- Daiichi Sankyo, Inc. (Basking Ridge, NJ)
- …with the CRO and the study team. Oversee the site qualification process.Monitor clinical trial performance and quality metrics and share with study team, ... regulations/EU Directive, and International Conference on Harmonization (ICH) guidelines.The Senior Clinical Study Manager will have routine interaction with key… more
- Daiichi Sankyo, Inc. (Basking Ridge, NJ)
- …immune disorders.Summary The purpose of this job is to oversee statistical vendor deliverables, perform programmatic review of analysis datasets and Table, Listing, ... and Figures (TLFs) generated by vendor , ensure deliverable quality, and expedite the preparation of oncology compound regulatory submission. It will also to maintain… more
- Daiichi Sankyo, Inc. (Basking Ridge, NJ)
- …learned, as appropriate.- Metrics:-When needed, help support the partnership with Clinical Trial Business Operations (CTBO)to:-monitor GCO processes and ... with minimum of 5 years' experience in pharmaceutical or biotechnology across clinical trial operations. Experience in training, process improvement, and project… more
- Daiichi Sankyo, Inc. (Basking Ridge, NJ)
- …and external data expertise to promote and implement best practices across the Clinical Trial lifecycle. Provide oversight and execution of the CDx development ... the collection of diverse external data types.Advises Study Data Manager on complex vendor management issues and...complex disease therapeutic area is a must.Working knowledge of Clinical trial data systems and/or EDC and… more
- Daiichi Sankyo, Inc. (Basking Ridge, NJ)
- …skills preferred.Excellent time management skills preferred.Experience with PH.1 - PH. IV clinical trial vendor contracts required.Experience with CRO ... Degree preferably in Life Sciences required Experience Qualifications4 or More Years in clinical trial outsourcing, health sciences or related field ( clinical… more
- Daiichi Sankyo, Inc. (Basking Ridge, NJ)
- …and International Conference on Harmonization (ICH) guidelines. Key focus is on providing clinical trial management support to study teams and tracking CRO and ... clinical studies, under the supervision of the Study Manager role the Study Associate Manager within...other vendor performance against project goals and milestones to monitor… more
- Daiichi Sankyo, Inc. (Basking Ridge, NJ)
- …and International Conference on Harmonization (ICH) guidelines. Key focus is on providing clinical trial management support to study teams and tracking CRO and ... clinical studies, under the supervision of the Study Manager role the Study Associate Manager within...other vendor performance against project goals and milestones to monitor… more
- Axelon Services Corporation (Princeton, NJ)
- …outsourcing strategies within a specific therapeutic area(s) and is accountable to support clinical trial vendor partnerships across select or multiple ... service categories of clinical trial activities in R&D. Key Responsibilities - Drive outsourcing activities by interfacing with operational teams, support groups… more
- IQVIA (New York, NY)
- **Elevate Your Career as a Clinical Trial Vendor Manager !** **About the Role:** Step into a world where your expertise in clinical vendor ... management becomes the catalyst for advancing medical breakthroughs. As a ** Clinical Trial Vendor Manager ** , you'll play a key role in our clinical … more
- J&J Family of Companies (Raritan, NJ)
- …(Phase I-IV); must have the ability to manage all aspects of execution of a clinical trial . 2-3 years' experience leading multiple aspects of a global ... Manager , Trial Delivery Management - 2406191849W **Description** The ...clinical trial Must possess excellent leadership skills and proven ability… more
- Regeneron Pharmaceuticals (Tarrytown, NY)
- …a Bachelor's Degree and minimum of 8 years of experience and success in a clinical trial /life sciences management role. Experience working with clinical drug ... The Senior Manager Development Operations & Portfolio Management (DO&PM) Vendor & Relationship Management (VRM) position is responsible to ensure that… more
- Regeneron Pharmaceuticals (Armonk, NY)
- …etc. + Oversees set-up and maintenance of study systems including but not limited to Clinical Trial Management System (CTMS), Trial Master File (TMF) etc. + ... Ensures compliance with the clinical trial registry requirements + Identifies outsourcing...collaborations + Applies advanced negotiation and interpersonal skills to vendor management + Advanced technical proficiency in trial… more
- Regeneron Pharmaceuticals (Armonk, NY)
- …etc. + Oversees set-up and maintenance of study systems including but not limited to Clinical Trial Management System (CTMS), Trial Master File (TMF) etc. + ... Ensures compliance with the clinical trial registry requirements + Identifies outsourcing...to build productive study teams and collaborations + Demonstrated vendor management experience + Technical proficiency in trial… more
- Regeneron Pharmaceuticals (Armonk, NY)
- …who have vendor management experience, as well as experience in clinical trial operations including developing key study documents. We also require ... based in Armonk, NY or Basking Ridge, NJ._ A Clinical Study Associate Manager (CSAM) role supports...Study Lead (CSL) by taking responsibility for areas of clinical trial delivery. This role applies to… more
- Pfizer (New York, NY)
- …, Study Start Up Project Manager , Site Intelligence Lead, Country Trial Manager , Site Care Partners, Site Excellence Partners, Site Relationship Partners, ... activities as applicable + Through the Site Care Partner/Country Trial Manager or pCRO supports the Country/investigator...Local Study Team (core members: (Lead) Site Care Partners Clinical Trial Assistant, ad hoc members: ICL,… more
- Regeneron Pharmaceuticals (Armonk, NY)
- …internally sourced studies and/or CRO/Partnered studies. Collaborates and interacts with clinical trial managers, development program managers, medical monitors, ... The **Sr Manager , Clinical Drug Supply & Logistics**...orders according to supply plans or as requested by Clinical Trial Management team, to ensure timely… more
- Daiichi Sankyo Inc. (Basking Ridge, NJ)
- …and external data expertise to promote and implement best practices across the Clinical Trial lifecycle. Provide oversight and execution of the CDx development ... of External data in Daiichi Sankyo R&D collaborating with Clinical and Medical teams, Functional Stakeholders, (QCP, Clinical...of diverse external data types. + Advises Study Data Manager on complex vendor management issues and… more
- Daiichi Sankyo Inc. (Basking Ridge, NJ)
- …+ Excellent time management skills preferred. + Experience with PH.1 - PH. IV clinical trial vendor contracts required. + Experience with CRO contracts ... preferably in Life Sciences required Experience Qualifications + 4 or More Years in clinical trial outsourcing, health sciences or related field ( clinical … more
- Daiichi Sankyo Inc. (Basking Ridge, NJ)
- …and International Conference on Harmonization (ICH) guidelines. Key focus is on providing clinical trial management support to study teams and tracking CRO and ... clinical studies, under the supervision of the Study Manager role the Study Associate Manager within...other vendor performance against project goals and milestones to monitor… more
- Daiichi Sankyo Inc. (Basking Ridge, NJ)
- …disorders. **Summary** The purpose of this job is to oversee statistical vendor deliverables, perform programmatic review of analysis datasets and Table, Listing, ... and Figures (TLFs) generated by vendor , ensure deliverable quality, and expedite the preparation of oncology compound regulatory submission. It will also to maintain… more
