Senior Scientist, DMPK
@ Atavistik BioSenior Scientist, DMPK
This job is still taking applications, but it's been up a while.
About the job
Atavistik Bio is a clinical-stage biotech advancing allosteric therapeutics using proprietary AMPS™ platform. The role focuses on designing and interpreting non-clinical DMPK data to support drug development.
Requirements
- PhD, PharmD or related
- 5+ years in bio/pharma industry
- Experience in drug development
- Strong communication skills
- Knowledge of pharmacokinetics
Qualifications
- PhD or PharmD degree
- Experience with regulatory submissions
- Understanding of drug metabolism
- CRO management skills
- Team-oriented and organized
Full job description
Company Summary:
Atavistik Bio is a privately-held clinical stage biotechnology company accelerating the discovery and development of transformative precision allosteric therapeutics to address serious unmet patient needs. Our proprietary AMPS™ platform allows us to rapidly unlock functional cryptic pockets across a broad range of target classes to accelerate the development of groundbreaking medicines. We have rapidly established an emerging pipeline of allosteric therapeutics with the potential to achieve superior efficacy and tolerability profiles by leveraging the power of allostery.
Atavistik Bio is led by an experienced team of drug hunters with a proven track record of developing marketed small molecule therapies and supported by top-tier investors, including The Column Group, Nextech Invest, Lux Capital, Regeneron Ventures, and RA Capital Management.
Position Summary:
We are seeking a Senior Scientist, DMPK, to join our R&D group and work with an enthusiastic team of highly skilled scientists in a fast-pace environment. Reporting to the Senior Director, DMPK, this individual will be responsible for the design, execution, reviewing and interpreting the non-clinical DMPK data. This work supports the progression of therapies from discovery through first in human and proof of concept clinical studies. This is a great opportunity to contribute to an efficient DMPK function while being part of an exciting early-stage company.
Key Responsibilities:
Required Qualifications:
- PhD., Pharm. D. or equivalent training in pharmacokinetics, pharmaceutical sciences, or related disciplines.
- 5+ years of experience in bio/pharmaceutical industry, combined with drug development.
- Excellent communication and collaborative skills to work on multiple project teams including chemists, biologists and platform scientists.
- Highly organized, self-motivated with a desire to succeed in a fast-paced organization.
- Solid understanding of drug metabolism, bioanalysis, pharmacokinetics, preclinical pharmacology, and PK/PD modeling.
- Expertise in SAR analysis and IVIVC.
- Expertise managing CROs, GLP and other regulated activities.
- Ability to operate objectively and independently as a leader and as a member of a team.
- Experience with regulatory submissions for small molecules with a focus on preclinical is a plus.
- Experience in nonclinical toxicology is a plus.
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