Research Scientist I
$43.10 - $64.11/hr
... FDA guidelines. Preferred Qualifications: Postdoctoral training (5+ years) in bioanalysis pharmacology medicinal or pharmaceutical chemistry areas. Proven record of UHPLC or LC-MS/MS-based assay ...
$43.10 - $64.11/hr
... FDA guidelines. Preferred Qualifications: Postdoctoral training (5+ years) in bioanalysis pharmacology medicinal or pharmaceutical chemistry areas. Proven record of UHPLC or LC-MS/MS-based assay ...
$43.10 - $64.11/hr
... FDA guidelines. Preferred Qualifications: Postdoctoral training (5+ years) in bioanalysis pharmacology medicinal or pharmaceutical chemistry areas. Proven record of UHPLC or LC-MS/MS-based assay ...
... FDA Investigational New Drug (IND) and one (1) Abbreviated New Drug Application (ANDA) approvals for clinical PET practice and research, in addition to over fifty (50) preclinical radiotracers for ...
... FDA Investigational New Drug (IND) and one (1) Abbreviated New Drug Application (ANDA) approvals for clinical PET practice and research, in addition to over fifty (50) preclinical radiotracers for ...
The company's diverse portfolio includes FDA-approved treatments for tardive dyskinesia, chorea ... include postdoc experience * Experience with parenteral drug product development, including ...
The company's diverse portfolio includes FDA-approved treatments for tardive dyskinesia, chorea ... include postdoc experience * Experience with parenteral drug product development, including ...
The company's diverse portfolio includes FDA-approved treatments for tardive dyskinesia, chorea ... above; may include postdoc experience * Advanced and comprehensive understanding of cGMP ...
The company's diverse portfolio includes FDA-approved treatments for tardive dyskinesia, chorea ... above; may include postdoc experience * Advanced and comprehensive understanding of cGMP ...
The company's diverse portfolio includes FDA-approved treatments for tardive dyskinesia, chorea ... above; may include postdoc experience * Advanced and comprehensive understanding of cGMP ...
The company's diverse portfolio includes FDA-approved treatments for tardive dyskinesia, chorea ... above; may include postdoc experience * Advanced and comprehensive understanding of cGMP ...
The company's diverse portfolio includes FDA-approved treatments for tardive dyskinesia, chorea ... include postdoc experience * Experience with parenteral drug product development, including ...
The company's diverse portfolio includes FDA-approved treatments for tardive dyskinesia, chorea ... include postdoc experience * Experience with parenteral drug product development, including ...
... FDA guidelines. Preferred Qualifications: Postdoctoral training (5+ years) in bioanalysis pharmacology medicinal or pharmaceutical chemistry areas. Proven record of UHPLC or LC-MS/MS-based assay ...
... FDA guidelines. Preferred Qualifications: Postdoctoral training (5+ years) in bioanalysis pharmacology medicinal or pharmaceutical chemistry areas. Proven record of UHPLC or LC-MS/MS-based assay ...
... postdoctoral work in drug development and 5+ years of successful functional area management ... Strong knowledge of nonclinical drug development, FDA and ICH guidelines and GLP/GMP regulations
... postdoctoral work in drug development and 5+ years of successful functional area management ... Strong knowledge of nonclinical drug development, FDA and ICH guidelines and GLP/GMP regulations
South San Francisco, CA · On-site
$235K - $256K/yr
... postdoctoral work in drug development and 5+ years of successful functional area management ... Strong knowledge of nonclinical drug development, FDA and ICH guidelines and GLP/GMP regulations
Quick apply
South San Francisco, CA · On-site
$235K - $256K/yr
... postdoctoral work in drug development and 5+ years of successful functional area management ... Strong knowledge of nonclinical drug development, FDA and ICH guidelines and GLP/GMP regulations
San Diego, CA · On-site
$110K - $151K/yr
The company's diverse portfolio includes FDA-approved treatments for tardive dyskinesia, chorea associated with Huntington's disease, classic congenital adrenal hyperplasia, hyperphagia in patients ...
San Diego, CA · On-site
$110K - $151K/yr
The company's diverse portfolio includes FDA-approved treatments for tardive dyskinesia, chorea associated with Huntington's disease, classic congenital adrenal hyperplasia, hyperphagia in patients ...
South San Francisco, CA · On-site
$235K - $256K/yr
... postdoctoral work in drug development and 5+ years of successful functional area management ... Strong knowledge of nonclinical drug development, FDA and ICH guidelines and GLP/GMP regulations
South San Francisco, CA · On-site
$235K - $256K/yr
... postdoctoral work in drug development and 5+ years of successful functional area management ... Strong knowledge of nonclinical drug development, FDA and ICH guidelines and GLP/GMP regulations
Represent the company in regulatory agency interactions (FDA, EMA, etc.) as the DMPK subject matter ... discipline; postdoctoral training preferred. * Proven track record supporting programs from ...
Represent the company in regulatory agency interactions (FDA, EMA, etc.) as the DMPK subject matter ... discipline; postdoctoral training preferred. * Proven track record supporting programs from ...
New York, NY · On-site
$214K - $245K/yr
... postdoc and/or industry experience; OR an M.S. with 5+ years of relevant experience. * R&D ... Experience supporting FDA regulatory submissions for ML-based software, including familiarity with ...
New York, NY · On-site
$214K - $245K/yr
... postdoc and/or industry experience; OR an M.S. with 5+ years of relevant experience. * R&D ... Experience supporting FDA regulatory submissions for ML-based software, including familiarity with ...
New York, NY · On-site +1
$120K - $165K/yr
... FDA. Who will love this job: * A structure-based drug designer who has experience in two of the ... with postdoctoral experience or 1 to 5 years industry experience Pay and perks: Schrodinger ...
New York, NY · On-site +1
$120K - $165K/yr
... FDA. Who will love this job: * A structure-based drug designer who has experience in two of the ... with postdoctoral experience or 1 to 5 years industry experience Pay and perks: Schrodinger ...
New York, NY · On-site
$120K - $165K/yr
... FDA. Who will love this job: * A structure-based drug designer who has experience in two of the ... with postdoctoral experience or 1 to 5 years industry experience Pay and perks: Schrödinger ...
New York, NY · On-site
$120K - $165K/yr
... FDA. Who will love this job: * A structure-based drug designer who has experience in two of the ... with postdoctoral experience or 1 to 5 years industry experience Pay and perks: Schrödinger ...
Syracuse, NY · On-site
$16 - $25/hr
... support a federally funded FDA study examining nicotine vaping and addiction. This project ... Coordinators work closely with faculty, postdoctoral researchers, and trainees and may contribute ...
Syracuse, NY · On-site
$16 - $25/hr
... support a federally funded FDA study examining nicotine vaping and addiction. This project ... Coordinators work closely with faculty, postdoctoral researchers, and trainees and may contribute ...
$100K - $160K/yr
Secure competitive extramural funding (e.g., NIH, USDA, NSF, DoD, FDA, foundations, industry ... Experience supervising students or postdoctoral scholars. Demonstrated interdisciplinary and ...
$100K - $160K/yr
Secure competitive extramural funding (e.g., NIH, USDA, NSF, DoD, FDA, foundations, industry ... Experience supervising students or postdoctoral scholars. Demonstrated interdisciplinary and ...
San Diego, CA · On-site
$97K - $132K/yr
The company's diverse portfolio includes FDA-approved treatments for tardive dyskinesia, chorea ... PhD in Analytical Chemistry or related discipline and some relevant experience; may include postdoc ...
San Diego, CA · On-site
$97K - $132K/yr
The company's diverse portfolio includes FDA-approved treatments for tardive dyskinesia, chorea ... PhD in Analytical Chemistry or related discipline and some relevant experience; may include postdoc ...
Washington, DC · On-site
Postdoctoral training in influenza immunology strongly preferred. * 10-15 years as principal ... Working knowledge of regulatory frameworks (FDA CBER, EMA CHMP), including immunogenicity data ...
Quick apply
Washington, DC · On-site
Postdoctoral training in influenza immunology strongly preferred. * 10-15 years as principal ... Working knowledge of regulatory frameworks (FDA CBER, EMA CHMP), including immunogenicity data ...
The company's diverse portfolio includes FDA-approved treatments for tardive dyskinesia, chorea ... postdoc experience * Thorough understanding of analytical chemistry and a well-developed ...
The company's diverse portfolio includes FDA-approved treatments for tardive dyskinesia, chorea ... postdoc experience * Thorough understanding of analytical chemistry and a well-developed ...
$25K - $30.3K
2% of jobs
$30.3K - $35.6K
3% of jobs
$35.6K - $41K
3% of jobs
$41K - $46.3K
11% of jobs
$48.1K is the 25th percentile. Wages below this are outliers.
$46.3K - $51.6K
16% of jobs
$51.6K - $56.9K
13% of jobs
The median wage is $57.4K / yr.
$56.9K - $62.2K
17% of jobs
$65.1K is the 75th percentile. Wages above this are outliers.
$62.2K - $67.5K
17% of jobs
$67.5K - $72.9K
13% of jobs
$72.9K - $78.2K
3% of jobs
$78.2K - $83.5K
1% of jobs
$25K
$59K
$83.5K
$43.10 - $64.11/hr
Full-time
Posted yesterday
As a Research Scientist, you will leverage your deep scientific knowledge to support and facilitate the organization's research programs and projects. You are expected to apply various scientific principles to drive innovation.
Every day you will design and execute rigorous laboratory research, contributing to ongoing studies through meticulous analysis. You will also actively support manuscript preparation and participate in grant writing.
To be successful in this role, you will possess proven scientific expertise, a strong track record in experimental execution and analysis. Your ability to plan research, contribute to publications, and assist in securing funding will be paramount.
The Ivy Brain Tumor Center at Barrow Neurological Institute is a non-conventional non-profit program offering state-of-the-art clinical trials for patients with the most aggressive form of brain cancer. It is home to the largest collection of Phase 0 trials for brain tumors in the world. Our multidisciplinary team of brain tumor specialists and scientists are accelerating drug discovery and precision medicine in neuro-oncology to identify the most promising first-in-class therapies for brain tumor patients.
To facilitate the development of brain targeting therapeutics via neuro-pharmacokinetic characterization of various molecules through preclinical and clinical studies. Principal Duties and Responsibilities: We are looking for an individual to join the Pharmacokinetics (PK) Lab as a Research Scientist. The candidate should have a strong background in chemical/pharmaceutical sciences with a strong research experience in translational studies. Candidates should demonstrate significant experience in LC-MS/MS-based method development and validation in compliance with CAP/CLIA regulations and/or FDA guidelines and competency in pharmacokinetic data analysis. The candidate should be able to work well in highly collaborative environment and have excellent communication skills. Potential areas of application include bioanalysis method validation drug development drug pharmacokinetics biomarker analysis and PK modeling.
Key responsibilities include
Development validation and implementation of analytical methods for various drugs drug candidates metabolites and biomarkers employing UHPLC and LC-MS/MS techniques.
Planning and conducting preclinical pharmacokinetic studies including drug formulations administration through various routes tissue perfusion harvesting and analysis.
Performing biochemical and physicochemical characterization of various molecules.
Performing pharmacokinetic data analyses and interpretation.
Oversight and implementation of multiple research projects.
Facilitates research activities in partnership with laboratory PI leveraging scientific experience.
Manuscript preparation and publishing.
Development of research projects assistance with grant proposals and applications.
Supervision and training of laboratory personnel including post-doctoral fellows PhD and undergrad students.
Preparation and delivery of research presentations at local meetings national and international conferences.
General operation maintenance and troubleshooting of lab equipment including UHPLC and LC-MS/MS.
Preparation and maintenance of required laboratory safety documentation and adherence to the guidelines and regulations in compliance with CAP/CLIA regulations and FDA guidelines.
Preferred Qualifications:
Postdoctoral training (5+ years) in bioanalysis pharmacology medicinal or pharmaceutical chemistry areas.
Proven record of UHPLC or LC-MS/MS-based assay development and validation in compliance with CAP/CLIA regulations and/or FDA guidelines.
Experience in pharmacokinetic study design execution data analyses and interpretation.
Experience in biomedical research (cellular techniques and preclinical efficacy studies).
Experience with maintenance and troubleshooting of LC and MS systems.
Excellent organizational and analytical skills.
Ability to work independently and cohesively as part of a team.
Additional Requirements Recommendation letters Education Ph.D. or equivalent degree (MD DVM PharmD etc.) in Pharmaceutical Sciences Chemistry Biochemistry Medical Sciences or in related disciplines.
Job RequirementsRequired
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Why SJHMC?
This is an invitation to join a family of dedicated professionals at the forefront of medical innovation, united by the power of humankindness.