Job Description Summary
#LI-Hybrid
Job Description
Key Responsibilities:
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)
Contribute to project/program level plans (Sr. Clinical Sciences Trial Leader)
May mentor junior team members
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.
Clinical Sciences Trial Leader level: Leadership potential and well-developed interpersonal skills.
Sr. Clinical Sciences Trial Leader level: Demonstrated leadership experience and well-developed interpersonal skills.
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:
Novartis is committed to working with and providing reasonable accommodation to all individuals. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the recruitment process, or in order to receive more detailed information about the essential functions of a position, please send an e-mail to inclusion.switzerland@novartis.com and let us know the nature of your request and your contact information. Please include the job requisition number in your message
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 ModelDiscover exciting opportunities in sports technology. Join innovative companies transforming the sports industry through data, media, and cutting-edge tech.
Salary: $140000-200000
🤖 This salary estimate is calculated by AI based on the job title, location, company, and market data. Use this as a guide for salary expectations or negotiations. The actual salary may vary based on your experience, qualifications, and company policies.
Interested in building your career at Novartis? Get future opportunities sent straight to your email.
Create AlertDiscover similar positions that might interest you
Novartis
Novartis
Novartis
Novartis
Novartis
Novartis