- BeOne Medicines (Emeryville, CA)
- **General Description:** Reporting to the Head/Director of Clinical Trial Diversity, the Associate Director will operationalize BeOne's clinical trial ... embed diversity into study design and site selection. The Associate Director will build trusted partnerships with sites, communities,...internal operations under the leadership of the Head of Clinical Trial Diversity + Primary focus is… more
- Parexel (Columbus, OH)
- …associated with the set-up, running and close-out of sites in a clinical trial . **Key Accountabilities:** **Oversight of Monitoring Responsibilities and Study ... **Job Purpose:** The Senior Clinical Research Associate (Sr. CRA) is... + Manage assigned operational aspects for implementation of clinical trial activities at assigned investigator sites… more
- Parexel (Pierre, SD)
- …activities associated with the set-up, running and close-out of sites in a clinical trial . **Monitoring Responsibilities and Study Conduct:** + Ensure proper ... The Senior Clinical Research Associate (Sr. CRA) is... + Manage assigned operational aspects for implementation of clinical trial activities at assigned investigator sites… more
- BeOne Medicines (Emeryville, CA)
- …with CRAs to ensure data collection is met per contractual guidelines - Works with Clinical Trial Oversight Managers (CTOMs) and Clinical Study Team (CST) to ... responsible for the management and oversight of their assigned clinical study sites to ensure data quality ...CTMS and data management systems **Other Qualifications:** - Understands clinical trial processes with a thorough knowledge… more
- Terumo Neuro (Aliso Viejo, CA)
- …close-out with strong regulatory and GCP compliance. + Collaborate with Medical Affairs, Clinical Quality Assurance, Clinical Data Management and Clinical ... **13125BR** **Title:** Associate Director, Clinical Research (US Remote)...Support & Collaboration + Assist in developing and implementing clinical trial strategies aligned with business priorities.… more
- Teleflex (Minneapolis, MN)
- …device are a required asset. **Principal Responsibilities** - Establish and maintain clinical trial sites for interventional cardiology studies. - Train site ... driven by our purpose to improve the health and quality of people's lives. Through our vision to become...is a senior-level position that provides field support for clinical studies involving both peripheral vascular and coronary products,… more
- Stony Brook University (Commack, NY)
- …II - Medical Records **Required Qualifications (as evidenced by an attached resume):** Associate 's Degree (foreign equivalent or higher). In lieu of an Associate ... working with medical records and database systems. Experience with performing quality assurance checks. Experience compiling data into reports. Familiar with the… more
- Lilly (Indianapolis, IN)
- …to make life better for people around the world. **Purpose:** The purpose of the Clinical Trial Quality Associate - Global Medicines Quality ... development and implementation of the strategy for **Good Clinical Practice (GCP)** quality systems and activities...functional areas such as medical writing, regulatory affairs, or clinical trial management + Ability to work… more
- Abbott (Austin, TX)
- …and liberate more than 500,000 people with diabetes from routine fingersticks. The ** Associate Manager of Clinical Trial Reimbursement** is responsible for ... help more than 10,000 people have healthier hearts, improve quality of life for thousands of people living with...implementing and managing clinical trial reimbursement processes to secure Medicare and private payer… more
- Bristol Myers Squibb (Princeton, NJ)
- …decision-making throughout execution. You will apply a strong foundation in both clinical trial science and applied analytics - from understanding protocol ... team of 3-5 analysts and senior analysts within a trial delivery context, ensuring coordinated, high- quality , and...trial strategy is required + Prior exposure to clinical trial delivery processes and data-driven decision… more
- Sumitomo Pharma (St. Paul, MN)
- …Specialist will be responsible for ensuring that SMPA studies have comprehensive and quality Trial Master Files (TMFs) ready for audits and inspections. ... Partnering with the Associate Director, Clinical Business Operations, the specialist...the study TMF. **Key Responsibilities** + Responsible for overall quality , maintenance, and completeness of Trial Master… more
- Takeda Pharmaceuticals (Boston, MA)
- …considered. + Enable a compliant quality system in safety and clinical trial delivery systems via CPMQ continual improvements projects. Actively participate ... of my knowledge. **Job Description** **About the role:** The Associate Director, Clinical & Quality ...represent in continual improvement projects, related to safety and clinical trial delivery in partnership with GDO,… more
- IQVIA (Philadelphia, PA)
- …owning local trial activites at the regional level._** **Additional Information** Associate Clinical Project Managers (aCPM)/Local Trial Managers are an ... inspection readiness, and uphold GCP, SOP, and local regulatory standards. **_Two years of clinical trial management experience is required within a role that is… more
- University of Utah (Salt Lake City, UT)
- …Additionally, the role includes mentoring research managers and coordinators to streamline clinical trial processes and deliver high- quality outcomes, ... investigators, industry sponsors, CROs, and external stakeholders. + Negotiate and manage clinical trial budgets and contracts to align with department and… more
- ICON Clinical Research (PA)
- …a Clinical Research Associate , with a strong understanding of clinical trial processes and regulatory requirements. + Proven ability to manage multiple ... Senior Clinical Research Associate ICON plc is...will play a critical role in overseeing and managing clinical trial activities to ensure they are… more
- ThermoFisher Scientific (Middleton, WI)
- …research portfolio, our work spans laboratory, digital and decentralized clinical trial services. Your determination to deliver quality and accuracy will ... study systems are updated per agreed study conventions (eg Clinical Trial Management System, CTMS). Performs QC...perform the job (comparable to 2+ years as traveling clinical research associate ). Valid driver's license where… more
- ThermoFisher Scientific (Alachua, FL)
- …research portfolio, our work spans laboratory, digital and decentralized clinical trial services. Your determination to deliver quality and accuracy will ... to ensure the acceptability of qualified investigative sites. Initiates clinical trial sites according to the relevant...(comparable to **10 Months - 2 years as traveling clinical research associate ** ). Valid driver's license… more
- Abbott (Des Plaines, IL)
- …working mothers, female executives, and scientists. **The Opportunity** This position of **Senior Associate Clinical Quality ,** works out of our **Lake ... teams in order to eliminate compliance risks; and Represents Clinical Quality at project / protocol deviation... Quality role in medical device area and/or clinical trial environment. + Prefer GCP audit… more
- Taiho Oncology (Princeton, NJ)
- …sciences is preferred. Knowledge, Skills, and Abilities: + 2 years of relevant clinical trial support or site management experience in the pharmaceutical, ... studies and alignment with internal TMF procedures. + Monitors Trial Master File related KPIs and performs quality...to multi-task and effectively prioritize in order to ensure clinical trial goals. + Recognize potential obstacles… more
- Grifols Shared Services North America, Inc (Research Triangle Park, NC)
- …Oversees the clinical feasibility assessment, strategic planning, and operations of clinical trial programs or studies. Executes on these global programs or ... services in more than 110 countries and regions. The Associate Director of Clinical Operations serves as...Supplies to ensure timely manufacturing, packaging, labeling, shipping of clinical trial supplies for which the incumbent… more
