- Actalent (Basking Ridge, 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
- 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 (Morristown, NJ)
- …including the creation of scopes of work and trial feasibility activities. + Monitor clinical trial performance and quality metrics, ensuring issues are ... + Minimum of 7 years experience in Pharma/biotech. + Experience in clinical trial study start-up and enrollment boosting activities. + Experience overseeing CROs… 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
- 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
- Regeneron Pharmaceuticals (Basking Ridge, NJ)
- …+ Ensure the design, implementation and maintenance of electronic case report forms, clinical trial . + database and electronic edit checks are performed ... - provides oversight of lead Data Manager(s) on assigned clinical data management studies in specific therapeutic areas to...Oversee all DM activities across all stages of the trial from study start-up through archiving. To include but… more
- Bristol Myers Squibb (Madison, NJ)
- …+ Articulating clinical development strategy + Analyzing, interpreting, and acting on Clinical Trial data to support development, and + Serving as principal ... research in academic or industry setting including education where applicable + Clinical trial leadership experience (eg, study director, etc.) within… more