1

Freelance Assay Development Scientist Jobs in Rochester, NY

We are seeking a contract position as a Research & Development Technologist/Scientist to work in a team environment working on developing a new assay for our VITROS analyzer systems. You will perform ...

... complete assay testing experiments aimed for the development of new VITROS in vitro diagnostic ... We are seeking a contract position as a Research & Development Technologist/Scientist to work in a ...

... complete assay testing experiments aimed for the development of new VITROS in vitro diagnostic ... We are seeking a contract position as a Research & Development Technologist/Scientist to work in a ...

About R&D Roles at Danaher Are you driven by curiosity, discovery, and a desire to contribute to ... Conducting laboratory studies to evaluate assay performance under guidance from scientific staff

About R&D Roles at Danaher Are you driven by curiosity, discovery, and a desire to contribute to ... Conducting laboratory studies to evaluate assay performance under guidance from scientific staff

About R&D Roles at Danaher Are you driven by curiosity, discovery, and a desire to contribute to ... Conducting laboratory studies to evaluate assay performance under guidance from scientific staff

About R&D Roles at Danaher Are you driven by curiosity, discovery, and a desire to contribute to ... Conducting laboratory studies to evaluate assay performance under guidance from scientific staff

Freelance Assay Development Scientist information

See Rochester, NY salary details

$20

$38

$60

How much do freelance assay development scientist jobs pay per hour?

As of Aug 8, 2026, the average hourly pay for freelance assay development scientist in Rochester, NY is $38.15, according to ZipRecruiter salary data. Most workers in this role earn between $27.98 and $45.53 per hour, depending on experience, location, and employer.

What is a freelance assay development scientist?

A Freelance Assay Development Scientist is an independent scientific professional who specializes in designing, optimizing, and validating assays for research, diagnostics, or drug development projects. Unlike in-house scientists, freelancers typically work on a contract basis for multiple clients, providing expertise in assay development across various platforms such as ELISA, PCR, or cell-based assays. Their responsibilities may include troubleshooting existing assays, developing new methodologies, and ensuring that assays meet required sensitivity, specificity, and reproducibility standards. This role requires strong analytical skills, knowledge of relevant technologies, and the ability to work autonomously. Freelance assay development scientists often collaborate remotely with research organizations, biotech companies, and academic institutions.

What are the key skills and qualifications needed to thrive as a freelance assay development scientist?

To thrive as a Freelance Assay Development Scientist, you need a strong background in biochemistry, molecular biology, or a related field, often with an advanced degree and practical laboratory experience. Familiarity with analytical instruments (such as HPLC, ELISA, or PCR), data analysis software, and quality control standards is typically required. Excellent problem-solving skills, self-motivation, and effective communication are crucial for managing projects independently and collaborating with clients. These capabilities ensure the development of reliable assays, client satisfaction, and the ability to adapt to varied project requirements in a competitive freelance environment.

What are some common challenges freelance assay development scientists face when managing multiple client projects?

Freelance assay development scientists often juggle several projects with varying requirements and timelines. A common challenge is balancing the need for clear communication with clients while maintaining rigorous documentation and data integrity across different assays. Additionally, freelancers must be adept at troubleshooting unexpected technical issues independently and quickly adapting methods to meet each client's unique specifications. Effective time management and transparent updates are key to building trust and ensuring project success.
What are popular job titles related to Freelance Assay Development Scientist jobs in Rochester, NY? For Freelance Assay Development Scientist jobs in Rochester, NY, the most frequently searched job titles are:
What job categories do people searching Freelance Assay Development Scientist jobs in Rochester, NY look for? The top searched job categories for Freelance Assay Development Scientist jobs in Rochester, NY are:
What cities near Rochester, NY are hiring for Freelance Assay Development Scientist jobs? Cities near Rochester, NY with the most Freelance Assay Development Scientist job openings:

Research & Development Specialist

Rochester Regional Health

Rochester, NY • On-site

$70K - $80K/yr

Full-time

Posted 26 days ago


Rochester Regional Health rating

7.3

Company rating: 7.3 out of 10

Based on 218 frontline employees who took The Breakroom Quiz

305th of 887 rated healthcare providers


Job description

Job Title: Research & Development Specialist
Department: Research & Development
Location: Onsite; Rochester, NY
Hours Per Week: 40
Schedule: Monday - Friday
SUMMARY
The Research & Development Specialist will be responsible for the execution of analytical /technical activities and ensures their quality for ACM Global Laboratories. The Research & Development Specialist will develop comprehensive policies and procedures for test development, method validation and implementation, while supporting other departments as needed.
RESPONSIBILITIES
  • Facilitate assay development, conduct instrument validations and implement new testing to meet the needs of clinical trials protocols, clients and regulatory requirements.
  • Develop validation plans, validation summary reports, stability study summary reports, correlation plans and correlation summary reports to meet regulatory requirement.
  • Prepare Standard Operating Procedures for newly developed test procedures and relevant documentation, as necessary.
  • Research and identify suppliers of laboratory consumables and equipment options for new tests to support clinical trials opportunities.
  • Comply with policies for the safe, secure and confidential processing and storage of patient and other laboratory information
  • Perform the investigation and corrective action for assay troubleshooting and proficiency testing failures.
  • Responsible for assay / panel pre-validation and validation and correlation testing globally.
  • Ensures all methods and validations are done according to all applicable regulatory guidelines, including but not limited to Good Clinical Practice (GCP), Good Laboratory Practice (GLP), Good Clinical Laboratory Practice (GCLP), College of American Pathologists (CAP) etc.
  • Provide supporting information to Scientific Affairs in the evaluation of appropriate testing and/or methodology. Liaise with technical staff on feasibility of testing for new study requirements. Provide pricing as needed to Proposals team.
  • Provide supportive information for consultation and technical support to clinical trials clients and operational staff. Responsible for communications (meetings, calls audits etc.) with clients and formulate responses as required.
  • Assess the impact of manufacturer / vendor communications and complete associated documentation.
  • Provide study management and direction of laboratory teams for the implementation of analytical method validations.
  • Document and ownership of any quality documentation (Note to File, Quality Event, CAPA, deviation, change control) as appropriate within the required timeframes.
  • Participation in all activities that seek to ensure compliance with GCP guidelines and accreditation schemes (e.g. CAP).
  • Preparation of documentation for and participation in internal and external audits (client and regulatory).
  • Perform any other duties as assigned

REQUIRED QUALIFICATIONS
  • BS in Life Sciences
  • 3+ years in Laboratory experience

PREFERRED QUALIFICATIONS
  • NYS Medical Technologist License
  • Experience in Microsoft Office
  • EP Evaluator experience

EDUCATION:
BS (Required)
LICENSES / CERTIFICATIONS:
PHYSICAL REQUIREMENTS:
S - Sedentary Work - Exerting up to 10 pounds of force occasionally Sedentary work involves sitting most of the time, but may involve walking or standing for brief periods of time. Jobs are sedentary if walking and standing are required only occasionally and all other sedentary criteria are met.
For disease specific care programs refer to the program specific requirements of the department for further specifications on experience and educational expectations, including continuing education requirements.
Any physical requirements reported by a prospective employee and/or employee's physician or delegate will be considered for accommodations.
PAY RANGE:
$70,000.00 - $80,000.00
CITY:
Rochester
POSTAL CODE:
14624
The listed base pay range is a good faith representation of current potential base pay for a successful full time applicant. It may be modified in the future and eligible for additional pay components. Pay is determined by factors including experience, relevant qualifications, specialty, internal equity, location, and contracts.
Rochester Regional Health is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, creed, religion, sex (including pregnancy, childbirth, and related medical conditions), sexual orientation, gender identity or expression, national origin, age, disability, predisposing genetic characteristics, marital or familial status, military or veteran status, citizenship or immigration status, or any other characteristic protected by federal, state, or local law.

What Rochester Regional Health employees say

Pay

Benefits

Hours and flexibility

Workplace

Get the full story on Breakroom