- Merck & Co. (North Wales, PA)
- …(eg, study team, country teams, vendors, committees) in support of clinical study objectives.Accountable for managing any study specific partners ... Material(s):n/aRequired Skills:Adaptability, Adaptability, Clinical Data, Clinical Operations, Clinical Research, Clinical Study Design, Clinical … more
- Merck & Co. (North Wales, PA)
- …experienceDegree in life sciences, preferred. Experience in planning and executing clinical studies in ophthalmology highly preferredAs an Equal Employment ... the operational planning and execution of one or more clinical trials. In this position, you will have the...Trial Team lead. Leads and directs teams in key study planning, development, and execution elements (eg operational reviews,… more
- Syneos Health Careers (Morrisville, NC)
- …Responsibilities Project Leadership and Delivery: *Manages a project as a project manager overseeing interdisciplinary clinical research studies and ensures ... Description Clinical Project Manager II - post-trial...Medicine, Pharmacy, Nursing or equivalent combination of education and experience . * Clinical research organization (CRO) and relevant… more
- Lutheran Services Carolinas (Charlotte, NC)
- …you must be fluent in Spanish for this position. The Post Release and Home Studies Program Case Manager works with Unaccompanied Children (UCs) who are fleeing ... NC This role is required to serve only Home Studies , completing up to 3 reports simultaneously. The role...in social work, or other relevant degree or equivalent experience ; Master's degree preferred Experience : At least… more
- Merck & Co. (Rahway, NJ)
- …operational/executional arms within the business.-- - - Working independently, the Protocol Clinical Supplies Project Manager ( Protocol CSPM) designs strategic ... - Responsible and accountable for establishing the timelines for clinical supply needs per study and providing...Clinical Practices (GCP) is highly desirable. - Preferred Experience and Skills: - - - Results-orientation with the… more
- Merck & Co. (Rahway, NJ)
- …Management Section of the GCS Planning organization. -Working independently, the Inventory Manager Clinical Supplies Project Manager (IM CSPM) creates ... strategic and operational plans associated with the downstream activities of clinical supplies for their assigned studies . -The primary function of the IM CSPM… more
- Virtua (Voorhees, NJ)
- Experience in Modified Barium Swallow Study (MBSS) and Videofluoroscopic Swallow Studies (VFSS) preferred. Opportunity for 20 - 40 hours a week Per Diem. ... determine prognosis, provide intervention, and update plan of care. Assists manager /supervisor with clinical and operational issues. Works with manager to… more
- Merck & Co. (Rahway, NJ)
- …teams and the operational/executional arms within the business.-- - - The Program Clinical Supplies Project Manager (Program CSPM) serves as the primary ... ensures proper allocation of drug product as needed across studies within assigned program(s) . - Responsible for identifying...Clinical Practices (GCP) is highly desirable. - Preferred Experience and Skills: - - Proficiency in using supply… more
- UMKC (Kansas City, MO)
- …equipment and supporting technologies. The Simulation Technician collaborates with the Director of Clinical Simulation, the Clinical lab manager and other ... Qualifications: Bachelor's degree in a health-related or technical field. Prior experience working in simulation, healthcare education, or clinical environments.… more
- Boston Scientific (Marlborough, MA)
- …(CTM) will be responsible for the design, planning, execution and leadership of clinical studies worldwide for BSC's Coronary Therapies portfolio. The Senior CTM ... Writes study protocols, protocol amendments, informed consents, clinical study project timelines and scientific papers...throughout the development and implementation of local or global clinical studies . May lead studies … more
- Merck & Co. (North Wales, PA)
- …related study materials (eg, ICF documents / amendments); Partners with the Study Manager on study deliverables.Ensuring CRF design supports data ... clinical drug development, project management, and/or medical field experience OR Master's Degree +3 year of pharmaceutical, ...Data, Clinical Operations, Clinical Outcomes, Clinical Research, Clinical Study Design,… more
- Merck & Co. (Rahway, NJ)
- …study materials (e . g . , ICF documents/ amendments); Partners with the Study Manager on study deliverables. Ensuring CRF design supports data collection ... Experience Bachelor's Degree +5 years of pharmaceutical , clinical drug development, project management , and/or medical field... Clinical Data Interpretation, Clinical Operations, Clinical Research, Clinical Study Design,… more
- The University of Chicago (Chicago, IL)
- …such as ACRP, SoCRA or the Graham School Clinical Trials. Experience : Experience coordinating multiple studies (eg, investigator initiated, industry ... administration of the compliance, financial and other related aspects of the clinical study . Responsibilities Research Conduct/ Study Management: Manages… more
- Duke University (Durham, NC)
- …Management: Records participant accrual information and consent documentation for non-complex studies in clinical research management system. Uses clinical ... in regulatory and institutional policies and processes; applies appropriately in study documentation, protocol submissions, and SOPs. May train others in these… more
- Planned Parenthood (Minneapolis, MN)
- …Qualifications: 1-3 years of experience in clinical research, including coordinating clinical research studies from start up to close out Experience ... will be under the general supervision of the Research Manager . This position will focus on research study...and optimize research protocols and procedures Ensure compliance with clinical study protocols, and proper completion/submission of… more
- Eisai, Inc (Nutley, NJ)
- …Environment Implementation of new programs, enhancements & support of Eisai Clinical Computing Environment Support study migration, program validation, technical ... is your profile, we want to hear from you. The Associate Director, Clinical Programming must have expertise in addressing technical challenges in the programming… more
- Recursion (Salt Lake City, UT)
- …leading 2-3 outsourced programs, simultaneously. Represent Data Management function in Clinical Study Meetings, ensuring proactive alignment of expectations ... sets, and sophisticated analytics. We are seeking a Lead, Clinical Data Manager who can lead and... who can lead and oversee end to end Clinical Data Management activities on assigned studies … more
- Syneos Health Careers (Morrisville, NC)
- Description Clinical Trial Manager - Real World Late Phase Syneos Health(R) is a leading fully integrated biopharmaceutical solutions organization built to ... Oversee the development, coordination, and implementation of Phase 1 clinical research studies at the organization's facilities,...field; advanced degree preferred Minimum of 5 years of experience in clinical trial management, with a… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …GxP audits assigned. Support conduct of document audits including eTMF, Clinical Study Reports and Common Technical Document submission.ResponsibilitiesSupport ... audit program for clinical studies and vendors as applicable for...including, but not limited to Common Technical Document (CTD), Clinical Study Report (CSR) and Nonclinical … more
- Profound Research (Las Vegas, NV)
- …Providing Advanced Therapeutic Options Our Vision: Creating the Absolute Best Patient-Physician Experience in Clinical Research Our Values: Compassion: We value ... degree or BS / BA in Life Sciences or related discipline. -8+ years prior experience as a clinical research coordinator -3-5 years of direct line management… more
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