Meditrial
Clinical Project Manager, MD
Berlin, Germany
Full time
Industry: Lifesciences Industry: Pharma, Medtech, Digital Health
Job Functions: Clinical Trial Management (from study approval to study close-out)
Work Location: Meditrial GmbH - Charlottenburg, Berlin
Requested Experience: Minimum 5 years experience in Healthcare, Biotech, Medtech
To learn more: www.meditrial.net
The Project Manager is responsible for setting up, coordinating and leading clinical trials with medicines, or medical devices, leading a clinical project team consisting of Clinical Trial Assistants (CTA), Clinical Start-up specialists, Clinical Research Associates (CRA) and Data Managers. The role also manages vendors such as central laboratories or clinical sites and monitor the progress of the clinical studies providing regular updates to internal and if applicable external stakeholders, such as the sponsor / client
The Project Manager is ultimately responsible for ensuring that projects are completed just in time within budget and with high level of quality and efficiency ensured by Meditrial standards.
Preferred Experience
Job Functions: Clinical Trial Management (from study approval to study close-out)
Work Location: Meditrial GmbH - Charlottenburg, Berlin
Requested Experience: Minimum 5 years experience in Healthcare, Biotech, Medtech
To learn more: www.meditrial.net
The Project Manager is responsible for setting up, coordinating and leading clinical trials with medicines, or medical devices, leading a clinical project team consisting of Clinical Trial Assistants (CTA), Clinical Start-up specialists, Clinical Research Associates (CRA) and Data Managers. The role also manages vendors such as central laboratories or clinical sites and monitor the progress of the clinical studies providing regular updates to internal and if applicable external stakeholders, such as the sponsor / client
The Project Manager is ultimately responsible for ensuring that projects are completed just in time within budget and with high level of quality and efficiency ensured by Meditrial standards.
Preferred Experience
- Over 5 + years of experience in clinical trial management medical device or drug
- Initiating and managing clinical projects in accordance with all relevant guidelines, legislation and SOPs;
- Monitoring the progress of the clinical trial in relation to the project plan and previously defined performance indicators in terms of quality and budget;
- Identify risks and develop and implement plans to mitigate risks in collaboration with team members and other stakeholders;
- Act as a daily point of contact for the sponsor and all members of the project team while conducting progress status updates;
- Reporting the progress to the internal project team, the internal and if applicable external stakeholders;
- Negotiating contracts with research centers and clinical budget;
Skillset
- Master’s degree in life science, healthcare management, preferred degrees include Medical Engineering, PharmD, MD, and/or PhD
- Excellent communication, negotiation and organizational skills;
- Language skills: fluent English and German are mandatory
- Previous Experience as a CRA is a plus
- Leadership skills;
- Knowledge of Good Clinical Practice (GCP)
How to apply
Meditrial
Meditrial is a leading provider of clinical trial services and digital cloud-based solutions for the lifesciences industry. As a Clinical Research Organization (CRO), Meditrial is renowned as the go-to partner by companies developing breakthrough innovations that require a clearly defined path to first-in-man and pivotal clinical studies. Established in 2008, today Meditrial is a trusted resource for large corporations as well as start-ups requiring support and resources to execute trials in the Uniteef States and Europe. Headquartered in Zürich, Meditrial has offices in Berlin, Rome, London and New York.
Learm more: www.meditrial.net - www.catchtrial.com - www.mastertrial.com
Despite the everchanging regulation and increasing difficulty to obtain approval for clinical investigations, Meditrial has a remarkable record of 100% success in assisting clients to execute studies in medical centers of excellence throughout Europe and United States. Meditrial's software solutions allow customers to successfully manage large global trials and registries while monitoring the results in large number of patients.
Meditrial’s core strength lies in its clinical experts’ proficiency, alongside with its integrated digital platform for elearning, data capture and analytics. The organization provides a set of systems and tools to minimize complexity of clinical trials and regulatory approvals Meditrial is extremely proud to be one of the first—and very few—CROs certified by ISO 9001, ISO 13485 and ISO 27001 for information security.
Learm more: www.meditrial.net - www.catchtrial.com - www.mastertrial.com
Despite the everchanging regulation and increasing difficulty to obtain approval for clinical investigations, Meditrial has a remarkable record of 100% success in assisting clients to execute studies in medical centers of excellence throughout Europe and United States. Meditrial's software solutions allow customers to successfully manage large global trials and registries while monitoring the results in large number of patients.
Meditrial’s core strength lies in its clinical experts’ proficiency, alongside with its integrated digital platform for elearning, data capture and analytics. The organization provides a set of systems and tools to minimize complexity of clinical trials and regulatory approvals Meditrial is extremely proud to be one of the first—and very few—CROs certified by ISO 9001, ISO 13485 and ISO 27001 for information security.
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