- Lilly (Indianapolis, IN)
- …better for people around the world. **Purpose** : The Clinical Development Trial Lead (CDTL), Associate Director / Director independently leads the ... with quality, and within scope and budget. The CDTL Associate Director / Director consistently demonstrates independent...Understand the scope of work required to complete the clinical trial successfully. Monitor the status and… more
- Lilly (Indianapolis, IN)
- …as all other duties as assigned. ** ** _Clinical Plan_ _and Trial_ _Options and Clinical Trial Protocols_ + As the Medical leader on a cross-functional ... least three (3) yearsthat provides adequate background relevant to clinical trial design of PhII to Phase...and Reimbursement + New Product Planning + Global Marketing director or manager + Global patient safety **External Contacts**… more
- Lilly (Indianapolis, IN)
- …listed below as well as all other duties as assigned. **_Clinical Plan Options and Clinical Trial Protocols_** + As the Medical leader on a cross-functional ... three (3) years that provides adequate background relevant to clinical trial design of PhII to Phase...and Reimbursement + New Product Planning + Global Marketing director or manager + Global patient safety **External Contacts**… more
- Lilly (Indianapolis, IN)
- …**Purpose:** The purpose of the Medical Device Safety Scientist Associate Director role is to leverage clinical and scientific expertise working across ... process + Provide safety input and review for device related documents including clinical investigator brochures (IB), clinical trial protocols, and… more
- Merck (Indianapolis, IN)
- …**Quantitative Pharmacology and Pharmacometrics -** **Immune/Oncology** **(QP2-IO)** team in the role of Associate Director QP2-IO team is part of the Global ... of drug development and effective communication skills. As a subject matter expert, the Associate Director within the QP2-IO Group will work closely with teams… more
- Merck (Indianapolis, IN)
- …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… more
- Sumitomo Pharma (Indianapolis, IN)
- …used for investigational clinical trials and/or commercial phases. The Associate Director ensures compliance with GMPs, SMPA procedures and applicable ... ** Associate Director , GMP Quality Control** Sumitomo...and/or Quality Control function for marketed pharmaceutical products or clinical trial materials. Review regulatory IND, IMPD,… more
- Lilly (Indianapolis, IN)
- …satisfaction. 4. Scientific Data Dissemination and Exchange * Ensures timely dissemination of clinical trial data. * Help to ensure the critical analysis of ... to support communities through philanthropy and volunteerism. **Purpose:** The Sr. Director -Medical is delegated various responsibilities by the Associate … more
- Sanofi Group (Indianapolis, IN)
- …Medical and Tactical Plans. + In coordination with the Field Medical Training Associate Director , ensure MSLs have robust scientific knowledge and communication ... This position reports to the US Sr. Field Medical Director , Immunology (Non-Alliance). **Main Job Responsibilities:** + Demonstrate value...the R&D Field Medical Lead, oversee MSL support of clinical trial programs. + Manage MSL resources… more
- Lilly (Indianapolis, IN)
- …scientific interpretation of critical data analyses. + Ensures timely dissemination of clinical trial data, including but not limited to manuscripts, abstracts, ... clinical research activities, including technical review of all team protocols, trial level safety reviews, and clinical study reports. + Promotes innovation… more