- Teleflex (Morrisville, NC)
- …electronic data capture and management, and study analysis through publication of scientific publications and regulatory study reports. Experience and comfort ... Business Acumen to lead and develop their Clinical Medical Affairs team to consistently deliver high value results and...functional budget. * Ensure the team works with the Regulatory lead and Medical Director to create… more
- Astrix Technology (Boston, MA)
- …+ Collaborate with cross-functional teams, including preclinical, clinical operations, and regulatory affairs , to integrate and execute clinical strategy. + ... **Senior Medical Director ** Clinical Boston, MA, MA, US Pay Rate...Ensure clinical initiatives are aligned with organizational goals and scientific advancements. + Design and direct early-phase clinical trials,… more
- Stanford University (Stanford, CA)
- …, student affairs , external relations, and human resources. Additionally, the Director of Finance and Administration works with the Chair and other faculty and ... Director of Finance and Administration, Department of Obstetrics...particular, we are focused on innovative translational medicine; bringing scientific results from the bench to the bedside. Our… more
- J&J Family of Companies (Spring House, PA)
- …the TA (TA R&D, Clinical Development, DPDS) and partnering functions ( Regulatory , Global Development, Medical Affairs , Commercial). * Share responsibility, ... Sub** **Function:** Translational Discovery & Development Biomarkers **Job Category:** Scientific /Technology **All Job Posting Locations:** Spring House, Pennsylvania, United… more
- Bristol Myers Squibb (Princeton, NJ)
- …and in their personal lives. Read more: careers.bms.com/working-with-us . The Associate Director (AD) for US Medical Pulmonary will provide deep disease state ... economics and outcomes research (HEOR) to ensure accuracy, currency, scientific balance and compliance with internal policies and procedures. **RESPONSIBILITIES**… more
- Bristol Myers Squibb (San Diego, CA)
- …team and closely collaborate with Clinical Operations, Clinical Development, Biometrics, and Regulatory Affairs . + Contribute to the design and execution of ... be the global leader in radiopharmaceuticals . The Senior Director - Clinical Pharmacology will be a key member...in Clinical Pharmacology, PK and PK/PD demonstrated by major Regulatory submission experience and/or scientific publications. +… more
- Surrozen (South San Francisco, CA)
- …with multidisciplinary teams including preclinical development, biostatistics, clinical operations, quality, regulatory affairs and CMC. As leader of the ... AMD/uveitic macular edema (UME). Reporting directly to the CEO, the Exec. Director /VP Clinical Development will contribute to and lead early clinical programs in… more
- AbbVie (Irvine, CA)
- … regulatory submissions. Responsibilities: + Based on strong medical and scientific experience, knowledge of compliance and regulatory requirements, Allergan ... committed to providing the most comprehensive science-based product offerings available. The Director I will provide direction and oversight to the design, planning… more
- AbbVie (North Chicago, IL)
- …added to our talent pipeline and considered for future opportunities. The Associate Director (AD) of Epidemiology in Pharmacovigilance & Patient Safety leads the ... scientific strategy for pharmacoepidemiology and real-world evidence to support...areas. They will design and interpret studies, contribute to regulatory submissions, and provide expertise in regulatory … more
- Astellas Pharma (Northbrook, IL)
- …modeling, adaptive designs, and hybrid or external controls-to improve efficiency, scientific rigor, and development impact. A key focus is designing studies ... and decision frameworks that balance exploration, safety, and speed with scientific rigor to inform go/no-go decisions and accelerate development. Experience in… more