Principal Bioanalytical Scientist at Jobot
Frederick, MD 21701
About the Job
NEW Principal Bioanalytical Scientist Opportunity!
This Jobot Job is hosted by: Audrey Block
Are you a fit? Easy Apply now by clicking the "Quick Apply" button
and sending us your resume.
Salary: $140,000 - $170,000 per year
A bit about us:
We are a well established, global CRO that works in oncology and rare diseases! We are hiring a principal bioanalytical scientist. Please contact me for more details!
Why join us?
Opportunity for growth into leadership
Competitive compensation package with bonus, 401k and more!
Work with an experienced team and grow in multiple areas of your career
Be a part of life changing science!
Job Details
Job Details:
We are seeking a highly skilled Principal Bioanalytical Scientist to join our team in the pharmaceutical industry. The ideal candidate will have a robust background in method development for large molecules, particularly in the areas of AD and PK. This role requires strong mentorship and leadership skills, excellent communication abilities, and a talent for troubleshooting complex analytical methods.
Key Responsibilities:
Method Development: Lead the design and optimization of bioanalytical methods for large molecules, ensuring compliance with regulatory standards and best practices.
Validation and Implementation: Oversee the validation of bioanalytical methods, ensuring they meet the required specifications and are implemented effectively in study protocols.
Data Analysis: Analyze bioanalytical data to support pharmacokinetic and toxicological assessments, providing critical insights for drug development.
Team Leadership: Mentor and guide junior scientists in their professional development, fostering a collaborative and innovative research environment.
Cross-Functional Collaboration: Work closely with pharmacologists, toxicologists, and other stakeholders to integrate bioanalytical findings into broader project goals.
Troubleshooting: Identify and resolve issues with bioanalytical methods, employing problem-solving skills to optimize assay performance and reliability.
Regulatory Compliance: Prepare and review documentation for regulatory submissions, ensuring adherence to GLP and other applicable guidelines.
Communication: Effectively communicate findings and strategies to both technical and non-technical audiences, including senior management and external partners.
Qualifications:
Ph.D. in Biochemistry, Pharmacology, Analytical Chemistry, or a related field, with 7+ years of experience in bioanalytical method development for large molecules.
Strong expertise in large molecule AD and PK methodologies, with a proven track record of successful project execution.
Demonstrated leadership experience, with the ability to mentor and inspire a team of scientists.
Excellent problem-solving skills, with a hands-on approach to troubleshooting complex analytical challenges.
Strong written and verbal communication skills, with the ability to present complex data clearly and concisely.
Familiarity with regulatory requirements and quality standards in the pharmaceutical industry.
Join our team and contribute to groundbreaking research in the pharmaceutical industry. We look forward to receiving your application!
Interested in hearing more? Easy Apply now by clicking the "Quick Apply" button.
This Jobot Job is hosted by: Audrey Block
Are you a fit? Easy Apply now by clicking the "Quick Apply" button
and sending us your resume.
Salary: $140,000 - $170,000 per year
A bit about us:
We are a well established, global CRO that works in oncology and rare diseases! We are hiring a principal bioanalytical scientist. Please contact me for more details!
Why join us?
Opportunity for growth into leadership
Competitive compensation package with bonus, 401k and more!
Work with an experienced team and grow in multiple areas of your career
Be a part of life changing science!
Job Details
Job Details:
We are seeking a highly skilled Principal Bioanalytical Scientist to join our team in the pharmaceutical industry. The ideal candidate will have a robust background in method development for large molecules, particularly in the areas of AD and PK. This role requires strong mentorship and leadership skills, excellent communication abilities, and a talent for troubleshooting complex analytical methods.
Key Responsibilities:
Method Development: Lead the design and optimization of bioanalytical methods for large molecules, ensuring compliance with regulatory standards and best practices.
Validation and Implementation: Oversee the validation of bioanalytical methods, ensuring they meet the required specifications and are implemented effectively in study protocols.
Data Analysis: Analyze bioanalytical data to support pharmacokinetic and toxicological assessments, providing critical insights for drug development.
Team Leadership: Mentor and guide junior scientists in their professional development, fostering a collaborative and innovative research environment.
Cross-Functional Collaboration: Work closely with pharmacologists, toxicologists, and other stakeholders to integrate bioanalytical findings into broader project goals.
Troubleshooting: Identify and resolve issues with bioanalytical methods, employing problem-solving skills to optimize assay performance and reliability.
Regulatory Compliance: Prepare and review documentation for regulatory submissions, ensuring adherence to GLP and other applicable guidelines.
Communication: Effectively communicate findings and strategies to both technical and non-technical audiences, including senior management and external partners.
Qualifications:
Ph.D. in Biochemistry, Pharmacology, Analytical Chemistry, or a related field, with 7+ years of experience in bioanalytical method development for large molecules.
Strong expertise in large molecule AD and PK methodologies, with a proven track record of successful project execution.
Demonstrated leadership experience, with the ability to mentor and inspire a team of scientists.
Excellent problem-solving skills, with a hands-on approach to troubleshooting complex analytical challenges.
Strong written and verbal communication skills, with the ability to present complex data clearly and concisely.
Familiarity with regulatory requirements and quality standards in the pharmaceutical industry.
Join our team and contribute to groundbreaking research in the pharmaceutical industry. We look forward to receiving your application!
Interested in hearing more? Easy Apply now by clicking the "Quick Apply" button.
Salary
140,000 - 170,000 /year
