- Merck & Co. (Rahway, NJ)
- …Material(s):n/aRequired Skills:Adaptability, Adaptability, Business, Business Risks, Change Management, Clinical Development, Clinical Research , ... Supply (GCS) organization is accountable for managing the 'end-to-end' integrated clinical supply chain across the full Company's Research & Development… more
- Merck & Co. (Rahway, NJ)
- …Management Section of the GCS Planning organization. -Working independently, the Inventory Manager Clinical Supplies Project Manager (IM CSPM) creates ... (GCS) organization is accountable for managing the 'end-to-end' integrated clinical supply chain across the full Research ...Hybrid Work Model Effective September 5, 2023, employees in office -based positions in the US will be working a… more
- Merck & Co. (Rahway, NJ)
- …managing the 'end-to-end' integrated clinical supply chain across the full c ompany's Research & Development Division portfolio of clinical trial s .- GCS is ... within the business.-- - - Working independently, the Protocol Clinical Supplies Project Manager ( Protocol CSPM)...Hybrid Work Model Effective September 5, 2023, employees in office -based positions in the US will be working a… more
- Merck & Co. (North Wales, PA)
- …and key strategic engagements. This includes the ability to:Solid knowledge of clinical research regulatory requirements (eg, GCP and ICH)Ability to manage ... (eg, ICF documents / amendments); Partners with the Study Manager on study deliverables.Ensuring CRF design supports data collection...Adaptability, Clinical Data, Clinical Operations, Clinical Outcomes, Clinical Research , … more
- Merck & Co. (Rahway, NJ)
- …tactical/scientific mentorship to other clinical scientists. Core Skills Solid knowledge of clinical research regulatory requirements (e . g . , GCP and ICH) ... . , ICF documents/ amendments); Partners with the Study Manager on study deliverables. Ensuring CRF design supports data... Clinical Data, Clinical Data Interpretation, Clinical Operations, Clinical Research , … more
- Merck & Co. (North Wales, PA)
- …managing any study specific partners and/or vendors.Core Skills: Solid knowledge of clinical research regulatory requirements (eg, GCP and ICH)Ability to manage ... Driving License:NoHazardous Material(s):n/aRequired Skills:Adaptability, Adaptability, Clinical Data, Clinical Operations, Clinical Research , Clinical… more
- Merck & Co. (North Wales, PA)
- …and key strategic engagements. This includes the ability to:--Strong knowledge of clinical research regulatory requirements (eg, GCP and ICH) Proven ability ... the strategy and leads the operational planning and execution of one or more clinical trials. In this position, you will have the opportunity to demonstrate your… more
- Merck & Co. (San Francisco, CA)
- …Director, DSCS Digital Implementation Project ManagerWithin the Development Sciences and Clinical Supply (DSCS) organization, the Digital Project Manager will ... or more of the areas of Drug Substance development, Drug Product development, Clinical Supply management or Analytical Research is critical for understanding… more
- ACROBiosystems Inc. (San Diego, CA)
- …proteins and critical reagents/assays to support drug development and clinical applications from target discovery and validation, candidate drug screening ... and optimization, CMC development, preclinical and clinical studies, commercial production, and companion diagnostics. We are committed to excellence in providing… more
- Merck & Co. (Rahway, NJ)
- …primarily for sterile operations under the remit of Our Company's Research Labs Pharmaceutical Sciences (Pharm Sci), Pharmaceutical Operations Engineering group ... Engineering Lead of the FLEx GMP facility within Pharmaceutical Operations and Clinical Supply (PSCS)The FLEx sterile facility supports the formulation and filling… more
- Merck & Co. (North Wales, PA)
- Job DescriptionIn Biostatistics and Research Decision Sciences (BARDS), a distinguished department within our renowned Research and Development division, ... BARDS and will work collaboratively with other leaders in Clinical Development and Global Regulatory Affairs.--The AVP provides leadership...and maintaining high performing teams both as a direct manager and a second line manager (ie,… more
- Merck & Co. (Durham, NC)
- …to manufacturing areas and operating under the direction of the Logistics Manager . Must adhere to current Good Manufacturing Practices, Standard Operating Procedures ... 3-4 years of cGMP warehouse experience, working knowledge of Microsoft Office and flexible work schedule.Preferred Experience and Skills:-SAP Subject Matter Expert,… more
- Merck & Co. (Minneapolis, MN)
- …that align with customer needs and business prioritiesPartner with Regional Sales Manager to develop and execute effective business strategy to reach and exceed ... organizational priorities for lasting successMeet with key opinion leaders in both clinical and university settings to discuss our Company's Animal Health portfolio… more
- Merck & Co. (Rahway, NJ)
- …allocating resources for cross-product delivery and coordinating with investment Manager to ensure appropriate coordination and forecasting.Communicate IT strategy ... and portfolio to key stakeholders in our Research & Development Division and IT.- Encourage a digital..., PR&D (Process R&D) and PSCS (Pharmaceutical Sciences and Clinical Supply) functions.Understanding of the business workflows across the… more
- BioAgilytix (Durham, NC)
- …is seeking a Scientist III to serve as Bioanalytical Project Manager (BPM)/Principal Investigator (PI), overseeing all aspects of bioanalytical studies-including ... we tackle challenges across the spectrum of drug discovery to clinical diagnostics, driving advancements that shape the future of healthcare.Essential… more
- Protara Therapeutics, Inc. (New York, NY)
- …needs via oral or enteral routes. Job Overview: The Clinical Trial Manager (CTM)/ Clinical Research Associate is responsible for providing oversight of ... trial services, with a primary focus on ensuring quality Clinical Research Associate (CRA) monitoring and data...upon business needs. Must be willing to travel to clinical trial sites and New York City office… more
- MicroVention (Aliso Viejo, CA)
- Job Description Responsible for coordinating clinical research activities in accordance with ICH Good Clinical Practices, FDA guidelines, local regulations, ... to address and resolve queries. Work closely with Project Manager (s) to ensure clinical studies are conducted...in related field. Minimum six (6) years of direct clinical research experience, preferably in the medical… more
- Mount Sinai Hospital (New York, NY)
- …source documentation and subject survival status. Educate new staff regarding overview of clinical research , office policy and procedures, data submission, ... related field 2 years of experience as a Clinical Research Coordinator, Study Coordinator, Data Manager , or similar role in clinical research Working… more
- University of Utah (Salt Lake City, UT)
- Announcement Details Open Date 05/19/2025 Requisition Number PRN41958B Job Title PS Manager , Clinical Research Working Title Clinical Trial & Post Award ... at the Huntsman Mental Health Institute (HMHI) seeks a Clinical Research Manger whose responsibilities include developing...the Title IX Coordinator, to the Department of Education, Office for Civil Rights, or both. To request a… more
- Anaheim Clinical Trials (Anaheim, CA)
- …have in-patient capability. We focus on quality people, teamwork, and highly experienced clinical research managers with a history of success. Along with an ... that promotes teamwork, positive leadership, and optimal work-life balance, CenExel Clinical Research also provides highly competitive compensation and a… more