate worldwide resources and apply multidisciplinary perspectives in resolving our client's unique challenges. Our client base includes global pharmaceutical companies, biotechnology companies, government agencies and hospitals and academic institutions around the world. At Charles River, we are passionate about our role in improving the quality of people's lives. Our mission, our excellent science and our strong sense of purpose guide us in all that we do, and we approach each day with the knowledge that our work helps to improve the health and well-being of many across the globe. We have proudly supported the development of 86% of the drugs approved by the FDA in 2021.

Industry

Scientific research and development services

Company size

10,000+ Employees

Headquarters location

Wilmington, MA, US

Year founded

1947