Position Summary:

This position will lead protein expression assays on tissues and liquid biopsies (circulating tumor cells, CTCs). Responsibilities include performing assay design and development, validation, and sample testing in a timely manner. Ensures assays are performed according to SOPs and supports development of new procedures and improvement of existing SOPs. Supervises assigned laboratory staff to ensure efficient organization, quality, development, and execution of project(s). Communicating results effectively to clients and develop lasting relationships to support future work.

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

Leads the development and implementation of protein expression services to support the translational research needs of Precision customers
Designs and performs experiments independently, and accurately analyzes and presents data
Conduct and support GCLP-compliant laboratory activities for sponsor clinical studies, ensuring adherence to study protocols, validated or qualified assay procedures, SOPs, data-integrity requirements, and established timelines while contributing to investigation of deviations and delivery of high-quality study data.
Maintains a high-quality output with the ability to build efficiency into improving productivity metrics
Coordinates with management to develop project timelines and deliver on these timelines
Trains and mentors’ junior staff in cell culture and antibody staining techniques, data analysis, collation, and presentation
Assists in establishing and improving all procedures and required SOP documentation
Responsible for trouble shooting and correcting scientific issues/problems
Responsible for ensuring that all experiments are performed on qualified equipment and that use and maintenance logs are up to date when performing experiments.
Maintains and supports safe lab practices and environment
Collaborate with other technical teams in resource sharing and providing technical expertise
Monitors project related expenses
Serves as a scientific resource to external clients and internal stakeholders
Assists with writing reports and presentations for clients as appropriate
Supervises assigned project related laboratory staff to ensure quality, development, and execution of project(s).
Other duties as assigned

Qualifications:

Minimum Required:

Ph.D. in cell biology, oncology, or related fields and 6+ years’ relevant laboratory experience OR
Master’s Degree and 10+ years’ in an academic core or industry is required

Other Required:

Experience in cell culture
Experience with manual staining and automated protocols (e.g. use of the Leica Bond autostainer) for multiplex Immunofluorescence (mIF) assays
Experience with Indica Halo or other digital pathology software
Ability to prioritize tasks and function in a team-oriented environment
Excellent communication, interpersonal, and organizational skills
Must have the ability to organize and analyze data, as well as prepare reports
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 GLP and/or ISO/CAP/CLIA standards
Experience supervising technical personnel

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

$100,600—$151,000 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 [email protected].

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

Reasonable estimate of the current range 100600 - 151000 USD

Precision for Medicine

Senior Scientist

About the Job

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About the Company

Precision for Medicine

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