- Abbott (Philadelphia, PA)
- …to work for diversity, working mothers, female executives, and scientists. **The Opportunity** The ** Associate Clinical Site Lead ** for the Philadelphia, ... clinical staff (eg, operations management, study team, Site Contracts Associate ), as needed. **Manage all...appropriate collaboration with Abbott clinical staff, eg Site CRA, Site Contract Associate .… more
- J&J Family of Companies (Trenton, NJ)
- …of day-to- day aspects of investigational site activities on assigned clinical trials. The Clinical Research Associate should ensure compliance ... Sr Clinical Research Associate - 2406209639W **Description**...+ Provide coaching and training to junior employees. + Lead in the investigation of all discrepancies in study… more
- Penn Medicine (Philadelphia, PA)
- …a Bachelors degree, and at least 2 years of related experience are encouraged to apply! Associate Clinical Analyst: + An Associate Clinical Analyst may ... reside in PA, NJ or DE. _The role involves on- site presence for the first 6 months with the...least 2 years of related experience are encouraged to apply! Associate Clinical Analyst: + An Associate… more
- Merck (North Wales, PA)
- …including those new to the organization therefore requiring someone who has built and lead clinical development plans from the ground up. They will also be ... **Job Description** The Associate Vice President (AVP)/Section Head, Global Clinical...including pipeline and licensed candidates. The Section Head may lead Product Development Teams (PDT) and manage PDT leaders… more
- Bristol Myers Squibb (Princeton, NJ)
- …implementation, planning, and execution of assigned clinical trial activities. Serves as Clinical Trial Lead for one or more trials + Successfully leads, ... team members + May support clinical development planning (collaboration with Clinical Development Lead / Clinical Trial Physician for provision and… more
- Bristol Myers Squibb (Princeton, NJ)
- …2/3 clinical study design and registrational strategy + **Accountable for the** Clinical Pharmacology Plan + ** Lead ** design of clinical pharmacology ... on cross-functional drug development teams, and regulatory submissions; serves as Clinical Pharmacology subject matter expert + ** Lead and participate**… more
- Bristol Myers Squibb (Princeton, NJ)
- …team! **Position Summary:** We are seeking a highly motivated and detail-oriented Associate Director - Product Manager with broad clinical data experience ... to join our IT team within the Clinical Data Ecosystem team. The successful candidate will play...enhancements based on user feedback, and business value + Lead the end-to-end product development lifecycle, from ideation to… more
- Merck (North Wales, PA)
- …and statistical analysis methods fundamental to effective pharmaceutical R&D. The Clinical Safety Statistics (CSS) group within BARDS supports proactive assessment, ... statistical representative and core member in the Risk Management Safety Teams. Lead and provide statistical support for related drug/vaccine projects in Clinical… more
- Bristol Myers Squibb (Princeton, NJ)
- …and execution of disease and product curricula utilized by the NP PA Clinical Specialist field team. This position is a headquarters-based position and will work ... US Field Enablement Team, and the WW Centre of Excellence. Specifically, the Associate Director will work in close partnership with colleagues from several functions… more
- Bristol Myers Squibb (Princeton, NJ)
- …of work across BMS and/or non-BMS programs. + Provides oversight of all clinical studies within assigned portfolio, via effective matrix management. + Represents the ... degree in relevant discipline + Minimum 8 years of global experience in clinical drug development or other related experience. + Broad clinical operational… more
- The Cigna Group (Philadelphia, PA)
- …Management + US Employer Strategy & Solutions + Digital & Analytics + Clinical Research & Innovation Every HSLDP Program associate 's experience is unique ... and cultivates The Cigna's Group next generation of leadership with these associate objectives in mind:** + Assume high-demand roles with increasing levels of… more
- Bristol Myers Squibb (Princeton, NJ)
- …provide leadership for all regulatory interactions with FDA/global regulatory authorities + Lead regulatory dossier submissions to global and/or FDA (IND, BLA, NDA, ... + Strong ability to work successfully in a matrix environment and to lead teams successfully toward drug approvals Other Qualifications: + Strong team player, using… more
- Bristol Myers Squibb (Princeton, NJ)
- …their personal lives. Read more: careers.bms.com/working-with-us . **Summary:** The CTI Lead is responsible day-to-day Cyber Threat Intelligence (CTI) operations, to ... and unique perspectives in an inclusive culture, promoting diversity in clinical trials, while our shared values of passion, innovation, urgency, accountability,… more
- Medtronic (Philadelphia, PA)
- …6 years of clinical , medical sales or medical imaging/navigation/robotics experience; + Associate 's Degree with a minimum 4 years of clinical , medical sales ... helping champion healthcare access and equity for all. You'll lead with purpose, breaking down barriers to innovation in...Day in the Life** At Medtronic, the Enabling Technology Clinical Consultant II - provides clinical , technical… more
- Medtronic (Philadelphia, PA)
- …of clinical evaluation best practices and regulatory agencies' guidelines on clinical evaluation requirements + May lead the development of policies, ... clinical department + Interface with regulators and may lead discussions and develop strategies with cross functional stakeholders...mathematics, mechanical concepts, science, or computing - OR- + Associate degree and a minimum 6 years of work… more
- Virtua Health (Moorestown, NJ)
- …care. + Teaches proper injectable protocol. + Collaborates with Front Desk Supervisors and Clinical Lead (s) to address other needs of the offices. + Identifies ... solutions to Front Desk Supervisors regarding office issues or problems. + Handles on site clinical patient complaints. + Organizes and assigns tasks to other … more
- Bristol Myers Squibb (Princeton, NJ)
- …is responsible for managing the end-to-end process for IC for BMS-sponsored clinical trials. This includes a centralized triage function for informed consent ... negotiations with global clinical trial sites, IRBs/ECs, and health authorities, as well...internal and external best practices and exploring technologies. The Associate Director (AD), Informed Consent Management role reports to… more
- Bristol Myers Squibb (Princeton, NJ)
- …. **Summary/Scope** Reporting to Senior Scientific Director Translational Medicine (TM), the TM Associate Director will be part of the late stage TM group. The ... individual will be responsible for TM and clinical biomarker activities to support drug development programs in neurodegeneration and neuropsychiatric indications.… more
- Bristol Myers Squibb (Princeton, NJ)
- …work and in their personal lives. Read more: careers.bms.com/working-with-us . Associate Director, TA (Therapeutic Area) Analysis Standards Leader is accountable for ... the TA, aligning cross-functionally and driving end to end standards. Associate Director, TA Analysis Standards Leader, independently leads improvement initiatives… more
- Bristol Myers Squibb (Princeton, NJ)
- …more: careers.bms.com/working-with-us . Employer: Bristol-Myers Squibb Company Position: Associate Medical Director, Eliquis Worldwide Medical Affairs (ref.# 4150) ... Location: 3401 Princeton Pike, Lawrenceville, NJ 08648 Duties: Lead research and strategic planning to determine and develop better understanding of unmet medical… more