Remote Director, Clinical Pharmacology

Allucent; Palmdale (CA); Hybride; USD 180 000 - 260 000; Plein temps

Avantages offerts par ce poste

Comprehensive benefits per location

Flexible working hours

Remote/hybrid working depending on loc

Leadership and mentoring opportunities

Buddy program

Résumé du poste

Allucent is seeking a Director, Clinical Pharmacology to independently lead Clinical Pharmacology activities within the Clinical Pharmacology, Modeling, and Simulation unit. The role involves strategic advisory duties for clients, designing and interpreting complex PK/PD studies, and reviewing regulatory documents such as INDs and NDAs.

Ideal candidates hold a PharmD or PhD with 8+ years of experience, and excel in cross-functional collaboration, with strong English communication.

Qualifications

• PharmD or Ph.D. in a relevant area.
• 8+ years of relevant work experience.
• Strong written and verbal communication skills in English.

Responsabilités

• Lead strategic clinical pharmacology advice to clients within a cross-functional team.
• Independently design, analyze, and interpret clinical pharmacology studies (PK/PD, DDI, BE/BA, SAD/MAD, etc.).
• Oversee development of PK/PD analysis plans, reports, and sections of study reports, INDs, and NDAs.

Connaissances

Leadership

Strategic advisory

Cross-functional collaboration

Communication

Formation

PharmD or PhD

Description du poste

At Allucent™, we are dedicated to helping small-medium biopharmaceutical companies efficiently navigate the complex world of clinical trials to bring life-changing therapies to patients in need across the globe.

We are looking for a Director, Clinical Pharmacology to join our A-team (office-based*/remote). As a Director, Clinical Pharmacology at Allucent, you are responsible for independently leading Clinical Pharmacology activities within the Clinical Pharmacology, Modeling, and Simulation unit of Allucent.

About The Role

As an expert in clinical pharmacology, you will:

• Take independent leadership in providing strategic clinical pharmacology advice to clients within a cross-functional team, covering overall drug development activities.
• Autonomously lead the design, analysis, and interpretation of clinical pharmacology studies (including renal, hepatic, TQT, ADME, DDI, BE/BA, SAD, MAD, etc.) and offer recommendations to enhance pharmacokinetic sampling and dosing strategies.
• Thoroughly assess the technical and scientific components of PK and PK/PD projects and programs for clients, with knowledge of noncompartmental analysis as well as population PK, PBPK, and QSP modeling.
• Oversee the development of statistical and PK analysis plans, standalone PK/PD reports, and PK/PD sections of clinical study reports, and take the lead in reviewing clinical protocols, clinical study reports, clinical pharmacology strategic plans, INDs, clinical pharmacology and safety sections of NDAs, Investigator Brochures, FDA briefing packages, and other clinical and regulatory documents.

To Be Successful You Will Possess

• PharmD or Ph.D. in a relevant area
• 8+ years of relevant work experience
• Strong written and verbal communication skills including good command of English language
• Client focused
• Ability to work in a fast-paced environment

Benefits Of Working At Allucent Include

• Comprehensive benefits package per location
• Competitive salaries per location
• Departmental Study/Training Budget for furthering professional development
• Flexible Working hours (within reason)
• Opportunity for remote/hybrid* working depending on location
• Leadership and mentoring opportunities
• Participation in our Buddy Program as a new or existing employee
• Internal growth opportunities and career progression
• Financially rewarding internal employee referral program

Disclaimers

• Our office-based work policy encourages a dynamic work environment, prescribing a minimum of 2 days in office per week for employees within reasonable distance from one of our global offices.