Clinical Country

vor 20 Stunden

Baar, Schweiz Biogen Vollzeit

**Job Description**:
**About the role**:
The **Clinical Country & Site Management - Medical Therapeutic Area Lead Neurovascular** (CCSM- M TA Lead) is a regional hub based role (**Cambridge, US** **or hybrid based in Baar, Switzerland**), responsible for line management of the CCSL-M role, along with representing the role on Product Development & Commercialization (PDC) and Research & Development Project Team (RDPT). You will be responsible for developing and implementing enhanced clinician to clinician site engagement strategies Biogen's neurovascular assigned program. You will coordinate and support the CCSL-M role as it executes on the strategy, and will coordinate communication, tracking and reporting back to the program and to the CCSM Regional Head. You will also serve as a key point of synergy and delivery of key local operational and scientific expertise used to drive, shape and understand enhanced clinician to clinician site engagement strategies and build them into program and study planning and align them with standard CCSL site engagement.

The TA Lead Neurovascular, as part of the CCSM management structure, will be tasked with regular engagement with CCSLs in the field to understand local site intelligence and local laws and regulations. They will also coordinate with the CCSL-M role to provide clinical/medical support to the CCSLs including coordinating support with individual site engagements as requested.

As TA Lead Neurovascular you will also meet regularly with the aligned Clinical Development Unit (DU) leads and Global Clinical Operations roles as needed to review and align on strategy and delivery of enhanced site management efforts across multiple modalities(site visits, calls, congresses, IM's etc).

**What you'll do**

1. Provide direct line management, leadership, prioritization, and support for CCSL-M role

2. Develop, lead and coordinate clinician to clinician enhanced site engagement activities on assigned programs

3. Interact with key internal stakeholders

4. Coordinate clinical/medical support for CCSLs in assigned programs

5. Participate in key program meetings (PDC, RDPT)

6. Coordination of investigator meetings and Congress activity with Clinical Development

**Qualifications**:

- Medical Degree and clinical experience in the respective TA (Neurovascular/ Stroke)
- Requires a minimum of 10+ years’ experience in clinical development, experience across multiple clinical operations disciplines including field-based site-facing clinical operations roles, clinical trial delivery via an outsourcing model; R&D project leadership experience preferred but not required
- Ability to collaborate across different functions
- Experienced people manager
- Strong understanding of cross functional drug development process and scientific/clinical knowledge/experience across assigned therapeutic area/DU
- Robust knowledge of GCP, clinical trial regulations and regulatory guidance pertinent to clinical trial conduct in assigned TA
- Strong interpersonal and communication skills, including experience working with various levels of senior management

Additional Information
**Why Biogen?**

Our mission to find therapies for neurological and rare diseases is a unique focus within our industry and this shared purpose is what connects us as a team. We work together to overcome obstacles and to follow the science. We are resilient as we strive to make an impact on our patients’ lives and on changing the course of medicine.

Together, we pioneer. Together, we thrive.

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