- Novo Nordisk Inc. (Plainsboro, NJ)
- … clinical trials 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...management systems and archiving systems. Relationships Reports to a Manager (or above) within NACD. Manages mutually beneficial relationships… more
- Novo Nordisk Inc. (Atlanta, GA)
- …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)
- Job DescriptionOverview:The Associate Director Publication (Pub) Manager is the central source of information regarding publication activities and is responsible ... development and implementation of global publication strategies and tactical plans. The Associate Director Pub Manager oversees compliance with our company's… 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, you...working a Hybrid work consisting of three total days on- site per week, generally Tuesday, Wednesday and either Monday… more
- Merck & Co. (North Wales, PA)
- …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 ... management, communication, and collaboration skills in support of our clinical trials. Job Responsibilities Responsible for the operational planning, feasibility,… 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, ... 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
- Legend Biotech USA, Inc. (Raritan, NJ)
- …systems processes within a cell therapy manufacturing facility to support both clinical and commercial requirements in a sterile GMP environment. This role will ... processes. Key Responsibilities Lead the CAPA program for the CAR-T manufacturing site . Oversee metrics, trending, and reporting of relevant quality systems records.… 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, ... 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
- Merck & Co. (Grand Rapids, MI)
- …with the in-scope customer team: Customer Team Leader, Key Account Manager , Nurse Educator, Field Reimbursement Associate , Medicare Account Executive, ... options on patients.- Understand the significance and use of clinical trials in multiple tumor types/therapies, both in impact...working a Hybrid work consisting of three total days on- site per week, generally Tuesday, Wednesday and either Monday… more
- Merck & Co. (Orlando, FL)
- …with the in-scope customer team: Customer Team Leader, Key Account Manager , Nurse Educator, Field Reimbursement Associate , Medicare Account Executive, ... impact of those options on patients.-Understand the significance and use of clinical trials in multiple tumor types/therapies, both in impact on promoted products… more
- PSG Global Solutions (El Paso, TX)
- …- Licensed Master Social WorkerLPC - Licensed Professional CounselorLAMFT - Licensed Associate Marriage and Family TherapistLCSW - Licensed Clinical Social ... The OpportunityDescriptionWe're looking for aT&S Counselor - On Site , working in the Healthcare Systems & Services industry in El Paso, Texas, United States.Content… more
- PSG Global Solutions (Boise, ID)
- …- Licensed Master Social WorkerLPC - Licensed Professional CounselorLAMFT - Licensed Associate Marriage and Family TherapistLCSW - Licensed Clinical Social ... The OpportunityDescriptionWe're looking for aT&S Counselor - On Site , working in the Healthcare Systems & Services industry in Boise, Idaho, United States.Content… more
- Actalent (Charlotte, NC)
- …Level Skills: CRA, Clinical Research Associate , sites, visits, monitor, Clinical research, Site Initiation Top Skills Details: CRA, Clinical Research ... + Perform routine and complex on- site and in-house site assessment for approximately 30-50 clinical sites with minimal to no guidance. Act as primary study… more
- University of Pennsylvania (Philadelphia, PA)
- …of health and wellness programs and resources, and much more. Posted Job Title Project Manager Multi- Site Clinical Research Job Profile Title Manager ... Project B Job Description Summary Job Description The Project Manager - Multi- Site Clinical Research is...full compliance with core grant mandates; work with the Associate Director for Quality Control and Compliance to ensure… more
- Vera Therapeutics (Brisbane, CA)
- Title: Clinical Trial Manager Associate Location: Brisbane, CA About Us: Vera Therapeutics (Nasdaq: VERA), is a late-stage biotechnology company focused on ... for patients suffering from immunological diseases. Position Summary: The Clinical Trial Manager Associate will...such as TMF review * May conduct, with oversight, site evaluation, initiation, monitor or co-monitor study sites, performing… more
- Merck (Boston, MA)
- … development teams and the operational/executional arms within the business. The Program Clinical Supplies Project Manager (Program CSPM) serves as the primary ... **Job Description** The Global Clinical Supply (GCS) organization is accountable for managing...working a Hybrid work consisting of three total days on- site per week, generally Tuesday, Wednesday and either Monday… more
- Compass Group, North America (Chicago, IL)
- Morrison Healthcare Position Title: Associate Director/ Clinical Nutrition Manager - Chicago, IL Pay Grade: 14 Reports To: Senior Director Job Details: This ... heavily focused on Food Service Operations in addition to Clinical RD oversight Morrison Healthcare is a leading national...Flexible Time Off + Holiday Time Off (varies by site /state) + Associate Shopping Program + Health… more
- Regeneron Pharmaceuticals (Armonk, NY)
- _This role is a hybrid position which means the individual must work on- site 3 days per week. Fully remote work is not possible for this role. The position can be ... Basking Ridge, NJ or Uxbridge, England._ The Assoc Mgr Clinical Study (CSAM) role supports the Clinical ...plan, monitoring plan, monitoring oversight plan, etc. + Reviews site level informed consents and other patient-facing study start-up… more
- UCLA Health (Inglewood, CA)
- …of the clinic. Under the leadership of the Chief Medical Officer, the Inglewood Site Clinical Director provides the majority of their primary care sessions at ... diagnostic and specialty referrals for our patients. The Inglewood site Clinical Director is an integral part...for two sites in a dyad relationship with the site manager . They work cooperatively with clinicians,… more
- WuXi AppTec (Natick, MA)
- **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
