Eu - Clinical Project Manager (Cpm)

vor 3 Wochen

Wien, Österreich Celerion Vollzeit

One of our key assets and greatest resources is the experience and expertise of our employees.

**We are looking for a (Senior) Clinical Project Manager (M/F)**

**in Vienna, Austria**

The main aim of the (Senior) Clinical Project Manager (CPM) is the operational management of studies or projects managed by Celerion.

**Essential Functions**
- Perform operational management activities, from project/study start (pre-study phase) to project/study closure in a performance-oriented and timely manner within the budget
- Manage Study Teams within Celerion in the area of clinical trials, clinical investigations, and other interventional or non-interventional studies, in adherence to Good Clinical Practice, international standards, and regulatory requirements
- Responsible that milestones and timelines are met and services delivered
- Responsible for the performance of the project/study with regards to the quality standards of Celerion and/or Sponsors/Clients wherever applicable
- Responsible for the performance of the project with regards to budget adherence and resource allocation
- Occasional clinical on-site monitoring may be required

JOB REQUIREMENTS

Bachelor’s degree in a biomedical-related field, life sciences or equivalent field
- Minimum of 3 years prior experience in clinical research
- Experience as Clinical Research Associate (CRA) and Clinical Project Coordinator (CPC)
- Minimum of 1 year prior employment-related experience in project scheduling, managing resources and coordinating team activities
- Excellent oral and written communication skills in English
- Demonstrates high level of organization, multi-tasking, judgement and analytical skills
- Good time management skills to ensure adherence to timelines
- Profound knowledge of Good Clinical Practice, 21 CFR Part 11, and other relevant regulatory requirements
- Commitment to continuous training and knowledge sharing; proactively keeping up to date with procedural industry standards and international regulatory developments in clinical research
- Ability to work well independently and as part of a team
- Self-motivated
- Maintains confidentiality of project information
- Computer literate
- Possess adequate knowledge and experience to train, instruct and guide CPCs and CRAs
- Possess a broad knowledge of clinical research methodology
- Ability to represent Celerion at investigator meetings and monitor trainings
- Demonstrate effectiveness in team leadership; foster a team environment and facilitate the building of positive, productive relationships with clients and at all levels within Celerion

Position Location: Home Office and Office based in Vienna, Austria or Berlin, Germany

Contract: Full-time

Start: As soon as possible

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