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Job Requirements of Scientist I:
-
Employment Type:
Contractor
-
Location:
Cambridge, MA (Onsite)
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Scientist I
Careers Integrated Resources Inc
Cambridge, MA (Onsite)
Contractor
Job Title: Scientist I
Job Location: Cambridge, MA- Onsite
Job Duration: 12 Months (possibility of extension)
Payrate: $58 - $62/ hr. on w2
Job Location: Cambridge, MA- Onsite
Job Duration: 12 Months (possibility of extension)
Payrate: $58 - $62/ hr. on w2
Main Responsibilities:
- Responsible for designing and performing in-vivo pharmacology experiments in support of project team goals.
- This includes study design, data collection and recording, communication of results, and report writing.
- Summarize and present study data to project teams within established timelines.
- Responsible for performing cigarette smoke induced COPD studies.
- Capacity to use established procedures and methodologies with the ability to transform Client approaches into routine practice.
- Must be a technical contributor.
- Ability to troubleshoot experiments.
- Support the development of disease relevant in-vivo models.
- Must be well organized and detail oriented.
- Must have meticulous record keeping skills according to Client quality guidelines.
- Maintain a thorough and compliant laboratory notebook.
- Must adhere to all federal, local, and Client animal welfare guidelines.
- Must be capable of working alone and in a team environment.
Education and Experience:
- Master’s Degree plus a minimum of 2 years of relevant research experience in a biopharmaceutical setting OR a Bachelor’s Degree plus a minimum of 3 to 5 years of relevant research experience in a biopharmaceutical setting.
- Experience with asthma, fibrosis, atopic dermatitis.
- Experience with in-vivo immunology models.
- Previous experience with models of respiratory disease, dermatitis models, and smoke-induced COPD models is a plus.
- Experience in various dosing methods, blood collection techniques, and tissue harvest are required.
- Experience with compound or reagent preparation.
Skills and Competencies:
- Ability to apply technical skills to complete assigned work as a competent technical contributor.
- Ability to design and perform in-vivo pharmacology experiments.
- Ability to work under moderate supervision with regular review of results and methods utilized.
- Ability to present study related results to project teams.
- Proven ability to work in a dynamic, customer-focused and results-oriented environment.
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