- Boehringer Ingelheim (Ridgefield, CT)
- **Description** **The Director , Study Management / Clinical Operations role is an On-site/Hybrid role, meaning it will be required to work from the ... Ridgefield, CT site 2-3 days per week.** The Director , Study Management / Clinical Operations is responsible for leading and supporting the planning,… more
- Otsuka America Pharmaceutical Inc. (Hartford, CT)
- …Under the direction of the Director /Associate Director of Clinical Management , the Senior Clinical Study Manager is responsible for the oversight ... and management of Otsuka clinical studies , including coordination with other relevant...with ESPs on study -level risk mitigation and management activities.** **Represent Clinical Management … more
- Bausch + Lomb (Hartford, CT)
- …parties the planning, implementation, management , execution and completion of clinical studies according to applicable regulations and guidance, ICH and ... **:** Is responsible for the implementation and oversight of clinical study operations by organizing and coordinating... objectives are being met and provide the operations director and/or senior management with timely updates… more
- Otsuka America Pharmaceutical Inc. (Hartford, CT)
- …regulatory submissions. You will lead study design, execution and reporting of ** clinical pharmacology** and studies . You will contribute to all phases of ... proof of concept (PoC), mass balance and drug interaction studies . The Director will author/review ** clinical...support drug development and regulatory packages **.** + Lead ** clinical pharmacology** activities related to study design,… more
- Medtronic (North Haven, CT)
- …and other duties may be assigned. + Provides leadership for the conduct of clinical studies as it applies to product approval, launch, adoption and maintenance. ... compassionate world. **A Day in the Life** The Sr. Clinical Research Director , Core Surgical Innovations (CSI)...within ethical guidelines. + The end result of the clinical studies must be a fair assessment… more
- Sumitomo Pharma (Hartford, CT)
- …PK/PD, clinical pharmacology and drug-metabolism expertise to project teams. + Design clinical pharmacology components of clinical studies . + Create ... reports/chapters of reports including those intended for regulatory submission. For example, clinical study reports (CSRs), investigator brochures (IB), new drug… more
- Otsuka America Pharmaceutical Inc. (Hartford, CT)
- …in preparation for a new drug. + Acts as the signatory on NDA submissions and clinical study and safety documents. + Involved in product life cycle management ... **Job Description** Otsuka is seeking a Director , Global Clinical Development (GCD), who...of experience at application). + A thorough knowledge of clinical medicine and science management . This entails… more
- Otsuka America Pharmaceutical Inc. (Hartford, CT)
- …in preparation for a new drug. + Be the signatory on NDA submissions and clinical study and safety documents. + Involved in product life cycle management ... the maintenance of everyday health We are seeking a Director , Global Clinical Development (GCD) who will...of experience at application). + In depth knowledge of clinical medicine and science management . This requires… more
- University of Connecticut (UConn) (Storrs, CT)
- …of Nursing is seeking applications to fill a full-time, 11-month, Assistant/Associate Clinical Professor, Graduate Track Director - Psychiatric Mental Health ... health: support for people with acute and chronic conditions, including symptoms and self- management ; and biobehavioral studies of sleep and pain. The School of… more
- Boehringer Ingelheim (Ridgefield, CT)
- …electronic data capture system; Project Management and Agile methods; and, Maintaining Clinical Data Management related study documents, including Data ... **Description** Associate Director , Principal Clinical Data Engineer at...teams and managing relationships with external vendors; Leading end-to-end clinical data management activities, including database specification,… more
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