- Option Care Health (Columbus, OH)
- …career. Option Care Health, Inc. is the largest independent home and alternate site infusion services provider in the United States. With over 6,000 team members ... patients with acute and chronic conditions in all 50 states. Through our clinical leadership, expertise and national scale, Option Care Health is re-imagining the… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …of clinical trials improvement/innovation projects for NACD and Novo Nordisk (eg, clinical trial site staff, IRBs, clinical research vendors). Manages ... of updates Ensures proactive risk identification and mitigation planning for assigned clinical trial sites Drives and tracks site activation and start-up… more
- Merck & Co. (Rahway, NJ)
- …and externally. Acts as primary site contact and site manager throughout all phases of a clinical research study, taking overall responsibility ... sites in a country.Under the oversight of the CRA manager or CRD, the person ensures compliance of study...site relationships through all phases of the trial.Performs clinical study site management/monitoring activities in compliance… more
- Merck & Co. (North Wales, PA)
- …the clinical trial team.Collaborates with the Medical Writer on clinical /scientific and regulatory documents.Partners with Study Manager on study ... drives scientific planning, strategy and execution of Phase 1-4 clinical studies. Under the direction of the Program Lead,...working a Hybrid work consisting of three total days on- site per week, generally Tuesday, Wednesday and either Monday… more
- Novo Nordisk Inc. (San Antonio, TX)
- …clinical trials and improvement/innovation projects for NACD and Novo Nordisk (eg, clinical trial site staff, clinical research vendors). Manages ... About the Department The Clinical , Medical and Regulatory (CMR) department at Novo...scientific integrity; regulatory and process compliance) for monitoring and site management activities. Takes ownership to deliver upon near-term… more
- Merck & Co. (North Wales, PA)
- …Clinical Trial Team (CTT)May work closely with the Medical Writer on clinical /scientific and regulatory documents and the Study Manager on study ... Job DescriptionOur Clinical Research and Pharmacovigilance team push the boundaries...working a Hybrid work consisting of three total days on- site per week, generally Tuesday, Wednesday and either Monday… more
- Daiichi Sankyo, Inc. (Basking Ridge, NJ)
- …collaborates with lead statistician on SAP update, as needed. Provides input to Clinical Operations on site issues. Contributes to development of CSR.External ... immune disorders. Summary Drafts development plans, protocol profile, protocol, and clinical sections of submission documents under guidance of CSL and/or Medical… more
- Catalent (Manassas, VA)
- …complex formulations to help create engaging new products consumers will love.The Site Procurement Manager is responsible for procurement leadership, sourcing ... and procuring materials, services, and capital for the site . The Site Procurement Manager ...sizes to advance new medicines from early development to clinical trials and to the market. Catalent produces more… more
- Daiichi Sankyo, Inc. (Basking Ridge, NJ)
- …planning and execution of clinical studies, under the supervision of the Study Manager role the Study Associate Manager within Clinical Operations, in ... and International Conference on Harmonization (ICH) guidelines. Key focus is on providing clinical trial management support to study teams and tracking CRO and other… more
- Option Care Health (Columbus, OH)
- …career. Option Care Health, Inc. is the largest independent home and alternate site infusion services provider in the United States. With over 6,000 team members ... and chronic conditions in all 50 states. Through our clinical leadership, expertise and national scale, Option Care Health...48 hours of receipt of payment. Notifies the Reimbursement Manager if there are overpayments and/or duplicate payments for… more
- Catalent (St. Petersburg, FL)
- Manager , QA (Product Development)Position SummaryThe Quality Assurance Department is responsible for providing Leadership and Quality Assurance Management support ... within at Catalent's St. Petersburg site . The Department has the responsibility for Quality aspects...Investigations, Deviations, Complaints, etc. The focus of each QA Manager may be dependent upon the needs of the… more
- Merck & Co. (Rahway, NJ)
- …case report form (CRF) data, lab data, other external data, biomarker data, and clinical outcomes assessments.2. Serves as project manager of all clinical ... Job DescriptionThe Trial Manager creates and ensures the successful execution of the clinical data management strategy for assigned trials within a specific… more
- Catalent (San Diego, CA)
- …, Quality AssurancePosition Summary:Catalent Pharma in San Diego, CA is hiring a Senior Manager of Quality Assurance (QA) at our Clinical Supplies facility. As a ... Leadership Team, you will partner with the General Manager to create and sustain a site ...manufacturing and stability storage and testing as well as Clinical Supply Services. At Catalent San Diego, we recruit… more
- Merck & Co. (North Wales, PA)
- Job DescriptionOverview:The Associate Director Publication (Pub) Manager is the central source of information regarding publication activities and is responsible for ... global publication strategies and tactical plans. The Associate Director Pub Manager oversees compliance with our company's publication policies and procedures and… more
- Catalent (Harman, WV)
- …has an opportunity to make a significant impact on the way that the Harman's site operates. The Manager , Supply Chain - Warehouse will lead a shift consisting ... Job Description: Manager , Supply Chain - WarehouseThe Manager ,...logistics, operational compliance, and inventory control.Assist in developing a site master plan and roadmap for supply chain which… more
- Merck & Co. (Rahway, NJ)
- Job Description Job Description: We are looking for a manager to lead and manage the validation and testing activities for our platform products. This role will need ... provide documentation and evidence of validation activities to regulatory authorities. Clinical systems knowledge highly preferred.#EligibleforERP MRLGCTO#ONEGDMSNOTICE FOR INTERNAL APPLICANTSIn… more
- Eisai, Inc (NJ)
- …is your profile, we want to hear from you. Job Summary The Senior Manager , Medical Writing will be the designated Lead Medical Writer for approximately 3-4 Programs. ... Writer, the incumbent ensures timely completion, accuracy and quality of all clinical and submission documentation across all aspects of the compounds' life cycle… more
- Lundbeck (New York, NY)
- …the way in creating positive customer experiences!As a Biopharmaceutical Area Sales Manager (BASM) you will be responsible for leading, developing, and managing a ... Others Achieves business objectives and sales results by observing Account Manager interactions with target customers, extended treatment team members, ancillary… more
- Lundbeck (White Plains, NY)
- …lead the way in creating positive customer experiences!As a BioPharmaceuticals Account Manager , you lead the promotion of our infusion product, driving demand ... creation by providing comprehensive clinical knowledge, executing sales and marketing strategies in the...Additional benefits information can be found on our career site .Why LundbeckLundbeck offers a robust and comprehensive benefits… more
- Merck & Co. (Ames, IA)
- …The position will require developing trial protocols, monitoring and summarizing clinical and marketing support trials specific to Ruminant animal health.- Position ... working a Hybrid work consisting of three total days on- site per week, generally Tuesday, Wednesday and either Monday...or Thursday, although the specific days may vary by site or organization, with Friday designated as a remote-working… more
