- Sumitomo Pharma (Trenton, NJ)
- …Master Files (TMFs) ready for audits and inspections. Partnering with the Associate Director, Clinical Business Operations, the specialist ensures accountable ... SMPA, visit our website https://www.us.sumitomo-pharma.com or follow us on LinkedIn. The Trial Master File (TMF) Specialist will be responsible for ensuring that… more
- Parexel (Trenton, NJ)
- …quality + Manage assigned operational aspects for implementation of clinical trial activities at assigned investigator sites from site activation through to ... Associate (Sr. CRA) is responsible for the site management, site monitoring and close-out of...the set-up, running and close-out of sites in a clinical trial . **Key Accountabilities:** **Oversight of Monitoring… more
- IQVIA (Parsippany, NJ)
- …owning local trial activites at the regional level._** **Additional Information** Associate Clinical Project Managers (aCPM)/Local Trial Managers are an ... inspection readiness, and uphold GCP, SOP, and local regulatory standards. **_Two years of clinical trial management experience is required within a role that is… more
- Parexel (Trenton, NJ)
- …quality + Manage assigned operational aspects for implementation of clinical trial activities at assigned investigator sites from site activation through to ... Associate (Sr. CRA) is responsible for the site management, site monitoring and close-out of...the set-up, running and close-out of sites in a clinical trial . **Monitoring Responsibilities and Study Conduct:**… more
- Taiho Oncology (Princeton, NJ)
- …biological sciences is preferred. Knowledge, Skills, and Abilities: + 2 years of relevant clinical trial support or site management experience in the ... team cultivating growth and learning. Position Summary: The Study Associate (SA) I is responsible for operational study support...to multi-task and effectively prioritize in order to ensure clinical trial goals. + Recognize potential obstacles… more
- System One (Basking Ridge, NJ)
- Job Title: Clinical Study Associate I Location: Basking Ridge, NJ Type: Contract - 1 year Contractor Work Model: Hybrid - must be able to go onsite 1-4 ... the life sciences industry? Joule is currently seeking a Clinical Study Associate to join an industry-leading...Oversight measures. + Support and assist the transmittal of trial and site level document to the… more
- Bristol Myers Squibb (Princeton, NJ)
- … development, the position is responsible for various aspects of ongoing clinical trial program-related activities within the relevant therapeutic area. These ... their personal lives. Read more: careers.bms.com/working-with-us . **Summary** The Associate Director of Clinical Science plays a...may be assigned. + Acquires and utilizes knowledge of clinical trial design to develop or oversee… more
- Merck (Rahway, NJ)
- …exposure to clinical drug development with emphasis on key elements of clinical trial planning, execution, data analysis and reporting of clinical ... Skills:** Clinical Development, Clinical Research, Clinical Sciences, Clinical Trial Planning,...working a Hybrid work consisting of three total days on- site per week, Monday - Thursday, although the specific… more
- IQVIA (Parsippany, NJ)
- …may be accountable for site financial management according to executed clinical trial agreement and retrieve invoices according to local requirement. ... in accordance with contracted scope of work and Good Clinical Practice. * Work with sites to adapt, drive,...site documents are available for filing in the Trial Master File (TMF) and verify that the Investigator's… more
- Bristol Myers Squibb (Princeton, NJ)
- …your application should be directed to Chat with Ripley. R1597891 : Associate Director, Oncology Clinical Biomarker Asset Lead, Translational Development ... will offer the greatest possible benefit to patients. **Position Summary** The Clinical Biomarker Asset Lead role will be responsible for development and execution… more