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IQVIA
IQVIA

Focused on health information technology and clinical research.

Global Site Contracts Manager at IQVIA

RoleLegal
LevelManager
LocationBarcelona
WorkHybrid
TypeFull-time
Posted1 day ago
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About the role

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.

At IQVIA, we believe that diversity, inclusion, and belonging empower our mission to accelerate innovation for a healthier world. We create a culture of belonging by valuing the perspectives of all talented employees worldwide and providing them with the opportunity to power smarter healthcare for everyone, everywhere. When our talented employees bring their authentic selves and their diverse experiences to work, they enable us to accomplish extraordinary things. Multifaceted thought processes spark innovation. Multi-talented collaboration harnesses innovation to deliver superior outcomes. Likewise, as part of this culture, IQVIA is committed to ensuring effective equality between women and men, integrating it as a strategic principle in its corporate and human resources policies.

Required skills

Contract management

Investigator grants

Budget planning

Sponsor communication

Process development

Clinical study start-up

Cross-regional coordination

Proposal support

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About IQVIA

IQVIA

IQVIA

Public

IQVIA Holdings, Inc. is an American company based in Durham, North Carolina, focused on health information technology and clinical research.

10,001+

Employees

Durham

Headquarters

$17B

Valuation

Reviews

10 reviews

3.9

10 reviews

Work-life balance

3.2

Compensation

3.8

Culture

4.2

Career

3.5

Management

3.8

72%

Recommend to a friend

Pros

Supportive management and colleagues

Flexible work arrangements and remote options

Great company culture and team environment

Cons

Heavy workload and long hours

High pressure and stress

Limited upward mobility

Salary Ranges

46 data points

Mid/L4

Mid/L4 · ANALYST

2 reports

$97,500

total per year

Base

$102,667

Stock

-

Bonus

-

$97,500

$97,500

Interview experience

3 interviews

Difficulty

2.7

/ 5

Duration

14-28 weeks

Experience

Positive 0%

Neutral 67%

Negative 33%

Interview process

1

Application Review

2

HR Screen

3

Behavioral Interview

4

Case Interview/Technical Interview

5

GM/Final Interview

6

Offer

Common questions

Behavioral/STAR

Case Study

Technical Knowledge

Past Experience