Table of Content
- Marken Overcomes Multiple Obstacles To Successfully Deliver Critical Stem Cell Samples Across The Globe
- Clinical Trial Manager (m/w/d) – Sponsor-Dedicated, Home-Office
- Seniority level
- (Senior) Clinical Research Associate - (m/w/d) (Germany, Home-based) - IQVIA MedTech, Cardiovascular, Medical Devices
- Utilization of Customs Warehouses in the Clinical Trial Supply Chain
- Clinical Science Associate (m/w/d)
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.
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.
Marken Overcomes Multiple Obstacles To Successfully Deliver Critical Stem Cell Samples Across The Globe
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.
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.
Clinical Trial Manager (m/w/d) – Sponsor-Dedicated, Home-Office
High School Diploma or GED and 2-5 yrs of experience. Works extensively with coverage analysis specialists, budget specialists, clinical research coordinators, principal investigators, various stakeholders of UW, the org, and SCCA, to assist with building of calendars in accordance with the protocol... Evaluate patients against specific genetic and clinical inclusion and exclusion criteria using various systems. Read and understand clinical trial protocols to identify high-fidelity patient matches for various cancer types in both oncology and...
You will monitor the progress of clinical studies at investigative sites or remotely, and ensure clinical trials are conducted, recorded, and reported in accordance with the protocol, standard operating procedures , ICH-GCP, and all applicable... Will monitor the progress of clinical studies at investigative sites or remotely, and ensure clinical trials are conducted, recorded, and reported in accordance with the protocol, standard operating procedures , ICH-GCP, and all applicable... Vaccine Trial Storage and Distribution Storage and distribution of clinical vaccine trials and treatments requires a single-source provider whose agility and tailored solutions set the highest quality standards. Cell and Gene Supply Chain Services Only Marken can seamlessly guide your cell and gene therapies through each stage of the pharmaceutical journey.
Seniority level
Track subject enrollment and identify R&R issues, maintain regular communication w/site staff. Document and communicate study site progress and issues/concerns to the project team. Assist other CRAs with study site issues/concerns/audits with the... E.g., manager -director means return search results for the term 'manager' but NOT when the term 'director' is present.
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...
Direct-to/From-Patient and Home Healthcare
Responsibilities include study planning, study start-up, study execution and study close-out.Delivers results that have direct impact on the successful completion of the study. Ensure overall site management while performing study related activities. The Clinical Research and Analytics role will have the critical responsibility of overseeing our efforts to measure and track the impact of Memora's care programs on delivering value to patients and care teams.
Clinical Drug Supply Chain Services We ensure the integrity of products during transport as it is a critical requirement of any client, and Marken is perfectly positioned to deliver your shipments safely and securely. Monitors the progress of clinical studies at investigative sites or remotely, ensuring clinical trials are conducted, recorded, and reported in accordance with the protocol, standard operating procedures, International Conference on Harmonization... You will monitor and own the progress of clinical studies at investigative sites and ensure that clinical studies are conducted, recorded, and reported per protocol, SOPs, ICH-GCP, and all applicable regulations and standards. The IQVIA Sponsor-Dedicated Clinical Trials Assistant Team is supporting the project teams in the execution of clinical trials. Joining the team provides the opportunity to work with the preparation and documentation of clinical research projects in different therapeutic areas.
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.
Assumes day-to-day accountability for the delivery of quality operations support for research studies and programs by managing the research team. Assumes accountability to measure and analyze key performance indicators/metrics for responsible clinical... May lead or support a study or studies, depending on size/complexity.
Evaluating pre-clinical and translational work for the purpose of generating early clinical development plans and Investigational New Drug applications. M.D or M.D./Ph.D from a recognized school of medicine required, preferably with demonstrated... Clinical Research Director will provide leadership to ensure all operations support quality patient care and clinical research and comply with all Command, federal, state, regulatory, Defense & Veterans Brain Injury Center & contractor... The Senior Trial Manager, Clinical Operations is responsible for conduct of global clinical studies. With minimal oversight, manages CRO and vendor performance to ensure that clinical studies are c... May accompany CRAs on site visits to assist with clinical monitoring duties upon completion of required training.
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.
Ranked sixth among medical schools in the nation, the School takes pr... Description Introduction The Clinical Trials Coverage Analyst is responsible for reviewing clinical research protocols, Informed Consent Forms, Clinical Trial Agreements, and other relevant study-r... We currently have the exciting opportunity to join the team as Clinical Trials Assistant (m/w/d) in full-time and work in our German headquarter in Frankfurt with the option to work from home partially.
Needs to review the security of your connection before proceeding. Collates materials for training and investigator meetings. Tracks site activation, enrolment and monitoring visits to projected plans, and escalate any issues or delays with site activation or deviations from monitoring plan. The Clinical Trial Manager is responsible for the delivery of all clinical aspects of the study.
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