USA-Scientist II (Scientific)#25-65728
Cambridge, MA
All On-site
Job Description
About the Job:
*** is a leading company in Global Healthcare that discovers, develops, produces, and markets innovative therapies to help protect health and enhance people's lives. We are seeking a highly motivated in-vivo pharmacologist to join the Type 2 Immunology Cluster within the Immunology and Inflammation Therapeutic Area located in Cambridge, MA. The ideal candidate will possess a strong background in in-vivo pharmacology, contributing technical skills and functional knowledge. The candidate will also be involved in the design, overall conduct, and the reporting of in-vivo pharmacology study results to project teams. The position is a hands-on, laboratory-based role that requires strong communication skills, attention to detail, a results-driven way of working, and ability to work both individually and in a team environment, and to work across functions. A successful candidate is expected to analyze, record and report data, be able to develop and learn new techniques, and be able to multi-task between multiple projects.
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.
Generate specific pharmacology reports based on studies performed to support IND submission.
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 *** quality guidelines. Maintain a thorough and compliant laboratory notebook.
Must adhere to all federal, local, and *** animal welfare guidelines.
Must be capable of working alone and in a team environment.
Qualifications:
Experience with in-vivo immunology models. Previous experience with models of respiratory disease, dermatitis models, and smoke induced COPD models is a plus.
Ability to apply technical skills to complete assigned work as a competent technical contributor.
Ability to design and perform in-vivo pharmacology experiments.
Experience in various dosing methods, blood collection techniques, and tissue harvest are required.
Experience with compound or reagent preparation.
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.
Education and Experience:
Master's Degree plus a minimum of 0 to 3 years of relevant research experience in a biopharmaceutical setting OR a Bachelor's Degree plus a minimum of 2 to 5 years of relevant research experience in a biopharmaceutical setting.
EEO:
Mindlance is an Equal Opportunity Employer and does not discriminate in employment on the basis of - Minority/Gender/Disability/Religion/LGBTQI/Age/Veterans.
Cambridge, MA
All On-site
Job Description
About the Job:
*** is a leading company in Global Healthcare that discovers, develops, produces, and markets innovative therapies to help protect health and enhance people's lives. We are seeking a highly motivated in-vivo pharmacologist to join the Type 2 Immunology Cluster within the Immunology and Inflammation Therapeutic Area located in Cambridge, MA. The ideal candidate will possess a strong background in in-vivo pharmacology, contributing technical skills and functional knowledge. The candidate will also be involved in the design, overall conduct, and the reporting of in-vivo pharmacology study results to project teams. The position is a hands-on, laboratory-based role that requires strong communication skills, attention to detail, a results-driven way of working, and ability to work both individually and in a team environment, and to work across functions. A successful candidate is expected to analyze, record and report data, be able to develop and learn new techniques, and be able to multi-task between multiple projects.
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.
Generate specific pharmacology reports based on studies performed to support IND submission.
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 *** quality guidelines. Maintain a thorough and compliant laboratory notebook.
Must adhere to all federal, local, and *** animal welfare guidelines.
Must be capable of working alone and in a team environment.
Qualifications:
Experience with in-vivo immunology models. Previous experience with models of respiratory disease, dermatitis models, and smoke induced COPD models is a plus.
Ability to apply technical skills to complete assigned work as a competent technical contributor.
Ability to design and perform in-vivo pharmacology experiments.
Experience in various dosing methods, blood collection techniques, and tissue harvest are required.
Experience with compound or reagent preparation.
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.
Education and Experience:
Master's Degree plus a minimum of 0 to 3 years of relevant research experience in a biopharmaceutical setting OR a Bachelor's Degree plus a minimum of 2 to 5 years of relevant research experience in a biopharmaceutical setting.
EEO:
Mindlance is an Equal Opportunity Employer and does not discriminate in employment on the basis of - Minority/Gender/Disability/Religion/LGBTQI/Age/Veterans.
Job ID: 486848897
Originally Posted on: 7/25/2025
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