Operationally and scientifically lead complex clinical studies
Drive and deliver aspects of global clinical trial execution from study design, set-up and recruitment to final reporting
Lead the matrix-management of robust global clinical trial teams, collaborating across the organization and externally with service providers/investigator sites
Drive the development of clinical study protocols, clinical operations execution plans and other required documents
Ensure quality conduct and document standards are applied across the clinical trial lifecycle
Lead clinical data review ( Sr. Clinical Sciences Trial Leader )
Support clinical data review ( Clinical Sciences Trial Leader )
Support optimization of standard methodologies in clinical trial operations and adopt an open learning and sharing environment
Unleash the value of data and digital within clinical studies Ultimately, YOU will help bring new technologies and therapies closer to our patients
Essential Requirements :
A minimum of BSc in life sciences is required. A MSc, PharmD or PhD is desired.
Clinical Sciences Trial Leader : 2-4 years' experience, in clinical trial management/operations, coupled with a broad knowledge of the drug development field; preferably within the pharma industry.
Sr. Clinical Sciences Trial Leader 4+ years' experience in clinical trial management/operations, coupled with a broad knowledge of the drug development field; preferably within the pharma industry.
A track record of collaborating with and influencing a wide range of people, and of building strong partnerships
Strong project management experience; excellent planning, prioritization and organizational skills; used to managing multiple priorities concurrently
High change agility, thriving in an open and dynamic environment.
Able to learn proactively, tackle issues and take accountability
Clear written and verbal expression of ideas; an active communicator
Desirable Requirements:
Experience in study design and protocol development/writing is highly desirable
This is a dual posting. The final level & title of the offer role would be determined by the hiring team based on the skills, experience & capabilities required to perform the role at the level the role has been offered.
Accessibility and accommodation:
Skills Desired
Auditing, Clinical Monitoring, Clinical Research, Clinical Study Reports, Clinical Trial Management Systems, Clinical Trials, Data Auditing, Data Management, Health Sciences, Lifesciences, Project Planning, Vendor Management, Waterfall Model
Benefits
Health insuranceRemote work options
Additional Information
Job Description Summary
#LI-Hybrid
Location: Basel
This role is based in Basel, Switzerland. Novartis is unable to offer
relocation support for this role: please only apply if this location is accessible for you.
We are Clinical Sciences and Innovation at Novartis. A dynamic group of Clinical Trial Leaders (Clinical Scientists) who plan and execute early phase trials worldwide. From First-in-Human to ph2a studies and beyond. We design and operationalize trials, ensuring they run smoothly, on time and - most importantly - with patients' interests to the fore.
Curious, unbossed and inspired; we are committed to flexibility in the workplace.
As a member of our team, you will support or lead the clinical science and operations of planning and executing translational medicine clinical trials. Collaborate across our global network. Partner with outstanding physicians and scientists. Build therapeutic area expertise. Revolutionize next-generation, digital and patient-centric trial design. Be always curious, innovative and inspiring.
This position will be located at the Novartis Headquarter in Basel and will not have the ability to be located remotely. This position may require up to 5% travel time as defined by the business.
Job Description
Novartis · Basel (city)