Clinical Project Manager
vor 3 Wochen
The Clinical Functional Service Partnerships (Clinical FSP) department at Pharmiweb is supporting our client's project team in the execution of clinical trials. We are seeking a skilled Local Trial Manager to join our Clinical Project Management team in a full-time, home-based position throughout Germany.
In this role, you will be accountable for the operational management of the component of a clinical trial, ensuring achievement of trial recruitment commitment, timelines, budget, and quality standards. Your responsibilities will include:
- Managing 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.
- Ensuring compliance with ICH-GCP and all other relevant regulatory regulations, as well as accordance with client SOPs and values.
- Collaborating with other functional groups within the company to support milestone achievement and to manage study issues and obstacles.
- Monitoring progress against contract and preparing/presenting project information proactively to stakeholders internally and externally.
- Achieving 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.
- Building the cross-functional project team and leading 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.
- Ensuring the financial success of the project, while optimizing speed, quality, and cost of delivery. Forecasting and identifying opportunities to accelerate activities to bring revenue forward.
- Participating 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.
- Adopting corporate initiatives and changes and serving as a change advocate when necessary.
Requirements:
- 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 the project management of clinical trials in different study phases and preferable in the therapeutic area oncology.
- Knowledge of applicable clinical research regulatory requirements, i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines.
- Fluent language 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 occasional business travel for client meetings.
Why Pharmiweb?
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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