Associate Clinical Development Director (Neurosciences)
Associate Clinical Development Director (Neurosciences)
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Job Description
Band
Level 5Job Description Summary
As our Clinical Development Director in Neurosciences you will be responsible for the scientific and clinical strategy of assigned clinical trials scientific monitoring and reporting of quality data. In addition you may be responsible for the clinical and scientific strategy of assigned sections of a clinical development program depending on the size and complexity.Job Description
our responsibilities include but are not limited to:
Provide clinical leadership medical and scientific strategic input and contribute to development of trial related documents (e.g. CTPs informed consent form case report forms data monitoring committee charters data analysis plan reports publications) for assigned clinical trial(s) consistent with Integrated Development Plan (IDP); develop materials for trial-related advisory boards data monitoring committees investigators meetings and protocol training meetings for Novartis local medical organizations.
Provide clinical and scientific input and contribute to clinical sections of trial and program level regulatory documents (e.g. Investigators Brochures Health Authority briefing books safety updates submission dossiers and responses to Health Authorities).
In collaboration with appropriate Clinical Trial Team (CTT) members: Ensure clinical support of trials as needed; conduct ongoing medical and scientific review of clinical trial data with Clinical Scientific Expert(s) with appropriate oversight from Medical Lead; manage patient safety reports on trial data to safety and clinical boards (e.g. Safety Management Team (SMT) GCT GPT) with appropriate oversight from Medical Lead; provide input into final analyses and interpretation including the development of the Clinical Study Report(s) (CSRs) publications and internal/external presentations.
Support Therapeutic Area Head (TAH) with contributing to peer-review of IDPs CTPs and other clinical documents across various indications and programs and support development of TA strategies as needed.
May contribute to the medical and scientific evaluation for Business Development & Licensing (BD&L) opportunities.
Contribute to talent and career development of CD associates through on-boarding coaching and/or mentoring support; develop and foster CD culture; and may contribute to the performance evaluation of CTT members.
Contribute to medical/scientific training of relevant Novartis stakeholders on the disease area and compound/molecule. May serve as speaker for franchise medical/scientific training.
Contribute to global initiatives (e.g. process improvement training SOP development other Clinical Development line function initiatives).
What youll bring to the role:
Advanced degree in life sciences/ healthcare (or clinically relevant degree) is required.
5 years of involvement in clinical research or drug development in an academic or industry environment spanning clinical activities in Phases I through IV; 2 or more years of contribution to and accomplishment in all aspects of conducting clinical trials (e.g. planning executing reporting and publishing) in a global/matrix environment in pharmaceutical industry.
Proven ability to interpret discuss and present efficacy and safety data relating to clinical trial(s) or program level.
Working knowledge of the disease area is desired with proven ability to interpret discuss and present efficacy and safety data relating to clinical trial(s) or program level
Working knowledge of GCP clinical trial design statistics and regulatory and clinical development processes.
This hybrid role can be based in London Dublin or Basel
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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 and let us know the nature of your request and your contact information. Please include the job requisition number in your message.
Skills Desired
Budget Management Clinical Research Clinical Trial Protocol Clinical Trials Coaching Cross-Functional Teams Data Analysis Learning Design Lifesciences Risk Management Risk MonitoringRequired Experience:
Director
Employment Type
Full-Time
