- Teva Pharmaceuticals (West Chester, PA)
- Associate Director , Global Clinical Quality Date: Jan 7, 2025 Location: West Chester, United States, Pennsylvania, 19380 Company: Teva Pharmaceuticals ... activities, and leads continuous improvement for clinical development activities. The Associate Director - Global Clinical Quality leads a portfolio… more
- Takeda Pharmaceuticals (Dover, DE)
- …to the best of my knowledge. **Job Description** **Objectives:** As part of the Global Evidence and Outcomes (GEO) team, this position is focused on documenting the ... innovative therapies across the oncology portfolio through: + Analysis of unmet clinical need and potential therapeutic preferences + Development of Clinical … more
- Takeda Pharmaceuticals (Dover, DE)
- …possible in order to bring life-changing therapies to patients worldwide. Join Takeda as Associate Director , Global Labeling Lead where you will be ... obtain labeling approval by Labeling Senior Management Cross-functional team ( Global Labeling Oversight Committee - GLOC) driving cross-functional collaboration and… more
- Merck (West Point, PA)
- **Job Description** The Global Clinical Supply organization is accountable for managing the 'end-to-end' integrated clinical supply chain across the full ... company Research Laboratories portfolio of clinical trials. Global Clinical Supply is accountable for the planning, sourcing, labeling, packaging and… more
- Takeda Pharmaceuticals (Dover, DE)
- …and direct the execution of diversity and inclusion strategy and tactics for global clinical trial programs. + Accountable for the co-creation and implementation ... and technologies that will ensure delivery of diverse participant populations in clinical trials representative of populations anticipated to be treated with the… more
- Takeda Pharmaceuticals (Dover, DE)
- …company that will inspire you and empower you to shine? Join us as an Associate Director , Data Configuration Engineer in our Cambridge, MA office. At Takeda, we ... and transformation templates for reuse for study level configuration tasks. The Associate Director Data Configuration Engineer (DCE) oversees a team that… more
- System One (King Of Prussia, PA)
- …meets industry and regulatory requirements for clinical trial coding. The Associate Medical Coding Director manages and oversees staff, strategic partners, ... Title: Associate Medical Coding Director Full Time...technology that supports efficient dictionary management processes and with Global Patient Safety and Clinical Development for… more
- Takeda Pharmaceuticals (Dover, DE)
- …innovation-driven company to inspire you and empower you to shine? Join us as an Associate Director , GCP Compliance based remotely reporting to the Director , ... research organization, including 6 or more years in compliance or clinical study management required. + Global /international experience required, including… more
- IQVIA (Wayne, PA)
- **Job Profile Summary** The Associate Strategic Account Management Director supports key client relationships within Clinical Trial Payments, driving client ... helping identify growth opportunities, and ensuring a seamless client experience. The Associate Director will collaborate with cross-functional teams to maintain… more
- Merck (West Point, PA)
- …component of decision-making at our Company, this position offers an opportunity for the Associate Director to drive pipeline impact across therapy areas. This ... Associate Director will work with scientists within...PK/PD models, exposure response (ER) models, model-based meta-analysis (MBMA), clinical trial simulations (CTS) and disease progression modeling into… more
- IQVIA (Wayne, PA)
- ** Associate Director , IQVIA Participant Payments (ADIPP)** The Associate Director , IQVIA Participant Payments (ADIPP) is responsible for directing a ... Experience & Education** **_Experience_** + 5-7 Years of prior experience with global participant payments, clinical trial payments, and/or other payment… more
- Takeda Pharmaceuticals (Dover, DE)
- …company to inspire you and empower you to shine? Join us as a Associate Director , Business Operations DMC Lead based remotely, reporting to the Executive ... Director , GDO Business Operations. At Takeda, we are transforming...maintain DMC/IRC R&D wide communication strategy. + Partner with Global Clinical Development Operations Process Excellence and… more
- Merck (Dover, DE)
- …enrollment and retention efforts to achieve study milestones + Upon request from Global Clinical Trial Operations (GCTO), + Recommends study sites and identifies ... **Job Description** **Role Summary** + The Oncology Regional Medical Scientific Director ( Associate RMSD) is a credentialed (ie, PhD, PharmD, DNP, MD)… more
- United Therapeutics (Dover, DE)
- …for cardiovascular and pulmonary diseases, and other orphan diseases. **How you'll contribute** The Associate Global PV Case Management Director plays a key ... successfully gained FDA approval for five medicines, we are always conducting new clinical trials, and we are working to create an unlimited supply of manufactured… more
- Publicis Groupe (Philadelphia, PA)
- …| Facebook: www.facebook.com/digitashealth| Twitter: www.twitter.com/digitas_health **Overview** The Associate Medical Director is a medical ... Digitas Health is the Agency of Now: the first global connected-health agency, purpose-built for marketing today. Digitas Health...used in marketing to HCPs. In this capacity, the Associate Medical Director has oversight for the… more
- Endo International (Malvern, PA)
- …for talented individuals to join our team. **Job Description Summary** The Associate Director , Commercial Development & Professional Relations will support the ... develop and deliver life-enhancing products through focused execution. Our nearly 3,000 global team members understand the important role we play in delivering… more
- Merck (West Point, PA)
- …Us:** The Discovery, Preclinical and Translational Medicine Operations (DPTM) is seeking an Associate Director to lead the Molecular lab within the Late ... IT platforms, and science to accelerate vaccines and enable late-stage clinical trials through the generation of timely, high-quality regulated bioanalytical data.… more
- IQVIA (Wayne, PA)
- …and modernize patient and consumer engagement to improve health outcomes. The ** Associate Director of Product Management, Healthcare Solutions** will manage, ... + Excellent communication and interpersonal skills required. IQVIA is a leading global provider of clinical research services, commercial insights and healthcare… more
- Takeda Pharmaceuticals (Dover, DE)
- …innovative opportunities to improve processes and infrastructure in line with global regulatory expectations and Global Regulatory Affairs (GRA) technology ... supporting Regulatory components of PSMF reporting, adapting strategies based on evolving global regulatory landscape. + Acts as a primary source for business RIM… more
- United Therapeutics (Dover, DE)
- …successfully gained FDA approval for five medicines, we are always conducting new clinical trials, and we are working to create an unlimited supply of manufactured ... Utilize advanced data programming skills (eg, SAS) to support HEOR and Global Medical Affairs (GMA) studies using Real-World Data (RWD) sources. Perform analytics… more