- Taiho Oncology (Princeton, NJ)
- … operations practices and processes ensuring consistent delivery across studies . Education/Certification Requirements: + Associate 's degree or equivalent. ... impactful results. The leadership and support provided by our Clinical Operations team are the cornerstone of...dynamic team cultivating growth and learning. Position Summary: The Study Associate (SA) I is responsible for… more
- Organon & Co. (Jersey City, NJ)
- …test articles, study records, etc.), and on-site monitoring of non- clinical studies at specific milestones. Additionally, this position will interface ... **Job Description** **The Position** The Non- Clinical Operations Lead within the Non-...Team (NCD), is responsible for operational oversight conduct outsourced non- clinical studies at contract research organizations (CROs),… more
- Sumitomo Pharma (Trenton, NJ)
- …Trial Master Files (TMFs) ready for audits and inspections. Partnering with the Associate Director, Clinical Business Operations , the specialist ensures ... and system work instructions. Provide support and guidance to study team members during the full lifecycle of the...ensure system validation is maintained. + Work closely with Clinical Operations and Regulatory Affairs to ensure… more
- Sumitomo Pharma (Trenton, NJ)
- …director is responsible for the leadership, development, and management of clinical studies while building and maintaining relationships with investigators ... highly motivated, and experienced individual for the position of ** Associate ** **Medical Director, Clinical Development - Oncology**...and study staff. + Responsible for leading clinical study teams, monitoring overall study… more
- Merck (Rahway, NJ)
- …operational plans for all clinical supply activities associated with the clinical studies in their assigned compound(s)/ program(s). The incumbent must have ... **Job Description** The Global Clinical Supply (GCS) organization is accountable for managing...ensures proper allocation of drug product as needed across studies within assigned program(s). + Responsible for identifying significant… more
- Bristol Myers Squibb (Princeton, NJ)
- …+ 5+ years of experience delivering niche technology products in area of Clinical Development (Retrospective Trial Design Intelligence, Digital Study Design, ... our diverse team! As the Product Manager for the Clinical Data Ecosystem within Global Drug Development (GDD) IT...for attracting, nurturing, mentoring, and overseeing the team's daily operations , and collaborating closely with GDD data teams. +… more
- Bristol Myers Squibb (New Brunswick, NJ)
- …to the hiring manager.** Temporary 6-Month Position - Pharmaceutical Development Technician, Clinical Supply Planning & Operations - 25 - CSO **Temporary ... a necessity to achieve departmental and company goals. **JOB FUNCTION - CLINICAL SUPPLY OPERATIONS INTEGRATED SUPPLY CHAIN** Assignments within Integrated Supply… more
- AbbVie (Florham Park, NJ)
- …YouTube, LinkedIn and Tik Tok (https://www.tiktok.com/@abbvie) . Job Description The Associate Director, Statistics - Immunology provides statistical leadership for ... clinical development and life-cycle management strategies for assigned projects....trials, patient safety, and global medical affairs (GMA). The Associate Director works in partnership with experts in multiple… more
- Sumitomo Pharma (Trenton, NJ)
- …relationships with colleagues, fostering collaboration, and idea sharing + Reviews nonclinical, clinical and CMC documentation (eg nonclinical study reports, ... general product development in the pharmaceutical industry + Experience reviewing nonclinical, clinical and CMC documentation (eg nonclinical study reports, … more
- Sumitomo Pharma (Trenton, NJ)
- …relationship with colleagues, fostering collaboration, and idea sharing + Reviews nonclinical, clinical and CMC documentation (eg nonclinical study reports, ... general product development in the pharmaceutical industry + Experience reviewing nonclinical, clinical and CMC documentation (eg nonclinical study reports, … more