8 дней назад
Scientist, Trial Support (Pharmacokinetics)
Мэтч & Сопровод
Для мэтча с этой вакансией нужен Plus
Описание вакансии
Текст:
TL;DR
Scientist, Trial Support (Pharmacokinetics): Supporting PK/PD research and clinical study data deliveries through sample management, bioanalytical reporting, and LIMS administration with an accent on clinical and nonclinical study operations, data integrity, and cross-functional coordination. Focus on defining studies in LIMS, managing clinical samples, reviewing technical documents, and tracking data-cleaning activities across multiple studies and service providers.
Location: Spring House, Pennsylvania, United States of America. Hybrid work is indicated, with remote work options considered on a case-by-case basis if approved by the company.
Company
Johnson & Johnson develops healthcare, Innovative Medicine, and MedTech solutions across the spectrum of disease prevention, treatment, and care.
What you will do
- Support pharmacokinetic/pharmacodynamic research projects and drug development programs.
- Coordinate clinical and nonclinical study deliveries, sample management, and bioanalytical data reporting.
- Partner with clinical operations, bioanalytical groups, compliance, central laboratories, clinical trial teams, and external providers.
- Review protocols, statements of work, lab manuals, and other study specifications.
- Define studies in LIMS, manage sample inventories, and support sample acquisition, storage, and disposition.
- Generate status reports, contribute to process and system optimization, and coach junior colleagues.
Requirements
- Bachelor’s degree with 3 years of relevant experience, master’s degree with 2 years, or PhD with 1 year of relevant experience.
- Experience in sample management and database systems such as Watson LIMS or LabVantage LIMS.
- Experience reviewing laboratory technical documents, including protocols, statements of work, and lab manuals.
- Experience in GLP/GCP environments.
- Strong communication, organization, attention to detail, and time-management skills.
Nice to have
- Experience with clinical data management, clinical pharmacology, pharmacometric modeling, study management, scientific research, and regulatory environments.
- Coaching experience and strong analytical or report-writing skills.
Culture & Benefits
- Work within multidisciplinary teams supporting medicines from discovery through post-market clinical development.
- Contribute to patient-focused healthcare innovation across Innovative Medicine and MedTech.
- Inclusive work environment focused on individual dignity, diversity, and equal opportunity.
- Remote work may be available on a case-by-case basis with company approval.
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