Do you want to work with a company that bridges the gap between disruptive discovery products and real-world patient reach? Would you like the opportunity to work for an organisation where innovation, people and entrepreneurship are the fundamentals of its success? If so, this role is for you.
As a Senior Clinical Scientist, you will provide scientific expertise to the design and delivery of Global clinical studies and programs for innovative new medicines. You will work as part of an organisation that identifies high-potential compounds for in-licensing, conducts clinical development and then partners with large pharma for commercialisation.
Reporting to the Oncology Medical Director, your role will include:
- Design and execute assigned clinical trial
- Work closely with clinical team members within the assigned project to execute activities associated with the conduct of clinical trials
- Contribute to the development of end-to-end clinical development strategy
- Protocol development with minimal guidance (writing, reviewing, resolution of cross-functional comments)
- Prepare and provide input to clinical study reports (CSRs) and clinical portions of Regulatory Documents (e.g., IB, DSUR, regulatory responses)
- Monitor, review and interpret safety and efficacy data of ongoing clinical trials
- Act as (clinical science expert) liaison to the cross-functional project core team, clinical study teams, CRO's, study sites and others
- Establish relationships with investigators, KOLs, partners and appropriate consultants
- Provide clinical scientific input to business development (e.g. due diligence) and marketing activities
- Perform literature research
- Develop and deliver presentations to internal and external stakeholders. Provide input in scientific communication plan and scientific publications
Skills and Experience Required:
- Design and execute assigned clinical trial
- Work closely with clinical team members within the assigned project to execute activities associated with the conduct of clinical trials
- Contribute to the development of end-to-end clinical development strategy
- Protocol development with minimal guidance (writing, reviewing, resolution of cross-functional comments)
- Prepare and/or provide input to clinical study reports (CSRs) and clinical portions of Regulatory Documents (e.g., IB, DSUR, regulatory responses)
- Monitor, review and interpret safety and efficacy data of ongoing clinical trials
- Act as (clinical science expert) liaison to the cross-functional project core team, clinical study teams, CRO's, study sites and others
- Establish relationships with investigators, KOLs, partners and appropriate consultants
- Provide clinical scientific input to business development (e.g. due diligence) and marketing activities
- Perform literature research
- Develop and deliver presentations to internal and external stakeholders. Provide input in scientific communication plan and scientific publications
Recruitment Process:
If this role interests you, then please apply now. You can submit your CV and cover letter highlighting your expertise as a Senior Clinical Scientist. We will send you a confirmation of acknowledgement, and please note feedback can take up to 2-3 weeks. Upon successful selection for an interview, the process will occur in the following three stages:
First stage: This will be an initial screening call with a Life Science People representative
Second stage: A video call with the Medical Director, Oncology along with selected key stakeholders over three days to go through your background and experience with the role
The Senior Clinical Scientist role is a full-time permanent position, paying up a competitive salary & benefits package. You will be working remotely for the interim, and once the restrictions lift, you will be required to be on-site 1-2 days a week in Vaud. Full details will be provided on application. In addition to a generous basic salary, the company offers the following benefits package:
Benefits:
- Pension
- Medical Insurance
- Travel Allowance
- Bonus
- Annual Holiday
