Principal Scientist, Dmpk

PTC Therapeutics is a global commercial biopharmaceutical company. For over 25 years our team has been deeply committed to a unified purpose: Extending life's moments for children and adults living with a rare disease.

At PTC, we cultivate an inclusive culture where everyone feels valued, respected, and empowered. We welcome candidates from all backgrounds to join our team, fostering a strong sense of belonging.

Visit our website to learn more about our company and culture!

Site: www.ptcbio.com

Job Description Summary:

The Principle Scientist, DMPK is responsible for planning and performing in vitro and in vivo ADME studies that contribute to PTC's research and development activities. The incumbent is also responsible for communicating experimental results to his/her supervisor and the project team.

The incumbent works cross-functionally with internal departments, and external resources as appropriate, as part of PTC's discovery science project teams.

The Principle Scientist, DMPK supports adherence to relevant regulatory requirements and company Standard Operating Procedures (SOPs) as appropriate.

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Job Description:

ESSENTIAL FUNCTIONS

Primary duties/responsibilities:

• Under limited direction plans, initiates and executes DMPK studies and interprets and communicates results as part of a multi-disciplinary team.

• Works with research and development teams in planning, scheduling and conducting DMPK studies per the development candidate nomination and IND/NDA timeline requirement.

• Serves as DMPK representative on project teams and interprets and presents data/results to cross-functional teams comprised of internal and external members.

• Performs hands-on in vitro and in vivo DMPK studies. These include, but may not be limited to, metabolic stability and metabolite profiling/identification, CYP inhibition and induction studies, pharmacokinetic studies and radiolabeled studies in lab animals and in humans.

• Documents experiment details in laboratory notebook and writes reports. Prepares relevant DMPK documents for development candidate nomination and IND/NDA purposes.

• Ensures the scientific quality of the experimental data.

• Provides direct oversight and/or leads interactions with the external Contract Research Organizations (CROs).

• Abides by all safety and regulatory guidelines.

• Contributes to general lab needs such as:

• Equipment maintenance

• Troubleshoot

• Performs other tasks and assignments as needed and specified by management.

• Minimum level of education and years of relevant work experience.

• PhD in Chemistry, Biology, Pharmaceutical science, Pharmacology or related scientific discipline and a minimum of 5 years of experience in drug metabolism OR a Master's degree in these same disciplines and a minimum of 6+ years of experience in drug metabolism.

KNOWLEDGE/SKILLS/ABILITIES REQUIRED

• Hands-on experience in conducting in vitro and in vivo DMPK studies.

• Demonstrated experience in drug metabolism and biotransformation, pharmacokinetics, pharmacodynamic and bioanalytical principles.

• Hands-on experience in using contemporary LC-MS/MS instruments.

• Demonstrated experience in developing protocols and writing study reports and other relevant documents for development candidate nomination and IND/NDA purposes.

• Ability to work on complex problems to produce experimental data across one or more projects.

• Ability to work effectively in a multi-disciplinary team environment.

• Proficiency with Microsoft Office.

• Excellent verbal and written communication skills.

• Ability to work independently and collaboratively in a fast-paced, matrixed, team environment consisting of internal and external team members.

• Analytical thinker with excellent problem-solving skills and the ability to adapt to changing priorities and deadlines.

• Excellent planning, organization and time management skills including the ability to support and prioritize multiple projects.

• Special knowledge or skills and/or licenses or certificates preferred.

• PhD

• Knowledge and experience in conducting radiolabeled studies.

• Hands on experience in operating and general troubleshooting of contemporary LC-MS instruments and automated liquid handlers.

• Prior experience with INDs and/or NDAs.

• Hands on experience with cell-based (hepatocytes and transporters, etc.) assays.

• Proficient in using WinNonlin or other pharmacokinetic software.

• Travel requirements

• 0-10%

• Laboratory based position.

Expected Base Salary Range

$153,500 - $185,000. The base salary offered will be contingent on assessment of candidate education level, background, and experience relative to the requirements of the position they are being considered for, as well as review of internal equity.

In addition to base salary, PTC employees are also eligible for short- and long-term incentives. All eligible employees may also enroll in PTC's medical, dental, vision, and retirement savings plans.

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EEO Statement:

PTC Therapeutics is an equal opportunity employer. We welcome applications from all individuals, regardless of race, color, national origin, gender, age, physical characteristics, social origin, disability, religion, family status, pregnancy, sexual orientation, gender identity, gender expression, disability, veteran status or any unlawful criterion under applicable law. We are committed to treating all applicants fairly and avoiding discrimination.

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