
Principal Pharmacometrician, FSP
- Durham, NC
- Permanent
- Full-time
- Home-based, remote work opportunities.
- Work/life balance.
- Collaborate on projects and innovations with industry leaders in the Pharma and CRO sectors.
- Cohesive team environment fostering a collaborative approach to study work.
- Variety of therapeutic areas, indications, and study phases.
- Job stability; long-term engagements and development opportunities.
- Career advancement opportunities.
- Contribute to development of protocols, statistical analysis plans, PK/PD analysis, PK/PD tables, listings and figures, and clinical study reports for Phase I-IV clinical pharmacology studies, such as dose tolerance, dose proportionality, mass balance, concept testing, bioavailability, thorough QTc, drug-drug interactions, and special population (age effects, renal disease, hepatic disease, gender effects, etc.), as well as population PK/PD studies.
- Consult with Clinical Pharmacology staff on study design, clinical development plans.
- Review analyses and documents prepared by CROs to help ensure accuracy and appropriateness.
- Prepare or review PK/PD sections of dossiers for product registration and communicate with regulatory agencies.
- Ensure quality and timely delivery of project PK/PD deliverables.
- Collaborate in cross functional teams that include Project Manager, CRA, Data Manager, Biostatistician, Programmer, and/or Medical Writer.
- Maintain awareness of overall developments in the field of Clinical Pharmacology and PK/PD based on current literature, application of new technology, attendance at professional meetings, etc.
- PharmD, Ph.D. in Pharmacology, Pharmacy, Pharmacokinetics, Pharmaceutics, Biology, or similar required
- Minimum of 3 years’ experience in Pharmacokinetics or Pharmacology for Clinical Research Organization or pharmaceutical environment
- Expert knowledge of pharmacometric concepts, including noncompartmental analysis and population PK modeling, current therapeutic environment, and drug development trends
- Strong understanding of the principles of the drug development process, ICH GCP, and applicable international and national regulatory requirements
- Good problem solving and analytical skills.
- Excellent computer skills, including proficiency with Microsoft Office, WinNonlin, and graphing, as well as NONMEM, R, and basic SAS programming.
- Excellent verbal and written communication skills and highly effective interpersonal, and organizational skills
- Ability to prioritize, and independently coordinate and manage PK/PD component of complex projects.
- Ability to interact in a cross-functional and multi-cultural team environment.
- Ability to establish and maintain effective working relationships with coworkers, managers and clients.