Site Contract Analyst IQVIA Biotech

Warsaw - Poland

Monthly Salary: Not Disclosed

Posted on: 14 hours ago

Vacancies: 1 Vacancy

Job Summary

Job Overview

Support the delivery of all required start-up contracting activities for selected sponsors studies or multi-protocol programs as determined by either the agreed algorithm or the Sponsors requirements including pre-award activities.

Essential Functions

Develop simple investigator grant estimates and proposal text to support the proposal development process.
Utilize and maintain contract and budget templates and 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 to successfully deliver the agreed project scope in compliance with sponsor requirements and/or the RSU Management Plan.
Provide specialist operational and financial contracting support to facilitate efficient business development and initiation and maintenance of clinical trials whilst enabling compliance with regulatory requirements.
Assist in the creation and/or review of core scientific technical and administrative documentation to support business development and enable study initiation and maintenance as required.
Contribute to the collection interpretation analysis and dissemination of accurate contracting intelligence to support assigned studies and the wider company as required.
Ensure overall contracting efficiency and adherence to project timelines and financial goals; report contracting performance metrics and out of scope contracting activities as required.
Comply with contract management and quality standards. Provide administrative and operational support to investigator site contract analysts managers and directors as required.
Ensure accurate completion and maintenance of internal systems (with emphasis on CTMS) databases tracking tools timelines and project plans.

Qualifications and Skills

Bachelors Degree in life sciences or health care
2 years relevant experience including demonstrable experience acting as a contract negotiator.
Relevant sponsor or clinical research organization clinical site contracting experience.
Good negotiating and communication skills.
Good interpersonal skills and a strong team player.
Strong technical writing skills.
Understanding of regulated clinical trial environment and knowledge of drug development process.
Knowledge and ability to apply GCP/ICH and applicable regulatory guidelines.
Knowledge of applicable regulatory requirements SOPs and companys Corporate Standards.
Good organizational and planning skills.
Strong knowledge of Microsoft Office and e-mail applications.
Ability to interpret pricing models and to prepare proposals bid grids and budgets.
Good understanding of clinical trial contract management.
Ability to establish and maintain effective working relationships with co-workers managers and sponsors.

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

Required Experience:

Job OverviewSupport the delivery of all required start-up contracting activities for selected sponsors studies or multi-protocol programs as determined by either the agreed algorithm or the Sponsors requirements including pre-award activities.Essential FunctionsDevelop simple investigator grant esti...

Job Overview

Essential Functions

Develop simple investigator grant estimates and proposal text to support the proposal development process.
Utilize and maintain contract and budget templates and 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 to successfully deliver the agreed project scope in compliance with sponsor requirements and/or the RSU Management Plan.
Provide specialist operational and financial contracting support to facilitate efficient business development and initiation and maintenance of clinical trials whilst enabling compliance with regulatory requirements.
Assist in the creation and/or review of core scientific technical and administrative documentation to support business development and enable study initiation and maintenance as required.
Contribute to the collection interpretation analysis and dissemination of accurate contracting intelligence to support assigned studies and the wider company as required.
Ensure overall contracting efficiency and adherence to project timelines and financial goals; report contracting performance metrics and out of scope contracting activities as required.
Comply with contract management and quality standards. Provide administrative and operational support to investigator site contract analysts managers and directors as required.
Ensure accurate completion and maintenance of internal systems (with emphasis on CTMS) databases tracking tools timelines and project plans.

Qualifications and Skills

Bachelors Degree in life sciences or health care
2 years relevant experience including demonstrable experience acting as a contract negotiator.
Relevant sponsor or clinical research organization clinical site contracting experience.
Good negotiating and communication skills.
Good interpersonal skills and a strong team player.
Strong technical writing skills.
Understanding of regulated clinical trial environment and knowledge of drug development process.
Knowledge and ability to apply GCP/ICH and applicable regulatory guidelines.
Knowledge of applicable regulatory requirements SOPs and companys Corporate Standards.
Good organizational and planning skills.
Strong knowledge of Microsoft Office and e-mail applications.
Ability to interpret pricing models and to prepare proposals bid grids and budgets.
Good understanding of clinical trial contract management.
Ability to establish and maintain effective working relationships with co-workers managers and sponsors.

Required Experience:

Key Skills

IVR
SOAP
Avaya
Solaris
Cost Accounting Standards
Database Design
Hibernate
ITIL
Weblogic
Express.js
Contracts
ASP

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About Company

IQVIA

IQVIA is the Human Data Science Company™. We are inspired by the industry we serve and provide solutions that enable life sciences companies to innovate with confidence, maximize opportunities and ultimately drive human health outcomes forward. Our approach is Human Data Science – a d ... View more

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