Global Site Contract Manager

IQVIA; Buenos Aires; On-site; ARS 1,000,000 - 1,800,000; Full time

Job summary

IQVIA seeks a Global Investigator Contract Manager to lead complex investigator grant estimates, contracting strategies, and coordination of investigator grants for multi-protocol studies. You will create templates, systems, and training, while collaborating with sponsors and RSU teams to ensure compliant, timely delivery and study initiation.

You will provide legal, operational, and financial contracting support, leveraging experience in GCP/ICH and regulatory guidelines to navigate a global

Qualifications

• Bachelor’s Degree in Life Science or related field.
• 5 years’ sponsor or clinical research organization contracting experience.
• Strong negotiating and communication skills.
• Ability to coordinate across complex projects.
• Excellent legal, financial and/or technical writing skills.
• GCP/ICH and regulatory guidelines knowledge.

Responsibilities

• Develop complex investigator grant estimates and contracting strategies.
• Coordinate investigator grants and proposal text for contracts.
• Develop templates, tools, processes, and training for contracting activities.
• Collaborate with sponsors, RSU regions and countries to deliver project scope.
• Provide specialist legal, operational, and financial contracting support.

Skills

Negotiation

Communication

Project coordination

Technical writing

Regulatory knowledge

Education

Bachelor’s Degree in Life Science or related field

Job description

Make an impact on patient health!IQVIA’s Global Site Activation Team of 2000 employees, drives best in class site and customer experience, with industry leading outcomes.We keep the patient at the forefront; ‘Always Impatient for the Patient’ and we excel in our collaboration with our external/internal customers.IQVIA’s Global Investigator Contracts Solutions team are a global network who manage the contract strategy and support delivery of all required start-up contracting activities for selected sponsors and for complex studies or multi-protocol programs as determined by the Sponsor’s requirements.

Job Overview

As a Global Investigator Contract Manager, you will be responsible for the development of complex investigator grant estimates, contracting strategies, coordination of investigator grants, as applicable and proposal text to support the proposal development process.You will also develop contract and budget templates and contracting systems, tools, processes, and training materials for selected sponsors and complex studies or multi-protocol programs according to the Scope of Work and Project Plan, within the agreed project strategy, as applicable to the position.Along with collaborating and communicating 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.Coupled with being able to 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 complex clinical trials, whilst ensuring compliance with regulatory requirements and local laws.You will create, publish and/or review core scientific, technical, and administrative documentation to support business development and enable study initiation and maintenance, as required. As well as assessing and reviewing the contracting landscape and contribute to the collection, interpretation, analysis, and dissemination of accurate contracting intelligence to support assigned studies and the wider company, as required.

Requirements

• Bachelor’s Degree in Life Science or related field
• 5 years’ relevant sponsor or clinical research organization, clinical site contracting experience, including demonstrable experience acting as an international contract expert
• Strong negotiating and communication skills with ability to challenge
• Ability to coordinate and collaborate across and within complex projects
• Excellent legal, financial and/or technical writing skills
• Thorough understanding of regulated clinical trial environment and knowledge of drug development process
• Knowledge and ability to apply GCP/ICH and applicable regulatory guidelines

Unleash your potential!

It takes passion to make the extraordinary possible for patients. Our culture of innovation and collaboration enables us to explore new possibilities and help improve health around the world.

When you join our diverse, global team, you’ll harness the power of unparalleled data, advanced analytics, cutting-edge technologies, and deep healthcare and scientific expertise to drive healthcare forward.

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.