Essential Functions Develop Coordinate the development of investigator grants and estimates, contracting strategies and proposal text to support the proposal development process.Develop contract language, payment languag…
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Full-time
bachelor degree
Posted 2d ago
~40 hrs/week
Responsibilities
Develop and coordinate investigator grants, contracting strategies, and budget templates to support clinical trial proposals. Provide legal and financial contracting support to study teams to ensure efficient site agreements and regulatory compliance.
Requirements
Requires a Bachelor's degree or 5 years of relevant clinical site contracting experience within a sponsor or CRO. Must be fluent in English and the local language with strong negotiation and legal writing skills.
Full job description
Essential Functions
Develop Coordinate the development of investigator grants and estimates, contracting strategies and proposal text to support the proposal development process.
Develop contract language, payment language and budget templates as required as applicable to the position
Utilize and maintain contracting systems, tools, processes, and training materials for selected sponsors, studies or multi-protocol programs according to the Scope of Work and Project Plan, within the agreed project strategy.
Ensure collaboration, including communication with sponsors, stakeholders and RSU regions and countries as applicable to the position, to successfully deliver the agreed project scope in compliance with sponsor requirements and/or the RSU Management Plan.
Provide specialist legal, operational and financial contracting support to the Study Teams, as applicable to site agreements to facilitate efficient business development and initiation and maintenance of clinical trials, whilst enabling compliance with regulatory requirements.
Ensure overall contracting efficiency and adherence to project timelines and financial goals as applicable to site agreements
Report contracting performance metrics and out of scope contracting activities as required.
Work with Quality Management to ensure appropriate contract management and quality standards. Mentor and coach colleagues as required including the delivery of training materials as required.
Qualifications
Bachelor's Degree Related field OR 5-year relevant sponsor or clinical research organization clinical site contracting experience
Good negotiating and communication skills with ability to challenge.
Strong understanding of regulated clinical trial environment and knowledge of drug development process.
Good understanding of clinical trial contract management.
Fluent in English and local language
IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com
IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.
IQVIA (NYSE:IQV) is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. IQVIA’s portfolio of solutions are powered by IQVIA Connected Intelligence™ to deliver actionable insights and services built on high-quality health data, Healthcare-grade AI™, advanced analytics, the latest technologies and extensive domain expertise. With approximately 88,000 employees in over 100 countries, including experts in healthcare, life sciences, data science, technology and operational excellence, IQVIA is dedicated to accelerating the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide.
IQVIA is a global leader in protecting individual patient privacy. The company uses a wide variety of privacy-enhancing technologies and safeguards to protect individual privacy while generating and analyzing information on a scale that helps healthcare stakeholders identify disease patterns and correlate with the precise treatment path and therapy needed for better outcomes. IQVIA’s insights and execution capabilities help biotech, medical device and pharmaceutical companies, medical researchers, government agencies, payers and other healthcare stakeholders tap into a deeper understanding of diseases, human behaviors and scientific progress, in an effort to advance healthcare. To learn more, visit www.iqvia.com.
Offices: 2400 Ellis Rd, Durham, North Carolina 27703, US
How many Science & Research jobs are open in Prague, Czechia right now?
There are currently 54 open science & research positions in Prague, Czechia listed on Clera. New openings are added daily as companies post roles.
Which companies are hiring for Science & Research roles in Prague, Czechia?
Companies currently hiring include Accenture, Sobi - Swedish Orphan Biovitrum AB (publ), VIVO Defence Services, Anyone App, MSD, among others. Browse the listings above to see every active employer.
Are there remote or hybrid Science & Research jobs in Prague, Czechia?
Yes — 24 of the 54 open science & research positions offer remote or hybrid work (6 remote, 18 hybrid).
How do I apply for Science & Research jobs in Prague, Czechia?
Each listing links directly to the employer's application page. Apply early — fresh listings get the most recruiter attention in the first two weeks.