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Clinical Data Manager
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Clinical Data Manager
vor 1 Tag
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Clinical Research Manager
vor 3 Wochen
Frankfurt am Main, Hessen, Deutschland IQVIA VollzeitJob SummaryIQVIA is seeking a highly skilled Clinical Research Manager to join our team in Germany. As a key member of our Clinical Functional Service Partnerships (Clinical FSP) department, you will play a critical role in supporting our client's project team in the execution of clinical trials.Key ResponsibilitiesEnsure that all services rendered adhere to...
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Clinical Research Manager
vor 3 Wochen
Frankfurt am Main, Hessen, Deutschland IQVIA VollzeitJob SummaryIQVIA is seeking a highly skilled Clinical Research Manager to join our team in Germany. As a key member of our Clinical Functional Service Partnerships (Clinical FSP) department, you will play a critical role in supporting our client's project team in the execution of clinical trials.Key ResponsibilitiesEnsure that all services rendered adhere to...
Clinical Project Manager
vor 3 Monaten
The IQVIA sponsor-dedicated Clinical Functional Service Partnerships (Clinical FSP) department is supporting our client's project team in the execution of clinical trials.
We currently offer the exciting opportunity to join the team as Clinical Project Manager (m/w/d) in full-time and work home-based throughout Germany , preferrable in the Munich/Bavaria area .
In this role you will be accountable for the operational management of the component of a clinical trial. Furthermore, you will need to gain an oversight to assures achievement of trial recruitment commitment, timelines, budget and quality standards.
Responsibilities might include:
- Manage the execution of clinical studies or assigned portion of clinical studies; including orchestration of local trial team, and integration with other functions as necessary throughout planning, conduct and closeout of trial.
- Ensure compliance with ICH-GCP and all other relevant regulatory regulations as well as accordance with client SOPs and values.
- Collaborate with other functional groups within the company where necessary to support milestone achievement and to manage study issues and obstacles.
- Monitor progress against contract and prepare/present project information proactively to stakeholders internally and externally.
- Achieve project quality by identifying quality risks and issues, responding to issues raised by project team and/or sub-team members and planning/implementing appropriate corrective and preventative action plans.
- Build the cross-functional project team and lead their efforts; responsible for managing cross-collaboration of the core team and for overall project delivery to support milestone achievement and to manage study issues and obstacles.
- Ensure the financial success of the project, while optimizing speed, quality and cost of delivery. Forecast and identify opportunities to accelerate activities to bring revenue forward.
- Participate in bid defense presentations in partnership with Business Development.
- May be assigned as the primary contact for vendors leading project vendor management and vendor management related activities as per project requirements.
- Adopt corporate initiatives and changes and serve as a change advocate when necessary.
Required knowledge, skills and experience:
- Bachelor's or higher-level degree preferable in life science.
- 5 years of prior relevant experience including project management experience or equivalent combination of education, training and experience.
- Expertise in covering clinical trials in phase Ib-III and in the therapeutic areas oncology and/or hematology .
- Knowledge of applicable clinical research regulatory requirements, i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines.
- Fluent languages skills in German on at least C1 level and good command of English .
- Computer skills including working knowledge of Microsoft Word, Excel and PowerPoint.
- Effective communication, organizational and planning skills.
- Planning, time management and prioritization skills while working on multiple projects.
- Excellent leadership skills, and the ability to establish and maintain effective working relationships with coworkers, managers and clients.
- Flexibility to business travel for client meetings and maybe occasional site visits.
We invite you to join IQVIA.
Why join us?
Ongoing development is vital to us enabling you to have the opportunity to progress your career, with the potential to move into other related areas to enhance your skill set. Our benefits package is competitive, our scope is international, and we genuinely care about our people and their success.
Whatever your career goals, we are here to ensure you get there
Please apply with your English CV, motivation letter and your certificates and reference letters.
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IQVIA is a leading global provider of advanced analytics, technology solutions and clinical research services to the life sciences industry. We believe in pushing the boundaries of human science and data science to make the biggest impact possible – to help our customers create a healthier world. Learn more at
IQVIA is a world leader in using data, technology, advanced analytics, and expertise to help customers drive healthcare – and human health – forward. Together with the companies we serve, we are enabling a more modern, more effective and more efficient healthcare system, and creating breakthrough solutions that transform business and patient outcomes.
To get there, it takes diverse skills and a curiosity to explore new possibilities. No matter your role, everyone at IQVIA, including our colleagues at Q2 Solutions, contributes to our shared goal of improving human health. Thank you for your interest in growing your career with us.
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