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Clinical Trial Coordinator
Vor 4 Tagen
The clinical trial coordinator will support the Senior Project Leader in all aspects of interventional and non-interventional studies in cardiovascular and oncology (study start up, study conduct, study closure, study results delivery).
***Key responsibilities**:
- Responsible for the day-to-day logistics of assigned study related tasks. The main activities include administrative tasks in the field of study coordination
- Initiate trial team activities such as trial documentation management, milestone tracking and identification, resolution and escalation of issues
- Participation in regular study meetings, organize meetings and coordinating internal and extermal communication. Responsible for the preparation of meeting agendas and minutes
- Ensure that the supervision of CROs and other 3rd party vendors are in line with the oversight plan according to the SOPs
- Responsible for the management of the Trial Master File and the conduct the Sponsor Qualty Control of uploaded documents in the TMF and update of trial related systems (CTMS)
- Close collaboration with Medical Affairs, DS Affiliates, and all other functional departements at DS
- Ensure the accurate conduct of the site selection process and coordinate the process with the affiliates
- Cooperate with the Senior Project Leader in budget control and forecasting
- Accompanying, faciliation and follow-up of bid defence meetings and RFP preparation (+ support allignment between the projects)
- Study related interactions with HCPs in Steering Committees, Data Safety Boards and Investigator Meetings
***Personal skills and professional experience**:
- University degree in medical Science
- Min 5+ years experience in scientific environment Solid scientific / clinical understanding flexibility, creativity and proactivity
- Able to practice adaptive change management and engagement in order to guarantee clinical operational excellence and continuous improvement
- Proven Project Management skills in a matrix environment
- Demonstrate empathy, respect and fairness
- Live a culture of cooperation and team-work and take action to prevent and solve conflicts
- Ability to work independently as well as part of a team
- Work proactively and assertively, encouraging others to act similarly
- Strong communication, negotiation, decision making and presentation skills
- Effective project planning, conduct and supervision abilities
- Analytical and systematic thinking, proactive problem identification, solution oriented, ability to drive project and clinical requirements
- Generally, manages work with limited supervision
**What we offer**:
**Working at Daiichi Sankyo**:
At Daiichi Sankyo in Europe, we offer a workplace where your voice is heard. Everything we do, we do with a high level of commitment and a clear focus on patients’ needs. We know that our bold ambition to change patients’ lives for the better can only be achieved through the power of collaboration and the exploration of new approaches. Thus, we encourage our colleagues across Europe to be courageous, to bring their ideas to the table and to embrace opportunities to grow. When you join our European family, you will be a part of a dynamic company where everyone, no matter their role, rolls up their sleeves and gets things done.
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