Associate Clinical Lead (m/w/d) - part time - sponsor dedicated

IQVIA™ is the leading human data science company focused on helping healthcare clients find unparalleled insights and better solutions for patients. Formed through the merger of IMS Health and Quintiles, IQVIA offers a broad range of solutions that harness the power of healthcare data, domain expertise, transformative technology, and advanced analytics to drive healthcare forward.

We are currently hiring an Associate Clinical Lead (m/w/d)in part time 32h/week for our sponsor dedicated department to work office-based in Frankfurt orhome-based in Germany.  

Clinical FSP Business:

IQVIA™ clinical FSP (=Functional Service Partnerships) business is unique.  Our teams are dedicated to a single sponsor partner, where the common goal is quality delivery for our clients.  We set ourselves apart with collaboration and face to face contact both at start up and during the clinical study.

Leadership recognises the skills, talent and experience of our clinical teams and strives to build upon this as the function evolves and grows.   Our managers understand the sponsors priorities and the individual aspects of each model.  Focus is given to career development from day one, including new hire orientation and onboarding, day to day problem solving and training and development.

Unique to the FSP model, our team contributes to the pipelines of the specific sponsor and therefore our CRAs are ‘indication and molecule experts’.  Additionally, IQVIA’s FSP business works with the Sponsors SOP’s, creating more continuity for both parties.

What we Offer:

Excellent salary and benefits package

Flexible working hours in a home-based role

We invest in keeping our teams stable, so workload is consistent

We offer genuine career development opportunities for those who want to grow as part of the organisation

We give the chance to work on cutting edge medicines, right at the forefront of new medicine development

Responsibilities:

• Ensure clinical delivery of assigned projects in compliance with regulatory requirements (International Conference on Harmonization (ICH)-Good Clinical Practice (GCP), protocol), customer requirements (contract), and internal requirements (policies, Standard Operating Procedures (SOPs), project plans).
• Accountable for meeting projects’ recruitment targets and ensuring appropriate recruitment strategies are in place.
• Contribute to the development of the project risk mitigation plan and manage clinical risks throughout the project’s lifecycle.
• Ensure clinical quality delivery by identifying quality standards/requirements, planning how compliance will be measured, monitoring and overseeing management of clinical quality issues.
• Manage clinical aspects of Project Finances including Estimate at Completion (EAC). Understand the scope of clinical delivery and create plans to deliver. Monitor and manage changes against baseline Estimate at Completion (EAC) and identify additional service opportunities or out of scope work.
• Identify clinical stakeholder landscape for the project and manage both internal and external stakeholders through effective communication and resolution management.
• Collaborate with the clinical team to support milestone achievements. Report to internal and external stakeholders as per project scope requirements.
• Resourcing and Talent Planning of the clinical team. Manage the clinical team at project level to successfully deliver the project through the establishment of high-quality operational plans and guidance and project related trainings.
• Conduct regular team meetings and communicate appropriately to achieve objectives.
• Support professional development by providing feedback to clinical team line managers on performance relative to project tasks.

  Become part of our team.

  We believe in hiring the best talent in the industry.

  To become part of our team, you should:

• Have a degree in Life Sciences or have equivalent education and experience.
• Hold at least 2-3 years of relevant Clinical Lead experience, including experience in EC / CA submissions
• Have in depth GCP knowledge as well as a broad protocol and therapeutic knowledge including Multiple Sclerosis
• Bring a solid understanding of project finances
• Possess strong communication skills, fluency in German and in English language is a must
• Be able to establish and maintain effective working relationships with coworkers, managers and clients.
• Show excellent computer skills including proficiency in use of Microsoft Word, Excel and PowerPoint
• Have excellent organizational and problem-solving skills and effective time management skills and ability to manage competing priorities

  Whatever your career goals, we are here to ensure you get there!

  We invite you to join IQVIA™.

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Join Us

Making a positive impact on human health takes insight, curiosity, and intellectual courage. It takes brave minds, pushing the boundaries to transform healthcare. Regardless of your role, you will have the opportunity to play an important part in helping our clients drive healthcare forward and ultimately improve outcomes for patients.

Forge a career with greater purpose, make an impact, and never stop learning.