hirly

Pfm

Principal Scientist

Houston, TX, USA

See how you match this job — and similar ones. Free.

Upload your resume and hirly scores it against this role at Pfm first, then against similar open jobs, and shows where you fit and why.

PDF or DOCX, up to 12MB. No sign-up to see your matches.

Get past the screening software and onto a recruiter's desk

hirly rewrites your resume for this job — matching the keywords and skills in the posting, moving your most relevant experience to the top, and writing a cover letter to fit. About 30 seconds.

  • Keywords matched to this posting
  • Fit score before you apply
  • Cover letter included
Tailor my resume for this job →

Apply from your AI assistant

Connect hirly to Claude and ask it to apply to this job. hirly tailors your resume, fills the employer’s form and asks before sending. ChatGPT: manual setup today.

Some employer sites stop an application at a CAPTCHA or sign-in and hand it back with a link. Applying needs a paid plan. Works with any assistant that supports MCP.

hirly's read of this role

Seniority
Lead / management
Stated salary
$110,700 – $166,100 per year
Country
US
Work mode
On-site / unstated
First seen by hirly
24 Oct 2026

Derived automatically from the posting. Upload your resume above to see how the role scores against it.

the posting

Position Summary:

The Principal Scientist will be instrumental in helping Precision achieve its goals of delivering exceptional services to Precision’s diverse, innovative, and global biopharmaceutical clients. Working closely with the assigned manager, the Principal Scientist will help support key scientific projects ensuring best practices are implemented to support timely delivery of client projects. Key components will be focused on the design and development of innovative qualified and validated molecular assays including, but not limited to, ddPCR, qPCR, Next Gen Sequencing, Nanostring, and FISH assays.

The successful candidate will assist and be a resource for scientist team members to design experimental plans and timelines, that match client specifications/requirements. The candidate should be able to communicate project plans and progress to the client, along with executing and reporting the work according to agreed timelines and under the appropriate regulations (GLP, CAP, CLIA etc.). A significant aspect of this role is the training and mentoring of junior scientists and team members in both laboratory techniques and in the analysis and presentation of data. This role will provide technical expertise to the laboratory and perform “hands on” experiments as needed for training and mentoring purposes.

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

Designs, implements, and troubleshoots molecular assays with the scientific team to meet client requirements

Oversees the scientists writing and implementing standard operating procedures (SOPs) to perform assays to meet client requirements and the level of regulatory compliance needed

Oversees the generation of technical reports and other communications required to present data to clients

Helps support the generation of posters and papers for submission to conference organizers and peer reviewed journals when applicable and approved by senior management

Reviews and edit client proposals, contract/proposals as needed

Trains and mentors scientific staff in the review and presentation of client data; supports client calls as the leading expert for the team

Trains and mentors technical staff on how to perform laboratory procedures. Devises and performs training and competency assessments to ensure staff can perform tasks independently

Maintains and supports safe lab practices and environment

Tracks and trends laboratory efficiency and quality

Performs duties with a high degree of independence, quality, and efficiency

Acts as internal expert on technical advances to anticipate and act as a thought leader to management on all matters related to their scope of work.

Initiates and/or recommends appropriate courses of action and identifies matters requiring policy interpretation or revision

Ensures scope of work and change orders are followed by technical team, and minimizes scope creep

Helps support the scheduling of work with the team, to ensure financial targets are being met by the lab staff

Qualifications:

Minimum Required:

Must have a Ph.D. in life sciences or relevant field (e.g. Molecular Biology)

At least 8 years related full-time laboratory experience

Other Required:

Strong bench scientist skills around molecular assays. Hands on sequencing, ddPCR, and qPCR experience is required.

Experience in validation/qualification of assays to CAP/CLIA/GLP or ISO guidelines

Strong organizational skills

Strong communication skills

Experienced technical report generation

The ability to see and differentiate between colors on the full color spectrum

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 :

10-15+ years’ experience as a molecular laboratorian in a leadership role with direct reports

Experience supervising or mentoring scientists or technical personnel

Industrial experience and/or management of outside collaborations is desirable

A solid understanding of current GxP or CAP/CLIA/ISO standards

Previous work experience in GLP or GCLP or CLIA regulatory compliance

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

$110,700 — $166,100 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.

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] .

Recruitment Fraud Warning: Please be aware that fraudulent individuals and websites may impersonate Precision Medicine Group or its affiliates and attempt to obtain personal, financial, or banking information through fake job postings or employment offers. Precision Medicine Group will never request payment, banking details, or other sensitive financial information as part of the recruitment process. If you believe you have been targeted by a recruitment scam, we encourage you to report the incident to your local law enforcement authorities, consumer protection agency, or relevant cybercrime reporting organization in your country. Please also notify us at [email protected] so we can investigate and take appropriate action.

Candidates must be legally authorized to work in the country of employment without employer sponsorship.

Original posting on Pfm's site ↗

Listed on hirly, a job board. hirly is not the employer: Pfm is hiring for this role.

Browse similar roles

Want this one?

Upload your resume and hirly rewrites it for this job and writes the cover letter — in about thirty seconds, before you sign up.

Tailor my resume for this job