- Sumitomo Pharma (Trenton, NJ)
- …execute corporate clinical strategy for global development projects in Oncology + Monitor clinical trial progress, identify and mitigate risks, and make ... from preclinical experiments to the end of the product's life cycle. + Clinical Trial Oversight: Develop and oversee clinical trial strategies, ensuring… more
- Actalent (Parsippany Troy Hills, NJ)
- …of work creation, and ensure compliance with quality measures and timelines. + Monitor clinical trial performance and quality metrics, escalating issues ... procedures for planning, conduct, close out, and reporting. + Monitor and reconcile study budgets, reviewing vendor invoices and...Qualifications + 7+ years of experience as a GLOBAL Clinical Trial Manager with a pharmaceutical or… more
- Actalent (Princeton, NJ)
- Job Title: Clinical Trial ManagerJob Description The Clinical Trial Manager acts as a vital operations leader within the global study team, ensuring ... study activities. Serving as the primary escalation point for site-related issues, the Clinical Trial Manager leads and coordinates efforts to maintain the… more
- Bristol Myers Squibb (Princeton, NJ)
- …pilots or new methods that keep the organization at the forefront of clinical trial innovation with a consultative mindset and approach **Cross-Functional ... **advanced analytics** (eg, forecasting, modeling, AI/ML) and strong understanding of clinical trial processes (feasibility, site selection, patient enrollment).… more
- Bristol Myers Squibb (Princeton, NJ)
- …implementation all study startup/conduct/close-out activities as applicable + Evaluate innovative trial designs (collaboration with Medical Monitor / Clinical ... Summary / Objective** + Responsible for implementation, planning, and execution of assigned clinical trial activities. Serves as Clinical Trial … more
- Daiichi Sankyo Inc. (Basking Ridge, NJ)
- …Provides medical input regarding country feasibility. Consulted on decisions related to clinical trial feasibility and contributes to the site feasibility ... are conducted by the Contract Research Organization (CRO) Medical Monitor (MM): + Provides oversight to the CRO MM...achieve the Target Product Profile (TPP) + Development of clinical sections of trial -level regulatory documents (eg,… more
- Otsuka America Pharmaceutical Inc. (Trenton, NJ)
- …of assigned trial (s), as assigned.** **Participates in ongoing review of clinical trial data focusing on data integrity, trending and consistency.** ... of programs (eg, Word, Excel, PowerPoint, Outlook, etc.)** **Good understanding of clinical trial related software (eg, eCRFs, IRT, CTMS, etc.).** **Ability… more
- Sanofi Group (Morristown, NJ)
- …pharmacovigilance and clinical operations team + Implements strategies to identify, monitor and resolve clinical program/ trial issues. + Responsible for ... requests and briefing packages for Regulatory agencies, extended synopsis/protocol for clinical trials, Investigator Brochure, Clinical Trial Authorization… more
- Actalent (Hackensack, NJ)
- …medical personnel. + Maintain accurate, complete, up-to-date records for each patient in clinical trial protocol. + Ensure appropriate billing for clinical ... research studies. Responsibilities + Assist the principal investigator in preparing proposed clinical trials by reviewing trial protocol and coordinating with… more
- Actalent (Hackensack, NJ)
- …medical personnel. + Maintain accurate records on each protocol and patient in the clinical trial management system. + Work with clinical research finance ... procedures, or inpatient stays as per study protocols. + Monitor study activities for compliance with protocols and regulations....to ensure appropriate billing of clinical trial activities. + Schedule, prepare, and assist with sponsor… more