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Freelance Real Time Pcr Jobs (NOW HIRING)

The Scientist III, Bioassay will demonstrate strong knowledge in cell-based potency assays, ELISA, real-time PCR, enzymatic activity assays, binding kinetic assays and other biochemical testing ...

New

Perform real-time PCR to detect and quantify pathogens in samples. * Troubleshoot various molecular biology techniques such as PCR. * Operate laboratory equipment (balances, centrifuges, microscopes ...

Research Associate II

Tempe, AZ · On-site

$60 - $80/hr

... and real time PCR, Next Generation Sequencing, protein extraction, assays for protein quantification and QC, western Blotting, ELISA and ELONA, sample preparation for mass spectrometry, aptamer ...

New

... and real time PCR, Next Generation Sequencing, protein extraction, assays for protein quantification and QC, western Blotting, ELISA and ELONA, sample preparation for mass spectrometry, aptamer ...

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Freelance Real Time Pcr information

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$14

$47

$132

How much do freelance real time pcr jobs pay per hour?

As of Sep 3, 2026, the average hourly pay for freelance real time pcr in the United States is $47.71, according to ZipRecruiter salary data. Most workers in this role earn between $24.28 and $61.78 per hour, depending on experience, location, and employer.

What is a freelance real time PCR specialist?

A Freelance Real Time PCR specialist is an independent professional who offers expertise in running and analyzing quantitative Polymerase Chain Reaction (qPCR) assays for clients, often in research, clinical, or diagnostic settings. They are skilled in designing experiments, preparing samples, operating Real Time PCR machines, interpreting data, and troubleshooting issues. As freelancers, they may work on a project basis for multiple laboratories or organizations, providing flexibility and specialized knowledge without long-term employment commitments.

What are the key skills and qualifications needed to thrive as a freelance real time PCR specialist?

To thrive as a Freelance Real-Time PCR Specialist, you need strong expertise in molecular biology, hands-on experience with PCR techniques, and at least a bachelor's degree in a relevant scientific field. Familiarity with real-time PCR instrumentation, analysis software (such as Applied Biosystems or Bio-Rad platforms), and relevant certifications (like GLP or CLIA compliance training) is highly valuable. Attention to detail, problem-solving ability, and effective communication with clients make candidates stand out in this freelance role. These skills ensure accurate results, efficient troubleshooting, and client satisfaction in delivering reliable molecular diagnostics or research services.

What are some common challenges freelance real time PCR specialists face when managing multiple projects for different clients?

Freelance real-time PCR specialists often juggle projects with varying protocols, timelines, and expectations, which can make workload management challenging. Balancing the need for high-quality, reproducible results with tight deadlines requires strong organizational and communication skills. Additionally, freelancers must ensure access to well-maintained equipment and reagents, sometimes coordinating with multiple laboratories or facilities. Building clear agreements with clients regarding data ownership, reporting standards, and troubleshooting support is also crucial for smooth project execution.

What is the difference between Freelance Real Time Pcr vs Freelance Laboratory Technician?

AspectFreelance Real Time PcrFreelance Laboratory Technician
CredentialsTypically requires certification in molecular biology or PCR techniquesRequires general laboratory training, often with a degree in biology or related field
Work EnvironmentPrimarily in labs performing PCR assays, often remotely or on a project basisIn various lab settings, handling multiple tests and equipment
Industry UsageUsed mainly in biotech, healthcare, and research for genetic testingCommon in clinical, research, and industrial laboratories

Freelance Real Time Pcr specialists focus on performing and analyzing PCR tests, often requiring specific molecular biology certifications. Freelance Laboratory Technicians have broader lab duties, working across various tests and equipment. Both roles are vital in laboratory settings but differ in specialization and scope.

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Cities with the most Freelance Real Time Pcr job openings:

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What states have the most Freelance Real Time Pcr jobs?

States with the most job openings for Freelance Real Time Pcr jobs include:

Infographic showing various Freelance Real Time Pcr job openings in the United States as of August 2026, with employment types broken down into 1% Internship, 1% As Needed, 73% Full Time, 21% Part Time, and 4% Contract. Highlights an 78% Physical, 2% Hybrid, and 20% Remote job distribution, with an average salary of $99,230 per year, or $47.7 per hour.

Scientist III - Bioassay

Alcami Corporation

Wilmington, NC • On-site

Full-time

Posted 8 days ago


Alcami rating

7.8

Company rating: 7.8 out of 10

Based on 9 frontline employees who took The Breakroom Quiz


Job description

At Alcami, we deliver reliable solutions that unlock the potential of transformative medicines from discovery to commercialization, through trusted partnership with our clients, recognized industry expertise and proven regulatory track record.
Are you interested in joining our team?
Job Summary
The Scientist III, Bioassay is accountable for driving results in a fast-paced environment by performing routine and non-routine testing in support of pharmaceutical product development and manufacturing. The Scientist III, Bioassay may also be required to work on method development and method validation projects. The Scientist III, Bioassay will demonstrate strong knowledge in cell-based potency assays, ELISA, real-time PCR, enzymatic activity assays, binding kinetic assays and other biochemical testing methods. Also, knowledge in techniques such as HPLC, icIEF, or CE-SDS is desirable. Strong problem-solving and troubleshooting skills along with proficiency in analyzing data, laboratory documentation, data presentation and collaboration will help ensure success in this position.
On-Site Expectations
  • 100% on-site position.
  • 1st Shift: Monday - Friday, 8:30am - 5:30pm.

Responsibilities
  • Performs laboratory analysis of pharmaceutical and biopharmaceutical products utilizing analytical instrumentation, analyzes and documents data in accordance with Alcami SOPs.
  • Documents results in electronic laboratory notebook.
  • Performs one or more of the following techniques: cell-based potency assays, ELISA, real-time PCR, enzymatic activity assays, binding kinetic assays and other biochemical testing methods.
  • Supports troubleshooting and problem solving activities for cell-based and biochemical tests.
  • Evaluates and interprets generated data.
  • Contributes to operational initiatives to support continued growth of the organization.
  • Develops and validates biological tests to determine purity, identity and potency of pharmaceutical and biopharmaceutical products.
  • Writes standard operating procedures (SOPs), test procedures, specifications and summary reports.
  • Maintains working knowledge of instrumentation, equipment, and scientific methodologies necessary to perform assigned tasks.
  • Assists in removal of hazardous waste, routine equipment cleaning, and restocking of consumable products and reagents.
  • Interacts with team members, management and clients to discuss data and project progress.
  • Ensures timely completion and compliance with cGMP and all other relevant company training requirements.
  • Effectively uses various laboratory software packages (SoftMax, ProCal, Master Control, ELN, etc.).
  • Maintains a safe, clean, and organized work environment free of safety hazards.
  • Safely handles potent compounds.
  • Ensures timely completion and compliance with cGMP and all other relevant company training requirements.
  • Other duties as assigned.

Qualifications
  • Associate's degree and 16+ years of related experience.
  • OR Bachelor's degree and 6+ years of related experience.
  • OR Master's degree with 2+ years of related experience.
  • OR PhD with 0+ years of experience required.
  • 2+ years of experience in Pharmaceutical, CDMO, or cGMP preferred.

Knowledge, Skills, and Abilities
  • Working knowledge of peptides, monoclonal antibodies, recombinant proteins is required, and knowledge of cell therapy and gene therapy is preferred.
  • Knowledge of Cell-based Bioassays required.
  • Working knowledge of Real-time PCR preferred.
  • Strong knowledge of ELISA/immunoassays required.
  • Working knowledge of Enzymatic Activity Assays preferred.
  • Working knowledge of Laboratory Documentation is required.
  • Working knowledge of cGMP in a pharmaceutical or regulated environment is preferred.
  • Strong verbal communications and presentation skills required.
  • Strong time management and organization skills required.
  • Strong knowledge of Laboratory equipment and safety required.
  • Good problem solving and trouble shooting ability required.
  • Proficiency with Microsoft Office (Word, Excel, PowerPoint) required.
  • Working knowledge of SoftMax and Empower preferred.

Travel Expectations
  • Up to 5% travel required.

Physical Demands and Work Environment
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. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. While performing the duties of this Job, the employee is regularly required to use hands to finger, handle, or feel; reach with hands and arms; talk or hear and smell. The employee is frequently required to sit. The employee is occasionally required to stand; walk and stoop, kneel, crouch, or crawl. The employee must regularly lift and/or move up to 10 pounds, frequently lift and/or move up to 25 pounds and occasionally lift and/or move up to 50 pounds. Specific vision abilities required by this job include close vision, distance vision, color vision, peripheral vision, depth perception and ability to adjust focus. While performing the duties of this Job, the employee is occasionally exposed to moving mechanical parts and vibration. The noise level in the work environment is usually very quiet.
While performing the duties of this job, the employee is frequently exposed to moving mechanical parts, fumes or airborne particles and toxic or caustic chemicals. The employee is occasionally exposed to wet and/or humid conditions; high, precarious places; risk of electrical shock and vibration. The noise level in the work environment is usually moderate. The employee will be required to wear the appropriate personal protective equipment for specific job duties to be performed. Such personal protective equipment may include, but not limited to safety eyewear, hearing protection, various types of respirators/breathing apparatus, lab coats, full protective body coverings, various types of gloves, etc. Other tasks involving elevated work may require the use of a body harness and lanyard. Additionally, the employee may be required to operate an industrial vehicle.

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