VP Clinical Pharmacology at Jobot
Waltham, MA 02451
About the Job
VP Clinical Pharmacology/DMPK
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: $350,000 - $400,000 per year
A bit about us:
We create new small molecule drugs to combat cancer and autoimmune diseases. Our primary areas of interest involve the selection of well-validated targets that have clear clinical development pathways, as well as the discovery of modulators with unique mechanisms of action. To achieve sustainable success, we are constantly building innovative data and screening platforms.
Why join us?
We're thrilled to offer a range of exciting benefits to prospective team members, including:
Tremendous potential for personal and professional growth, with opportunities to take on new challenges and expand your skill set
A dynamic and engaging work environment that is deeply collaborative and hands-on, allowing you to truly make a difference in the field of biotechnology
Competitive compensation, comprehensive benefits, and the possibility of bonuses, all designed to recognize your valuable contributions to our organization
Robust funding that provides a stable foundation for our ambitious projects and exciting research initiatives
A strong and supportive company culture, with frequent team events and a tight-knit community of colleagues who are passionate about what they do.
Job Details
Job Details:
We are seeking a dynamic and dedicated individual to join our team as the Vice President Clinical Pharmacology/DMPK. This is a unique opportunity to play a pivotal role in the development of innovative therapies that can change the lives of patients worldwide. The successful candidate will be involved in the strategic planning and execution of clinical pharmacology, DMPK (Drug Metabolism and Pharmacokinetics) and oncology programs. This role requires a deep understanding of drug development, a strategic mindset, and the ability to work collaboratively with cross-functional teams.
Responsibilities:
1. Provide strategic leadership and direction for the Clinical Pharmacology/DMPK function, ensuring alignment with overall company objectives.
2. Lead the design, execution, and interpretation of clinical pharmacology programs and DMPK studies.
3. Work closely with clinical development teams to integrate DMPK and clinical pharmacology principles into clinical development plans.
4. Oversee the preparation and review of clinical pharmacology sections of regulatory submissions.
5. Collaborate with cross-functional teams to ensure the successful execution of clinical trials.
6. Provide expert guidance on drug-drug interactions, pharmacokinetics, and pharmacodynamics.
7. Develop and maintain relationships with external partners, including regulatory agencies, academic institutions, and contract research organizations.
8. Stay abreast of the latest developments in clinical pharmacology, DMPK, and oncology, and incorporate this knowledge into strategic planning.
9. Foster a culture of scientific excellence, innovation, and teamwork within the Clinical Pharmacology/DMPK team.
Qualifications:
1. PhD in Pharmacology, Pharmaceutical Sciences, or a related field.
2. A minimum of 10 years of experience in clinical pharmacology and DMPK, within the pharmaceutical or biotech industry.
3. Proven experience in oncology drug development is essential.
4. Strong understanding of drug metabolism, pharmacokinetics, and clinical pharmacology principles.
5. Demonstrated experience in the design, execution, and interpretation of clinical pharmacology studies.
6. Excellent leadership skills, with a proven track record of leading cross-functional teams.
7. Strong strategic thinking and problem-solving abilities.
8. Excellent written and verbal communication skills, with the ability to effectively communicate complex scientific concepts to a variety of audiences.
9. Proven experience in preparing and reviewing clinical pharmacology sections of regulatory submissions.
10. Ability to work effectively in a fast-paced, dynamic environment.
11. Commitment to scientific excellence and the highest ethical standards.
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: $350,000 - $400,000 per year
A bit about us:
We create new small molecule drugs to combat cancer and autoimmune diseases. Our primary areas of interest involve the selection of well-validated targets that have clear clinical development pathways, as well as the discovery of modulators with unique mechanisms of action. To achieve sustainable success, we are constantly building innovative data and screening platforms.
Why join us?
We're thrilled to offer a range of exciting benefits to prospective team members, including:
Tremendous potential for personal and professional growth, with opportunities to take on new challenges and expand your skill set
A dynamic and engaging work environment that is deeply collaborative and hands-on, allowing you to truly make a difference in the field of biotechnology
Competitive compensation, comprehensive benefits, and the possibility of bonuses, all designed to recognize your valuable contributions to our organization
Robust funding that provides a stable foundation for our ambitious projects and exciting research initiatives
A strong and supportive company culture, with frequent team events and a tight-knit community of colleagues who are passionate about what they do.
Job Details
Job Details:
We are seeking a dynamic and dedicated individual to join our team as the Vice President Clinical Pharmacology/DMPK. This is a unique opportunity to play a pivotal role in the development of innovative therapies that can change the lives of patients worldwide. The successful candidate will be involved in the strategic planning and execution of clinical pharmacology, DMPK (Drug Metabolism and Pharmacokinetics) and oncology programs. This role requires a deep understanding of drug development, a strategic mindset, and the ability to work collaboratively with cross-functional teams.
Responsibilities:
1. Provide strategic leadership and direction for the Clinical Pharmacology/DMPK function, ensuring alignment with overall company objectives.
2. Lead the design, execution, and interpretation of clinical pharmacology programs and DMPK studies.
3. Work closely with clinical development teams to integrate DMPK and clinical pharmacology principles into clinical development plans.
4. Oversee the preparation and review of clinical pharmacology sections of regulatory submissions.
5. Collaborate with cross-functional teams to ensure the successful execution of clinical trials.
6. Provide expert guidance on drug-drug interactions, pharmacokinetics, and pharmacodynamics.
7. Develop and maintain relationships with external partners, including regulatory agencies, academic institutions, and contract research organizations.
8. Stay abreast of the latest developments in clinical pharmacology, DMPK, and oncology, and incorporate this knowledge into strategic planning.
9. Foster a culture of scientific excellence, innovation, and teamwork within the Clinical Pharmacology/DMPK team.
Qualifications:
1. PhD in Pharmacology, Pharmaceutical Sciences, or a related field.
2. A minimum of 10 years of experience in clinical pharmacology and DMPK, within the pharmaceutical or biotech industry.
3. Proven experience in oncology drug development is essential.
4. Strong understanding of drug metabolism, pharmacokinetics, and clinical pharmacology principles.
5. Demonstrated experience in the design, execution, and interpretation of clinical pharmacology studies.
6. Excellent leadership skills, with a proven track record of leading cross-functional teams.
7. Strong strategic thinking and problem-solving abilities.
8. Excellent written and verbal communication skills, with the ability to effectively communicate complex scientific concepts to a variety of audiences.
9. Proven experience in preparing and reviewing clinical pharmacology sections of regulatory submissions.
10. Ability to work effectively in a fast-paced, dynamic environment.
11. Commitment to scientific excellence and the highest ethical standards.
Interested in hearing more? Easy Apply now by clicking the "Quick Apply" button.
Salary
350,000 - 400,000 /year