At a Glance
- Tasks: Manage complex contracts and budgets for clinical trials, ensuring compliance and collaboration.
- Company: Join IQVIA, a leader in clinical research and healthcare intelligence.
- Benefits: Competitive salary, diverse team, and opportunities for professional growth.
- Other info: Dynamic work environment with a focus on innovation and collaboration.
- Why this job: Make a real impact on patient health while working with cutting-edge technologies.
- Qualifications: Bachelor’s degree in Life Science and 5 years of relevant experience required.
The predicted salary is between 40507 - 49509 £ per year.
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.
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.
- Developing 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.
- 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.
- Providing 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.
- Creating, publishing and/or reviewing core scientific, technical, and administrative documentation to support business development and enable study initiation and maintenance, as required.
- Assessing and reviewing the contracting landscape and contributing 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
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.
Location: London, United Kingdom; Lisbon, Portugal; Zagreb, Croatia; Athens, Greece; Belgrade, Serbia; Prague, Czech Republic; Sofia, Bulgaria; Bratislava, Slovakia; Madrid, Spain; Bucuresti, Romania
Type: Full time
Global Site Contract Manager employer: IQVIA
IQVIA in Livingston, Scotland is an excellent employer that fosters a collaborative team environment and prioritises employee growth through outstanding career development opportunities. Working as a Lab Operations Assistant here not only allows you to contribute to meaningful projects but also ensures you are part of a supportive workplace that values safety and professionalism.
