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

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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 myHR@precisionmedicinegrp.com .

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