Scientific Alliances Lead
at Novocure
Root, LU, Switzerland -
Start Date | Expiry Date | Salary | Posted On | Experience | Skills | Telecommute | Sponsor Visa |
---|---|---|---|---|---|---|---|
Immediate | 02 Dec, 2024 | Not Specified | 06 Sep, 2024 | 8 year(s) or above | Collaboration,Negotiation,Pharmaceutical Industry,Data Analysis,Interpersonal Skills,Strategic Thinking,Clinical Research,Partnerships,Leadership | No | No |
Required Visa Status:
Citizen | GC |
US Citizen | Student Visa |
H1B | CPT |
OPT | H4 Spouse of H1B |
GC Green Card |
Employment Type:
Full Time | Part Time |
Permanent | Independent - 1099 |
Contract – W2 | C2H Independent |
C2H W2 | Contract – Corp 2 Corp |
Contract to Hire – Corp 2 Corp |
Description:
Location:Root D4, CH, 6039
To join our Global Medical Affairs team, and located either in US or Switzerland, we are looking for a:
Responsibilities:
- Program Development:
- Define and structure a Cooperative Group and Academic Research Center program in collaboration with Global Medical Affairs, Pre-Clinical, Clinical and Product Development Teams
- Establish collaboration agreements to support evidence generation and information exchange.
- Identify, update, and maintain a database of key collaborative research groups worldwide.
- ISTs Management:
- Oversee the end-to-end process of ISTs, from proposal evaluation and approval to study execution and results dissemination.
- Serve as the primary point of contact for investigators, providing guidance and support throughout the trial lifecycle.
- Ensure ISTs are conducted in compliance with relevant regulations, guidelines, and company policies.
- Stakeholder Coordination:
- Facilitate the establishment of a coordinated global network of internal and external stakeholders.
- Enable efficiencies in the planning, implementation, and execution of supported clinical trials.
- Regulatory Compliance:
- Ensure all evidence generation activities comply with relevant regulations, guidelines, and industry standards.
- Maintain up-to-date knowledge of regulatory requirements and changes in the clinical research landscape.
- Develop and implement policies and procedures to ensure compliance and mitigate risks.
- Representation and Negotiation:
- Represent Novocure at global cooperative group meetings, scientific meetings, industry conferences, and other professional events.
- Lead or facilitate discussions and negotiations with Cooperative Group leadership and Academic Centers, as required.
- Process Improvement:
- Develop master agreements for work with cooperative groups.
- Simplify processes used to collaborate with external researchers
REQUIREMENT SUMMARY
Min:8.0Max:13.0 year(s)
Pharmaceuticals
Pharma / Biotech / Healthcare / Medical / R&D
Clinical Pharmacy
Graduate
A relevant scientific field
Proficient
1
Root, LU, Switzerland