- Taft College (Taft, CA)
- …MESA Program Director is responsible for the efficient and effective operations of the MESA program. This position requires a demonstrated ability to coordinate ... group study activities, working cooperatively with the Learning Center Director . Recruit and schedule speakers for meetings of MESA students. Plan, schedule,… more
- BeOne Medicines (Emeryville, CA)
- … Operations , Regulatory, Development, and corporate functions to embed diversity into study design and site selection. The Associate Director will build ... **General Description:** Reporting to the Head/ Director of Clinical Trial Diversity, the Associate ...site selection, and regulatory readiness. + Partner with Clinical Operations , Feasibility, and Medical Affairs colleagues to… more
- Seattle Children's (Seattle, WA)
- We are seeking a detail oriented and strategic Clinical Trial Operations Director to oversee clinical study operations within our healthcare ... oversee resourcing, developing, training, and managing a successful clinical trial operations team. This leader is responsible for the planning, oversight,… more
- Organon & Co. (Plymouth Meeting, PA)
- …the approved early development plans. The Clinical Pharmacology Lead will serve as the medical monitor and/or study director responsible for the execution ... (in conjunction with the TMED Operations Lead) and reporting thereof. The Director ...collaboration with the TMED operations lead and study biostatistician), analysis and interpretation of TMED studies… more
- Lundbeck (Deerfield, IL)
- Senior Director Head, Field Medical Neuro Rare Requisition ID: 7066 Location: Deerfield, IL, US Do you want to join a team where the mission is meaningful, the ... us on our journey of growth! **SUMMARY:** The Senior Director , Head of Field Medical - Rare...and balanced communication of product data. + Support post-marketing studies , real-world evidence generation, and publication planning. + Monitor… more
- CSL Behring (King Of Prussia, PA)
- …applicable to resolve issues with E2B submission + Review of interventional clinical trial studies and study specific reporting rules: . Review of study ... meaningful difference worldwide. We are looking for a **Associate Director ,** **Case Management Intake & Submissions** to join our...approval status and update reporting requirements as required. + Study setup of post marketing studies : Review… more
- Pfizer (Groton, CT)
- …assigned molecule(s)/indication(s) Responsible for scientific leadership and execution of clinical studies and delivering on innovative clinical study designs, ... working with and solid understanding of related disciplines, eg, Clinical Operations , Data Management, Safety, Biostatistics, Regulatory, Study Management,… more
- CSL Behring (King Of Prussia, PA)
- …of the program + providing clinical oversight and expertise during development of clinical studies + serves as medical monitor for assigned clinical trials or ... Plan (CDP), the Project Strategy Document (PSD), Investigator Brochures (IB), Clinical Study Protocols (CSP), Informed Consent Forms (ICF), Medical Monitoring… more
- Organon & Co. (Plymouth Meeting, PA)
- …and outcomes research sourced activities to support efficient, on-time execution of clinical studies and early clinical study operations . + Actively ... require a working knowledge of and skills in clinical operations , medical affairs, outcomes research, business ...development. + Knowledgeable of clinical operations and study management, and outcomes research studies for… more
- CSL Behring (King Of Prussia, PA)
- …the program** **providing clinical oversight and expertise during development of clinical studies ** **serves as medical monitor for assigned clinical trials or ... Plan (CDP), the Project Strategy Document (PSD), Investigator Brochures (IB), Clinical Study Protocols (CSP), Informed Consent Forms (ICF), Medical Monitoring… more