Associate Scientist, Biomarker/PK

CareAbout

Everett (WA)

On-site

USD 68,000 - 92,000

Full time

8 days ago

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Benefits offered by this job

Health/Dental/Vision Insurance Plans
401(k)/RRSP with Employer Match
Paid Vacation and Holidays
Paid Sick and Bereavement Leave
Telework when applicable

Job summary

Altasciences seeks an Associate Scientist to provide technical leadership in biomarker, pharmacokinetic, and ligand assay areas. You will plan and execute projects, acquiring facilities, equipment, and procedures for research efforts.

Under supervision, you will analyze study data for GLP and non-GLP preclinical studies, review molecular biology data, and write/peer-review protocols, SOPs, and data reports. You will assist with new assays and respond to client inquiries.

Qualifications

  • BS with 3 years or MS with 1 year or PhD in related field.
  • Experience with immunology, molecular biology, and/or cell biology/biochemistry/chemistry assays.
  • Ability to read and interpret safety rules, study documents, and write technical documents.
  • Strong technical writing and oral communication for diverse audiences.
  • Familiarity with GLP and analytical equipment such as chromatography, Luminex, RT-PCR.

Responsibilities

  • Oversee and maintain study conduct according to GLP regulations and SOPs.
  • Analyze study data and compile reports for GLP and non-GLP preclinical studies.
  • Collect and review molecular biology data per PI and SOPs.
  • Write and peer review protocols, SOPs, validation plans, and data reports.
  • Assist with development and implementation of new assays and projects.
  • Respond to client inquiries about scientific aspects of projects.

Skills

Scientific writing
Oral communication
Math skills
Independent work
GLP knowledge

Education

Bachelor's degree + 3 years experience
Master's degree + 1 year experience
PhD

Tools

Bioanalytical equipment

Job description

About The Role

As an Associate Scientist you will provide technical and scientific leadership in the area (e.g., biomarker, pharmacokinetic, ligand assay). Plan and execute projects, and identify and acquire the necessary facilities, equipment and procedures for research projects by performing the below duties.


What You’ll Do Here


  • Oversee and maintain study conduct according to GLP regulations and as described in the appropriate oversight documents (ex: SOPs, Study Protocol, and Analytical Study Plan).


  • Under supervision, critically analyze study or project data and compile into reports for internal and client sponsored GLP and non-GLP preclinical drug studies.


  • Collect and review molecular biology data according to the Contributing Scientist or Principal Investigator and the appropriate oversight documents (ex: Protocol, Analytical Study Plan, SOPs).


  • Write and peer review technical documents (ex: Protocols, SOP’s, validation plans, study forms, and data reports).


  • Assist with the development and implementation of new assays and projects to support internal and client sponsored studies.


  • Assist with responding to inquiries from clients and other relevant parties regarding scientific aspects of projects.



What You’ll Need to Succeed


  • BS with 3 years or MS with 1 year of experience or PhD, or an equivalent combination of education and experience in performing laboratory-based assays related to immunology, molecular biology, and/or cell biology/biochemistry/chemistry.


  • Ability to read and interpret documents such as safety rules, operating and maintenance instructions, software manuals, study documents, and procedure manuals. Advanced technical writing with the ability to write and present scientific articles and complex topics to people of different backgrounds and education levels. Ability to speak effectively before groups of customers or employees of the organization.


  • Intermediate to Advanced Math Skills.


  • Advanced technical writing and good oral communication skills; the ability to learn and understand complex theories and applications; the ability to read, analyze, and interpret complex documents; and the ability to work independently with minimal supervision.


  • Experience with GLP, knowledge of bioanalysis, and familiarity with analytical equipment e.g., chromatography, Luminex, RT-PCR equipment, preferred



Work Authorization & Sponsorship:

Applicants must be legally authorized to work in the United States. Altasciences is unable to provide sponsorship, sponsorship transfers, or visa maintenance for this position. All applicants must possess valid work authorization that does not require employer sponsorship now or in the future.


What We Offer

The pay range estimated for this position is $80,000 annually. Please note that hourly rates/salaries vary within the range based on factors including, but not limited to, prior relevant experience, skills, education, certification, location as well as internal equity and market data.


Benefits

Altasciences offers a wide variety of benefits to help our employees live healthy and fulfilling lives both at and outside of work.


Altasciences’ Benefits Package Includes:


  • Health/Dental/Vision Insurance Plans


  • 401(k)/RRSP with Employer Match


  • Paid Vacation and Holidays


  • Paid Sick and Bereavement Leave


  • Employee Assistance & Telehealth Programs


  • Telework when applicable.



Altasciences’ Incentive Programs Include:


  • Training & Development Programs


  • Employee Referral Bonus Program



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