Scientist (Bioanalytical)

Posted 5 Days Ago
Be an Early Applicant
Frederick, MD
83K-120K Annually
Senior level
Healthtech • Pharmaceutical
The Role
The Bioanalytical Scientist manages laboratory staff to perform and analyze assays supporting clinical research. The role involves designing experiments, improving productivity, maintaining safe lab practices, and collaborating with other teams. Responsibilities include troubleshooting, supporting new procedures, writing project reports, and representing the company in scientific discussions.
Summary Generated by Built In

Precision for Medicine 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. 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. Won’t you join us today as a Scientist, Bioanalytical?

Position Summary:

The Bioanalytical Scientist manages staff to accurately and efficiently perform assays to support ongoing services and contract activities. This role will perform assays according to SOPs and support development of new procedures and improvement of existing SOPs.

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

  • Design and perform experiments, independently and accurately analyze and present data
  • Responsible for high quality output with the ability to build efficiency into improving productivity metrics
  • Support development of projects in a timely manner in strict accordance with documented procedures
  • Perform assays according to defined protocol/SOP and support development of new procedures
  • Assist in establishing and improving all procedures and required SOP documentation
  • Responsible for troubleshooting 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 resource externally to clients and internally
  • Assists with writing, reviewing and editing contract and grant applications/proposals as appropriate
  • Assist with writing and reviewing project reports and editing contract proposals
  • Assists with writing and publishing papers, abstracts, techniques/or chapters to maintain the scientific standard and image of the company
  • May present completed work at appropriate scientific meetings and in publications
  • Carry out other duties/projects as assigned


Qualifications:

Minimum Required:

  • Master's Degree in life sciences or Bachelors in life science with 5+ years of relevant laboratory experience

Other Required:

  • Must have demonstrated expertise developing, troubleshooting, and performing bioanalytical assays in plate-based and cell-based assay formats, including pharmacokinetic (PK), biomarker, anti-drug antibody (ADA), neutralizing antibody (NAb) assays for protein/cell/gene-based therapeutics
  • Experience in different ligand binding technology platforms, such as ELISA, MSD, Quanterix, Luminex, Biacore/SPR
  • Strong background in leading bioanalytical and biomarker assay qualification and validation
  • Demonstrate an ability to working independently in planning, executing and analyzing data.
  • Solid understanding of current regulatory standards of bioanalytical assays
  • Experience in good documentation practices (GDP)
  • Proven experience managing, leading teams
  • Excellent communication, interpersonal, organizational and multi-tasking required
  • Must have the ability to independently organize and analyze data and prepare reports
  • Must possess strong computer skills, including experience with Prism, Microsoft Word, and Excel
  • 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:

  • D. in life sciences, with a minimum of 2 years post-doctoral training, industry experience or equivalent combination of education and experience preferred
  • Previous work experience in GLP or GCLP environment and a solid understanding of current GXP standards

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

Bioanalytical Assays
The Company
HQ: Bethseda, MD
396 Employees
On-site Workplace
Year Founded: 2012

What We Do

We founded Precision Medicine Group in 2012 because we believed there was a transformational opportunity to improve the process of bringing new drugs to market. It involves utilizing technology, data, and human expertise. It is a big challenge that requires diverse talents. Our model involves both nurturing and investing organically and acquiring capabilities that we do not have but critically need. Our core executive team is anchored to this model, building life science services that address fundamental changes in healthcare that are necessary for health and outcomes improvement.

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