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Clinical Trial Associates Or Senior Clinical Trial Associate

Clinical Trial Associates Or Senior Clinical Trial Associate
Empresa:

Precision Medicine Group


Detalles de la oferta

Clinical Trial Associates or Senior Clinical Trial Associates - CRO - Oncology REMOTE Precision for Medicine is a precision medicine CRO. Our uniquely integrated offering enables the science of precision medicine by combining novel clinical trial designs, industry-leading operational and medical authorities, advanced biomarker and data analytics solutions, and an unequivocal real passion for rare diseases and oncology.
We offer opportunities for both CTAs and Senior CTAs who will be providing administrative support to project teams in clinical operations. You will support several clinical programs and participate on a number of project teams as a valued member of the Project Team contributing towards efficient management of trials. Senior level CTAs serve as Subject Matter Experts with a focus on mentoring and training.
About You:
You are calm, thoughtful, and responsive when things don’t go as planned.
You are well-prepared, whether it be for an investigator meeting, site visit or project team update, always staying two steps ahead of the game.
You find quick and creative ways of overcoming difficulties.
You have an impeccable eye for detail.
You identify potential study risks and know how to mitigate them.
You are adept at handling conflict by using tried and true resolution strategies.
You are ambitious, collaborative, agile, and a standout colleague.
How we will keep you busy and support your growth:
Handling inventory, tracking, and shipping for clinical trials supplies (consisting of CRFs, study drug where applicable, and other supplies)
Assisting with preparation and shipment of Operating Manuals
Developing and maintaining the study specific investigator database for use with correspondence and mail merges
Updating and maintaining study tracking including a master team contact list
Preparing and distributing initial site start up packages and liaises with the sites to obtain required regulatory documents
Assisting team leaders in the production of study reports and updates
Serving as an office based point of contact for all sites during the course of the study as well as provides phone coverage for travelling team members
Preparing investigator budget payments and distributing to sites
Serving as administrator of the Trial Master File with direction from Project Management, including the preparation, maintenance, and archiving of the TMF
Identifying and processing Serious Adverse Events according to the procedures defined by the study team
Assisting with study start-up of clinical trials, including feasibility, investigator recruitment, collection of regulatory documents and general site management support
Qualifications:
UK GCSE or equivalent local level qualifications
Other Required :
Experience in a Clinical Trial Administration role or related discipline; CTAs will have 1-3 years and Sr. CTAs will have 3-5 years of experience
Working knowledge of ICH-GCP, SOPs, and regulatory guidance including a good knowledge of the regulatory and safety processes
Limited travel may be required for this position
Preferred :
CRO experience
About Precision for Medicine
Precision medicine is revolutionizing the attack on cancer—and we are passionate about helping our clients harness its power. We strike tumors on a molecular level using biomarkers to link specific mutations to specific treatments. We combine deep science with deep data from advanced technological platforms, then layer on specialized expertise in the design and execution of targeted, adaptive clinical trials. Ultimately, we deliver robust insights that inform real-time decisions—and optimize the oncology development pathway.
Any data provided as a part of this application will be stored in accordance with our Privacy Policy .
If you are an individual with a disability and require a reasonable accommodation to complete any part of the application process, or are limited in the ability or unable to access or use this online application process and need an alternative method for applying, you may contact Precision Medicine Group at ********** .
Are you authorized to work lawfully in the country/location for which you are applying? *
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Will you now or in the future require Precision Medicine Group to commence (sponsor) an immigration case in order to employ you (for example, work visa application or work visa transfer, or other-employment based immigration case)? This is sometimes called "sponsorship" for an employment-based visa status. *
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If sponsorship is required, confirm your current visa type:

Have you ever worked for Precision Medicine Group or one of its affiliated companies? *
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Have you ever interviewed with Precision Medicine Group or an affiliated company? *
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I certify that the information on this application, my resume and any supporting documentation I provide is complete and accurate to the best of my knowledge.If this application leads to employment, I understand that false or misleading information in my application, resume or interview may result in my release or termination of employment.I authorize the Company or its agents to confirm all statements contained in this application and/or resumes as it relates to the position I am seeking and to the extent permitted by federal, state, or local law. I agree to complete any required authorization forms for the background investigation.I authorize and consent to, without reservation, any party or agency contracted by this employer to furnish the above-mentioned information. I hereby release, discharge, and hold harmless, to the extent permitted by federal, state, and local law, any party delivering information to the Company or its duly authorized representative pursuant to this authorization from any liability, claims, charges or causes of action which I may have as a result of the delivery or disclosure of the above requested information and all other persons, corporations, or organizations furnishing such information.If hired I understand that I will be required to provide genuine documentation establishing my identity and eligibility to be legally employed in the United States. I also understand that the Company employs only individuals who are legally eligible to work in the United States.This application will remain active for 60 days. Any applicant wishing to be considered for employment after that time must reapply.UNDER MARYLAND LAW, AN EMPLOYER MAY NOT REQUIRE OR DEMAND, AS A CONDITION OF EMPLOYMENT, PROSPECTIVE EMPLOYMENT, OR CONTINUED EMPLOYMENT, THAT AN INDIVIDUAL SUBMIT TO OR TAKE A LIE DETECTOR OR SIMILAR TEST. AN EMPLOYER WHO VIOLATES THIS LAW IS GUILTY OF A MISDEMEANOR AND SUBJECT TO A FINE NOT EXCEEDING $100. *
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Precision Medicine Group has my consent to collect, store, and process my data for the purpose of considering me for employment, and for up to 1825 days thereafter. *

Requisitos


Conocimientos:
Clinical Trial Associates Or Senior Clinical Trial Associate
Empresa:

Precision Medicine Group


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