- IQVIA (Parsippany, NJ)
- **Position Overview:** IQVIA is seeking an experienced Associate Clinical Project Management Director/Trial Delivery Manager (TDM) to lead and coordinate ... global and regional clinical trial management activities. This role ensures the successful planning, execution, and closure of clinical trials, whether… more
- IQVIA (Parsippany, NJ)
- …and owning local trial activites at the regional level._** **Additional Information** Associate Clinical Project Managers (aCPM)/Local Trial Managers are ... to meet contractual requirements in accordance with SOPs, policies and practices. Clinical Project Management is focused on project delivery,… more
- Regeneron Pharmaceuticals (Warren, NJ)
- …practices and processes to achieve objectives. + Exhibit strong problem-solving, analytical, and project management skills. + Thrive in a matrix environment with ... The Associate Director, External Data Services, plays a critical...and industry best practices. This position collaborates closely with Clinical Data Management teams and External Data… more
- Bristol Myers Squibb (Madison, NJ)
- …Assure coherence between the global supply strategy, Project Team objectives and Clinical Supply Chain management objectives." + Provide overall project ... development, of the functions and processes relevant to drug development, and project management principles applicable to the biopharmaceutical environment. +… more
- System One (Basking Ridge, NJ)
- …SME, and may collaborate with team on CAPAs, including CAPA responses and approvals Project Management : + Collaborates with the PSL(s) and scientist lead to ... Job Title : Associate Director, Clinical Safety Scientist (Contingent...This position will proactively perform safety surveillance and risk management for assets in early/late stage clinical … more
- IQVIA (Parsippany, NJ)
- …per site basis. * If applicable, may be accountable for site financial management according to executed clinical trial agreement and retrieve invoices according ... Job Overview: Perform monitoring and site management work to ensure that sites are conducting...in accordance with contracted scope of work and Good Clinical Practice. * Work with sites to adapt, drive,… more
- Bristol Myers Squibb (Madison, NJ)
- …Responsibilities** Responsibilities will include, but are not limited to: ** Project Management and Leadership** + Provides clinical data management ... BMS R&D pipeline. This role may report into Director, Clinical Data Management or Associate ...+ At least 5 years of relevant industry experience. Project management certification (eg PMP) is desirable.… more
- J&J Family of Companies (Raritan, NJ)
- …+ Manages Medical Writing staff (ie, medical writers and reviewers, project management staff, librarians, medical information specialists, programmers, as ... management expertise **required** . + Certification or 2+ years of project management experience _preferred_ . + Experience developing and implementing… more
- Sanofi Group (Morristown, NJ)
- …to do advanced statistical analyses using SAS or R. + Demonstrated strong project management , interpersonal and communication skills. + Exhibited expertise to ... accelerate progress. Join our **Biostatistics Immunology & Inflammation as Statistical Project Leader ( Associate Director)** and you'll provide statistical… more
- Sanofi Group (Morristown, NJ)
- …software development lifecycle, design controls, labeling, software documentation, risk management , clinical evaluations, and usability. Ability to synthesize ... **Job Title:** GRA Device Lead ( Associate Director) - Digital Health **Location:** Cambridge, MA/...GRA Device Lead for DHTs and SaMDs on assigned project teams (early phase, late stage and marketed products)… more
- AbbVie (Florham Park, NJ)
- …Associate Director, Statistics - Immunology provides statistical leadership for clinical development and life-cycle management strategies for assigned ... statistical input to compound/drug development and drive alignment with functional management . Partner with other functions ( Clinical , Regulatory, Patient… more
- J&J Family of Companies (Raritan, NJ)
- …of the impacts of new and changing regulations on the company objectives to project and management teams. + Support GRA Diagnostics in becoming a first-in-class ... + Must have the ability to work independently, managing daily activities and project deliverables with limited management oversight. + The ability to present… more
- Sanofi Group (Morristown, NJ)
- …Health Authority responses + Monitor and implement regulatory documentation requirements ** Project Management ** + Lead cross-functional initiatives as Subject ... **Job Title:** Principal Medical Writer Associate Director **Location** : USA, Remote. Proximity to...our teams accelerate progress. Global Medical writing and Document management serves to generate timely, high quality, cost effective… more
- IQVIA (Bridgewater, NJ)
- …is highly preferred + People leadership experience is required. + Proven client and project management experience is required. + Ability to monitor team outputs, ... ** Associate Creative Director, Copy** **Overview** Wanna know what's...to work collaboratively with other capabilities such as Account Management , Project Excellence, and more + Participate… more
- Sanofi Group (Morristown, NJ)
- **Job Title:** GRA Device Associate **Location:** Cambridge, MA/ Morristown, NJ/ Washington DC **About the Job** Are you ready to shape the future of medicine? The ... and Manufacturing & Supply, Regulatory Health Authorities, and others. As GRA Device Associate in the GRA Device Digital and Diagnostic team you'll contribute to… more
- Bristol Myers Squibb (Madison, NJ)
- …and in their personal lives. Read more: careers.bms.com/working-with-us . ** Associate Director, Global Regulatory Strategy, Neuroscience** **Position Summary:** The ... + Prepare content for regulatory strategic documentation and Regulatory Project Reviews. Align regulatory plans with commercial and development plans… more
- Sanofi Group (Morristown, NJ)
- **Job Title:** Associate Director Quantitative Data Modeling **Location:** Morristown, NJ **About the Job** Are you ready to shape the future of medicine? The race ... to regulatory submissions and interactions from first-in-human studies through life-cycle management . This position, based in Morristown, NJ, requires the successful… more
- AbbVie (Florham Park, NJ)
- …The Associate Director will independently lead all aspects of project planning, such as coordination, setting time lines, gaining cross functional team ... and recommendations, presenting interim and final results, and communicating all project progress/initiatives to Brand Teams, Senior Management , and/or Vendors,… more
- Bristol Myers Squibb (Madison, NJ)
- …+ Excellent communication, strategic thinking, and problem-solving skills. + Experience with project management tools and Lean Six Sigma methodologies is a ... personal lives. Read more: careers.bms.com/working-with-us . **Position Summary** The Associate Director, Breyanzi Product Champion, leads the technical agenda for… more
- Gilead Sciences, Inc. (Parsippany, NJ)
- …leaders and teams. + May participate on other Sub-teams (eg, Study Management , Clinical , Nonclinical, Biomarkers) or assign such to other colleagues ... and help create possible, together. **Job Description** As an Associate Director, Global Regulatory Affairs, you will act as...documents for submission to regulatory authorities. + Provides matrix management and leadership to project teams. +… more