Clinical Research Scientist for Investigator

Vor 2 Tagen

Munich, Deutschland Daiichi-Sankyo Europe Vollzeit

**Passion for Innovation. Compassion for Patients.**:
**Clinical Research Scientist for Investigator Initiated Studies (M/F/x)**:
**The position**:
The Clinical Research Scientist for Investigator Initiated Studies (IIS) will be responsible for the oversight and daily management of IIS & Collaborative Research Programs (CR) in Oncology and Specialty Medicine, ensuring compliance with policies & process requirements.

**Roles and Responsibilities**:

- Work with global and local medical/clinical colleagues in daily management of IIS/CR
- Manage and maintain the IIS submission portal and user access requests
- Ensure the IIS proposals are reviewed and approved by the regional team
- Work collaboratively with legal/compliance/regulatory and IIS /CR institution/principal investigator on contract (agreement) request, development in accordance with fair market value (FMV), negotiation and execution
- Coordinate the trial medication supply with the Supply Chain from Daiichi Sankyo and manage the trial medication orders, support the shipments and the returns
- Be contact person for the Leading Physician and support the Sponsor with all relevant material to run the IIS/CR in line with regulations
- Establish and maintain a strong partnership with Global Clinical Operations Team and cross-functional partners to manage the IIS & CR programs
- Deliver appropriate IIS/CR updates on a regular basis to global functions
- Responsible for budget management and forecasting of all IIS/CR programs and manages clinical study milestones, invoices, payments and needs assessment as well as to ensure dissemination of all IIS evidence generated

***Personal skills and professional experience**:

- University degree in medical Science
- Min 3 years experience in scientific environment
- Solid scientific / clinical understanding flexibility, creativity and proactivity
- Ability 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
- Proactive problem identification, solution oriented, ability to drive project and clinical requirements
- Generally, manages work with limited supervision
- Ability to work in English - fluent written and spoken

**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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