Study Manager Salary at Basf Se BETA

Your New Company! At Altasciences we all move in unison to assist and work in the discovery, development, and manufacturing of new drug therapies to get them faster to people who need them. No matter your role, we all play an important part and you will have a significant impact on the health and well-being of people across the globe. By living our values of Employee Development, Customer Focus, Quality and Excellence, Respect and Integrity, we look to foster a passionate and collaborative work environment and we are looking for talented and enthusiastic people, like you, to join our growing team! Whether you're a recent college graduate or seeking your next career opportunity, it's time to discover your future at Altasciences. We are better together and together We Are Altasciences. About The Role Works under the guidance of designated Study Director(s), Contributing Scientists and Principal Investigators, as appropriate, to provide administrative and professional support for accurate

**The Opportunity** The Clinical Trial Supply (CTS) Senior Study Manager manages the end-to-end supply chain for assigned clinical studies throughout the multi-year study lifecycle. The CTS Senior Study Manager independently leads clinical studies to ensure compliant, supply of study medication and ancillary materials for our patients. Responsibilities include determining kit design and blinding, forecasting demand of investigational product and ancillary supplies, establishing, and managing the depot network and distribution to clinical sites, and ensuring final return and destruction. The CTS Senior Study Manager also leads process improvement projects for the clinical supply chain and may have direct reports. **The Role** + Give input to and oversee the implementation of multi-year clinical supply strategies and plans for assigned simple to complex clinical studies. + Gather and documents requirements for clinical supplies based on protocol attributes and clinical assumptions. Influ

Overview: Velocity Clinical Research is an owned and integrated research site organization, providing excellence in patient care, high quality data and fully integrated research sites. At Velocity, we align our values and behaviors to give our employees the best chance of delivering on our brand promise: to bring innovative medical treatments to patients. We are committed to making clinical trials succeed by generating high quality data from as many patients as possible, as quickly as possible while providing exemplary patient care at every step. As an employee of Velocity, you are the most integral part of our mission. For talented candidates who perform at a high level, Velocity will invest to support career advancement and reward performance. Whether you are new to clinical research or are an industry veteran, we invite you to apply to Velocity. Benefits include medical, dental and vision insurance, paid time off and company holidays, 401(k) retirement plan with company-match, and a

Welcome to West Liberty University! Mission Statement West Liberty University is a public university with a rich history of providing students with a comprehensive education form undergraduate to graduate degrees. Through experiential learning and personalized support, we empower students toward scholarly exploration, creative expression, and economic opportunity. The Opportunity West Liberty University is seeking applications for a Program Coordinator in the Office of Graduate Studies. The position reports to the Dean of Graduate Studies and focuses on supporting current master's degrees as well as new and emerging programs. The position works closely with Program Directors and Deans to assist with administrative aspects of graduate recruitment and admissions, curriculum management, and student services. The position interfaces with the administrative systems and protocols at the departmental, college, and university levels, including the CRM, Banner, Sakai and related work flow syste

Location : Fresno, CA Job Type: Full-time, tenure track Job Number: 2024-00362 Department: School of Arts and Sciences Opening Date: 12/18/2024 Position Summary Department: School of Arts & Sciences Reports To: Dean Status/Time Commitment: Full-time with faculty rank, Tenure-Track, 9- or possibly a 10-month appointment Rank: Assistant or Associate Professor Start Date: 07/01/2025 Committee will begin reviewing applications by February 15, 2025. All applications received before February 15, 2025, will be given full consideration. Department/School Summary: The School of Arts and Sciences prepares students for a life of service through rigorous academic programs in the liberal arts, social sciences, science, technology, and math, and biblical and ministry studies. The Department of Biblical, Ministry, Philosophy and Liberal Arts/Studies specifically trains and prepares students for both professional and vocational goals as well as serving the entire undergraduate population with signific

Job Description Job Description Emerson Clinical Research Institute (ECRI) is a network of research sites focused on working with community based clinics in the D.C, VA, and MD area. We conduct phase II-IV clinical research studies in community clinics. These clinics are focused on providing health care services to the minority populations, that don't otherwise have access to research opportunities. Our studies are industry sponsored research protocols in for adults and pediatric patients (study participants). We are looking for an Ophthalmology Technician that is ready to take the next step up in their carrier. Here you won’t be doing standard work. This position will allow the candidate to be fully engaged in the development of new medical treatments. The candidate will work doing BCVA, OCT, FA and a variety of other procedures, in order to support work in the conduct of clinical research. The second part of this position the candidate will learn to manage a clinical research protoco

**General Description:** _Line management responsibilities:_ + Provides leadership, management, and/or mentorship to clinical study managers at various levels for assigned portfolio + Collaborates effectively with internal and external stakeholders within the region as well as with global stakeholders to ensure the needs of the business are met. + Contributes to overall Clinical Operations strategy for the region and is accountable for performance against key metrics + Contributes to resourcing and capability development related to regional study management + Ensures alignment of regional resources and deliverables with overall portfolio goals **Essential Functions of the job:** **Regional Leadership** _Line management responsibilities:_ + Provides leadership to the team of Operations Managers and Operations Associates in charge of regional study management, including mentoring, coaching and managing performance + Collaborates with peers in the regional Clinical Operations leadership t

POSITION RESPONSIBILITIES: Implement study protocols; Perform data collection and quality control of study data; Oversee the process by which participants are recruited into the study, adherence to research protocols in obtaining informed consent, blood drawing and testing, data collection and management and participant confidentiality; Develop and implement methods to track and follow-up with study participants; Assist with coordinating data safety monitoring and produce quarterly reports; Oversee questionnaires for completeness and accuracy; Arrange meetings of study partners, develop meeting agendas, and facilitate meeting; Implement quality control procedures; Assist in the preparation of grants for future studies; Develop and manage REDCap database. QUALIFICATIONS: Bachelors degree is required. Minimum Salary Range: USD $58,500.00/Yr. Maximum Salary Range: USD $58,500.00/Yr. About Us: This position is in the Division of Nephrology, with a primary assignment to the clinical studies