- Bristol Myers Squibb (Princeton, NJ)
- …Manager (GTM), Clinical Trial Managers (CTMs) Clinical Trial Monitors (CTMos), Study Start-up Specialists, Site Contract Leads, Vendor Operations ... and non-drug (Lab kits, ECG) importation to support study site + Complete all payment activities including preparing invoices,...work experience. + Experience in the use of industry Clinical Trial Management Systems and Clinical… more
- Bristol Myers Squibb (Princeton, NJ)
- … Clinical Research or related work + Experience in the use of industry Clinical Trial Management Systems + Additional complex software application related to ... and non-drug (Lab kits, ECG) importation to support study site + Complete all payment activities including preparing invoices,...clinical trial research (ie electronic data capture… more
- Taiho Oncology (Princeton, NJ)
- …of timelines, budget, recruitment and country/ site selection strategies, and provision of clinical trial materials. + Serves as main study contact for the ... Associate Director, Clinical Operations Pleasanton, CA,...sites. + Responsible for the financial management of the clinical trial in conjunction with his/her supervisor… more
- ThermoFisher Scientific (Bridgewater, NJ)
- … clinical research portfolio, our work spans laboratory, digital and decentralized clinical trial services. Your determination to deliver quality and accuracy ... Impactful Work:** Performs and coordinates all aspects of the clinical monitoring and site management process. Conducts...study systems are updated per agreed study conventions (eg Clinical Trial Management System, CTMS). Performs QC… more
- Actalent (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 ... the supervision of the Study Manager role the Study Associate Manager within Clinical Operations, in adherence... system, Clinical project management, cro, irb, clinical study, regulatory documents, clinical trial… more
- Regeneron Pharmaceuticals (Basking Ridge, NJ)
- …supports the Clinical Study Lead (CSL) by taking responsibility for areas of clinical trial delivery in Clinical Experimental Sciences. This role applies ... plan, monitoring plan, monitoring oversight plan, etc. + Reviews site level informed consents and other patient-facing study start-up...maintenance of study systems including but not limited to Clinical Trial Management System (CTMS) and … 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 Clinical Operations, in adherence to the protocol, Good … more
- Gilead Sciences, Inc. (Parsippany, NJ)
- …the TMF technical capabilities and oversight of standardization, training, quality, and timely clinical trial documentation across the clinical program. The ... impact. Join Gilead and help create possible, together. **Job Description** The Associate Director, Clinical Records & Information Management will partner with… more
- WuXi AppTec (Plainsboro, NJ)
- **Overview** The Clinical Research Associate III Senior Oncology performs and coordinates aspects of field-based and office-based monitoring and data quality ... clinical monitoring and required reporting, including pre-study visits, site invitation visits, routine monitoring visits (both onsite and...or supervisor, including but not limited to mentoring of Clinical Research Associate (CRA) I and II… more
- IQVIA (Parsippany, NJ)
- …may be accountable for site financial management according to executed clinical trial agreement and retrieve invoices according to local requirement. ... copies/originals (as required) site documents are available for filing in the Trial Master File (TMF) and verify that the Investigator's Site File (ISF)… more
- IQVIA (Parsippany, NJ)
- …may be accountable for site financial management according to executed clinical trial agreement and retrieve invoices according to local requirement. ... site documents are available for filing in the Trial Master File (TMF) verify that the Investigator's ...**MINIMUM RECRUITMENT STANDARDS:** + **2.5 years of clinical research coordination experience at site level**… more
- Insight Global (Perth Amboy, NJ)
- …documentation is a must Bachelor's Degree, science / nurse background Expertise of modern clinical trial site technologies (eg, eReg, eSource, eConsent) null ... Job Description The CRA anticipates and proactively solves study-related clinical site issues as they occur and initiates, recommends and communicates corrective… more
- AbbVie (Florham Park, NJ)
- …knowledge of database concepts. + Experienced in the life sciences domain and clinical trial processes + Demonstrated ability to influence others without direct ... bringing people, process, and technology together to generate business value from clinical trials data. Our operational model is exemplified through execution and… more
- Bristol Myers Squibb (Princeton, NJ)
- …projects * Efficiently plans, coordinates, and delivers complete, high quality and reliable clinical trial data in a timely manner for assigned projects * ... R&D pipeline . This role may report into Director, Clinical Data Management or Associate Director, ...functional study team members to ensure on-going review of trial data currency , quality and completeness * Represents… more
- Daiichi Sankyo Inc. (Basking Ridge, NJ)
- …with Daiichi Sankyo QA on audit activities + Provide oversight of the transmittal of trial and site level documents to the Daiichi Sankyo Document Control Center ... will be responsible for ensuring the delivery execution of clinical studies in one or more geographic regions in...primarily a tactical study delivery role, reporting into an Associate Director or above responsible for Operational Study Strategy.… more
- Bristol Myers Squibb (Princeton, NJ)
- …- Supervise and coordinate the work assignments and performance of Trial Manager, Trial Specialist and Trial Associate staff assigned NRDG trials in the ... personal lives. Read more: careers.bms.com/working-with-us . **Title: Senior Manager, Clinical Operations Position** **Responsibilities:** + 7-10 years of pharmaceutical… more
- Regeneron Pharmaceuticals (Basking Ridge, NJ)
- …internally sourced studies and/or CRO/Partnered studies. Collaborates and interacts with clinical trial managers, development program managers, medical monitors, ... orders according to supply plans or as requested by Clinical Trial Management team, to ensure timely...compliant shipment and delivery to investigator sites. Works with Clinical Logistics Associate to complete this activity… more
- Bristol Myers Squibb (Berkeley Heights, NJ)
- …the development and implementation of innovative strategies and technologies for clinical trial programming. A ssociate Director develop collaborative ... the development and implementation of innovative strategies and technologies for clinical trial programming + Independently develops, validates, troubleshoots,… more
- Bristol Myers Squibb (Princeton, NJ)
- …and ethical standards + Ensures active participation of FM in providing input on clinical trial site selection and feasibility based on their knowledge ... insight generation and patients' access to medicine. The Regional Associate Director (RAD) role is field-based and focused on...in their geography + Ensures FM team's execution of clinical trial support activities (as per established… more
- Bristol Myers Squibb (Madison, NJ)
- …aligned medical communications plans; adjust communications plans in accordance with clinical trial results/milestones and changes in the healthcare landscape ... Professional (CMPP), and ISMPP active member highly desired + Understanding of clinical trial design and execution, statistical methods and clinical… more