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- (Senior) Clinical Research Coordinator (80-100%)
- Patient-Centric Supply Chain & Drug Storage Solutions
- How to Evaluate a Clinical Supply Chain Partner to Meet Your Vaccine Trial Needs
- Senior Scientific Expert Polymer Development (m/f/d) - limited for 12 months
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- UPS HEALTHCARE CONTINUES INVESTMENT IN PERSONALIZED MEDICINE
Remember the dash must have a space before it, but none before the term you want to filter out. About BioIntelliSense BioIntelliSense is ushering in a new era of continuous health monitoring and clinical intelligence for Remote Patient Monitoring and Screening (COVID-19/Infection). To verify your email address and activate your job alert.
Save this job with your existing LinkedIn profile, or create a new one. Seeking a Social Science Research Professional/Research Program Coordinator for a research group at the University focused on clinical, translational and epidemiologic studies of infectious diseases. Overview CommonSpirit Health was formed by the alignment of Catholic Health Initiatives and Dignity Health. With more than 700 care sites across the U.S. from clinics and hospitals to home-ba... Our client, a world-leading Pharmaceutical Company in Peapack, NJ is currently looking for a Sourcing Specialist / Clinical Trial Vendors / REMOTE WORK to join their expanding team.
(Senior) Clinical Research Coordinator (80-100%)
As Manager of Clinical Systems , you will get the opportunity to work with the industry's largest vendors, build your knowledge of eCOA, and be part of project teams delivering some of the largest and most important clinical trials in the industry. Work in multiple therapeutic areas to ensure compliance, data quality, monitor patient recruitment, and more. Must have a bachelor's degree and five years of direct experience. Work closely with clinical leadership to define KPIs that measure team performance and capacity. You will also work closely with teams across the company that support clinical operations. At least 2 years of experience in a quantitative role in...
If lead, accountable for the clinical/scientific execution of the protocol. BS/BA in Life Sciences with 7+ yrs clinical research experience. In.indeed.com needs to review the security of your connection before proceeding.
Patient-Centric Supply Chain & Drug Storage Solutions
Assist with the tracking and management of Case Report Forms , queries and clinical data flow. Assist the clinical team with the preparation, handling, distribution, filing, and archiving of clinical documentation and reports according to the scope of work and standard operating procedures. If so, please click "Applied for Job" to save it to your "Application History" page. If not, click on "Did Not Apply" to return to the job post.
Discover Your Career at Emory University Emory University is a leading research university that fosters excellence and attracts world-class talent to innovate today and prepare leaders for the futu... Uk.indeed.com needs to review the security of your connection before proceeding. Ongoing development is vital to us enabling you to have the opportunity to progress your career, with the potential to move into other related areas to enhance your skill set. Our benefits package is competitive, our scope is international, and we genuinely care about our people and their success. Save time and find higher-quality jobs than on other sites, guaranteed.
How to Evaluate a Clinical Supply Chain Partner to Meet Your Vaccine Trial Needs
The CTM oversees the clinical portion of the budget, develops monitoring plans & tools, trains CRAs, drives enrolment and study start-up activities... Produce and distribute status, tracking and financial reports for internal and external team members and senior management. 5 years of related experience or equivalent combination of education... This individual will be responsible for providing coordination and administrative support for a clinical research trial run within the Real-World Evidence Division.
Assist in the organization, implementation and completion of clinical research studies in compliance with all applicable laws and regulations, institutional/ departmental guidelines, standards of Good clinical Practice , and within budget. Facilitate clinical evidence reviews with cross functional team to align on clinical evidence strategies, document / track decisions and risks, and write PMCF Plans. Support development and drafting of clinical study protocols, registry plans... At TE, you will unleash your potential working with people from diverse backgrounds and industries to create a safer, sustainable and more connected world. Au.indeed.com needs to review the security of your connection before proceeding. CLINICAL TRIAL ASSISTANT II At TE, you will unleash your potential working with people from diverse backgrounds and industries to create a safer, sustainable and more connected world.
Senior Scientific Expert Polymer Development (m/f/d) - limited for 12 months
We recommend you enter a location since many remote jobs have city, state or country requirements. Holden Comprehensive Cancer Center is seeking a Clinical Research Specialist. To coordinate clinical study activities of the Clinical Trials Support Core ; participate in the design, executio... Clinical point of contact for scientific issues/questions for internal and external stakeholders (e.g., IRB, sites). Sets up/supports SAC, DMC, and adjudication committees.
Lead business development opportunities - identify and generate new project opportunities, clarify customers challenges and needs, be able to develop a compelling, differentiated proposal to solve these issues, and win new work. How to Apply A cover letter is required for consideration for this position and should be attached as the first page of your resume. The cover letter should address your specific interest in the po... Job Description Data Entry Administrative Assistant - Online Remote Work At Home Position (Part Time / Full Time) - Be Part of Our Focus Group Panel Now! School of Medicine Established in 1930, Duke University School of Medicine is the youngest of the nation's top medical schools.
You will also have the opportunity to train and mentor junior staff members. Is responsible for overall conduct of clinical studies in support of Veterinary Medicine Research & Development companion animal research and development projects i.e., budgeting, investigator/site selection, protocol development/writing... Storage and Distribution Global GMP Depot Network Our expansive network supports the regional requirements of worldwide clinical trials. Responsible for the execution and adaptation of clinical data management plans and processes for collection, management, reporting and analysis of data on behalf of project teams and sponsors. Collaborate with multi-functional project teams and...
Accountable for the end-to-end performance and project management for assigned protocols in a country in compliance with ICH/GCP and country regulations, quality standards, and adverse event reporting requirements internally and externally. All Transport Options, One Logistics Provider Marken has the flexibility to design the best supply chain solution for every customer, ensuring your clinical trial materials are delivered with the utmost care and efficiency. The Clinical Trial Leader provides clinical trial oversight to the assigned clinical trial ensuring deliverables are met in terms of quality, compliance and timing. Strong external vendor and CRO management skills are critical for this role and this... Senior CRAs handle appropriately sized clinical trials, and support Project Managers with trials that are larger in scope.
You will be involved in data management, creation of study related documents and correspondence with internal departments, research sites and our client. Complete onsite and remote monitoring activities in accordance with ICH-GCP guidelines, applicable regulations, SOPs, and study processes. Activities include qualifying potential investigative sites, initiating clinical trials, maintaining study files. Duties include leading the clinical elements of trials & coordinating staff activities. Must have at least 18 months' experience leading clinical trial operations. A nursing qualification, life science degree, or related exp. is required.
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