Scientist

Posted 18 Days Ago
Be an Early Applicant
Frederick, MD
83K-120K Annually
Senior level
Biotech
The Role
The Cellular Assay Scientist is responsible for developing, validating, and performing clinical assays in an accredited laboratory, specifically focusing on neutralizing antibody assays. This role entails designing experiments, analyzing data, improving lab procedures, and ensuring compliance with safety standards. Collaboration with technical teams and supporting equipment qualifications are also key responsibilities.
Summary Generated by Built In

Position Summary:

The Cellular Assay Scientist participates in assay development, validation, and execution in a timely manner.  Performs clinical assays in CLIA/CAP/ISO accredited clinical immunology laboratory. and support development of new procedures and improvement of existing SOPs. Prepares critical reagents and involves in reagent lot-to-lot evaluation.

Essential functions of the job include but are not limited to: 

  • Perform Neutralizing Antibody Assay primarily, as well as, other immunocellular assays
  • Design and perform experiments, independently and accurately analyze and present data
  • High quality output is essential with the ability to build efficiency into improving productivity metrics
  • Assist in establishing and improving all procedures and required SOP documentation
  • Responsible for trouble shooting and correcting routine scientific issues/problems
  • Identify, update and implement emerging laboratory techniques
  • Maintain and support safe lab practices and environment
  • Work collaboratively with other technical teams in resource sharing and providing technical expertise
  • Support new equipment operational qualifications and performance checks
  • Monitor Product and Service/R&D related project expenses
  • Act as a scientific technology platform lead internally
  • Write and prepare SOP, abstracts or draft scientific study report
  • May present completed work at appropriate scientific meetings and in publications
  • Other duties as assigned

Qualifications:

Minimum Required:

  • Master’s Degree in life sciences or related field
  • 5 years of relevant laboratory experience

Other Required:

  • Expert level mammalian cell culture and plate-based cellular assay experience
  • Excellent communication, interpersonal, and organizational skills required
  • Must have the ability to organize and analyze data, as well as, prepare data reports
  • Must possess strong computational skills, preferably experienced with Word, Excel, Power Point, and GraphPad Prism
  • Excellent use of judgment and discretion required
  • Extended work hours may be occasionally necessary in order to meet business demands
  • Ability to lift and carry between 1-15 lbs.; Ability to lift up to 50 lbs. overhead with assistance; frequently required to sit, grasp, and use right/left finger dexterity; May be exposed to a cold freezer environment (Freezer temperatures range between -20ºC -196ºC)
  • Must be able to read, write, speak fluently and comprehend the English language


Preferred:

  • A solid understanding of current GXP or CAP/CLIA/ISO standards with industry working experience in cell/gene therapy field.
  • Demonstrated skills with assays used for immune monitoring such as primary cell based assays, ELISpot, NAb, ELISA and Mesoscale

Precision is required by law in some states or cities to include a reasonable estimate of the compensation range for this role. This compensation range takes into account the wide range of factors that are considered in making compensation decisions including but not limited to: skill sets, experience and training, licensure and certifications, and other business and organizational needs. The disclosed range estimate has not been adjusted for the applicable geographic differential associated with the location at which the position may be filled. At Precision, it is not typical for an individual to be hired at or near the top of the range for their role and compensation decisions are dependent on the facts and circumstances of each case. This role is also eligible for a discretionary annual bonus, health insurance, retirement savings benefits, life insurance and disability benefits, parental leave, and paid time off for sick leave and vacation, among other benefits.

Reasonable estimate of the current range

$83,400$119,750 USD

Any data provided as a part of this application will be stored in accordance with our Privacy Policy. For CA applicants, please also refer to our CA Privacy Notice.

Precision Medicine Group is an Equal Opportunity Employer. Employment decisions are made without regard to race, color, age, religion, sex, sexual orientation, gender identity, national origin, disability, veteran status or other characteristics protected by law. © 2020 Precision Medicine Group, LLC

If you are an individual with a disability and require a reasonable accommodation to complete any part of the application process or are limited in the ability or unable to access or use this online application process and need an alternative method for applying, you may contact Precision Medicine Group at [email protected].

It has come to our attention that some individuals or organizations are reaching out to job seekers and posing as potential employers presenting enticing employment offers. We want to emphasize that these offers are not associated with our company and may be fraudulent in nature. Please note that our organization will not extend a job offer without prior communication with our recruiting team, hiring managers and a formal interview process.


Top Skills

Elisa
Elispot
Graphpad Prism
Excel
Microsoft Powerpoint
Microsoft Word
The Company
HQ: Bethesda, MD
1,114 Employees
On-site Workplace

What We Do

Precision is the first global precision medicine clinical research services organization, purpose-built to improve the clinical research and development process for new therapeutics. Our novel approach integrates clinical operations excellence, with laboratory expertise, and advanced data sciences to inform every step. This maximizes our clients’ insight into patient biology, delivering more predictable trial outcomes and accelerating clinical development. We apply our expertise to trials at all stages—from early development through approval—with embedded experience in oncology and rare disease. With over 2000 dedicated professionals and 35 offices worldwide, we stand ready to help accelerate life-changing treatments anywhere around the globe.

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