Study Supervisor

at  Altasciences

Everett, Washington, USA -

Start DateExpiry DateSalaryPosted OnExperienceSkillsTelecommuteSponsor Visa
Immediate18 Jan, 2025USD 33 Hourly19 Oct, 2024N/AGood communication skillsNoNo
Add to Wishlist Apply All Jobs
Required Visa Status:
CitizenGC
US CitizenStudent Visa
H1BCPT
OPTH4 Spouse of H1B
GC Green Card
Employment Type:
Full TimePart Time
PermanentIndependent - 1099
Contract – W2C2H Independent
C2H W2Contract – Corp 2 Corp
Contract to Hire – Corp 2 Corp

Description:

Your New Company!
At Altasciences we all move in unison to assist and work in the discovery, development, and manufacturing of new drug therapies to get them faster to people who need them. No matter your role, we all play an important part and you will have a significant impact on the health and well-being of people across the globe. By living our values of Employee Development, Customer Focus, Quality and Excellence, Respect and Integrity, we look to foster a passionate and collaborative work environment and we are looking for talented and enthusiastic people, like you, to join our growing team! Whether you’re a recent college graduate or seeking your next career opportunity, it’s time to discover your future at Altasciences.
We are better together and together We Are Altasciences.
About the Role
Study Supervisors supervise study procedures and research assignments. They will coordinate duties of personnel and study teams and assists with sample and data collection for research studies.

What You’ll Do Here

  • Ensure assigned studies have appropriately trained staff, necessary supplies and forms, or electronic systems for data collection
  • Trains staff on technical procedures including injections, blood draws, collection of samples, catheterization, and more
  • Monitor study progress during the in-life phases, verifying adherence to study guidelines and timelines
  • Participates in study planning meetings
  • Create, review, and revise Standard Operating Procedures (SOP) relating to animals, technical procedures and facility issues
  • Monitor and report changes in animal behavior or health, and problems with animal room
  • Monitor and maintain animals and facilities in accordance to applicable laws and regulations
  • Monitor and report problems with data collection or equipment
  • Set up study equipment
  • Record raw study data into templates for use by study directors
  • Operate and maintain selected laboratory equipment; ensure equipment is GLP compliant
  • Maintain organization and cleanliness of work area including cleaning and disinfecting procedure rooms and preparation areas
  • Provide technical knowledge to training team in developing training manuals and guidelines
  • Ensure animals are housed in accordance with federal and established guidelines
  • Ensure study conduct as described in protocol (e.g., dosing, treatments, surgery schedule, necropsy schedule)
  • Document study procedures and results in study notebooks complying with GLP regulations
  • Perform QC review study and facility data in a timely manner
  • Complete daily research data
  • Assign and oversee personnel duties necessary to complete daily schedules
  • Schedule and assign appropriate animal species for studies according to the study scientist or study director
  • Schedule animal and procedure rooms, and surgery suites
  • Report information regarding clinical problems with the animals, data collection or equipment to project scientist
  • Assist staff supervisors in developing and completing training plans for team members
  • Meets regularly with functional team members and communicate study needs and goals

What We Offer
The pay range estimated for this position is $25.21 - $33.61 (per hour rates or 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.
Altasciences offers a wide variety of benefits to help our employees live healthy and fulfilling lives both at and outside of work.

What You’ll Need to Succeed

  • BA/BS specializing in science and/or equivalent experience
  • 3+ years working in a research environment
  • LATG certification preferred
  • Intermediate computer skills including proficiency with Microsoft Office suite; adapts easily to new software
  • English proficiency both written and verbal; general reading, writing and verbal communication skills
  • Intermediate maths skills as related to analyzing scientific data
  • Work cross functionally on process improvements

Responsibilities:

  • Ensure assigned studies have appropriately trained staff, necessary supplies and forms, or electronic systems for data collection
  • Trains staff on technical procedures including injections, blood draws, collection of samples, catheterization, and more
  • Monitor study progress during the in-life phases, verifying adherence to study guidelines and timelines
  • Participates in study planning meetings
  • Create, review, and revise Standard Operating Procedures (SOP) relating to animals, technical procedures and facility issues
  • Monitor and report changes in animal behavior or health, and problems with animal room
  • Monitor and maintain animals and facilities in accordance to applicable laws and regulations
  • Monitor and report problems with data collection or equipment
  • Set up study equipment
  • Record raw study data into templates for use by study directors
  • Operate and maintain selected laboratory equipment; ensure equipment is GLP compliant
  • Maintain organization and cleanliness of work area including cleaning and disinfecting procedure rooms and preparation areas
  • Provide technical knowledge to training team in developing training manuals and guidelines
  • Ensure animals are housed in accordance with federal and established guidelines
  • Ensure study conduct as described in protocol (e.g., dosing, treatments, surgery schedule, necropsy schedule)
  • Document study procedures and results in study notebooks complying with GLP regulations
  • Perform QC review study and facility data in a timely manner
  • Complete daily research data
  • Assign and oversee personnel duties necessary to complete daily schedules
  • Schedule and assign appropriate animal species for studies according to the study scientist or study director
  • Schedule animal and procedure rooms, and surgery suites
  • Report information regarding clinical problems with the animals, data collection or equipment to project scientist
  • Assist staff supervisors in developing and completing training plans for team members
  • Meets regularly with functional team members and communicate study needs and goal


REQUIREMENT SUMMARY

Min:N/AMax:5.0 year(s)

Pharmaceuticals

Pharma / Biotech / Healthcare / Medical / R&D

Clinical Pharmacy

Graduate

Proficient

1

Everett, WA, USA