- 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
- Organon & Co. (Jersey City, NJ)
- …seven years of working experience with or within a healthcare/consumer care industry project management , clinical operations or outcomes research function ... position is responsible for working alongside the Director of Clinical /Pre- Clinical /TMED/Outcomes Research (OR) R&D Procurement & Supplier Management in… more
- Merck (Rahway, NJ)
- …Description** **Position Description:** ** Associate Director, DSCS Digital Implementation Project Manager** Within the Development Sciences and Clinical ... Digital Project Manager, will be responsible for implementing improved project management methodologies across DSCS Digital use-cases. The ideal candidate… 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
- Sanofi Group (Morristown, NJ)
- …to do advanced statistical analyses using SAS or R. + Demonstrated strong project management , interpersonal and communication skills. + Exhibited expertise to ... **Job Title:** Statistical Project Leader ( Associate Director) **Location:** Morristown,...and Decision Science (EGDS) group** at Sanofi unites Biostatistics, Clinical Statistical Modeling, and Real-World Evidence to revolutionize data-driven… more
- Merck (Rahway, NJ)
- … Practice (GCP) studies, and occasionally Good Laboratory Practice (GLP) studies. The Associate Principal Scientist is the primary clinical study team leader and ... Principal Scientist can also be responsible for several effectiveness studies within a project , participating as the clinical representative in project teams… more
- Bristol Myers Squibb (Summit, NJ)
- …activity in line with key business milestones & budget. + Utilize standard project management tools and Scrum methodology for tracking and status reporting. ... highly desired + Analysis and simplification of complex operational issues + Project management execution, expertise in its principles and application, the… 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...contracted scope of work and regulatory requirements, ie, Good Clinical Practice (GCP) and International Conference on Harmonization (ICH)… more
- Merck (Rahway, NJ)
- **Job Description** The Associate Principal Scientist, Device Risk Management Lead, is a crucial member of our team, responsible for spearheading risk ... and Activities:** The Associate Principal Scientist, Device System - Device Risk Management will be responsible for device risk management activities in the… more
- Merck (Rahway, NJ)
- …present ideas to senior leadership + Excellent communication, presentation, negotiation, project management , and organizational skills + Experience with leading ... Devices Design, Negotiation, Process Manufacturing, Product Design, Production Process Development, Project Management , Quality Management Systems (QMS) {+… more
- Merck (Rahway, NJ)
- …deliverables for R&D projects (data, analyses, tables, graphics, listings) + Strong project management skills; leadership at a program level; determines approach ... position is a key collaborator with statistics and other project stakeholders in ensuring that project plans...understanding of statistical terminology and concepts. + Familiarity with clinical data management concepts + Experience in… more
- AbbVie (Florham Park, NJ)
- …The Associate Director, Statistics provides statistical leadership for clinical development and life-cycle management strategies for assigned projects. ... statistical input to compound/drug development and drive alignment with functional management . Partner with other functions ( Clinical , Regulatory, Patient… 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
- 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)
- …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
- Organon & Co. (Jersey City, NJ)
- …Affairs, Pharmacovigilance, Regulatory Affairs, etc.) + At least three years of experience in project management . + Proficient with MS Project , MS Timeline, ... understanding of and application of principles, concepts, practices, and standards of pharmaceutical project management . + Worked on programs in one or more… 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
- 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
- Merck (Rahway, NJ)
- …integrity guidelines, engineering standards, and regulatory issues. Provides technical, project management and system leadership. **Education Minimum ... Process Development, Process Control Automation, Process Optimization, Product Formulation, Project Management , Quality Control Management , Regulatory… more