- 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
- Evolent (Hartford, CT)
- …the mission. Stay for the culture. **What You'll Be Doing:** Seeking a detail-oriented ** Clinical Rules Management , Associate Director ** who will play a ... will be responsible for the design, implementation, support, and maintenance of our clinical rules management systems. The ideal candidate will have a strong… 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
- Stony Brook University (Stony Brook, NY)
- Clinical Study Coordinator - Cancer Clinical Trials **Position Summary** At Stony Brook Medicine, a ** Clinical ** ** Study Coordinator** is a valuable ... communication skills while adhering to our high standard of excellence. **Duties of a Clinical Study Coordinator may include the following but are not limited… 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
- 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
- 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
- Merck (Hartford, CT)
- …questions from investigators and provides information regarding participation in Company-sponsored clinical studies **Scientific Congress Support** + Engages in ... approved, in-development, and active Company-sponsored trials and/or investigator-sponsored research studies . The Regional Medical Scientific Director serves as… more
- Otsuka America Pharmaceutical Inc. (Hartford, CT)
- …**and** ** Clinical Management .** **Manages project timelines** **for studies and** **projects and collaborates with** ** study teams** **and** **vendors ... ** studies and projects** **by managing all aspects of study deliverables related to** **S** **tatistical** **P** **rogramming** **including validation plans.**… more
- Fairfield University (Fairfield, CT)
- …Center, including the provision of supervisory and administrative oversight of staff, clinical services, and outreach initiatives. The Director will work closely ... Director will ensure that all ethical, legal, and clinical expectations are met relative to medical services, EMR...the development of the SHC Quality Improvement activities and studies + Oversee the SHC Risk Management … more
- Sunrise Senior Living (Suffolk County, NY)
- …Suffolk County Metro Area **Job ID** 2025-224991 **JOB OVERVIEW** The Resident Care Director (RCD) serves as the nursing clinical leader for the community ... services for the residents. + Serves as the CLIA Director as applicable for the community and according to...clinical team members and is responsible for performance management , evaluations, and engagement. + Completes direct report team… more
- Kelly Services (New Haven, CT)
- …the day-to-day activities associated with the implementation and conduct of clinical studies + Understanding and experience of study start-up and close out + ... I (CRC I) will oversee the execution of research studies according to established study protocols. Responsibilities...Experience of working on multiple study protocols + Solid understanding of clinical … more
- The Cigna Group (Bloomfield, CT)
- **Overall** Responsible for leading clinical strategy development and product management for pharmacy utilization management and the coordination of rebate ... contracting efforts to ensure alignment across formulary, utilization management , SafeGuard, and other trend solutions. **Essential Functions:** + Ability to manage… more
- Norstella (Hartford, CT)
- … trial operations and confidence in dealing with stakeholders responsible for clinical study success * Experience selling market intelligence, consulting, custom ... Global Account Director , Strategic Solutions Company: Citeline Location: Remote, United...the world's leading providers of data and intelligence on clinical trials, drug treatments, medical devices and what's new… more
- Merck (Hartford, CT)
- …engagers, bispecifics) in Oncology, authoring regulatory documents (investigational new drugs/INDs, clinical study reports (CSRs), clinical trial ... and Pharmacometrics -** **Immune/Oncology** **(QP2-IO)** team in the role of Director , Quantitative Systems Pharmacology (QSP). QP2-IO team is part of the… more
- Merck (Hartford, CT)
- …and biologics in Oncology, authoring regulatory documents (investigational new drugs/INDs, clinical study reports (CSRs), clinical trial applications ... the role of Director . QP2-IO team is part of the Global Clinical Development organization and has oversight over drug development aspects related to clinical… more
- Merck (Hartford, CT)
- **Job Description** **Role Summary:** + The Global Director Medical Affairs (GDMA) is responsible for supporting the execution of scientific & medical affairs plans ... regions. + Serves as an impactful member of Product Development Team sub-teams (eg, Clinical , V & I, Commercial, Publications). + Contributes to the development of a… more
- Merck (Hartford, CT)
- …and biologics in Oncology, authoring regulatory documents (investigational new drugs/INDs, clinical study reports (CSRs), clinical trial applications ... role of Associate Director QP2-IO team is part of the Global Clinical Development organization and has oversight over drug development aspects related to … more