Study Director, Associate Scientist

Reposted 2 Days Ago
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18447, Olyphant, PA, USA
In-Office
Mid level
Information Technology • Analytics • Biotech
The Role
Serve as single point of control for nonclinical studies: plan, coordinate, interpret, analyze, document and report results under GLP. Support protocol development, IACUC submissions, client interactions, QA audits, milestone tracking, and data archiving. Begin in training then assume Study Director duties with mentorship.
Summary Generated by Built In

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

Direct and participate in the planning, organization, conduct, and interpretation of animal research according to the regulations, protocols, standards and guidelines, such as USDA, FDA, GLP, GCP, etc. Be responsible for monitoring of studies and providing updates to both Sponsors and management. Ensure that the employees are performing the study according to protocols and Standard Operating Procedures (SOP's).

 

What You'll Do Here:

  • Serve as Study Director (SD) and take SD responsibilities. Participate in research projects including, but not limited to, protocol development, preparation and administration of test article, collecting and processing samples or tissues from animals, reporting, etc.
  • Plan an outline of research procedures to be followed during the course of the experiment. Writing protocols and reports as well as reviewing study schedules. Communicate with clients regarding up-dates, amendments, deviations, study results, etc. Provide his/her supervisor with timely updates on any study issues.
  • Assist in ensuring that personnel allocated to performing research activities for their studies have a clear understanding of the research protocol, activities to be performed, and are properly trained to conduct the procedures. Monitor the study to ensure all activities are conducted appropriately according to the study schedule, and data are appropriately recorded.
  • Utilize appropriate sources of information (the internet, archives, and government agencies, etc.) to collect, record, and analyze information useful for the research projects.
  • Prepare study reports, communicate with Sponsors, publications in scientific journals, submission to regulatory agencies, or for use in further applied or theoretical research activities.
  • All other duties as assigned.

 

What You'll Need to Succeed:

  • Ph.D. or M.S. in biology, toxicology, or related life sciences fields
  • A BS/BA in a relevant field (e.g. Animal Science, Biology, or related field) with a minimum of two years related experience: or equivalent combination of education and experience.
  • Strong written and verbal communication skills

 

What We Offer:

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

 

Altasciences' Incentive Programs Include:

  • Training & Development Programs
  • Employee Referral Bonus Program
  • Annual Performance Review

#LI-TA1

MOVING IN UNISON TO DELIVER A BIG IMPACT WITH A PERSONAL TOUCH

Altasciences is an equal opportunity employer committed to diversity and inclusion. Our goal is to attract, develop and retain highly talented employees from diverse backgrounds, allowing us to benefit from a wide variety of experiences and perspectives. All qualified applicants will receive consideration for employment without regard to age, race, color, religion, creed, sex, sexual orientation, gender identity, national origin, disability or any other protected grounds under applicable legislation. Reasonable accommodations for persons with disabilities during the recruitment process are available upon request. Join us at Altasciences!

Skills Required

  • BSc or equivalent degree in toxicology or related field
  • 2-4 years relevant industry experience with Bachelors (or up to 2 years with Masters/PhD)
  • Ability to read, analyze, interpret complex scientific and regulatory documents (English)
  • Knowledge or willingness to learn and apply GLP and applicable regulatory guidance
  • Excellent verbal and written communication skills
  • Well-developed interpersonal skills and ability to build trusting relationships
  • Ability to manage multiple conflicting priorities and work independently
  • Relevant industry experience
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The Company
HQ: Laval, Quebec
1,832 Employees
Year Founded: 1995

What We Do

Outsourcing made easy with a one-stop solution to early-phase drug development. We are an integrated drug development solution company, offering pharmaceutical and biotechnology companies a proven, flexible approach that removes the need for multiple service providers during the early stages of drug development. Whether for one study or an end-to-end program, we help you reach critical decision-making milestones sooner by improving speed and ease from lead candidate selection to clinical proof of concept, and beyond. When partnering with Altasciences, you can experience up to 40% in time savings thanks to our integrated, one-stop solution offering. We strive to create a true partnership with our clients, our partners, and our colleagues that enables a mutually supporting relationship built on a combination of excellent science and solid communication. Helping sponsors get better drugs to the people who need them, faster, for over 25 years. Our full-service offering is always tailored to your specific research needs: - Preclinical research - Clinical pharmacology - Drug formulation - Manufacturing and analytical services - Bioanalysis - Program management - Medical writing - Biostatics - Data management - And so much more!

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